Mediators of Inflammation

Volume 2014 (2014), Article ID 914326, 9 pages

http://dx.doi.org/10.1155/2014/914326

Research Article

Myocardial Gene Expression of T-bet, GATA-3, Ror-t, FoxP3, and Hallmark Cytokines in Chronic Chagas Disease Cardiomyopathy: An Essentially Unopposed T H1-Type Response

Luciana Gabriel Nogueira,1,2,3 Ronaldo Honorato Barros Santos,⁴ Alfredo Inácio Fiorelli,⁴ Eliane Conti Mairena,1,2,3 Luiz Alberto Benvenuti,⁵ Edimar Alcides Bocchi,⁶ Noedir Antonio Stolf,⁴ Jorge Kalil,1,2,3 and Edecio Cunha-Neto1,2,3

¹Laboratory of Immunology, Heart Institute (InCor), University of São Paulo School of Medicine, 05403-000 São Paulo, SP, Brazil

²Division of Clinical Immunology and Allergy, University of São Paulo School of Medicine, 01246-903 São Paulo, SP, Brazil

³Institute for Investigation in Immunology (iii), INCT, University of São Paulo School of Medicine, 05403-000 São Paulo, SP, Brazil

⁴Division of Surgery, Heart Institute (InCor), University of São Paulo School of Medicine, 05403-000 São Paulo, SP, Brazil

⁵Division of Pathology, Heart Institute (InCor), University of São Paulo School of Medicine, 05403-000 São Paulo, SP, Brazil

⁶Transplantation and Heart Failure Unit, Heart Institute (InCor), University of São Paulo School of Medicine, 05403-000 São Paulo, SP, Brazil

Received 15 May 2014; Accepted 8 July 2014; Published 24 July 2014

Academic Editor: Christophe Chevillard

Copyright © 2014 Luciana Gabriel Nogueira 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.

Background. Chronic Chagas disease cardiomyopathy (CCC), a late consequence of Trypanosoma cruzi infection, is an inflammatory cardiomyopathy with prognosis worse than those of noninflammatory etiology (NIC). Although the T cell-rich myocarditis is known to play a pathogenetic role, the relative contribution of each of the functional T cell subsets has never been thoroughly investigated. We therefore assessed gene expression of cytokines and transcription factors involved in differentiation and effector function of each functional T cell subset (1/2/17/Treg) in CCC, NIC, and heart donor myocardial samples. Methods and Results. Quantitative PCR showed markedly upregulated expression of IFN-γ and transcription factor T-bet, and minor increases of GATA-3; FoxP3 and CTLA-4; IL-17 and IL-18 in CCC as compared with NIC samples. Conversely, cytokines expressed by 2 cells (IL-4, IL-5, and IL-13) or associated with Treg (TGF-β and IL-10) were not upregulated in CCC myocardium. Expression of 1-related genes such as T-bet, IFN-γ, and IL-18 correlated with ventricular dilation, FoxP3, and CTLA-4. Conclusions. Results are consistent with a strong local 1-mediated response in most samples, possibly associated with pathological myocardial remodeling, and a proportionally smaller FoxP3⁺CTLA4⁺ Treg cell population, which is unable to completely curb IFN-γ production in CCC myocardium, therefore fueling inflammation.

