Journal of Immunology Research

Volume 2014 (2014), Article ID 696812, 11 pages

http://dx.doi.org/10.1155/2014/696812

Clinical Study

Uncomplicated Diverticular Disease: Innate and Adaptive Immunity in Human Gut Mucosa before and after Rifaximin

Rossella Cianci,¹ Simona Frosali,¹ Danilo Pagliari,¹ Paola Cesaro,² Lucio Petruzziello,² Fabio Casciano,¹ Raffaele Landolfi,¹ Guido Costamagna,² and Franco Pandolfi¹

¹Department of Medical Science, Catholic University of the Sacred Heart, ‘A. Gemelli’ University Hospital, Largo A. Gemelli, 8-00168 Rome, Italy

²Endoscopy Unit, Catholic University of the Sacred Heart, ‘A. Gemelli’ University Hospital, Largo A. Gemelli, 8-00168 Rome, Italy

Received 16 April 2014; Revised 12 June 2014; Accepted 18 June 2014; Published 16 July 2014

Academic Editor: Anis Larbi

Copyright © 2014 Rossella Cianci 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/Aim. Uncomplicated diverticular disease (UDD) is a frequent condition in adults. The pathogenesis of symptoms remains unknown. Bacteria are able to interact with Toll-like receptors (TLRs) and to induce inflammation through both innate immunity and T-cell recruitment. We investigated the pattern of TLRs 2 and 4 and the intestinal homing in patients with UDD before and after a course of Rifaximin. Methods. Forty consecutive patients with UDD and 20 healthy asymptomatic subjects were enrolled. Among UDD patients, 20 were assigned to a 2-month course of treatment with Rifaximin 1.2 g/day for 15 days/month and 20 received placebo. Blood sample and colonic biopsies were obtained from patients and controls. The samples were collected and analyzed at baseline and at the end of treatment. Flow cytometry was performed using monoclonal antibodies (CD3, CD4, CD8, CD103, TCR-gamma/delta, CD14, TLR2, and TLR4). Results. In UDD, TLR2 and TLR4 expression on immune cell subpopulations from blood and mucosa of the affected colon are altered as compared with controls. Rifaximin treatment induced significant modifications of altered conditions. Conclusions. Our data show the role of TLRs in the development of inflammation in UDD. TLRs distribution is altered in UDD and these alterations are reversed after antibiotic treatment. This trial is registered with ClinicalTrials.gov: NCT02068482.

1. Introduction

Colon diverticulosis is a frequent condition in adults in Western countries and several patients experience clinical symptoms even when diverticulosis is not complicated by diverticulitis. This condition is being referred to as uncomplicated diverticular diseases (UDD) [1]. UDD symptoms pathogenesis remains unknown, but alterations in the diet and gut microbiota may be involved and could be responsible for “chronic low mucosal inflammation” [2]. Intestinal motility exerts a major control on gut microflora through the sweeping of luminal contents [3]. An alteration of the intestinal motility, especially decreasing anaerobic bacteria, can influence intestinal inflammation and be beneficial in both clinical and experimental models of colitis [4]. Rifaximin is beneficial to mice colitis [5]. Animal data indicate that a reduced load of bacteria may be useful in the prevention of colitis in susceptible individuals [5]. Although there is no supporting evidence from placebo-controlled trials, recommendations for management of acute episodes of UDD include medical treatment with broad-spectrum antibiotics [6, 7]. We have recently shown that both central and mucosal immunity are altered in UDD with increased recruitment of CD103 lymphocytes; treatment with Rifaximin ameliorates clinical symptoms (when present) and reduces CD103 levels, suggesting decreased mobilization of mucosal homing [8].

Rifaximin is an antibiotic that acts locally in the gastrointestinal tract with a broad spectrum of antibacterial activity. Fecal concentrations of Rifaximin are known to largely exceed the minimum inhibitory concentration values of pathogenic enteric bacteria. Rifaximin, instead of other systemic absorbed antibiotics, acts in the gastrointestinal tract modifying the gut microbiota (at the concentrations used, its action is mainly directed to pathobionts and much less to physiological gut flora). Furthermore, at the same time, Rifaximin, being a nonabsorbed antibiotic, has only little systemic effects [9].

To better understand the mechanisms involved, we reasoned that Rifaximin treatment may reverse immune system alteration by reducing bacteria related activation. Bacteria activate the immune system through specific receptors referred to as Toll-like receptors (TLRs) [10]. Bacterial lipopeptides (BLP) and lipopolysaccharides (LPS) are recognized by TLR2 and TLR4, respectively.

