Journal of Immunology Research
Volume 2019 (2019), Article ID 4103819, 14 pages
https://doi.org/10.1155/2019/4103819

Review Article

Sex-Related Differences in Immune Response and Symptomatic Manifestations to Infection with Leishmania Species

Ryan D. Lockard,¹ Mary E. Wilson,2,3 and Nilda E. Rodríguez¹

¹Department of Biology, University of Northern Iowa, Cedar Falls, IA 50614, USA
²Departments of Internal Medicine and Microbiology, University of Iowa, Iowa City, IA 52242, USA
³Veterans Affairs Medical Center, Iowa City, IA 52240, USA

Correspondence should be addressed to Nilda E. Rodríguez; nilda.rodriguez@uni.edu

Received 25 May 2018; Revised 22 October 2018; Accepted 11 December 2018; Published 10 January 2019

Academic Editor: Martin Holland

Copyright © 2019 Ryan D. Lockard et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Worldwide, an estimated 12 million people are infected with Leishmania spp. and an additional 350 million are at risk of infection. Leishmania are intracellular parasites that cause disease by suppressing macrophage microbicidal responses. Infection can remain asymptomatic or lead to a spectrum of diseases including cutaneous, mucocutaneous, and visceral leishmaniasis. Ultimately, the combination of both pathogen and host factors determines the outcome of infection. Leishmaniasis, as well as numerous other infectious diseases, exhibits sex-related differences that cannot be explained solely in terms of environmental exposure or healthcare access. Furthermore, transcriptomic evidence is revealing that biological sex is a variable impacting physiology, immune response, drug metabolism, and consequently, the progression of disease. Herein, we review the distribution, morbidity, and mortality among male and female leishmaniasis patients. Additionally, we discuss experimental findings and new avenues of research concerning sex-specific responses in cutaneous and visceral leishmaniasis. The limitations of current therapies and the emergence of drug-resistant parasites underscore the need for new treatments that could harness the host immune response. As such, understanding the mechanisms driving the differential immune response and disease outcome of males versus females is a necessary step in the development of safer and more effective treatments against leishmaniasis.

1. Introduction

1.1. Leishmaniasis

Leishmania are parasitic protozoa endemic in 98 tropical and subtropical countries. Worldwide, 12 million people are infected with Leishmania spp. and an additional 350 million are at risk of infection [1, 2]. Leishmania spp. are intracellular parasites that cause a spectrum of human diseases called leishmaniasis, including cutaneous (CL), mucocutaneous (ML), and visceral leishmaniasis (VL) as prominent forms [1, 3]. Post-kala-azar dermal leishmaniasis (PKDL) is a complication of VL, and there are several additional disseminated forms of cutaneous disease [1, 2]. Leishmania spp. life stages include the promastigote form, which converts to the infective metacyclic form in the gut of a phlebotomine sand fly vector, and the obligate intracellular amastigote present in the phagocytes of a mammalian host. Leishmania spp. have a number of mechanisms to subvert the microbicidal activity of the host macrophages [4]. Progressive leishmaniasis is characterized by replication of amastigotes and the spread of parasites to additional macrophages, leading to localized or disseminated disease manifestations [3].

VL is the most severe clinical form of leishmaniasis, and symptomatic VL is often fatal if left untreated. Up to 500,000 new cases of VL are estimated on a yearly basis, along with about 50,000 reported deaths [2]. Treatment modalities for VL are complicated by high cost, toxicity, and the need for lengthy and often parenteral administration. An increasing concern is the emergence of drug-resistant Leishmania parasites in some endemic areas, particularly among L. donovani strains in India [2, 5, 6]. These limitations highlight the importance of developing new approaches to therapy. In particular, approaches that synergize with the host immune response as well as natural determinants of susceptibility provide potential targets to interfere with disease progression.

1.2. Biological Sex as a Variable in Physiology and Disease

Large-scale transcriptomic studies are shedding light on the various ways that biological sex impacts physiology and as a consequence, disease outcomes. Males and females have a similar number of genes, differing only in those encoded by the sex chromosomes. However, in various tissues, the expression of many transcripts can differ significantly between the sexes. In humans, this includes the brain, heart, liver, and peripheral blood mononuclear cells. Furthermore, the number of biased transcripts and their respective fold difference varies from tissue to tissue between both sexes [7–11].

Sex-related differences in immunophysiology may underlie distinct male or female susceptibility to certain cancers and autoimmune conditions as well as infectious diseases, including several that are caused by parasites [8, 12–16]. Both pathogen and host factors likely drive these dichotomous rates in disease [16–18]. It cannot be excluded that social dynamics and gender-associated behavior might play roles in the disposition to seek medical care and consequently, disease outcome [13, 14, 16, 17]. However, often these sex differences cannot be explained by environmental exposure or healthcare access, suggesting a physiological basis [13, 14, 16–20]. Biological differences between the sexes have been shown in animal models and in a number of human disease states. Furthermore, sex-associated differences have been observed in cells of male versus female origin, strongly supporting a role for biological sex in disease development [7, 9–12, 16–19].

In this review, we will explore epidemiological patterns of sex-related differences in cutaneous and visceral leishmaniasis, in addition to other manifestations of symptomatic infection. We also outline ongoing efforts to elucidate the immune mechanisms contributing to sex-specific responses in disease.

2. Cutaneous Leishmaniasis

2.1. Epidemiological Evidence of Sex Bias in Old World CL

Old World CL is caused primarily by L. aethiopica, L. major, and L. tropica, while in the New World, L. mexicana and species of the Leishmania (Viannia) (V.) subgenus are largely responsible for causing CL [21, 22]. Differential incidence of CL between the sexes has been reported in multiple endemic regions of the Old World. Whether CL is more common in males versus females appears to differ depending on multiple variables. It is likely that a complex interaction between environmental, host gender and biological factors, and the infective Leishmania species, determines whether there is a sex bias and, if so, the direction of the bias [23–29].

2.2. Sex-Dependent Differences in Experimental Models of Old World CL

During infection with the Old World species L. major, the resistant and susceptible phenotypes of C57BL/6 and BALB/c murine models are determined by their respective Th1- and Th2-mediated CD4+ T cell responses [30, 31]. Sex biases have been documented in murine L. major infection; however, whether it is males or females that develop more severe disease is highly dependent on the model. This suggests that sex-dependent responses are driven by factors that are differentially expressed in male versus female mice and their distinct interactions with parasites [32–34].

Studies using wild-type (WT) C57BL/6 mice showed that a low-dose L. major inoculum, which resembles natural infection, resulted in higher parasite burdens and parasite spread to the spleens of female than male mice. In addition, cells from draining lymph nodes showed that females have a cytokine profile resembling Th2 responses, with higher interleukin (IL)-4 and lower interferon-γ (IFN-γ) than male mice. Interestingly, in this study, neither macrophages, dendritic cells, nor lymphocytes were involved in driving the biased cytokine profile and disease outcome. The authors hypothesized that factors present at the time of inoculation or shortly thereafter might be involved in driving the higher susceptibility of females. These could include stromal tissue, fibroblasts, keratinocytes, and/or hormones [31]. Several other lines of evidence support a role for keratinocytes and hormones in mediating sex-specific differences at the inoculation site. First, many skin diseases show a sex bias in prevalence, severity, and mortality [35, 36]. Second, sex hormones are known to mediate differences in skin structure and physiology between males and females [35, 36]. Third, keratinocytes and sebaceous glands can synthesize sex hormones [36, 37]. In particular, keratinocytes can synthesize sex steroids de novo, which in turn can exert autocrine and paracrine effects in various targets, including immune cells, potentially contributing to sex-related immune responses [37]. Furthermore, studies in other systems have shown that IL-6, a cytokine produced by keratinocytes and stromal cells, among others, can skew T cell responses away from Th1- and towards Th2-type responses [38, 39]. Overall, these studies suggest complex host-pathogen interactions at the inoculation site, although further studies will be necessary to dissect the factors contributing to sex-biased responses at the earliest stages of infection.

Additional factors with the potential to drive sex-dependent responses during or shortly after Leishmania inoculation include tissue-specific differences in resident immune cell populations. For example, in C57BL/6 mice, males have more resident neutrophils and nonclassical monocytes in the spleens than their female counterparts, whereas there are twice as many macrophages, B cells, and CD4+ T cells in the pleural and peritoneal cavities of females than males [40, 41]. However, no sex differences were observed in the bone marrow [40]. It is possible that variations in cellular composition might be driven by tissue-specific chemokines [41].

Sex-dependent differences have also been shown in immune cell infiltration. For example, a model of acute inflammation showed higher neutrophil and monocyte recruitment in male than female C57BL/6 mice [40]. Moreover, sex-dependent responses have been observed in eosinophil infiltration during L. major infection, although the role of eosinophils in leishmaniasis is complex [33, 42]. In vitro studies suggested that eosinophils are microbicidal toward L. major and L. amazonensis and increased numbers of eosinophils in vivo correlate with resistance to murine L. mexicana and L. infantum infection [42]. In contrast, Slapnickova et al. found a significant correlation between eosinophil infiltration and increased parasite loads in male mice but not female mice infected with L. major. This suggests a male-specific detrimental role for eosinophils [33].

Murine host polymorphic genes associated with eosinophil infiltration into lymph nodes mapped to four autosomal loci, two of which showed a cooperative effect (Lmr15, chr 11; Lmr26; chr 9) and two of which apparently functioned independently (Lmr14, chr 2; Lmr25, chr 5). Interestingly, Lmr14 was associated with eosinophil infiltration in male mice but not female mice. The positive correlation between parasite load and higher eosinophil infiltration in males was suggested to reflect the chronic inflammatory state in L. major infection [33]. These results form part of a growing number of studies showing the potential involvement of autosomal genes in controlling pathogen tropism, immune responses, and the sex-dependent outcome of infection [13, 16, 33]. In summary, it can be speculated that at the inoculation site, qualitative and quantitative differences in cellular composition and inflammatory signals will affect the development and maintenance of the immune response and the outcome of infection between males and females [2, 33, 42].