1. Introduction

Approximately 8 million people are infected with the protozoan parasite Trypanosoma cruzi [1] in Central and South America, with an estimated 300,000 cases in the USA alone due to migration. T. cruzi is a major cause of heart disease and cardiovascular-related deaths in endemic areas located in Latin America, with approximately 50,000 fatalities per year due to chronic Chagas cardiomyopathy (CCC) [2]. CCC, the most important clinical consequence of Chagas disease, is an inflammatory cardiomyopathy that affects around 30% of infected individuals and occurs 5–30 years after acute infection, while ca. 60% of those infected remain asymptomatic (ASY) [3]. The reasons why it takes so long after infection for development of full-blown CCC are still unknown. One-third of patients developing CCC present a particularly lethal form of dilated cardiomyopathy with significant left ventricular dysfunction, and shorter survival than cardiomyopathies of noninflammatory etiology (NIC) [4]. CCC is characterized by a diffuse mononuclear cell myocarditis, with significant heart fiber damage, prominent fibrosis, and scarcity of T. cruzi parasites (reviewed in [5]). The inflammatory infiltrate of CCC heart lesions is mainly composed by CD4+ and CD8+ T cells and macrophages [6, 7]. The occurrence of myocarditis is correlated with clinical severity, ASY patients having minimal inflammation [8]. Evidence suggests that the presence or intensity of myocarditis plays a major pathogenic role in CCC development and severity.

The immune response to T. cruzi is triggered by persistent infection with an obligatory intracellular parasite. During acute T. cruzi infection, T. cruzi pathogen-associated molecular patterns (PAMPs) trigger innate immunity in multiple cell types [9], which release proinflammatory cytokines, such as IL-1, IL-6, IL-12, IL-18, and TNF-α, activating cascades of inflammatory cells [10] (reviewed [11]). Antigen-presenting cells subsequently elicit a strong T cell and antibody response against T. cruzi,where IL-12 and IL-18 drive the differentiation of IFN-γ-producing T. cruzi-specific TH1-type T cells which migrate to sites of T. cruzi-induced inflammation, including the myocardium, in response to locally produced chemokines [11–13]. The TH1-type T cell and antibody responses lead to control—but not complete elimination—of tissue and blood parasitism, establishing a low-grade chronic persistent infection by T. cruzi.

As a result of persistent infection, both CCC and ASY chronic Chagas disease patients show a skewed TH1-type immune response [13–15] with reduced production of IL-4 by PBMC, but those who develop Chagas cardiomyopathy display a particularly strong TH1-type immune response with increased numbers of IFN-γ-producing T cells in peripheral blood mononuclear cells (PBMC) [16–18] as well as plasma TNF-α in comparison with uninfected or ASY patients [14, 19].

In addition, CCC patients display a reduced number of CD4⁺CDIL-10⁺ T cells and CD4⁺CDFoxP3⁺ regulatory T cells in their peripheral blood as compared to patients in the ASY form of Chagas disease, suggesting that such cells may play a role in the control of the intensity of inflammation in chronic Chagas disease [14, 20, 21]. Furthermore, PBMC from CCC patients displayed increased numbers of CD4⁺CDFoxP3⁺CTLA-4⁺ T cells and decreased numbers of CD4⁺CDIL-10⁺ T cells as compared to ASY patients. These reports suggest that a smaller CD4⁺CD25⁺ Treg compartment displays a deficient suppressive activity in CCC patients, leading to uncontrolled production of TH1 cytokines [22]. Regarding TH17 cells in Chagas disease, a recent study showed a lower frequency of circulating CD4⁺IL-17⁺ T cells in CCC patients as compared with ASY patients and noninfected individuals [23].

The exacerbated TH1 response observed in the PBMC of CCC patients is reflected on the CD4⁺ and CD8⁺TH1-type T cell-rich myocardial inflammatory infiltrate, with mononuclear cells predominantly producing IFN-γ and TNF-α, with lower production of IL-4, IL-6, IL-7, and IL-15 [6, 7, 14, 16, 24, 25]. It has recently been shown by our group that CCL5⁺, CXCL9⁺, CCR5⁺, and CXCR3⁺ mononuclear cells were abundant in CCC myocardium, and mRNA levels of the TH1-chemoattracting chemokines CXCL9, CXCL10, CCL3, CCL4, and CCL5 and their receptors were also found to be upregulated in CCC heart tissue [26]. Significantly, the intensity of the myocardial infiltrate was positively correlated with CXCL9 mRNA expression; moreover, a single nucleotide polymorphism in the CXCL9 gene, associated with a reduced risk of developing severe CCC in a cohort study, was associated with reduced CXCL9 expression and intensity of myocarditis in CCC [26]. These results are consistent with a major role of locally produced TH1-chemoattractant chemokines in the accumulation of CXCR3/CCR5⁺TH1 T cells in CCC heart tissue. Significantly, CCC patients display increased numbers of T. cruzi-specific CXCR3⁺ and CCR5⁺ T cells coexpressing IFN-γ in the PBMC as compared to ASY subjects [27].