TLRs are involved in the generation of innate and adaptive immunity [11, 12]. Recent studies have shown that T cells also express certain types of TLRs [13, 14]. These TLRs can function as costimulatory receptors that complement T cell receptor- (TCR-) induced signals to enhance effector T cell activation [15]. Thus, TLRs also participate in adaptive immune response. No data have been reported on TLRs in humans affected by UDD. We therefore investigated TLR2, TLR4, and intestinal homing in UDD before and after a course of Rifaximin.

2. Material and Methods

The local Ethics Committee approved the study protocol and a written informed consent was obtained according to the principles of the Declaration of Helsinki (1983).

2.1. Patients’ Recruitment

Over a period of 6 months, 40 consecutive patients with UDD (abdominal pain in the lower abdominal quadrant and change in bowel habit) and 20 healthy asymptomatic subjects undergoing screening colonoscopy for colorectal cancer were enrolled. The 40 patients with UDD were randomly assigned into two groups:

(i)20 patients with UDD were assigned to a 2-month treatment with Rifaximin 1.2 g/day for 15 days/month.(ii)20 patients with UDD on the same time received placebo.

Colonoscopy with multiple biopsies and blood samples were taken from patients and controls and repeated in patients at the end of the 2-month Rifaximin treatment or placebo course. Control healthy group was matched for gender, age, and body mass index (BMI) to the other two groups of patients.

Inclusion criteria in UDD patients group were as follows: endoscopic evidence of extensive diverticula limited to the sigmoid and descending colon; continuous gastrointestinal symptoms for at least 3 months; and age ≥18 years.

Exclusion criteria were as follows: inflammatory bowel diseases (IBD); mucosal inflammation at endoscopy and histology; present or past episodes of acute diverticulitis; colonic surgery; intestinal and extraintestinal cancer; use of antibiotics, anti-inflammatory drugs, probiotics, PPI, steroids, or fibers in the previous 12 weeks; hematological diseases; and pregnancy.

Acute diverticulitis was excluded on the basis of clinical signs and laboratory data.

Each patient underwent an abdominal ultrasonography to exclude abdominal masses or abscesses. Patients’ identification was performed by the presence of left colonic diverticula, whilst controls had a normal colon.

2.2. Colonic Mucosa

Bioptic tissue samples were incubated with 100 UI/mL of human recombinant interleukin-2 (IL-2) to allow lymphocyte growth as previously described [8]. When tissue infiltrating lymphocytes (TILs) reached a sufficient number to perform the immunophenotype, surface markers were studied by immunofluorescence.

2.3. Peripheral Blood

Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Hypaque according to standard procedures.

Whole blood cells (WBC), for granulocytes analysis, were isolated from EDTA-treated blood through red cell lysis. Briefly, 1 mL of venous blood was incubated with 1 mL of PBS and 10 mL of isotonic NH₄Cl solution (155 mM NH₄Cl, 10 mM KHCO₃, 0.1 mM EDTA, and pH 7.4) for 10 min. Next, after two washes in PBS, the cells were stained as described below.

2.4. Flow Cytometry

PBMC, WBC, and TILs were stained for 30 min at 4°C with the following anti-human monoclonal antibodies (mAb): PE-Cy7 or PE conjugated-CD3 (clone SK7), PE-Cy7 or PE conjugated-CD4 (clone SK3), PE-Cy7 or PE conjugated-CD8 (clone SK1), FITC conjugated-CD103 (clone Ber-ACT8), PE conjugated-TCRgd (clone 11F2), PE-Cy7 conjugated-CD14 (clone M5E2), Alexa 482 conjugated-TLR2 (clone 11G7) (all from BD, San Diego, CA), and APC conjugated-TLR4 (clone HTA125) (eBiosciences, San Diego, CA).

2.5. Gating Strategy

Each analysis was performed using at least 100.000 cells that were gated in the region of the lymphocyte-monocyte population or in granulocytes population, as determined by light-scatter properties (forward scatter versus side-scatter).

Flow analysis was performed by a standardized 3- or 4-colour analysis protocol that was gated on cell stained with one fluorochrome, followed by 2-colour analysis of cells stained with the prescribed remaining fluorochromes.

Quadrants of dot plot were set using appropriate isotype controls for each antibody. Appropriate fluorochrome-conjugated isotype-matched mAbs (Beckman Coulter) were used as control for background staining in each flow acquisition. In these assays, careful colour compensation was performed before cell analysis. Expression of TLRs in lymphocytes was performed analysing at least 500 events. Mean fluorescence intensity (MFI) was calculated only for positive events after subtraction of specific isotype control MFI. All samples were analyzed with a FACS Calibur and CellQuest software (BD, Franklin Lakes, NJ).

2.6. Statistical Analysis

The statistical analysis was carried out using the GraphPad 6.0 statistical package. The Mann-Whitney U test was applied to the continuous variables, the changes observed in unpaired groups, and the Wilcoxon test in paired groups.