Sex-based differences have also been described in patients and in animal models of infection with L. tropica, another Old World species. In addition to cutaneous lesions, L. tropica infection can result in VL, simultaneous VL and disseminated CL, or viscerotropic disease, a hybrid of cutaneous and visceral symptoms that is defined by the systemic spread of parasites [32, 43–45]. Epidemiological data suggest that different clinical syndromes due to L. tropica infection vary also in their sex bias. CL, the most common presentation of L. tropica infection, seems to be more prevalent among females in some endemic areas, whereas males are more likely to develop viscerotropic leishmaniasis [26, 28, 44]. However, the mechanisms responsible for the spectrum of disease manifestations and the variation in sex-dependent outcomes have been elusive, due in part to the lack of an apt animal model [32].

Recently, Kobets et al. developed a suitable model to study the intersection between genotype, sex-dependent differences, and Leishmania species-specific responses. They used nine recombinant congenic mouse strains from STS/A (CcS/Dem) on a BALB/c background to examine the progress of L. major and L. tropica infection [32]. Compared to L. tropica, infection with L. major progressed faster and showed increased pathology in all but one of the strains of mice. In some, but not all strains, males developed larger skin lesions than females. However, during infection with L. tropica, females of most strains formed larger skin lesions. This did not correlate with higher parasite burdens in draining lymph nodes of females, suggesting the involvement of other host factors, such as inflammatory mediators, in the sex-associated differences in skin lesions. For example, the greatest skin pathology to L. tropica infection was shown by females of the strain CcS-16, which also showed the highest expression of the C-C motif chemokine ligands (CCL) CCL3 and CCL5. These chemokines have been associated with resistance to L. major, although CCL3 has been related with chronic progressive L. mexicana disease [32]. The specific effects of CCL3 and CCL5 in L. tropica infection merit further study.

The complex interactions between genotype, parasite species, and sex-based disease manifestations are well illustrated in the CcS-11 mouse strain. This strain showed only moderate susceptibility to L. major-induced lesions but succumbed to L. tropica infection. By week 14, female mice developed small lesions that healed into nodules; however, by weeks 32-42, about half the animals had died. Males were more resistant to skin pathology as they developed only small or no nodules, yet most male mice died earlier, by week 18. Histopathological examination showed no parasite dissemination into the spleen of CcS-11 mice. In contrast, L. tropica visceralizes to the spleens of BALB/c mice and several other recombinant strains used in this study [32, 43]. Together, these results suggest that the differential response to infection between males and females, if present, includes a combination of factors such as host genetic background, organ-specific responses, and the Leishmania species.

2.3. Epidemiological Evidence of Sex Bias in New World CL

Unlike Old World CL, data from the New World document a higher incidence of CL in males than females in Mexico and Colombia [46–48]. Similar reports from across Brazil show that males develop cutaneous manifestations of leishmaniasis at higher rates than females [49–53]. A nationwide study found increased CL in males versus females under age 1. The predominance in male infants could be driven by minipuberty, a transient postnatal increase in sex steroid levels that shows clear hormonal differences between boys and girls and has been implicated in other sex-biased infectious diseases [54, 55]. Overall, the prevalence of CL among males increased at puberty, reached its highest level in adulthood, and decreased in the elderly population. This occurred despite the fact that males likely do not experience increased parasite exposure, suggesting that the observed sex dichotomy has a biological basis [54, 56]. Together, these studies support the hypothesis that inherent biological factors, perhaps together with gender-related behavior, place males at higher risk of New World CL.

2.4. Sex-Dependent Differences in Experimental Models of New World CL

2.4.1. L. mexicana

Mice lacking the IL-4 receptorα (Rα) are resistant and do not form lesions during L. mexicana infection. Since IL-4Rα is a common subunit in the IL-4 and IL-13 receptors, these results suggest that either IL-4, IL-13, or both are involved in susceptibility [30]. To identify the critical cell populations, Bryson et al. studied infection in global- and CD4+ T cell-specific IL-4Rα-deficient mice in a BALB/c background and compared these results to that in WT mice. These data show that IL-4Rα from CD4+ T cells, but not from neutrophils and macrophages, is implicated in disease progression by facilitating Th2 responses. Strikingly, the splenocyte cytokine response differed between CD4+ T cell-specific IL-4Rα-deficient male and female mice. Splenocytes from males expressed higher levels of IL-4, IL-5, IL-10, and immunoglobulin G1 (IgG1). This occurred despite the fact that mice of both sexes curtailed disease progression. However, while females healed the initial small lesions, sex-specific, IL-4Rα-independent production of IL-4 led to lesion persistence in males [30].

In humans, L. mexicana infection can result in localized CL (LCL) with ulcers at the site of parasite inoculation or anergic diffuse cutaneous leishmaniasis (ADCL). ADCL is characterized by high parasite loads, suppressed cutaneous delayed-type hypersensitivity, and disfiguring nodules throughout the body. Innate immunity has been implicated in parasite dissemination in ADCL [3, 45]. Natural killer (NK) cells, components of innate immunity, have the potential to activate innate and adaptive immune responses and thus could play a role in the differential manifestations of LCL versus ADCL. Peripheral blood and tissue samples showed higher numbers of NK cells in LCL than ADCL patients. In addition, LCL patients showed increased expression of IFN-γ and tumor necrosis factor (TNF) in nonstimulated and lipophosphoglycan (LPG) stimulated NK cells, with greater levels in females than males [45]. Increased NK cell numbers and their associated production of IFN-γ and TNF facilitate macrophage activation and parasite control and might contribute to the increased resistance of females to L. mexicana infection [34, 45].

The aforementioned studies showed how differences in the immune response contribute to L. mexicana susceptibility among males. Although some sex-specific immune responses may be determined by the male or female genotype, some are modulated by circulating sex hormones [13, 16]. Several studies discussed herein have examined sex steroids as a variable in infection using animal models of leishmaniasis [34, 57–59]. Additionally, a role for sex steroids in disease progression is implied by the epidemiological data [54, 60–62].

In addition to modulating host susceptibility, sex hormones could directly affect pathogens [16, 19, 63, 64]. Treatment of L. mexicana promastigotes with physiological doses of dihydrotestosterone (DHT), the main circulating androgen in males, increased parasite growth [13, 64]. In addition, DHT-treated parasites increased the macrophage infection rate and parasite load and were more resistant to the macrophage microbicidal attack. Furthermore, male BALB/c mice infected with DHT-treated parasites developed larger lesions and contained more parasites per area than those infected with nontreated parasites [64]. Overall, these results suggest that interactions between sex steroids, parasite virulence, immune responses, and host susceptibility determine the final outcome of Leishmania infection.

2.4.2. Leishmania (Viannia) Species

Sex differences in the severity of experimental leishmaniasis are not limited to species of the L. Leishmania subgenus (L. major, L. mexicana). Studies in hamster models of cutaneous infection with either L. (V.) guyanensis or L. (V.) panamensis led to higher parasite loads in males than females. Although overall infection severity was higher with L. (V.) guyanensis, the sex dichotomy was most pronounced in L. (V.) panamensis-infected animals [59].

A potential role for sex steroids in driving the differential responses to L. (V.) panamensis was investigated in studies of estrogen-treated male or testosterone-treated female hamsters. There was an increase in the size of lesions of hamsters treated with testosterone, whereas estrogen treatment had no discernible effects. This was consistent with the observation that the augmented size and necrosis of lesions due to L. (V.) panamensis developed only in adult male hamsters that have reached biological maturity. These sex differences correlated with the abundance of skin lesion transcripts encoding IL-4, IL-10, and transforming growth factor-β (TGF-β), but not IFN-γ or IL-12 [59]. L. (V.) guyanensis infection resulted in a contrasting pattern, in that adult males developed an increase in necrosis but not in lesion size compared to juvenile males. Furthermore, adult female hamsters had smaller lesions than juveniles infected with L. (V.) guyanensis, consistent with a protective role for estrogen [59]. Similar sex-based differences have been observed in other infectious disease models including Staphylococcus aureus, in which female resistance to dermonecrosis is associated with estrogen and its downstream effects [35].

3. Visceral Leishmaniasis

3.1. Epidemiological Evidence of Sex Bias in Old World VL

VL, known in some endemic areas as kala-azar, is a systemic disease characterized by enlargement of the spleen and liver as well as progressive immunosuppression [2, 65]. VL is caused by L. infantum in the New World and either L. infantum or L. donovani in the Old World [2, 21, 65]. Considering VL patients from Brazil, East Africa, India, and Nepal, Harhay and colleagues concluded that despite variations in the ratios of males-to-females, males accounted for more cases of VL across all regions. These observations could result from parasite, host, societal factors, or some combination of these variables [5]. An illustration is VL caused by L. donovani in the Indian subcontinent and other areas, where gender and biological factors could contribute to variations in disease severity between the sexes [34, 61, 66–72]. Reports from India are uncertain regarding a sex bias in PKDL, a cutaneous complication sometimes observed after VL treatment; whereas some studies indicate no difference, others show a greater incidence of PKDL in males [69, 73, 74]. In India, conclusions about the involvement of biological factors are complicated by the likely underreported numbers of adult females with symptomatic VL, which may result from gender disparities in healthcare access in the region [61]. However, in some endemic areas (e.g., Northeast Brazil), studies provide evidence that the male predominance in VL prevails even in situations of similar infection rates between the sexes, as discussed herein [60, 75].

Sex-associated differences in antileishmanial IgG titers have also been reported, although not always in the same direction. Among VL patients from India, males had higher IgG titers whereas Sudanese females with VL had higher serologic titers than males. In both populations, sex differences were observed in subjects aged 16 or older, raising the possible involvement of sex hormones [76]. Although the physiologic consequence of serologic differences is not known, elevated leishmania-specific IgG has been identified as a marker of subjects who will progress from asymptomatic to symptomatic VL [77].

3.2. Sex-Dependent Differences in Experimental Models of Old World VL

Several studies have set out to investigate the mechanisms underlying the sex bias observed in Old World VL epidemiological data. Compared to females, male hamsters infected with L. donovani exhibited higher parasite loads. Furthermore, in both sexes, estradiol lowered whereas testosterone increased infection [78]. In murine macrophages, testosterone has been shown to promote L. donovani uptake and parasite load, and decrease p38 mitogen-activated protein kinase (MAPK) activation, which may lead to a lower antimicrobial response and promote parasite survival [79–82]. In contrast, exposure to 17β-estradiol has no impact on parasite load [81]. Overall, these results implicate sex hormones in the modulation of L. donovani infection. The potentially detrimental effects of testosterone would likely hold more significance in the infection of males than females.