Although the presence of heart-infiltrating TH1-type T cells has been well documented, relatively little is known about the presence or relative proportion of the other functional T cell subsets in CCC heart tissue, which may ultimately determine the local inflammatory status. Although studies with PBMC have established significant differences in the frequency of functional T cell subset differences between CCC and ASY, it does not necessarily follow that those findings will all apply to CCC heart tissue. The presence of different Treg populations in CCC heart tissue has been suggested by the findings of Foxp3 expression and TGF-β signaling (through Smad4 detection) in CCC compared to ASY heart tissue [28, 29]. Regarding production of IL-4 in CCC myocardium, there are conflicting results, where IL-4-producing mononuclear cells were either undetectable [14], prominent in autopsy samples [25], or outnumbered by IFN-γ-producing T cells [30]. So far, TH17 cells have not yet been studied in human CCC myocardium.

We believe the elucidation of the balance of functional T cell lineages in CCC myocardium is of paramount importance to understand the pathogenesis of CCC, including the key elements for disease progression.

In order to evaluate the relative contribution of each functional T cell subset in the CCC myocardial inflammatory infiltrate, we assessed the mRNA expression of lineage-specifying transcription factors associated with differentiated TH1/TH2/TH17 T cells (T-box expressed in T cells (T-bet), GATA-binding protein-3 (GATA-3), and retinoid-related orphan receptor γt (RORγ-T), respectively [31, 32] and the corresponding effector cytokines (IFNγ, IL-4, IL-5, IL-13, IL-17, and IL-23), along with genes associated with regulatory T cell function (FoxP3, TGF-β, CTLA-4, and IL-10), and proinflammatory and/or TH1-inducing cytokines (IL-1, IL-6, IL-12p35, IL12p40, IL-18, and IL-23) in myocardial samples from CCC and NIC patients as well as heart donor controls.

2. Methods

2.1. Ethics Statement

The protocol was approved by the Institutional Review Board of the School of Medicine, University of São Paulo (Protocol number 739/2005) and written informed consent was obtained from the patients. In the case of samples from heart donors, written informed consent was obtained from their families.

2.2. Patients and Sample Collection

All Chagas disease patients were considered serologically positive for antibodies against T. cruzi on the basis of results of at least 2 of 3 independent tests as described [18]. All Chagas disease and NIC patients underwent standard electrocardiography and 2-dimension and M-mode echocardiography in the hospital setting as described [18]. Patients with CCC presented with typical electrocardiographic findings such as right bundle branch block and/or left anterior division hemiblock [33], in addition to ventricular dysfunction classified on the basis of left ventricular ejection fraction <40%. Myocardial left ventricular free wall heart samples were obtained from end-stage heart failure CCC patients (Table 1) and end-stage heart failure patients with noninflammatory cardiomyopathies (NIC, five patients with idiopathic dilated cardiomyopathy and three patients with ischemic cardiomyopathy, all seronegative for T. cruzi; Table 1). Control adult heart tissue from the left ventricular-free wall was obtained from nonfailing donor hearts (N, Table 1) not used for cardiac transplantation due to size mismatch with available recipients. This sample set is the same previously studied for myocardial chemokine expression [26]. Hearts were explanted at the time of heart transplantation at the Heart Institute-InCor, School of Medicine, University of São Paulo, São Paulo, SP, Brazil. For mRNA extraction, samples were quickly dissected, and myocardial tissue was frozen in liquid nitrogen and stored at −80°C.