The Kruskal-Wallis test H was applied to evaluate whether significant differences exist between different samples and also for comparisons between independent samples. When appropriate, the correction for multiple comparisons was applied to the statistical significance.

3. Results

Demographic and clinical features of UDD patients and controls are summarized in Table 1. No statistical differences in smoking habits, alcohol daily intake, and body mass index (BMI) were observed between the two groups.

Table 1: Demographic and clinical characteristics of UDD patients and controls.

UDD patients ()
Controls ()

Gender (male/female)
21/19
5/16

Age, median (range), years
67.5 (39–84)
53 (20–78)

Smoking habit (yes)
8
7

Alcohol intake (>60 g/day)
18
7

Weight, mean (range) (Kg)
70.38 (52–100)
66.14 (52–84)

Height, mean (range) (m)
1.66 (1.41–1.80)
1.67 (1.50–1.80)

Body mass index (range)
22.6 (17–24)
22 (17–22)

Good compliance to Rifaximin (>90% of the appropriate dose) was observed in all patients. A statistically significant decrease in symptoms was observed in patients two months after treatment. No adverse events to the drug or complications were observed.

3.1. Expression of TLRs

In peripheral blood, at baseline, both the percentages of TRL2 and TRL4 lymphocytes were significantly higher ( and , resp.) in patients than in controls (Figures 1(a) and 1(b)).

(a)

(b)

(c)

(d)

(e)

Figure 1: Expression of TLRs in lymphocytes. (a, b) TLR2 and TLR4 in peripheral blood lymphocytes, at baseline and after Rifaximin and placebo treatments. (c, d) TLR2 and TLR4 in sigma mucosa lymphocytes at baseline and after Rifaximin and placebo treatments. (e) TLR2 and TLR4 in transverse mucosa lymphocytes at baseline and after Rifaximin treatment. The values reported in box-and-whiskers plots show the minimum, the 25th percentile, the median, the 75th percentile, and the maximum. In particular, the whiskers go down to the smallest value (minimum) and up to the largest one (maximum), the top and bottom of the box are the 25th and 75th percentiles, and the line in the middle of the box is the median corresponding to 50th percentile (, , patients versus control (health or baseline)); , between treatments. Healthy control (CTR), UDD patients (PZ), before Rifaximin (BR), after Rifaximin (AR), before placebo (BP), and after placebo (AP).

After Rifaximin treatment (AR), the percentages of TRL2 and TRL4 lymphocytes in patients remained similar to basal values obtained before Rifaximin treatment (BR). However, TLR2 and TLR4 increased significantly ( and , resp.) in patients who received placebo treatment (after placebo or AP), as compared with patients who received Rifaximin treatment (Figures 1(a) and 1(b)). These data suggest that, in the lack of antimicrobial treatment, patient with UDD experiences an increase of TLRs expression.

In the sigmoid mucosa, at baseline, the percentages of TRL2 lymphocytes were lower () in patients than in controls, while TLR4 showed no significant differences (Figures 1(c) and 1(d)). In patients after Rifaximin, in a pattern similar to that observed in the peripheral blood, patients expressed significantly reduced percentages of both TLR2 and TLR4 ( and , resp.) in comparison to values observed in placebo treated patients (Figures 1(c) and 1(d)). Our data suggest that Rifaximin treatment contributes to maintain stable levels of TLRs and this is possibly related to the control of intestinal microflora.

Since the transverse mucosa of patients with UDD is supposed to be normal, lymphocytes in the transverse mucosa were studied as controls. In fact, no significant differences were observed before and after Rifaximin treatment (Figure 1(e)).

For a better understood role of TLR2 and TLR4 we also analyzed the subpopulations CD4 and CD8 lymphocytes as reported in Table 2.

Table 2: TLRs phenotype in CD4 and CD8 lymphocytes subpopulation.

PBMC
Sigma
Transverse

CD4 TLR2
CD8 TLR2
CD4 TLR4
CD8 TLR4
CD4 TLR2
CD8 TLR2
CD4 TLR4
CD8 TLR4
CD4 TLR2
CD8 TLR2
CD4 TLR4
CD8 TLR4

CTR

PZ

BR

AR

BP

ND
ND
ND
ND

AP

ND
ND
ND
ND

The values are reported as Mean ± SEM , , patients versus control (health or baseline); , between treatments. Healthy control (CTR), UDD patients (PZ), before Rifaximin (BF), after Rifaximin (AR), before placebo (BP), and after placebo (AP).

TLR2 and TLR4 were analyzed in PBMC and sigma mucosa of same patient. To clarify the way in which the modulation of TLR2 and TLR4 in PBMC and sigma mucosa occurred, we compared the modulation of TLR2 and TLR4 expression between PBMC and gut in the different patient groups (BR and AR and BP and AP) (Figure 2). We observed the same trend of TLRs modulation in both the mucosa and the PBMC.