3.3. Epidemiological Evidence of Sex Bias in New World VL

In Brazil, where L. infantum is endemic, the epidemiological data have largely shown a male predominance in VL [54, 83–88]. In addition, one nationwide study found higher levels of discontinued therapy among male VL patients. It is unknown whether gender-related behavior explains higher rates of treatment cessation among men or if sex-related biological differences lead to more adverse effects, and thus, higher treatment withdrawal [86]. In the same study, males () represented a greater number of deaths caused by VL compared to females (), similar to other reports from Brazil as well as in Southern Iraq where L. donovani is endemic [84–86, 89, 90]. Furthermore, morbidity and mortality associated with HIV and Leishmania coinfection in Brazil and Spain are reported to be higher in males [84, 85, 87, 89, 91]. However, epidemiological studies cannot always discern whether differences between males and females are due to gender-related or biological factors.

Data from the state of Rio Grande do Norte, Brazil, have consistently demonstrated a male bias in VL [60, 62, 92]. Lutzomyia longipalpis, the sand fly vector of L. infantum, is peridomestic, and males and females have similar rates of infection [60, 62, 93]. However, after the age of ten, males were more likely to develop symptomatic disease than females. This age range approximately corresponds with the start of puberty [60, 62]. An expanded analysis of 1,967 cases of VL reported from across the state showed the same pattern of male bias in disease after puberty. Likewise, a nonsignificant male bias among VL subjects under the age of 1 may be related to minipuberty, which has been implicated in other studies of leishmaniasis [54, 62]. Overall, males accounted for 66% of symptomatic cases [62]. Other studies in Brazil have found comparable rates of infection between the sexes but did not always differentiate between early childhood and postpubertal patients [54, 94–96]. Those studies could be complicated by the fact that VL has been a disease predominant in children under the age of 10, although this epidemiological pattern is now changing [97]. The increased frequency of disease in postpubertal males could result from a combination of factors, including biological variables such as the anti-inflammatory properties of testosterone and sex-based genetic differences, possibly in combination with gender-related behavioral patterns [54, 62, 86, 87, 98, 99].

3.4. Sex-Dependent Differences in Experimental Models of New World VL

Collectively, epidemiological studies of New World VL support the concept that the interaction between gender-based behavior and biological sex could determine the outcome of disease. Experimental studies are necessary to elucidate the biological aspects of sex-dependent responses to infection with visceralizing species of Leishmania.

3.4.1. Sex-Dependent Differences at the Macrophage Level: Receptors, Parasite Load, and Potential Implications for Leishmaniasis

(1) Macrophage Receptors. Phagocytic and antimicrobial differences in macrophages of male versus female origin have been shown in various infectious diseases including Cryptococcus neoformans, group B streptococci, and Paracoccidioides brasiliensis [19, 20, 41]. Recently, our group examined infection levels in C57BL/6 macrophages of male and female origin. In the initial hour of infection with LcJ, a clonal line of a Brazilian L. infantum strain, macrophages from male mice showed higher percent of infection and parasite load. Leishmania uptake is mediated by various receptors including mannose, fibronectin, Fcγ receptor, complement receptor-1 (CR1), and CR3 [100–104]. The observation of sex-biased uptake of LcJ promastigotes suggests receptor differences in C57BL/6 macrophages of male versus female origin [62]. Recognition by macrophage receptors is among the earliest interactions between Leishmania and its host, and parasite survival is impacted by differential uptake [100, 104]. As such, sex-specific differences at this stage could have a major impact on infection outcome.

Transcriptomic data have shown differential expression of surface and downstream signaling molecules in macrophages of male versus female origin. These differences are far more extensive than those originating only from the sex chromosomes. Many variations arise from dissimilar regulation in epigenetics and gene expression [7, 10, 105]. For example, mouse macrophages from males and females showed over 30% of genes differentially expressed. Additionally, transregulation of expression quantitative trait loci was mostly sex specific. The differential gene expression was independent of exogenously added sex steroids, as these were ex vivo experiments [105]. However, it cannot be ruled out that endogenous sex hormones could have induced long-lasting epigenetic changes nor can it be excluded that there were intracrine or autocrine effects of sex hormones released by macrophages in vitro [37]. Overall, these data showed a strong effect of biological sex in both gene expression and transregulation, thus, supporting the rationale of segregating data analysis by sex [37, 105].

Likewise, macrophages from male and female donors differentially express various transcripts including CD14, cell surface adhesion proteins, signaling molecules, transcription factors, and Toll-like receptors (TLRs) [7, 10, 12, 13, 41, 106]. To facilitate their survival, Leishmania spp. interact with TLR-2, TLR-9, and TLR/IL-1R signaling cascades [107, 108]. Similarly, L. infantum increases the transcripts of phagocytosis receptors implicated in parasite survival while decreasing those associated with parasite clearance [109]. Differential use of macrophage receptors leads to distinct entry and parasite survival [100, 103, 104]. As such, future studies should examine whether sex differences in the types or abundance of receptors involved in parasite recognition and entry contribute to the differential responses of male- versus female-derived macrophages.

(2) Parasite Load. As we previously showed that LcJ and WT L. infantum promastigotes could utilize different entry pathways, the sex-biased uptake of attenuated parasites led us to examine the kinetics of infection using a WT strain of L. infantum from Brazil [62, 100]. Uptake and parasite load of WT promastigotes were similar between C57BL/6 macrophages of male and female origin in the initial 24 hours. In contrast, by 72 hours, parasite loads were higher in macrophages from males. Thus, despite similar uptake of WT parasites, macrophages from females contained the infection better [62].

While more comprehensive studies are necessary to determine the mechanisms underlying these sex-dependent differences, the 72-hour kinetics implicate the involvement of nitric oxide (NO) [62, 110]. Related studies with L. mexicana showed increased NO production by female-derived DBA/2 macrophages leading to better control of infection [34, 58]. Furthermore, treatment with estrogen increased NO and microbicidal activity in L. mexicana-infected DBA/2 macrophages from both sexes [34, 58]. Sex-dependent responses in L. mexicana infection could depend on the host genotype, as studies with C57BL/6 macrophages did not show the same results [57, 58]. Thus, sex-dependent antimicrobial responses are determined by the combination of the host genotype, sex hormones, and Leishmania species [34, 57, 58]. Collectively, these results indicate that inherent differences at the macrophage level, which may be further modulated by sex hormones, could be factors driving the sex dichotomy in disease.

3.4.2. Sex-Dependent Differences in Granuloma Formation: Potential Implications for VL

To further explore the mechanisms mediating sex differences, we examined liver parasite loads in L. infantum-infected BALB/c and C57BL/6 mice. In both strains, male mice had higher parasite burdens than females, suggesting that across genetic backgrounds, males are more susceptible to L. infantum infection [62]. In the mouse model, containment of parasite growth in the liver correlates with the induction of Th1-mediated immune responses, which interact with TLR7 in the formation of liver granulomas [2, 110–112].

Immune cells from females have higher expression of TLR7, a gene present in the X chromosome. In humans and mice, females avoid doubling the expression of genes encoded on the X chromosome by inactivating the second copy [7, 13, 113, 114]. However, this is not a comprehensive shutdown and at least 15% of the genes in the second X chromosome escape inactivation, either partially or completely [7, 10, 12, 13, 113]. The X chromosome contains a high number of immune-related genes, and incomplete gene inactivation could facilitate some amplified immune responses in females [9, 12]. Escaping gene inactivation might not be random, and it has been proposed that some genes, such as TLR7, are biased to be overexpressed in females [7, 9, 13]. Thus, it can be speculated that female tissues will respond to infections with stronger granuloma formation. In agreement with this notion, the BALB/c and C57BL/6 models of Mycobacterium tuberculosis infection have shown that lung granulomas form earlier and reach a larger size in female than in male mice [115, 116]. Furthermore, castration of male BALB/c mice improved granuloma formation and survival, implying an adverse effect of testosterone in granuloma development [115]. Taken together, these studies suggest that females could more readily initiate and maintain granulomatous immune responses. Whether granulomas contribute to the sex-biased responses observed in L. infantum infection deserves further investigation.

3.4.3. Sex-Dependent Differences in Cytokine Responses

In the mouse model of L. major infection, a distinct dichotomy of Th1- or Th2-mediated responses results in cure or disease, respectively. The immune responses implicated in experimental CL systems involving other Leishmania species as well as in VL are more complex. Similar to experimental models of CL, other than L. major BALB/c mice, a clear-cut Th2 response is absent in L. infantum-infected animals or VL patients. Nonetheless, Th1 responses have been associated with resolution of either asymptomatic or symptomatic infection in all models and infections examined [65, 117].

In response to anti-CD3 and anti-CD28 stimulation, naive T cells from female donors produce more IFN-γ and express higher levels of IL-12Rβ, as well as molecules associated with higher cytotoxic activity [14, 118]. Furthermore, animal infection models and vaccination studies in humans have shown that females have increased expression of several molecules involved in the TLR pathway and Th1 responses, including TLR8, myeloid differentiation primary response 88 (MyD88), and nuclear factor-kappaB (NFκB) [13, 114]. Overall, T cells from females displayed a stronger proinflammatory profile, which became increasingly more so with repeated stimulation. In contrast, T cells from males displayed a mixed profile, with the inflammatory cytokine IL-17A, the eosinophil-recruiting cytokine IL-5, and the anti-inflammatory cytokine IL-10 [118]. Interestingly, about half of the genes overexpressed in T cells from females had estrogen-responsive elements (EREs), suggesting a regulatory role for sex steroids [13, 16, 114, 118]. However, the mechanisms underlying sex-biased T cell immune responses have not been elucidated.