Table 1: Characteristics of patients and control heart donors whose samples were used in this study.

CCC
NIC
N

14
8
6

Age
47.2 ± 14.6
53.3 ± 7.5
32.2 ± 12.8

Sex (M/F)
5/9
0/9
0/6

EF
26.50 ± 8.96
22.73 ± 6.28
ND

Fibrosis
Moderate to intense
Moderate to intense
0

LVDD
71.64 ± 7.48
75.86 ± 15.84
ND

Hypertrophy
Yes
Yes
No

Myocarditis
Moderate to intense
Absent
0

Age (years); M (male); F (female); CCC (chronic Chagas cardiomyopathy); NIC (noninflammatory cardiomyopathy). Normal heart donors (N) were subject to ventilator and vasoactive drugs and had been under life support for an average of 48 hours. Characterization of the samples as myocarditis, fibrosis, and hypertrophy; reference values for the presence of myocarditis and fibrosis: absent; slight; moderate; intense; hypertrophy: Y (yes), N (no). ND (not done); EF (left ventricular ejection fraction) ≥ 55%; LVDD (left ventricle diastolic diameter); reference value: diameter 39–55 mm.

2.3. RNA Isolation, Reverse Transcription, and Quantitative Real-Time Polymerase Chain Reaction (Real-Time qPCR)

Total RNA was extracted from  mm myocardial samples using the Trizol method (Life Technologies Inc., Grand Island, NY). The RNA was quantified using NanoDrop Spectrophotometry (Thermo Scientific) and treated with Rnase-free DNase I (USB, Ohio, USA). cDNA was obtained from 5 μg total RNA using Super-script II Reverse Transcriptase (Invitrogen, Carlsbad, CA, USA). We designed forward and reverse primers for real-time qPCR assays using the Primer Express software (Applied Biosystems, Foster City, CA, USA; see Table S1 in supplementary materials available online at http://dx.doi.org/10.1155/2014/914326). Real-time qPCR reactions were carried out in an ABI Prism 7500 Sequence Detection system (Applied Biosystems) using the SYBR Green PCR Master Mix (Applied Biosystems), as described in [6]. PCR efficiency was measured in myocardial tissue for all real-time PCR primers. All the samples were tested in triplicate with the glyceraldehyde 3-phosphate dehydrogenase (GAPDH, reference gene) whose expression was previously shown to display little variance among human myocardial tissue samples [24], as the reference gene for normalization of data, and relative expression of each mRNA was calculated with the method [34], using expression in six normal donor hearts as calibrator. A ratio between expression values of the T-bet and GATA-3 genes was calculated as previously reported [32].

2.4. Statistical Analysis

Values of the relative expression of each mRNA in the CCC and NIC groups were compared with the Mann-Whitney test and performed using the GraphPad Prism 5 software. Correlation analysis was performed by Spearman’s rank correlation test with SPSS version 14.0 software (SPSS, Chicago, III).

3. Results

3.1. Patient and Sample Features

As previously observed with the same sample set studied here [26], while myocardial sections from both cardiomyopathy groups displayed cardiomyocyte hypertrophy and fibrosis upon histopathological analysis, lymphocytic myocarditis was only observed among samples from CCC patients (Table 1). No significant differences were found in age, ejection fraction (EF), or left ventricular diastolic diameter (LVDD) between the two groups. We have also previously observed positive correlations between the intensity of lymphocytic myocarditis and fibrosis and between EF and myocardial expression of ANP and BNP [26]. Myocardial tissue samples are rich in CD4+ and CD8+ T cells (photograph in [26]).