(a)

(b)

(c)

(d)

Figure 2: Modulation of TLR2 and TLR4 lymphocytes in PBMC and gut. (a, b) The comparison of modulation of TLR2 and TLR4 expression in the different patient groups between PBMC and gut (before and after placebo or Rifaximin). (c-d) Modulation of TLR2 and TLR4 expression observed in a single representative patient. The values reported in box-and-whiskers plots show the minimum, the 25th percentile, the median, the 75th percentile, and the maximum. In particular, the whiskers go down to the smallest value (minimum) and up to the largest one (maximum), the top and bottom of the box are the 25th and 75th percentiles, and the line in the middle of the box is the median, corresponding to 50th percentile, evaluated before Rifaximin (BR), after Rifaximin (AR), before placebo (BP), and after placebo (AP).

We observed coexpression of TRL2 and TLR4 on lymphocyte in both PBMC and sigma mucosa of the same patient. Moreover, we reported that the modulation of TLR2 and TLR4 correlated in PBMC (95% confidence interval 0.21 to 0.447; ; ) and in transverse mucosa (95% confidence interval 0.052 to 0.687; ; ), but not in sigma mucosa (95% confidence interval −0.334 to 0.256; ; ).

The phenotype of TLR lymphocytes was also evaluated for the CD4 and CD8 lymphocytes subpopulations to better understand the effect of Rifaximin in UDD patients; the results are summarized in Table 2. We show that both TLR2-CD8 and TLR2-CD4 cells were increased in patients PBMC as compared to controls. In the sigma mucosa, after Rifaximin, TLR4-CD4 cells were significantly reduced.

In peripheral blood, at baseline, no changes were found in TRL2 monocytes (CD14+) percentages. The percentages of TRL4 monocytes were lower () in patients with respect to controls (Figures 3(a) and 3(b)). After Rifaximin treatment the percentages of TRL2/CD14+ increased significantly () with respect to before Rifaximin (Figure 3(a)); no changes were found in TRL4 monocytes percentages (Figure 3(b)).

(a)

(b)

(c)

(d)

(e)

(f)

Figure 3: Expression of TLRs in monocytes and granulocytes. (a, b) Percentage of TLR2 and TLR4 monocytes in peripheral blood, at baseline and after Rifaximin and placebo treatments. (c, d) Median of fluorescence (MFI) of TLR2 and TLR4 monocytes in peripheral blood at baseline and after Rifaximin and placebo treatments. (e, f) MFI of TLR2 and TLR4 granulocytes in peripheral blood at baseline and after Rifaximin and placebo treatments. The values reported in box-and-whiskers plots show the minimum, the 25th percentile, the median, the 75th percentile, and the maximum. In particular, the whiskers go down to the smallest value (minimum) and up to the largest one (maximum), the top and bottom of the box are the 25th and 75th percentiles, and the line in the middle of the box is the median corresponding to 50th percentile (, , and patients versus controls (health or baseline)). Healthy control (CTR), UDD patients (PZ), before Rifaximin (BR), after Rifaximin (AR), before placebo (BP), and after placebo (AP).

Analysis of MFI showed that, in monocytes, the TLR4 MFI baseline was significantly lower than control (), while after Rifaximin treatment no change was found (Figure 3(d)). On the other hand, TLR2 MFI was increased after placebo (), while remained unchanged in the after Rifaximin patients. In granulocyte populations, at baseline TRL2 MFI decreased (), while TLR2 MFI increased after placebo () (Figure 3(e)). All these findings suggest that Rifaximin treatment contributes to maintain stable levels of TLRs and possibly related to the control of intestinal microflora.

We did not find any correlation between TLRs expression in lymphocytes and monocytes; instead, we found correlations for both TLR2 and TLR4 in monocytes and granulocytes; in fact, the direct associations were found between MFI monocytes and MFI granulocytes in UDD patients at T0 (TLR2 correlation coefficient: 0.530, ; TLR4 correlation coefficient: 0.478, ).

3.2. CD103 Lymphocytes

CD103 is a gut homing receptor present on the surface of lymphocytes and marks gut-homing recruitment of lymphocytes. We analyzed CD103 expression in peripheral blood and in sigmoid and transverse mucosa TILs.

Considering both mucosal CD4 and CD8/CD103 cells, no significant variations were observed between patients and controls in colonic tissue (data not shown). In peripheral blood, in UDD patients, we found an increased recruitment of CD103 lymphocytes (as reported in our previous work (8)). When we evaluated CD4/CD103 and CD8/CD103 in sigma mucosa before and after Rifaximin treatment, we did not find any change. However, in patients treated with placebo the percentage of CD8/CD103 lymphocytes was lower after placebo () than before placebo (Figure 4(b)). This suggests that Rifaximin may keep a constant homing flux to the sigma of the CD8 cells.