Cytokine expression assays in male and female C57BL/6 mice infected with L. infantum showed no difference in the serum levels of IL-12, a type 1 cytokine [2, 62]. In contrast, males had higher levels of serum TNF and IL-10, two cytokines implicated with exacerbated VL [2, 62, 65, 119–121]. Examination of cytokine expression in splenocytes showed that females have higher levels of the proinflammatory cytokine IL-1β, and IFN-γ, a key type 1 cytokine important for protective or curative immune responses. No sex-dependent difference was observed in IL-4, consistent with the observation that type 2 responses do not drive VL susceptibility [62, 65, 117]. A sex-based difference was also observed in splenocyte-derived IL-6 and IL-17, with males showing higher expression [62]. Our results are in agreement with animal models of inflammation in which splenocytes cultured from females produced higher IL-1, whereas splenocytes from males released higher levels of TNF and IL-6 [122].

IL-6 is a pleiotropic cytokine produced by many cell types [12, 38, 39]. As a consequence, its role in leishmaniasis has not been fully delineated. However, IL-6 has been implicated in the modulation of macrophage and T cell responses. For example, IL-6 has the potential to drive macrophages away from M1 (classical) activation leading to lower microbicidal activity and inhibition of proinflammatory cytokines, which could facilitate parasite growth [39, 109]. In addition, IL-6 facilitates type 2 cellular immune responses whereas it suppresses type 1 immunity by interfering with IFN-γ signaling [38].

Peripheral blood mononuclear cells from male donors have higher basal levels of IL-6 than cells from females, and this difference further increases upon stimulation [123]. In experimental L. donovani infection, IL-6 decreases IFN-γ leading to increased liver parasite load [124]. Similarly, among L. infantum-infected VL patients, IL-6 correlates with disease severity and death risk, both of which show a male predominance [86, 125]. An association between elevated IL-6 levels and more severe disease in males has also been documented among hepatocarcinoma patients [12, 15, 63].

In concert with TGF-β, IL-6 facilitates the induction of Th17-type effector cells, the main producers of IL-17 [39, 117, 120, 126, 127]. There is a balance between the development of Th17 and the differentiation of regulatory T cells (Tregs) in humans, and IL-6 appears to be a pivotal regulator of this equilibrium. IL-6 has been reported to inhibit the Treg-associated transcription factor FOXP3, and in combination with TGF-β, it has been shown to downregulate FOXP3 protein levels. On the other hand, TGF-β promotes Treg differentiation, possibly in a dose-dependent manner [126, 127]. There is abundant TGF-β in the organs of BALB/c mice as well as bone marrow of VL patients infected with L. infantum, although recent studies have shown that progressive visceral leishmaniasis in humans and mouse models is associated with IL-10-producing CD4+ T cells [128–132]. In addition to the well-studied type 1 CD4+ T cells, the ultimate outcome of chronic VL is the sum of the effects of adaptive cell populations expanded in the host, including B cells, CD8+ T cells, and CD4+ T cells expressing IFN-γ and inhibitory IL-10, as well as Tregs and Th17 cells.

Studies of IL-17 in VL have shown mixed results, with some studies suggesting a protective role whereas others suggest that it is detrimental to the host [117, 120]. IL-17A, the most studied member of the IL-17 family, is implicated in the expansion and recruitment of neutrophils. However, the ultimate effect of neutrophils in Leishmania spp. infection varies according to the tissue infected, the timing of recruitment, and their persistence at the infection site [2, 120]. Further examination of the effects of IL-17A in VL showed lower parasite load in the spleen and liver of L. donovani-infected IL-17A-/- C57BL/6 mice. The absence of IL-17A led to increased IFN-γ production by CD4+ T cells and lower neutrophil recruitment. These results suggest that IL-17A facilitates VL progression by impairing IFN-γ responses while supporting damaging inflammation [117].

Furthermore, studies from our group and others suggest a link between IL-17 and sex-specific responses. For example, male donors have higher numbers of Th17-type cells in peripheral blood than females. In addition, naive and stimulated T cells from males secrete more IL-17 than those from females [118, 133]. Similarly, male C57BL/6 mice infected with L. infantum released significantly higher levels of IL-17 than females. Additionally, IL-6 increased slightly in C57BL/6 males [62]. IL-6 induces the development of Th17-type cells, and consequently, can facilitate IL-17 production [120]. Thus, higher IL-6 and IL-17 expression may converge to influence pathways underlying sex-dependent responses.

4. Transcriptomic Evidence of Sex-Dependent Immune Responses: Potential Implications for Leishmaniasis

Accumulating transcriptomic evidence is increasing our knowledge of sex-based differences in immunity [7, 106]. In a comprehensive study, Piasecka et al. examined transcriptional profiles from 500 males and 500 females before and after stimulation of whole blood samples with various microbial challenges. Of the 560 immune-related genes examined, 509 (91%) showed significant sex differences in response to at least one stimulus. One hundred eighty-one (36%) of the sex-biased genes were differentially expressed only after stimulation. Thus, some sex-specific differences in the immunotranscriptome are present in basal conditions while others are inducible [106].

In a similar study, microarrays of mononuclear blood cells of over 5,200 healthy human subjects showed about 1,000 transcripts differentially expressed between the sexes [7]. Many female predominant transcripts were associated with the Kyoto encyclopedia of gene and genome pathways termed as cytokine stimulus, response to interferon 1, and lymphocyte differentiation, whereas male predominant transcripts were related to the pathway named lysosomes [7, 134]. Some of the transcriptional differences decreased in postmenopausal women or increased in women using hormone-based contraceptives, suggesting a role for sex steroids. However, the number and magnitude of the most significantly changed transcripts did not correspond with the hormone status, indicating that sex-based transcriptional differences are driven by multiple mechanisms [7, 9].

Differences between male and female transcriptomes are highlighted by a meta-analysis of 22 microarray studies involving 2,500 healthy subjects. Samples from 15 tissues showed over 3,000 transcripts differentially expressed. The major differences were found in the brain and the heart. The liver, a target organ in VL, also showed a significant number of sex-biased transcriptional differences. Global analysis of the transcripts overexpressed in one sex or the other revealed that about one-third contained hormone-responsive elements, including androgen response elements, estrogen response elements, or both. Some of the differences were due to genes on sex chromosomes. However, almost two-thirds of the dichotomous transcripts were found in autosomal chromosomes and did not contain sex steroid binding sites [10]. It has been proposed that these transcripts could be controlled by sex-specific epigenetic modifications [10, 11]. Data from VL epidemiological studies show a higher male bias at puberty, coinciding with the spike of sex hormones, and a moderate bias into older age; these observations could be associated with the cumulative effects of sex steroids and sex-biased epigenetics [54, 60–62].

Similarly, a study of sex-associated differences in liver cell transcriptomes from equal numbers of male and female subjects () showed over 1,200 transcripts differentially expressed between the sexes. Transcripts involved in lipid and drug metabolism showed the highest magnitude differences between males and females [11]. Given the expanding literature on the association between dyslipidemia and inflammatory states and the recent recognition of dyslipidemia in animals and humans with VL, these differences deserve exploration in the context of VL [135–137]. Furthermore, other studies have shown extensive sex-dependent differences in the expression of genes encoding enzymes involved in liver metabolic pathways, including the drug-metabolizing enzymes cytochrome P450s (CYPs) [8, 15, 138]. Differential expression of various CYPs results in distinct pharmacokinetics and pharmacodynamics between males and females [138]. Overall, vast transcriptome differences in the liver, an organ involved in VL pathogenesis as well as drug and lipid metabolism, emphasize the importance of tracking experimental and clinical differences in male versus female subjects.

5. Sex-Related Differences in the Outcome of Antileishmanial Treatment

Higher rates of treatment failure or more adverse effects among males have been shown in several studies. For example, in Colombia, male CL patients were more likely to maintain measurable parasite burdens following treatment with either miltefosine or meglumine antimoniate, although these results were not statistically significant [139]. In a related study of 318 CL patients in Belo Horizonte, Brazil, three times more males () than females () experienced relapse following treatment with meglumine antimoniate. However, in a hazard risk analysis, sex was not significantly associated with relapse [140].

In studies from the Indian subcontinent, male patients were at a greater risk of VL relapse after treatment with either miltefosine or liposomal amphotericin B [6, 141]. The differential responses between males and females could be due to male-biased healthcare access [141]. Sex differences in relapse rates might also result from biological factors such as differential drug metabolism and variations in immune responses [6]. In Nepal and Bihar, India, relapse rates following miltefosine treatment were higher among males of all ages and the sex difference was most pronounced after the age of 9. Furthermore, the authors could not identify gender-based differences in adherence to treatment protocol that would explain the sex-biased risk. Together, these results suggest an intrinsic male susceptibility to symptomatic VL [6].

Drug teratogenicity and decreased access to healthcare could potentially contribute to a lower rate of antileishmanial therapy among females in some endemic areas [61, 142]. In a study of PKDL patients in Bangladesh, miltefosine-induced corneal keratopathy was reported only in males. The authors suggest that increased treatment access could contribute to the male bias in this complication, although it cannot be excluded that biological differences might have played a role in the adverse effects observed among males [143].

A study from Kolkata, India, indicated no sex differences in the prevalence of VL but a significantly higher PKDL incidence in postpubertal males compared to females, as well as a more protracted course of PKDL among males. While this observation could be confounded by gender-related norms in health care use, studies of skin disease and wound healing in mice and humans have shown that estrogen promotes, whereas testosterone decreases skin healing [35, 36, 74]. There was also a significant positive correlation between levels of plasma testosterone and antileishmanial IgG in PKDL patients as measured by ELISA [74]. Increased levels of antileishmanial IgG have been implicated in the severity of PKDL [144]. Interestingly, after treatment with miltefosine, PKDL patients were found to have significantly lower plasma testosterone levels. A decrease in testosterone levels by miltefosine treatment may reduce the immunosuppressive effects of androgens, promoting an immune response more appropriate for parasite killing and disease resolution [13, 36, 74]. The authors concluded that these data highlight the importance of closely monitoring progression to PKDL in male VL patients, especially among pubertal and adult patients [74].