3.2. Expression of TH1, TH2, and TH17 T Cell Lineage-Specific of Transcription Factors on Heart Tissue from CCC Patients

We evaluated the expression of the transcription factors associated with the TH1, TH2, and TH17 effector T cell lineages. The expression of mRNA encoding the transcription factors T-bet and GATA-3 was 10 and 2-fold higher in CCC samples than in NIC samples, respectively ( and , resp.; Figure 1). However, the expression of RORγ-T mRNA, the master transcription factor for TH17 cells, was not significantly different in the myocardium of CCC patients when compared to heart of NIC patients and control individuals (Figure 1). The ratio of relative expression of T-bet/GATA-3, a putative index of TH1/TH2 imbalance [32], was significantly higher in the CCC than in the NIC group (Figure 2), indicating once again the skewed TH1/TH2 balance in CCC myocardium.

Figure 1: Expression of mRNA encoding transcription factors T-bet, Gata-3, and Rorγ-T in myocardium. Real-time qPCR analysis of mRNA expression in CCC and NIC myocardium. After normalization to GAPDH mRNA, relative increase was plotted in comparison to N group and data were calculated with the method, as described in Methods section. The horizontal bar stands for the median; dotted lines indicate twofold increase or decrease of expression as compared with the control group.

Figure 2: The ratio of mRNA encoding transcription factors T-bet and Gata-3 in myocardium. The ratio of relative expression of T-bet/GATA-3 in CCC and NIC group. The ratio of relative expression was plotted in comparison to N group and data were calculated with the method, as described in Methods section.

3.3. Hallmark , and Cytokine Expression in CCC Patient Myocardial Tissue

Given the evidence for the expression of T-bet and GATA-3 mRNA in CCC myocardium, indicative of the presence of TH1 and TH2 cells, we also evaluated mRNA expression of hallmark TH1, TH2, and TH17 cytokines. Expression levels of IFN-γ and the proinflammatory and pro-TH1 cytokine IL-18 were 42- and 3-fold higher in the heart tissue of CCC than NIC patients ( and , resp.; Figure 3). We observed a positive correlation between T-bet expression with that of IFN-γ and IL-18; significantly, mRNA expression of T-bet was also positively correlated with left ventricular diastolic diameter (LVDD), an index of global systolic ventricular dysfunction (Table 2). TH2 cytokines IL-4, IL-5, and IL-13 were undetectable in all samples, while IL-17 expression was 3-fold higher among CCC than NIC samples () (Figure 3 and data not shown). However, expression of other proinflammatory cytokines such as IL-1β, IL-12p40, IL23p19, and IL-27, which also has regulatory functions [35], was undetectable in all samples tested (data not shown), while expression of IL-6 and IL-12p35 both in the CCC and NIC groups was similar to that found in control samples (Figure 3).

Table 2: Correlation of mRNA expression of T cell lineage-associated molecules against each other and versus LVDD on heart tissue from CCC patients using Spearman’s rank correlation.

mRNA expression

T-bet versus LVDD
0.043
0.546

T-bet versus Foxp3
0.047
0.538

T-bet versus CTLA-4
0.0001
0.903

IFN- versus Foxp3
0.004
0.714

IFN- versus CTLA-4
0.004
0.710

IL-18 versus T-bet
0.045
0.543

IL-18 versus IFN-
0.002
0.749

IL-18 versus Foxp3
0.009
0.670

IL-18 versus CTLA-4
0.007
0.648

Foxp3 versus CTLA-4
0.001
0.771

Figure 3: Myocardial expression of cytokine mRNA. Real-time qPCR analysis of mRNA expression in CCC and NIC myocardium. After normalization to GAPDH mRNA, relative increase was plotted in comparison to N group and data were calculated with the method, as described in Methods section. The horizontal bar stands for the median. Dotted lines indicate twofold increase or decrease of expression as compared with the control group.