(a)

(b)

(c)

Figure 4: Expression of CD103 in lymphocytes of sigma mucosa. (a) Percentage of CD103 in CD4 lymphocytes subpopulation after Rifaximin and placebo treatments. (b) Percentage of CD103 in CD8 lymphocytes subpopulation after Rifaximin and placebo treatments. (c) Percentage of TCR-gamma/delta CD103 lymphocytes subpopulation after Rifaximin and placebo treatments. The values reported in box-and-whiskers plots show the minimum, the 25th percentile, the median, the 75th percentile, and the maximum. In particular, the whiskers go down to the smallest value (minimum) and up to the largest one (maximum), the top and bottom of the box are the 25th and 75th percentiles, and the line in the middle of the box is the median corresponding to 50th percentile ( before versus after treatments in patients); before Rifaximin (BR), after Rifaximin (AR), before placebo (BP), and after placebo (AP).

The gamma/delta T cells are abundant in the gut mucosa. We therefore evaluated these cells in combination with the homing marker CD103 in TILs derived from sigma of UDD patients.

After treatment with Rifaximin the percentages of the sigma CD103 TCR-gamma/delta lymphocytes decreased significantly () with respect to the before Rifaximin percentages, while no differences were found in patients treated with placebo (Figure 4(c)).

No correlations were found between TLRs and CD103 expression in TCR-gamma/delta lymphocytes.

4. Discussion

We have investigated bacterial ligands TLR2 and TLR4 and other markers in peripheral blood and mucosa and on lymphocytes, monocytes, and granulocytes of patients with UDD before and after antibacterial treatment. Several abnormalities of TLRs can be reversed by Rifaximin treatment.

We showed that UDD induces significant modifications of TLR2 and TLR4 expression on several immune system cell subpopulations isolated from both peripheral blood and affected mucosa as compared with controls. Since TLR2 and TLR4 are receptors for ligands present on bacterial walls, we reasoned that antibiotic treatment could reverse colonic inflammation associated with UDD. Rifaximin treatment induced significant modifications of several altered conditions: either restoring the values observed in controls, or limiting the deviations from normal range observed after 2-month placebo treatment. Diverticula, even when not acutely inflamed, represent an anatomical abnormality where excessive growth of bacteria occurs. This may lead to clinical symptoms. We have previously shown that both clinical symptoms and immunological abnormalities can be ameliorated by a short course of Rifaximin [8].

TLR2 and TLR4 are not constitutively expressed on human T cell surface, but their expression requires activation of T cells by TCR complex [16]. We have previously reported increased CD25+ cells in UDD peripheral blood [8]. Accordingly, we showed that TLR2 and TLR4 lymphocytes in the peripheral blood are increased in patients versus controls suggesting more activated circulating T cells in peripheral blood.

TLRs are involved in the activation of NF-kB [17]. Moreover, NF-B is a critical factor in antibacterial defense [18] and activates the secretion of proinflammatory cytokines resulting in a Th1 response [19]. Thus, Rifaximin keeping under control the activation of TLRs may also limit the triggering of Th1 adaptive immune response. These findings suggest that Rifaximin also has a systemic action on immune system.

In the sigmoid mucosa, percentages of TLR2 and TLR4 lymphocytes are decreased in patients and remain stable after Rifaximin, while we observed an increase of these populations after placebo. It may be suggested that in UDD immunotolerance to commensal bacteria and short-term TLRs activation impairment might be related to increased inflammation that leads to the development of symptoms in UDD. No differences were observed in modulation of TLR2 and TLR4 lymphocytes between PBMC and sigma mucosa. However, data showing that TLR2 and TLR4 increase in time in after placebo patients suggest that the TLRs defect is not constitutive, but it is limited to the stage of early activation. This mechanism can be the result of a lack of lymphocytes activation since TLR2 is expressed in activated cells [16]. Alternatively, lymphocytes in UDD patients recognize the antigens through adaptive immune response, which requires time to be activated, rather than through innate immunity. Thus, our results of reduced TLR2 expression in sigmoid mucosa could be explained by the delayed activation. In fact, in after placebo patients TLR2 expression is increased. It is interesting to note that we observed a reduced TLR2 expression only in TILs and not in peripheral blood. Our data are similar to evidences in the pleural fluid of patients with tuberculosis infection [19] and filariasis [20], suggesting that downregulation of TLRs at the site of infection and not in the periphery may be connected with a reduction in the secretion of proinflammatory cytokines [19]. Alternatively, an involvement of the T regulatory cells (Tregs) could be proposed [21]. The agonists of TLRs may enhance Tregs proliferation, rendering Tregs transiently nonsuppressive [22].