6. Concluding Remarks

The ultimate outcome of Leishmania infection will depend on a multitude of host-pathogen interactions and the development, or lack thereof, of immune responses that restrict parasite growth [2, 65]. Accumulating evidence shows sex-associated differences in the initiation and maintenance of immune responses [7, 13, 114, 118]. There are clearly social and epidemiological factors that contribute to differences in disease prevalence between the sexes in various endemic areas. Nonetheless, collective data from experimental models and studies of human infection suggest that there are also biological predispositions leading to sex-specific parasite burden and symptomatic disease during infection with Leishmania spp. Many epidemiological reports cannot easily differentiate between gender-related exposure and sex-based susceptibility. However, in Brazilian neighborhoods with peridomestic exposure, the data suggest that there are biological factors underlying the observed male bias in VL, as discussed herein [62]. In different endemic areas, whether a sex bias is present or not and whether males or females are more susceptible likely depend on the combination of the infecting species, epidemiological variables, and host biological factors. The molecular mechanisms underlying unique immune responses to infection are just beginning to be explored.

The increasing concern of drug-resistant pathogens, including but not limited to Leishmania spp., underscores the importance of developing therapeutic approaches that target host factors associated with disease progression. We propose that effective control and treatment of leishmaniasis and other infectious diseases should take into account the influence of biological sex in pathogenesis, immune response, and drug metabolism.

Abbreviations

ADCL: | Anergic diffuse cutaneous leishmaniasis
CCL: | C-C motif chemokine ligand
CL: | Cutaneous leishmaniasis
CR: | Complement receptor
CYP: | Cytochrome P450
DHT: | Dihydrotestosterone
EREs: | Estrogen-responsive elements
IFN-γ: | Interferon-γ
IL: | Interleukin
Ig: | Immunoglobulin
LCL: | Localized cutaneous leishmaniasis
LPG: | Lipophosphoglycan
LPS: | Lipopolysaccharide
L. (V.): | Leishmania (Viannia)
MAPK: | Mitogen-activated protein kinase
ML: | Mucocutaneous leishmaniasis
MyD88: | Myeloid differentiation primary response 88
NFκB: | Nuclear factor-κB
NK cells: | Natural killer cells
NO: | Nitric oxide
PKDL: | Post-kala-azar dermal leishmaniasis
R: | Receptor
TGF-β: | Transforming growth factor-β
Th: | Helper T cell
TLRs: | Toll-like receptors
TNF: | Tumor necrosis factor
Treg: | Regulatory T cell
VL: | Visceral leishmaniasis
WT: | Wild type.

Conflicts of Interest

The authors declare no conflicting financial interests.

Acknowledgments

This work was supported in part by funds from the Graduate College, University of Northern Iowa (RDL, NER) and the College of Humanities, Arts and Sciences, University of Northern Iowa (RDL, NER). Additional funds were provided by grants 5I01BX001983 and 2I01BX000536 from the Department of Veterans’ Affairs (MEW) and NIH grants R01 AI076233 (MEW) and NIH Tropical Medicine Research Center P50 AI-30639 (MEW).

References

J. Alvar, I. D. Velez, C. Bern et al., “Leishmaniasis worldwide and global estimates of its incidence,” PLoS One, vol. 7, no. 5, article e35671, 2012.

E. O. de Freitas, F. M. S. Leoratti, C. G. Freire-de-Lima, A. Morrot, and D. F. Feijó, “The contribution of immune evasive mechanisms to parasite persistence in visceral Leishmaniasis,” Frontiers in Immunology, vol. 7, p. 153, 2016.

B. M. Scorza, E. M. Carvalho, and M. E. Wilson, “Cutaneous manifestations of human and murine Leishmaniasis,” International Journal of Molecular Sciences, vol. 18, no. 6, article 1296, 2017.

G. Arango Duque and A. Descoteaux, “Leishmania survival in the macrophage: where the ends justify the means,” Current Opinion in Microbiology, vol. 26, pp. 32–40, 2015.

M. O. Harhay, P. L. Olliaro, M. Vaillant et al., “Who is a typical patient with visceral leishmaniasis? Characterizing the demographic and nutritional profile of patients in Brazil, East Africa, and South Asia,” The American Journal of Tropical Medicine and Hygiene, vol. 84, no. 4, pp. 543–550, 2011.

B. Ostyn, E. Hasker, T. P. C. Dorlo et al., “Failure of miltefosine treatment for visceral leishmaniasis in children and men in South-East Asia,” PLoS One, vol. 9, no. 6, article e100220, 2014.

R. Jansen, S. Batista, A. I. Brooks et al., “Sex differences in the human peripheral blood transcriptome,” BMC Genomics, vol. 15, no. 1, p. 33, 2014.

A. Maggi and S. Della Torre, “Sex, metabolism and health,” Molecular Metabolism, vol. 15, pp. 3–7, 2018.

S. Marttila, J. Jylhava, T. Nevalainen et al., “Transcriptional analysis reveals gender-specific changes in the aging of the human immune system,” PLoS One, vol. 8, no. 6, article e66229, 2013.

B. T. Mayne, T. Bianco-Miotto, S. Buckberry et al., “Large scale gene expression meta-analysis reveals tissue-specific, sex-biased gene expression in humans,” Frontiers in Genetics, vol. 7, p. 183, 2016.

Y. Zhang, K. Klein, A. Sugathan et al., “Transcriptional profiling of human liver identifies sex-biased genes associated with polygenic dyslipidemia and coronary artery disease,” PLoS One, vol. 6, no. 8, article e23506, 2011.

S. Jaillon, K. Berthenet, and C. Garlanda, “Sexual dimorphism in innate immunity,” Clinical Reviews in Allergy & Immunology, vol. 30, 2017.

S. L. Klein and K. L. Flanagan, “Sex differences in immune responses,” Nature Reviews Immunology, vol. 16, no. 10, pp. 626–638, 2016.

J. G. Markle and E. N. Fish, “SeXX matters in immunity,” Trends in Immunology, vol. 35, no. 3, pp. 97–104, 2014.

W. C. Tsai, S. D. Hsu, C. S. Hsu et al., “MicroRNA-122 plays a critical role in liver homeostasis and hepatocarcinogenesis,” The Journal of Clinical Investigation, vol. 122, no. 8, pp. 2884–2897, 2012.

L. G. vom Steeg and S. L. Klein, “SeXX matters in infectious disease pathogenesis,” PLoS Pathogens, vol. 12, article e1005374, no. 2, 2016.

H. Bernin and H. Lotter, “Sex bias in the outcome of human tropical infectious diseases: influence of steroid hormones,” The Journal of Infectious Diseases, vol. 209, Supplement 3, pp. S107–S113, 2014.

M. Muenchhoff and P. J. R. Goulder, “Sex differences in pediatric infectious diseases,” The Journal of Infectious Diseases, vol. 209, Supplement 3, pp. S120–S126, 2014.

E. E. McClelland, L. M. Hobbs, J. Rivera et al., “The role of host gender in the pathogenesis of Cryptococcus neoformans infections,” PLoS One, vol. 8, no. 5, article e63632, 2013.

C. F. Pinzan, L. P. Ruas, A. S. Casabona-Fortunato, F. C. Carvalho, and M. C. Roque-Barreira, “Immunological basis for the gender differences in murine Paracoccidioides brasiliensis infection,” PLoS One, vol. 5, no. 5, article e10757, 2010.

I. Kevric, M. A. Cappel, and J. H. Keeling, “New World and Old World Leishmania infections: a practical review,” Dermatologic Clinics, vol. 33, no. 3, pp. 579–593, 2015.

R. D. Pearson and A. Q. Sousa, “Clinical spectrum of Leishmaniasis,” Clinical Infectious Diseases, vol. 22, no. 1, pp. 1–13, 1996.

N. Aara, K. Khandelwal, R. A. Bumb et al., “Clinco-epidemiologic study of cutaneous leishmaniasis in Bikaner, Rajasthan, India,” The American Journal of Tropical Medicine and Hygiene, vol. 89, no. 1, pp. 111–115, 2013.

S. Bamba, A. Gouba, M. K. Drabo, D. Nezien, M. Bougoum, and T. R. Guiguemde, “Epidemiological profile of cutaneous leishmaniasis: retrospective analysis of 7444 cases reported from 1999 to 2005 at Ouagadougou, Burkina Faso,” The Pan African Medical Journal, vol. 14, p. 108, 2013.

B. Faucher, C. Pomares, S. Fourcade et al., “Mucosal Leishmania infantum leishmaniasis: specific pattern in a multicentre survey and historical cases,” The Journal of Infection, vol. 63, no. 1, pp. 76–82, 2011.

M. Hakkour, A. Hmamouch, M. M. El Alem et al., “New epidemiological aspects of visceral and cutaneous leishmaniasis in Taza, Morocco,” Parasites & Vectors, vol. 9, no. 1, p. 612, 2016.

D. Moein, D. Masoud, M. Saeed, and D. Abbas, “Epidemiological aspects of cutaneous Leishmaniasis during 2009-2016 in Kashan City, Central Iran,” The Korean Journal of Parasitology, vol. 56, no. 1, pp. 21–24, 2018.

R. Reithinger, M. Mohsen, K. Aadil, M. Sidiqi, P. Erasmus, and P. G. Coleman, “Anthroponotic cutaneous leishmaniasis, Kabul, Afghanistan,” Emerging Infectious Diseases, vol. 9, no. 6, pp. 727–729, 2003.

E. Turan, Y. Yeşilova, H. A. Sürücü et al., “A comparison of demographic and clinical characteristics of Syrian and Turkish patients with cutaneous Leishmaniasis,” The American Journal of Tropical Medicine and Hygiene, vol. 93, no. 3, pp. 559–563, 2015.

K. J. Bryson, O. R. Millington, T. Mokgethi, H. A. McGachy, F. Brombacher, and J. Alexander, “BALB/c mice deficient in CD4⁺ T cell IL-4Rα expression control Leishmania mexicana load although female but not male mice develop a healer phenotype,” PLoS Neglected Tropical Diseases, vol. 5, no. 1, article e930, 2011.

M. R. Fischer, C. Kunz, K. Dietze-Schwonberg, B. Lorenz, and E. von Stebut, “Myeloid cells do not contribute to gender-dependent differences in disease outcome in murine cutaneous leishmaniasis,” Cellular Immunology, vol. 308, pp. 13–18, 2016.

T. Kobets, H. Havelkova, I. Grekov et al., “Genetics of host response to Leishmania tropica in mice - different control of skin pathology, chemokine reaction, and invasion into spleen and liver,” PLoS Neglected Tropical Diseases, vol. 6, no. 6, article e1667, 2012.