3.4. Expression of Molecules Associated with Regulatory T Cell Function on Heart Tissue from CCC Patients

We next analyzed the expression of genes associated with regulatory T cell function in myocardial samples from the three groups. mRNA expression of FoxP3 and CTLA-4 was 3- and 5-fold higher in the heart tissue of CCC than in NIC patients, respectively ( and , resp.; Figure 4). On the other hand, there was no significant difference in the expression of IL-10 and TGF-β in myocardial samples of CCC patients when compared to those of NIC patients and control individuals (Figure 4). We found a significant (, ) positive correlation between the mRNA expression of FoxP3 and CTLA-4 (Table 2), which is consistent with coexpression in the same cell population. Expression of genes associated with TH1 cells, such as IFN-γ, T-bet, and IL-18, was positively correlated with the Treg-associated molecules FoxP3 and CTLA-4; T-bet expression correlated highly significantly with CTLA-4 (, ) (Table 2).

Figure 4: Expression of Foxp3, CTLA-4, IL-10, and TGF-β in myocardium. Real-time qPCR analysis of mRNA expression in CCC and NIC myocardium. After normalization to GAPDH mRNA, relative increase was plotted in comparison to N group and data were calculated with the method, as described in Methods section. The horizontal bar stands for the median. Dotted lines indicate twofold increase or decrease of expression as compared with the control group.

4. Discussion

We report that CCC myocardial tissue displays significantly increased expression of mRNA encoding IFN-γ and T-bet, with less prominent increase in expression of IL-17, GATA-3, FoxP3, and CTLA-4. Among proinflammatory cytokines only IL-18, but not IL1β, IL-6, IL-12, IL-23, and IL-27, displayed increased expression in CCC heart tissue. mRNA expression of the cytokines IL-4, IL-5, and IL-13, and cytokines associated with regulatory T cells, such as IL-10 and TGF-β, was either similar to controls or undetectable. TH1-associated genes such as T-bet, IFN-γ, and IL-18 expression levels were found to correlate among themselves, as well as with FoxP3, CTLA-4, and, in the case of T-bet, with ventricular dilation. Transcription factor and cytokine expression patterns are consistent with a predominant TH1-type inflammatory infiltrate, with antagonized TH2 cells and a proportionately smaller FoxP3⁺CTLA-4⁺ Treg cell population which fails to completely suppress IFN-γ production and TH1 inflammation in CCC myocardium. The correlation of T-bet and ventricular dysfunction further points out the role of inflammatory TH1 responses in pathological myocardial hypertrophy/remodeling leading to disease progression.

The finding that the expression of T-bet is significantly upregulated in CCC myocardial tissue corroborates the predominance of TH1-type of heart-infiltrating T cells in the CCC myocardium. The finding that the median IFN-γ mRNA expression was over 40-fold upregulated in CCC myocardial tissue is in line with previous studies of heart-infiltrating T cell lines and immunohistochemical studies [14, 25, 36]. Our group has recently shown that expression of IFN-γ- inducible chemokines CXCL9 and CXCL10 may be directly involved in the recruitment of large numbers of CCR5⁺ and CXCR3⁺TH1-type T cells to CCC myocardium [24, 26], suggesting that the local production of IFN-γ and IFN-γ inducible chemokines leads to the recruitment of effector TH1-type T cells into heart tissue. The correlations between the TH1-associated genes T-bet, IFN-γ, and IL-18 and CCR5, CXCR3, and their IFN-γ-dependent chemokine ligands were described previously in the same sample set (Table S2) [26]. Although we measured static mRNA levels in a single time point, this can be a sign of a positive feedback loop. Increased numbers of cells capable of local production of IFN-γ and also IFN-γ-dependent chemoattractant molecules may result in the migration of additional CCR5+, CXCR3+, IFN-γ producing T1-type T cells. The correlation between T-bet expression levels and the left ventricular diastolic diameter, an index of ventricular dilation and disease severity, is consistent with the idea that the TH1-type T cell compartment is a determinant factor in CCC progression. In support of this idea, associations between the intensity of the inflammatory infiltrate and disease progression have been previously described in Chagas disease patients [8] and in the chronic Syrian hamster model of CCC where the number of mononuclear cells also correlated with ventricular dilation (ECN and JK, unpublished data). This is further corroborated by the positive correlation between the intensity of lymphocytic myocarditis and fibrosis [26] and may be the pathogenetic translation of the ability of IFNγ to directly induce ANF expression in cardiomyocytes [24], the first step in the pathological hypertrophy pathway. Accordingly, a recent report has described that IFN-γ overexpressing transgenic mice develop mononuclear cell myocarditis, culminating in dilated cardiomyopathy [37].