Finally, we have shown as Rifaximin controls the activation of TLRs in TILs. This may limit the triggering of Th1 adaptive immune response. Limiting the activation of Th1 immune response, involved in the pathogenesis of several inflammatory diseases [23, 24], may be a mechanism by which Rifaximin acts as an anti-inflammatory agent in addition to its antibiotic effect [25].

We have also shown that both TLR2-CD8 and TLR2-CD4 cells were increased in patients PBMC as compared to controls. We hypothesize that, as in UDD bacterial infections are more frequent, lymphocytes expressing TLR2 and TLR4 are already mobilized and ready to mount the immune-response. After Rifaximin, TLR-CD4 cells are significantly reduced in sigmoid mucosa, thus confirming the indirect role of the antibiotic on mucosal immunity. In fact, the reduced number of TLR4-CD4 lymphocytes may be related to the fact that, after antibiotic treatment, there is a reduced need of TLR4-CD4 cells which are important in immune responses against bacteria. CD4 cells are instrumental in starting immune response to produce specific antibodies, cell to cell cross talking through production of cytokines, delivering activation signals and induction of activation markers. The TLR2-CD4 cells are also reduced, but this reduction is not significant. This suggests a similar trend for both TRL2-CD4 and TLR4-CD4 cells. However our data show that Rifaximin prevalently acts on TLR4-CD4 cells. Only further studies may clarify the different responses of CD4 cells to the antibiotic.

Monocytes and granulocytes are essential cells in the innate immune response and reflect the level of inflammation [26]; we therefore analyzed TLRs expression in peripheral blood monocytes and granulocytes.

In monocytes, TLR4 was decreased in peripheral blood both as percentages of cells and MFI, in patients versus controls. These conditions were not modified by Rifaximin. Then, we hypothesized that a defect in TLR4 expression predisposes to diverticular disease by impairing antibacterial defense. This could be related to genetic polymorphism of TLR4 as described by other authors [27, 28]. This reinforces the possibility that, in UDD, the increased bacterial load may contribute to the development of symptoms related to UDD.

Instead, both percentages and MFI of TLR2 monocytes in patients were similar to controls. After Rifaximin TLR2 monocytes were increased in percentage, while TLR2 expression was stable. These results suggest that Rifaximin limits the increase of TLR2 expression, probably in relation to its bactericide action on pathogenic flora. This was reinforced by the increase of MFI expression after placebo, both in monocytes and in granulocytes, which could be related to a stimulation of proinflammatory cytokine and TLR-ligands due to increased bacterial load. Our finding may reflect increased activation of monocytes, as reported [26].

Finally, CD103 cells are lymphocytes homing to the gut tissue [23]. Sigma’s CD103 cells are normal in UDD (data not shown). After placebo, we observed a significant decrease of these cells, while after Rifaximin their percentage remained unchanged, suggesting that Rifaximin can maintain intestinal homing within the normal range. Moreover, the decrease of CD103 cells can be due to cell death, which may be related to insufficient recruitment.

Furthermore, we analyzed the involvement of gamma-delta T cells both in peripheral blood and in tissue. Gamma-delta T cells exert a regulatory function. These cells are a minor population in the peripheral blood but constitute a major population among intestinal intraepithelial lymphocytes [29]. Thus, we focused on gamma-delta T cells expressing the intestinal homing receptor CD103 [23].

After Rifaximin, mucosal CD103 positive gamma-delta T-cells were reduced and our data suggest that homing gamma-delta cells directly correlate with gut inflammation in UDD and their reduction supports the anti-inflammatory activity of Rifaximin either through the bacterial load reduction or because Rifaximin has been showed to have a direct anti-inflammatory activity, as already reported above. The gamma-delta T cells may be considered as a marker of inflammation, similar to Tregs, as reported in other papers of our group [21, 23, 30]. While our data clearly show the reduction of inflammatory-related features after Rifaximin, only further studies will demonstrate if these effects are due to reduced bacterial growth or due to intrinsic anti-inflammatory activity recently observed with Rifaximin [25]. It is interesting to note that, in the mice, gamma-delta activation is associated with Th17 cells acting through ligation of TLR2 and TLR4 [31].

In summary, we have described a vast immunological pattern of several innate and adaptive cells markers including TLRs, which may be involved in the pathogenesis and clinical course of the diverticular disease, and we have showed its variations before and after the antibiotic therapy with Rifaximin. We suggest that TLRs are modified by the presence of pathogenic flora in UDD. The role of pathogenic flora is supported by the finding that Rifaximin acts in the gut mucosa homeostasis by limiting the activation of TLRs. Furthermore, Rifaximin may also have a luminal anti-inflammatory function modulating the adaptive immune response in an inhibitory sense. Rifaximin keeps under control TLRs expression in peripheral blood suggesting that, in addition to its activity in gut mucosa, it may also have a systemic action on immune system.