M. Slapnickova, V. Volkova, M. Cepickova et al., “Gene-specific sex effects on eosinophil infiltration in leishmaniasis,” Biology of Sex Differences, vol. 7, no. 1, p. 59, 2016.

H. Snider, C. Lezama-Davila, J. Alexander, and A. R. Satoskar, “Sex hormones and modulation of immunity against leishmaniasis,” Neuroimmunomodulation, vol. 16, no. 2, pp. 106–113, 2009.

M. J. Castleman, S. Pokhrel, K. D. Triplett et al., “Innate sex bias of Staphylococcus aureus skin infection is driven by α-hemolysin,” The Journal of Immunology, vol. 200, no. 2, pp. 657–668, 2018.

H. Dao Jr. and R. A. Kazin, “Gender differences in skin: a review of the literature,” Gender Medicine, vol. 4, no. 4, pp. 308–328, 2007.

K. B. Rubinow, “An intracrine view of sex steroids, immunity, and metabolic regulation,” Molecular Metabolism, vol. 15, pp. 92–103, 2018.

S. Diehl and M. Rincon, “The two faces of IL-6 on Th1/Th2 differentiation,” Molecular Immunology, vol. 39, no. 9, pp. 531–536, 2002.

C. A. Hunter and S. A. Jones, “IL-6 as a keystone cytokine in health and disease,” Nature Immunology, vol. 16, no. 5, pp. 448–457, 2015.

E. Kay, L. Gomez-Garcia, A. Woodfin, R. S. Scotland, and J. R. Whiteford, “Sexual dimorphisms in leukocyte trafficking in a mouse peritonitis model,” Journal of Leukocyte Biology, vol. 98, no. 5, pp. 805–817, 2015.

R. S. Scotland, M. J. Stables, S. Madalli, P. Watson, and D. W. Gilroy, “Sex differences in resident immune cell phenotype underlie more efficient acute inflammatory responses in female mice,” Blood, vol. 118, no. 22, pp. 5918–5927, 2011.

N. E. Rodriguez and M. E. Wilson, “Eosinophils and mast cells in leishmaniasis,” Immunologic Research, vol. 59, no. 1-3, pp. 129–141, 2014.

H. Mahmoudzadeh-Niknam, S. S. Kiaei, and D. Iravani, “Viscerotropic growth pattern of Leishmania tropica in BALB/c mice is suggestive of a murine model for human viscerotropic leishmaniasis,” The Korean Journal of Parasitology, vol. 45, no. 4, pp. 247–253, 2007.

A. Abdoli, N. Maspi, F. Ghaffarifar, and V. Nasiri, “Viscerotropic leishmaniasis: a systematic review of the case reports to highlight spectrum of the infection in endemic countries,” Parasitology Open, vol. 4, pp. 1–14, 2018.

I. C. Caneda-Guzman, N. Salaiza-Suazo, E. A. Fernandez-Figueroa, G. Carrada-Figueroa, M. Aguirre-Garcia, and I. Becker, “NK cell activity differs between patients with localized and diffuse cutaneous leishmaniasis infected with Leishmania mexicana: a comparative study of TLRs and cytokines,” PLoS One, vol. 9, no. 11, article e112410, 2014.

C. M. Lezama-Davila, S. Oghumu, A. R. Satoskar, and A. P. Isaac-Marquez, “Sex-associated susceptibility in humans with chiclero's ulcer: resistance in females is associated with increased serum-levels of GM-CSF,” Scandinavian Journal of Immunology, vol. 65, no. 2, pp. 210-211, 2007.

D. A. Medina-Morales, M. E. Machado-Duque, and J. E. Machado-Alba, “Epidemiology of cutaneous Leishmaniasis in a Colombian municipality,” The American Journal of Tropical Medicine and Hygiene, vol. 97, no. 5, pp. 1503–1507, 2017.

G. Munoz and C. R. Davies, “Leishmania panamensis transmission in the domestic environment: the results of a prospective epidemiological survey in Santander, Colombia,” Biomedica, vol. 26, Supplement 1, pp. 131–144, 2006.

A. F. Brilhante, L. A. K. Melchior, V. L. B. Nunes, C. de Oliveira Cardoso, and E. A. B. Galati, “Epidemiological aspects of American cutaneous leishmaniasis (ACL) in an endemic area of forest extractivist culture in western Brazilian Amazonia,” Revista do Instituto de Medicina Tropical de São Paulo, vol. 59, article e12, 2017.

C. S. Gosch, C. P. Marques, B. S. Resende et al., “American tegumentary leishmaniasis: epidemiological and molecular characterization of prevalent Leishmania species in the state of Tocantins, Brazil, 2011-2015,” Revista do Instituto de Medicina Tropical de São Paulo, vol. 59, article e91, 2017.

L. H. Guimarães, A. Queiroz, J. A. Silva et al., “Atypical manifestations of cutaneous Leishmaniasis in a region endemic for Leishmania braziliensis: clinical, immunological and parasitological aspects,” PLOS Neglected Tropical Diseases, vol. 10, no. 12, article e0005100, 2016.

M. A. Marlow, M. da Silva Mattos, M. E. Makowiecky et al., “Divergent profile of emerging cutaneous leishmaniasis in subtropical Brazil: new endemic areas in the southern frontier,” PLoS One, vol. 8, no. 2, article e56177, 2013.

M. L. Turetz, P. R. Machado, A. I. Ko et al., “Disseminated leishmaniasis: a new and emerging form of leishmaniasis observed in northeastern Brazil,” The Journal of Infectious Diseases, vol. 186, no. 12, pp. 1829–1834, 2002.

F. Guerra-Silveira and F. Abad-Franch, “Sex bias in infectious disease epidemiology: patterns and processes,” PLoS One, vol. 8, no. 4, article e62390, 2013.

T. H. Johannsen, K. M. Main, M. L. Ljubicic et al., “Sex differences in reproductive hormones during mini-puberty in infants with normal and disordered sex development,” The Journal of Clinical Endocrinology & Metabolism, vol. 103, no. 8, pp. 3028–3037, 2018.

L. Soares, F. Abad-Franch, and G. Ferraz, “Epidemiology of cutaneous leishmaniasis in central Amazonia: a comparison of sex-biased incidence among rural settlers and field biologists,” Tropical Medicine & International Health, vol. 19, no. 8, pp. 988–995, 2014.

C. M. Lezama-Davila, A. P. Isaac-Marquez, J. Barbi, H. E. Cummings, B. Lu, and A. R. Satoskar, “Role of phosphatidylinositol-3-kinase-γ (PI3Kγ)-mediated pathway in 17β-estradiol-induced killing of L. mexicana in macrophages from C57BL/6 mice,” Immunology and Cell Biology, vol. 86, no. 6, pp. 539–543, 2008.

C. M. Lezama-Davila, A. P. Isaac-Marquez, J. Barbi, S. Oghumu, and A. R. Satoskar, “17β-estradiol increases Leishmania mexicana killing in macrophages from DBA/2 mice by enhancing production of nitric oxide but not pro-inflammatory cytokines,” The American Journal of Tropical Medicine and Hygiene, vol. 76, no. 6, pp. 1125–1127, 2007.

B. L. Travi, Y. Osorio, P. C. Melby, B. Chandrasekar, L. Arteaga, and N. G. Saravia, “Gender is a major determinant of the clinical evolution and immune response in hamsters infected with Leishmania spp,” Infection and Immunity, vol. 70, no. 5, pp. 2288–2296, 2002.

S. M. B. Jeronimo, P. Duggal, R. F. S. Braz et al., “An emerging peri-urban pattern of infection with Leishmania chagasi, the protozoan causing visceral leishmaniasis in northeast Brazil,” Scandinavian Journal of Infectious Diseases, vol. 36, no. 6-7, pp. 443–449, 2004.

S. Jervis, L. A. C. Chapman, S. Dwivedi et al., “Variations in visceral leishmaniasis burden, mortality and the pathway to care within Bihar, India,” Parasites & Vectors, vol. 10, no. 1, p. 601, 2017.

N. E. Rodriguez, I. D. Lima, U. Gaur Dixit et al., “Epidemiological and experimental evidence for sex-dependent differences in the outcome of Leishmania infantum infection,” The American Journal of Tropical Medicine and Hygiene, vol. 98, no. 1, pp. 142–145, 2018.

L. G. Vom Steeg and S. L. Klein, “Sex steroids mediate bidirectional interactions between hosts and microbes,” Hormones and Behavior, vol. 88, pp. 45–51, 2017.

L. Sanchez-Garcia, A. Wilkins-Rodriguez, N. Salaiza-Suazo, J. Morales-Montor, and I. Becker, “Dihydrotestosterone enhances growth and infectivity of Leishmania mexicana,” Parasite Immunology, vol. 40, no. 3, 2018.

M. E. Wilson, S. M. B. Jeronimo, and R. D. Pearson, “Immunopathogenesis of infection with the visceralizing Leishmania species,” Microbial Pathogenesis, vol. 38, no. 4, pp. 147–160, 2005.

M. A. A. Ahmed, A. A. Ahmed, S. M. Omar, G. K. Adam, T. M. Abdallah, and A. A. Ali, “Epidemiology of visceral leishmaniasis among children in Gadarif hospital, eastern Sudan,” BMC Public Health, vol. 16, no. 1, p. 1234, 2016.

S. Ali Shah, A. Khattak, M. Ghori, and Z. Batool, “Clinical and hematological presentation of visceral leishmaniasis in children in a tertiary care hospital,” Journal of Medical Science, vol. 20, pp. 94–97, 2012.

A. Das, M. Karthick, S. Dwivedi et al., “Epidemiologic correlates of mortality among symptomatic visceral Leishmaniasis cases: findings from situation assessment in high endemic foci in India,” PLoS Neglected Tropical Diseases, vol. 10, no. 11, article e0005150, 2016.

V. N. R. Das, A. Ranjan, K. Pandey et al., “Clinical epidemiologic profile of a cohort of post-kala-azar dermal leishmaniasis patients in Bihar, India,” The American Journal of Tropical Medicine and Hygiene, vol. 86, no. 6, pp. 959–961, 2012.