The modest expression of GATA-3, together with the observed lack of expression of IL-4, IL-5, and IL-13, hallmark effector TH2 cytokines, suggests that TH2 cells may be relatively rare in the CCC myocardial infiltrate and failing to produce TH2 cytokines, thus being nonfunctional possibly due to antagonism by IFN-γ [38]. Our findings are in contrast with previous immunohistochemistry studies that, in spite of showing a majority of mononuclear cells staining with anti-IFN-γ, disclose a minority of mononuclear cells producing IL-4 in CCC myocardium [25, 30] but are in agreement with a previous study with T cell lines derived from CCC myocardium [13]. At any event, STAT4 mRNA was overexpressed in CCC patients with heart failure as compared with STAT6 levels in patients with presence or absence of heart failure [30], a further indication of TH1 signaling [24]. The correlation found between GATA-3 expression and CCR4 (Table S2) may suggest that infiltrating TH2 cells effectively possess such a phenotype.

In the absence of RORγ-T expression, the finding of low-grade expression of IL-17 suggests that there may be little or no differentiated TH17 cells in CCC heart tissue. At any event, the correlation found between IL-17 expression and CCR4 (Table S2) may suggest that such putative infiltrating TH17 cells effectively possess this phenotype. This may be in concert with the recent finding that CCC patients with low ejection fraction similar to the ones examined here had lower IL17⁺ T cells in their PBMC than CCC patients without ventricular dysfunction [23].

Our finding of a modest increase in the mRNA expression of FoxP3 and CTLA-4, with no significant modulation of TGF-β and IL-10 expression, is in line with previous studies showing that FoxP3+ cells are significantly less abundant in myocardial sections from CCC than in ASY patients or noninfected individuals, suggesting that reduced numbers of Treg cells could be one important cause for the prevalent TH1 response in CCC heart tissue [29]. Araujo et al. [21] have previously shown that PBMC from CCC patients displayed increased numbers of CD4⁺CDFoxp3⁺CTLA-4⁺ T cells and decreased numbers of CD4⁺CDIL-10⁺ T cells, as compared to ASY patients, consistent with our findings in regulatory T cell molecules in CCC heart tissue [22]. Recently, CTLA-4 was found to be expressed in mononuclear cells infiltrating heart tissue sections from chronically infected subjects with severe myocarditis [39]. The finding that expression of FoxP3 and CTLA-4 displayed positive correlations with TH1 chemokine receptors CCR5 and CXCR3 and their ligands, along with T-bet, IFN-γ, and IL-18 (Table S2), is in line with previous findings and indicates for the first time that the FoxP3⁺ CTLA4⁺ Treg compartment bears a relationship with the TH1 infiltrate. However, in case the Treg compartment was effectively controlling the TH1 infiltrate in at least some samples, one would expect to find a negative correlation between markers of the two T cell populations. Data thus suggest that a proportional but comparatively smaller or less functional FoxP3⁺ CTLA-4⁺ Treg compartment, possibly also bearing chemokine receptors CCR5 and/or CXCR3 [38], migrated to CCC heart tissue in a partially failed attempt to control TH1-driven inflammation. However, since both FoxP3 and CTLA-4 can be transiently expressed in activated human T cells, we cannot formally exclude that the increased expression was merely due to the presence of activated T cells belonging to other functional subsets [40, 41]. Our findings of lack of upregulation of TGF-β in situ are in apparent contrast with the immunohistochemical study by Araúijo-Jorge et al. [33] who have identified a low number of TGF-β ⁺ mononuclear cells infiltrating CCC myocardium. However, that report failed to show values from healthy control tissue samples, so it is not possible to assess whether the detected values were above baseline. A recent report showed that circulating TGF-β1 could be detected in CCC serum samples [42] which could be the source of activation of the TGF-β1 signaling pathway in CCC myocardium [28].