We have shown that, in UDD, TLRs and several immune cell populations are altered in patients with respect to controls, suggesting that in UDD inflammation is present even in the absence of severe clinical symptoms.

Abbreviations

AP: | After placebo
AR: | After Rifaximin
BP: | Before placebo
BR: | Before Rifaximin
MFI: | Mean fluorescence intensity
TILs: | Tissue infiltrating lymphocytes
TLRs: | Toll-like receptors
UDD: | Uncomplicated diverticular diseases
WBC: | Whole blood cells.

Conflict of Interests

The authors have no conflict of interests.

Authors’ Contribution

Rossella Cianci, Danilo Pagliari, Simona Frosali, and Franco Pandolfi ideated the experiment, analyzed the samples, analyzed the data, and wrote and corrected the paper. Rossella Cianci and Franco Pandolfi coordinated the project. Paola Cesaro and Lucio Petruzziello recruited patients, performed colonoscopies, and collected histological samples. Fabio Casciano analyzed part of samples. Raffaele Landolfi and Guido Costamagna participated in discussion of results and in writing and correcting the paper.

Acknowledgments

The authors wish to thank Dr. Bernardo Toraldo (Rome) for his help in the design and execution of the study. This work was supported in part by “linea D1” from Catholic University.

References

W. Kruis, E. Meier, M. Schumacher, O. Mickisch, R. Greinwald, and R. Mueller, “Randomised clinical trial: Mesalazine (Salofalk granules) for uncomplicated diverticular disease of the colon—a placebo-controlled study,” Alimentary Pharmacology and Therapeutics, vol. 37, no. 7, pp. 680–690, 2013.

E. Isolauri, Y. Sutas, P. Kankaanpää, H. Arvilommi, and S. Salminen, “Probiotics: effects on immunity,” The American Journal of Clinical Nutrition, vol. 73, supplement 2, pp. 444S–450S, 2001.

G. Barbara, V. Stanghellini, G. Brandi et al., “Interactions between commensal bacteria and gut sensorimotor function in health and disease,” The American Journal of Gastroenterology, vol. 100, no. 11, pp. 2560–2568, 2005.

C. Fiocchi, “Inflammatory bowel disease: etiology and pathogenesis,” Gastroenterology, vol. 115, no. 1, pp. 182–205, 1998.

S. Fiorucci, E. Distrutti, A. Mencarelli, M. Barbanti, E. Palazzini, and A. Morelli, “Inhibition of intestinal bacterial translocation with rifaximin modulates lamina propria monocytic cells reactivity and protects against inflammation in a rodent model of colitis,” Digestion, vol. 66, no. 4, pp. 246–256, 2002.

A. A. Sheth, W. Longo, and M. H. Floch, “Diverticular disease and diverticulitis,” The American Journal of Gastroenterology, vol. 103, no. 6, pp. 1550–1556, 2008.

L. B. Ferzoco, V. Raptopoulos, and W. Silen, “Acute diverticulitis,” The New England Journal of Medicine, vol. 338, no. 21, pp. 1521–1526, 1998.

R. Cianci, F. Iacopini, L. Petruzziello, G. Cammarota, F. Pandolfi, and G. Costamagna, “Involvement of central immunity in uncomplicated diverticular disease,” Scandinavian Journal of Gastroenterology, vol. 44, no. 1, pp. 108–115, 2009.

C. Blandizzi, G. C. Viscomi, A. Marzo, and C. Scarpignato, “Is generic rifaximin still a poorly absorbed antibiotic? A comparison of branded and generic formulations in healthy volunteers,” Pharmacological Research, vol. 85, pp. 39–44, 2014.

S. Akira, “Toll-like receptor signaling,” The Journal of Biological Chemistry, vol. 278, no. 40, pp. 38105–38108, 2003.

D. Werling, O. C. Jann, V. Offord, E. J. Glass, and T. J. Coffey, “Variation matters: TLR structure and species-specific pathogen recognition,” Trends in Immunology, vol. 30, no. 3, pp. 124–130, 2009.

C. Pasare and R. Medzhitov, “Toll-like receptors: linking innate and adaptive immunity,” Advances in Experimental Medicine and Biology, vol. 560, pp. 11–18, 2005.

G. Liu and Y. Zhao, “Toll-like receptors and immune regulation: their direct and indirect modulation on regulatory CD4+ CD25+ T cells,” Immunology, vol. 122, no. 2, pp. 149–156, 2007.