S. Rijal, S. Uranw, F. Chappuis et al., “Epidemiology of Leishmania donovani infection in high-transmission foci in Nepal,” Tropical Medicine & International Health, vol. 15, Supplement 2, pp. 21–28, 2010.

S. P. Singh, A. Picado, M. Boelaert et al., “The epidemiology of Leishmania donovani infection in high transmission foci in India,” Tropical Medicine & International Health, vol. 15, Supplement 2, pp. 12–20, 2010.

Y. Wondimeneh, Y. Takele, A. Atnafu, G. Ferede, and D. Muluye, “Trend analysis of visceral leishmaniasis at Addis Zemen health center, Northwest Ethiopia,” BioMed Research International, vol. 2014, Article ID 545393, 5 pages, 2014.

V. N. R. Das, R. N. Pandey, N. A. Siddiqui et al., “Longitudinal study of transmission in households with visceral Leishmaniasis, asymptomatic infections and PKDL in highly endemic villages in Bihar, India,” PLoS Neglected Tropical Diseases, vol. 10, no. 12, article e0005196, 2016.

D. Mukhopadhyay, S. Mukherjee, S. Ghosh et al., “A male preponderance in patients with Indian post kala-azar dermal leishmaniasis is associated with increased circulating levels of testosterone,” International Journal of Dermatology, vol. 55, no. 5, pp. e250–e255, 2016.

A. L. M. Lima, I. D. de Lima, J. F. V. Coutinho et al., “Changing epidemiology of visceral leishmaniasis in northeastern Brazil: a 25-year follow-up of an urban outbreak,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 111, no. 10, pp. 440–447, 2017.

T. Bhattacharyya, D. E. Bowes, S. El-Safi et al., “Significantly lower anti-Leishmania IgG responses in Sudanese versus Indian visceral leishmaniasis,” PLoS Neglected Tropical Diseases, vol. 8, no. 2, article e2675, 2014.

R. Kumar and S. Nylén, “Immunobiology of visceral leishmaniasis,” Frontiers in Immunology, vol. 3, p. 251, 2012.

Anuradha, R. Pal, and J. C. Katiyar, “Sex-influenced population kinetics of Leishmania donovani in hamsters,” Indian Journal of Experimental Biology, vol. 28, no. 9, pp. 876–879, 1990.

G. Yin, Z. Guo, L. Yin, J. Zhao, Z. Qiao, and W. Frank, “Effect of testosterone on Leishmania donovani infection levels of murine bone marrow derived-macrophages,” Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi, vol. 16, no. 4, pp. 251–255, 1998.

H. Zhang, J. Zhao, P. Wang, and Z. Qiao, “Effect of testosterone on Leishmania donovani infection of macrophages,” Parasitology Research, vol. 87, no. 8, pp. 674–676, 2001.

L. Liu, W. P. Benten, L. Wang et al., “Modulation of Leishmania donovani infection and cell viability by testosterone in bone marrow-derived macrophages: signaling via surface binding sites,” Steroids, vol. 70, no. 9, pp. 604–614, 2005.

L. Liu, L. Wang, Y. Zhao, Y. Wang, Z. Wang, and Z. Qiao, “Testosterone attenuates p38 MAPK pathway during Leishmania donovani infection of macrophages,” Parasitology Research, vol. 99, no. 2, pp. 189–193, 2006.

L. F. B. Diniz, C. D. Freire de Souza, and R. Feliciano do Carmo, “Epidemiology of human visceral leishmaniasis in the urban centers of the lower-middle São Francisco Valley, Brazilian semiarid region,” Revista da Sociedade Brasileira de Medicina Tropical, vol. 51, no. 4, pp. 461–466, 2018.

F. R. Martins-Melo, M. da Silveira Lima, A. N. Ramos, C. H. Alencar, and J. Heukelbach, “Mortality and case fatality due to visceral leishmaniasis in Brazil: a nationwide analysis of epidemiology, trends and spatial patterns,” PLoS One, vol. 9, no. 4, article e93770, 2014.

F. R. Martins-Melo, M. da Silveira Lima, C. H. Alencar, A. N. Ramos Jr, and J. Heukelbach, “Epidemiological patterns of mortality due to visceral leishmaniasis and HIV/AIDS co-infection in Brazil, 2000-2011,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 108, no. 6, pp. 338–347, 2014.

L. L. dos Reis, A. A. da Silva Balieiro, F. R. Fonseca, and M. J. F. Gonçalves, “Changes in the epidemiology of visceral leishmaniasis in Brazil from 2001 to 2014,” Revista da Sociedade Brasileira de Medicina Tropical, vol. 50, no. 5, pp. 638–645, 2017.

D. A. Zacarias, N. Rolao, F. A. de Pinho et al., “Causes and consequences of higher Leishmania infantum burden in patients with kala-azar: a study of 625 patients,” Tropical Medicine & International Health, vol. 22, no. 6, pp. 679–687, 2017.

I. J. M. Cavalcante and M. R. Vale, “Epidemiological aspects of visceral leishmaniasis (kala-azar) in Ceará in the period 2007 to 2011,” Revista Brasileira de Epidemiologia, vol. 17, no. 4, pp. 911–924, 2014.

F. R. P. Bruhn, M. H. F. Morais, N. C. P. Bruhn, D. L. Cardoso, F. Ferreira, and C. M. B. M. Rocha, “Human visceral leishmaniasis: factors associated with deaths in Belo Horizonte, Minas Gerais state, Brazil from 2006 to 2013,” Epidemiology and Infection, vol. 146, no. 5, pp. 565–570, 2018.

Z. H. Gani, M. K. Hassan, and A. M. Jassim, “Sero-epidemiological study of visceral leishmaniasis in Basrah, Southern Iraq,” The Journal of the Pakistan Medical Association, vol. 60, no. 6, pp. 464–469, 2010.

Z. Herrador, A. Gherasim, B. C. Jimenez, M. Granados, J. V. San Martin, and P. Aparicio, “Epidemiological changes in leishmaniasis in Spain according to hospitalization-based records, 1997-2011: raising awareness towards leishmaniasis in non-HIV patients,” PLoS Neglected Tropical Diseases, vol. 9, no. 3, article e0003594, 2015.

I. D. Lima, J. W. Queiroz, H. G. Lacerda et al., “Leishmania infantum chagasi in northeastern Brazil: asymptomatic infection at the urban perimeter,” The American Journal of Tropical Medicine and Hygiene, vol. 86, no. 1, pp. 99–107, 2012.

M. E. C. Dorval, E. T. Oshiro, A. F. Brilhante et al., “Sandflies in an urban area of transmission of visceral leishmaniasis in midwest Brazil,” Parasite, vol. 23, p. 35, 2016.

J. Â. B. Crescente, F. T. Silveira, R. Lainson, C. M. C. Gomes, M. D. Laurenti, and C. E. P. Corbett, “A cross-sectional study on the clinical and immunological spectrum of human Leishmania (L.) infantum chagasi infection in the Brazilian Amazon region,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 103, no. 12, pp. 1250–1256, 2009.

L. H. Dos Santos Marques, I. C. Marques Da Rocha, I. A. Reis et al., “Leishmania infantum: illness, transmission profile and risk factors for asymptomatic infection in an endemic metropolis in Brazil,” Parasitology, vol. 144, no. 4, pp. 546–556, 2017.

E. C. Moreno, M. N. Melo, O. Genaro et al., “Risk factors for Leishmania chagasi infection in an urban area of Minas Gerais state,” Revista da Sociedade Brasileira de Medicina Tropical, vol. 38, no. 6, pp. 456–463, 2005.

I. D. Lima, A. L. M. Lima, C. O. Mendes-Aguiar et al., “Changing demographics of visceral leishmaniasis in northeast Brazil: lessons for the future,” PLoS Neglected Tropical Diseases, vol. 12, no. 3, article e0006164, 2018.

R. L. Ursine, J. V. Dias, H. A. Morais, and H. H. Pires, “Human and canine visceral leishmaniasis in an emerging focus in Aracuai, Minas Gerais: spatial distribution and socio-environmental factors,” Memórias do Instituto Oswaldo Cruz, vol. 111, no. 8, pp. 505–511, 2016.

V. S. Belo, G. L. Werneck, D. S. Barbosa et al., “Factors associated with visceral leishmaniasis in the Americas: a systematic review and meta-analysis,” PLoS Neglected Tropical Diseases, vol. 7, no. 4, article e2182, 2013.

N. E. Rodriguez, U. Gaur Dixit, L. A. Allen, and M. E. Wilson, “Stage-specific pathways of Leishmania infantum chagasi entry and phagosome maturation in macrophages,” PLoS One, vol. 6, no. 4, article e19000, 2011.

N. E. Rodriguez, U. Gaur, and M. E. Wilson, “Role of caveolae in Leishmania chagasi phagocytosis and intracellular survival in macrophages,” Cellular Microbiology, vol. 8, no. 7, pp. 1106–1120, 2006.

R. Polando, U. G. Dixit, C. R. Carter et al., “The roles of complement receptor 3 and Fcγ receptors during Leishmania phagosome maturation,” Journal of Leukocyte Biology, vol. 93, no. 6, pp. 921–932, 2013.

R. E. Polando, B. C. Jones, C. Ricardo, J. Whitcomb, W. Ballhorn, and M. A. McDowell, “Mannose receptor (MR) and Toll-like receptor 2 (TLR2) influence phagosome maturation during Leishmania infection,” Parasite Immunology, vol. 40, no. 4, article e12521, 2018.

N. Ueno, C. L. Bratt, N. E. Rodriguez, and M. E. Wilson, “Differences in human macrophage receptor usage, lysosomal fusion kinetics and survival between logarithmic and metacyclic Leishmania infantum chagasi promastigotes,” Cellular Microbiology, vol. 11, no. 12, pp. 1827–1841, 2009.

J. M. Bhasin, E. Chakrabarti, D. Q. Peng, A. Kulkarni, X. Chen, and J. D. Smith, “Sex specific gene regulation and expression QTLs in mouse macrophages from a strain intercross,” PLoS One, vol. 3, no. 1, article e1435, 2008.