The selective increase of IL-18 in the absence of any other proinflammatory cytokine in CCC myocardium is intriguing, since most proinflammatory cytokines are produced in response to shared stimuli, like Toll-like receptor ligands and IFN-γ [43]. The longer half-life of the IL-18 mRNA [44] could partially explain our findings. The positive correlation between the mRNA expression of IL-18 and IFN-γ is consistent with the described positive feedback loop between the two cytokines [45]. IL-18 has been reported to induce ANP gene expression and hypertrophy in cardiomyocytes, as previously described for IFN-γ, TNF-α, IL-1β, and CCL2 [24, 46]. IL-18 also induces fibroblast expression of fibronectin, a prominent extracellular matrix protein [47], a mechanism possibly involved in myocardial fibrosis.

Since all our CCC myocardium samples came from clinically similar end-stage patients submitted to transplantation, it could be argued that possessing a more or less intense expression of T-bet, a TH1-associated expression profile or even a more significant inflammatory infiltrate by itself, may not be relevant for the progression of CCC. However, CCC is not a monogenic disease, and it is likely that the progression to overt inflammatory dilated cardiomyopathy may result from the combined effect and inadequate counterregulation of relevant genes and environmental factors. Polymorphisms in multiple innate immunity/inflammatory genes have been found to associate with risk for developing CCC (reviewed in [5, 11]). In addition to interference by other genes, differential myocardial resilience, including responses to hypertrophic/fibrogenic factors occurring in CCC heart tissue (IL1β, TNF-α, IFN-γ, IL18, CCL2,and CCL21)(reviewed in [5]), could explain why these few patients presenting less intense inflammation and a lower expression of TH1 cytokines can nevertheless develop end-stage cardiomyopathy. Our group has recently observed that polymorphisms in the promoter region that bind to transcription factors of the cardiac actin gene, a cardiomyocyte gene associated with muscle contraction and resilience, whose dysfunction or altered expression levels lead to cardiomyocyte malfunction and apoptosis [48] associate with CCC development [49]. In the Syrian hamster model of chronic Chagas disease cardiomyopathy, although the intensity of chronic inflammation correlated with ventricular dilation, intensity of myocarditis was similar in hamsters dying from chronic T. cruzi-induced dilated cardiomyopathy and survivors euthanized 11 months after infection [5], suggesting the existence of additional factors related to disease progression or death from CCC.

It is likely that the interplay between the Treg and TH1-type T cell populations is key towards the control of myocardial inflammation in chronic Chagas disease. Our findings suggest that the myocarditis in the chronic cardiac form of Chagas disease is related to a strong TH1 response in most cases, associated with a balanced regulatory T cell response and an antagonized TH2 response. Our results are consistent with the hypothesis that a putative FoxP3⁺ and CTLA-4⁺ Treg heart-infiltrating T cell population fails to control the exacerbated IFN-γ production by TH1-type T cells in the majority of end-stage CCC cases.

5. Conclusion

The TH1-type T cell-rich mononuclear infiltrate plays a major role in the development and progression of chronic CCC. We found increased expression of TH1-associated genes in CCC myocardial tissue, with minor upregulation, similar or even undetectable levels of mRNAs encoding associated TH2, TH17 and Treg associated genes. Our results show a limited role of TH2-type T cells, and are consistent with the hypothesis that a putative FoxP3⁺ and CTLA4⁺ Treg heart-infiltrating T cell population fails to control the exacerbated IFN-γ production by TH1-type T cells in the majority of end-stage CCC cases.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors thank Dr. Priscila Teixeira for helping in heart tissue collection and Dr. João Santana Silva for providing the sequences of the IL-17 primer.

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