I. Caramalho, T. Lopes-Carvalho, D. Ostler, S. Zelenay, M. Haury, and J. Demengeot, “Regulatory T cells selectively express toll-like receptors and are activated by lipopolysaccharide,” Journal of Experimental Medicine, vol. 197, no. 4, pp. 403–411, 2003.

A. Cottalorda, B. C. Mercier, F. M. Mbitikon-Kobo et al., “TLR2 engagement on memory CD8+ T cells improves their cytokine-mediated proliferation and IFN-γ secretion in the absence of Ag,” European Journal of Immunology, vol. 39, no. 10, pp. 2673–2681, 2009.

M. Komai-Koma, L. Jones, G. S. Ogg, D. Xu, and F. Y. Liew, “TLR2 is expressed activated T cells as a costimulatory receptor,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 9, pp. 3029–3034, 2004.

I. Siddique and I. Khan, “Mechanism of regulation of Na-H exchanger in inflammatory bowel disease: role of TLR-4 signaling mechanism,” Digestive Diseases and Sciences, vol. 56, no. 6, pp. 1656–1662, 2011.

L. Zhao, M. Kwon, S. Huang et al., “Differential modulation of nods signaling pathways by fatty acids in human colonic epithelial HCT116 cells,” Journal of Biological Chemistry, vol. 282, no. 16, pp. 11618–11628, 2007.

C. Prabha, P. Rajashree, and D. D. Sulochana, “TLR2 and TLR4 expression on the immune cells of tuberculous pleural fluid,” Immunology Letters, vol. 117, no. 1, pp. 26–34, 2008.

S. Babu, C. P. Blauvelt, V. Kumaraswami, and T. B. Nutman, “Cutting edge: diminished T cell TLR expression and function modulates the immune response in human filarial infection,” Journal of Immunology, vol. 176, no. 7, pp. 3885–3889, 2006.

G. Cammarota, F. Pandolfi, R. Cianci, D. Pagliari, R. Landolfi, and S. Kunkel, “Cellular mediators of inflammation: tregs and T H 17 cells in gastrointestinal diseases,” Mediators of Inflammation, vol. 2009, Article ID 132028, 2009.

P. T. Liu, S. Stenger, H. Li et al., “Toll-like receptor triggering of a vitamin D-mediated human antimicrobial response,” Science, vol. 311, no. 5768, pp. 1770–1773, 2006.

R. Cianci, G. Cammarota, and G. Frisullo, “Tissue-infiltrating lymphocytes analysis reveals large modifications of the duodenal immunological niche in coeliac disease after gluten-free diet,” Clinical and Translational Gastroenterology, vol. 3, p. e28, 2012.

T. Olsen, R. Rismo, G. Cui, R. Goll, I. Christiansen, and J. Florholmen, “TH1 and TH17 interactions in untreated inflamed mucosa of inflammatory bowel disease, and their potential to mediate the inflammation,” Cytokine, vol. 56, no. 3, pp. 633–640, 2011.

A. Mencarelli, M. Migliorati, M. Barbanti et al., “Pregnane-X-receptor mediates the anti-inflammatory activities of rifaximin on detoxification pathways in intestinal epithelial cells,” Biochemical Pharmacology, vol. 80, no. 11, pp. 1700–1707, 2010.

R. Salomão, P. S. Martins, M. K. C. Brunialti et al., “TLR signaling pathway in patients with sepsis,” Shock, vol. 30, supplement 1, pp. 73–76, 2008.

A. Abu-Maziad, K. Schaa, E. F. Bell et al., “Role of polymorphic variants as genetic modulators of infection in neonatal sepsis,” Pediatric Research, vol. 68, no. 4, pp. 323–329, 2010.

D. M. Agnese, J. E. Calvano, S. J. Hahm et al., “Human toll-like receptor 4 mutations but not CD14 polymorphisms are associated with an increased risk of gram-negative infections,” Journal of Infectious Diseases, vol. 186, no. 10, pp. 1522–1525, 2002.

A. S. Ismail, K. M. Severson, S. Vaishnava et al., “Gammadelta intraepithelial lymphocytes are essential mediators of host-microbial homeostasis at the intestinal mucosal surface,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 21, pp. 8743–8748, 2011.

R. Cianci, D. Pagliari, R. Landolfi et al., “New insights on the role of T cells in the pathogenesis of celiac disease,” Journal of Biological Regulators and Homeostatic Agents, vol. 26, no. 2, pp. 171–179, 2012.

A. Zuo, D. Liang, H. Shao, W. K. Born, H. J. Kaplan, and D. Sun, “In vivo priming of IL-17+ uveitogenic T cells is enhanced by Toll ligand receptor (TLR)2 and TLR4 agonists via γ δ T cell activation,” Molecular Immunology, vol. 50, no. 3, pp. 125–133, 2012.