B. Piasecka, D. Duffy, A. Urrutia et al., “Distinctive roles of age, sex, and genetics in shaping transcriptional variation of human immune responses to microbial challenges,” Proceedings of the National Academy of Sciences of the United States of America, vol. 115, no. 3, pp. E488–E497, 2018.

N. Parmar, P. Chandrakar, P. Vishwakarma, K. Singh, K. Mitra, and S. Kar, “Leishmania donovani exploits Tollip, a multitasking protein, to impair TLR/IL-1R signaling for its survival in the host,” The Journal of Immunology, vol. 201, no. 3, pp. 957–970, 2018.

A. Saha, M. Basu, and A. Ukil, “Recent advances in understanding Leishmania donovani infection: the importance of diverse host regulatory pathways,” IUBMB Life, vol. 70, no. 7, pp. 593–601, 2018.

N. E. Rodriguez, H. K. Chang, and M. E. Wilson, “Novel program of macrophage gene expression induced by phagocytosis of Leishmania chagasi,” Infection and Immunity, vol. 72, no. 4, pp. 2111–2122, 2004.

K. R. Gantt, T. L. Goldman, M. L. McCormick et al., “Oxidative responses of human and murine macrophages during phagocytosis of Leishmania chagasi,” The Journal of Immunology, vol. 167, no. 2, pp. 893–901, 2001.

A. Paun, R. Bankoti, T. Joshi, P. M. Pitha, and S. Stager, “Critical role of IRF-5 in the development of T helper 1 responses to Leishmania donovani infection,” PLoS Pathogens, vol. 7, no. 1, article e1001246, 2011.

M. E. Wilson, M. Sandor, A. M. Blum et al., “Local suppression of IFN-gamma in hepatic granulomas correlates with tissue-specific replication of Leishmania chagasi,” The Journal of Immunology, vol. 156, no. 6, pp. 2231–2239, 1996.

C. Ainsworth, “Genetics: sex and the single cell,” Nature, vol. 550, no. 7674, pp. S6–S8, 2017.

S. L. Klein, “Immune cells have sex and so should journal articles,” Endocrinology, vol. 153, no. 6, pp. 2544–2550, 2012.

E. I. Bini, D. Mata Espinosa, B. Marquina Castillo et al., “The influence of sex steroid hormones in the immunopathology of experimental pulmonary tuberculosis,” PLoS One, vol. 9, no. 4, article e93831, 2014.

J. Dibbern, L. Eggers, and B. E. Schneider, “Sex differences in the C57BL/6 model of Mycobacterium tuberculosis infection,” Scientific Reports, vol. 7, no. 1, article 10957, 2017.

C. Terrazas, S. Varikuti, J. Kimble, E. Moretti, P. N. Boyaka, and A. R. Satoskar, “IL-17A promotes susceptibility during experimental visceral leishmaniasis caused by Leishmania donovani,” The FASEB Journal, vol. 30, no. 3, pp. 1135–1143, 2016.

A. Hewagama, D. Patel, S. Yarlagadda, F. M. Strickland, and B. C. Richardson, “Stronger inflammatory/cytotoxic T-cell response in women identified by microarray analysis,” Genes & Immunity, vol. 10, no. 5, pp. 509–516, 2009.

P. Bhattacharya, S. Ghosh, S. A. Ejazi et al., “Induction of IL-10 and TGFβ from CD4⁺CD25⁺FoxP3⁺ T cells correlates with parasite load in Indian kala-azar patients infected with Leishmania donovani,” PLoS Neglected Tropical Diseases, vol. 10, no. 2, article e0004422, 2016.

S. D. C. Goncalves-de-Albuquerque, E. S. R. Pessoa, L. A. M. Trajano-Silva et al., “The equivocal role of Th17 cells and neutrophils on immunopathogenesis of Leishmaniasis,” Frontiers in Immunology, vol. 8, p. 1437, 2017.

S. Roy, D. Mukhopadhyay, S. Mukherjee et al., “An IL-10 dominant polarization of monocytes is a feature of Indian visceral Leishmaniasis,” Parasite Immunology, vol. 40, no. 7, article 12535, Article ID e12535, 2018.

G. Meneses, M. Rosetti, A. Espinosa et al., “Recovery from an acute systemic and central LPS-inflammation challenge is affected by mouse sex and genetic background,” PLoS One, vol. 13, no. 8, article e0201375, 2018.

E. Da Pozzo, C. Giacomelli, C. Cavallini, and C. Martini, “Cytokine secretion responsiveness of lymphomonocytes following cortisol cell exposure: sex differences,” PLoS One, vol. 13, no. 7, article e0200924, 2018.

H. W. Murray, “Accelerated control of visceral Leishmania donovani infection in interleukin-6-deficient mice,” Infection and Immunity, vol. 76, no. 9, pp. 4088–4091, 2008.

P. L. Dos Santos, F. A. de Oliveira, M. L. Santos et al., “The severity of visceral Leishmaniasis correlates with elevated levels of serum IL-6, IL-27 and sCD14,” PLoS Neglected Tropical Diseases, vol. 10, no. 1, article e0004375, 2016.

Z. Gao, Y. Gao, Z. Li et al., “Synergy between IL-6 and TGF-β signaling promotes FOXP3 degradation,” International Journal of Clinical & Experimental Pathology, vol. 5, no. 7, pp. 626–633, 2012.

A. Kimura and T. Kishimoto, “IL-6: regulator of Treg/Th17 balance,” European Journal of Immunology, vol. 40, no. 7, pp. 1830–1835, 2010.

C. F. Anderson, M. Oukka, V. J. Kuchroo, and D. Sacks, “CD4⁺CD25⁻Foxp3⁻ Th1 cells are the source of IL-10–mediated immune suppression in chronic cutaneous leishmaniasis,” Journal of Experimental medicine, vol. 204, no. 2, pp. 285–297, 2007.

K. R. Gantt, S. Schultz-Cherry, N. Rodriguez et al., “Activation of TGF-β by Leishmania chagasi: importance for parasite survival in macrophages,” The Journal of Immunology, vol. 170, no. 5, pp. 2613–2620, 2003.

R. Maurya, R. Kumar, V. K. Prajapati et al., “Brief definitive report: human visceral leishmaniasis is not associated with expansion or accumulation of Foxp3⁺ CD4 cells in blood or spleen,” Parasite Immunology, vol. 32, no. 7, pp. 479–483, 2010.

M. E. Wilson, T. J. Recker, N. E. Rodriguez et al., “The TGF-β response to Leishmania chagasi in the absence of IL-12,” European Journal of Immunology, vol. 32, no. 12, pp. 3556–3565, 2002.

M. E. Wilson, B. M. Young, B. L. Davidson, K. A. Mente, and S. E. McGowan, “The importance of TGF-β in murine visceral leishmaniasis,” The Journal of Immunology, vol. 161, no. 11, pp. 6148–6155, 1998.

L. P. Blanco, M. Plegue, W. P. Fung-Leung, and J. Holoshitz, “Gender-biased regulation of human IL-17-producing cells in vitro by peptides corresponding to distinct HLA-DRB1 allele-coded sequences,” Journal of Immune Based Therapies, Vaccines and Antimicrobials, vol. 2, no. 3, pp. 29–38, 2013.

I. Rabhi, S. Rabhi, R. Ben-Othman et al., “Comparative analysis of resistant and susceptible macrophage gene expression response to Leishmania major parasite,” BMC Genomics, vol. 14, no. 1, p. 723, 2013.

A. Descoteaux, N. Moradin, and G. Arango Duque, “Leishmania dices away cholesterol for survival,” Cell Host & Microbe, vol. 13, no. 3, pp. 245–247, 2013.

M. Khaleghi Einakchi, N. Sedaghat Sharifi, J. Khoshnegah, and M. Heidarpour, “Canine visceral leishmaniosis: the relationship of blood serum thyroid hormones, lipids, and lipoproteins with clinical status,” Parasitology Research, vol. 117, no. 12, pp. 3761–3765, 2018.

R. A. Lopez-Munoz, A. Molina-Berrios, C. Campos-Estrada et al., “Inflammatory and pro-resolving lipids in trypanosomatid infections: a key to understanding parasite control,” Frontiers in Microbiology, vol. 9, article 1961, 2018.

H. Chikada, K. Ida, E. Ando, Y. Inagaki, A. Sakamoto, and A. Kamiya, “Establishment and analysis of a mouse model that regulates sex-related differences in liver drug metabolism,” Laboratory Investigation, vol. 98, no. 11, pp. 1500–1511, 2018.

A. J. Martinez-Valencia, C. F. Daza-Rivera, M. Rosales-Chilama et al., “Clinical and parasitological factors in parasite persistence after treatment and clinical cure of cutaneous leishmaniasis,” PLoS Neglected Tropical Diseases, vol. 11, no. 7, article e0005713, 2017.

V. M. Passos, S. M. Barreto, A. J. Romanha, A. U. Krettli, A. C. Volpini, and M. F. Lima e Costa, “American cutaneous leishmaniasis: use of a skin test as a predictor of relapse after treatment,” Bulletin of the World Health Organization, vol. 78, no. 8, pp. 968–974, 2000.

S. Burza, P. K. Sinha, R. Mahajan et al., “Risk factors for visceral leishmaniasis relapse in immunocompetent patients following treatment with 20 mg/kg liposomal amphotericin B (Ambisome) in Bihar, India,” PLoS Neglected Tropical Diseases, vol. 8, no. 1, article e2536, 2014.

S. Sundar and P. L. Olliaro, “Miltefosine in the treatment of leishmaniasis: clinical evidence for informed clinical risk management,” Therapeutics and Clinical Risk Management, vol. 3, no. 5, pp. 733–740, 2007.

S. Maruf, P. Nath, M. R. Islam et al., “Corneal complications following post kala-azar dermal Leishmaniasis treatment,” PLoS Neglected Tropical Diseases, vol. 12, no. 9, article e0006781, 2018.

D. Mukhopadhyay, N. K. Das, S. De Sarkar et al., “Evaluation of serological markers to monitor the disease status of Indian post kala-azar dermal leishmaniasis,” Transactions of the Royal Society of Tropical Medicine & Hygiene, vol. 106, no. 11, pp. 668–676, 2012.