Background Helicobacter pylori-induced peptic ulceration is less likely to occur in patients with a strong gastric anti-inflammatory regulatory T cell (Treg) response. Migration of Tregs into the gastric mucosa is therefore important.
Objective To identify the homing receptors involved in directing Tregs to the gastric mucosa, and investigate how H pylori stimulates the relevant chemokine responses.
Design Gastric biopsy samples and peripheral blood were donated by 84 H pylori-infected and 46 uninfected patients. Luminex assays quantified gastric biopsy chemokine concentrations. Flow cytometry was used to characterise homing receptors on CD4+CD25hi Tregs. H pylori wild-type and isogenic mutants were used to investigate the signalling mechanisms behind CCL20 and IL-8 induction in gastric epithelial cell lines. Transwell assays were used to quantify Treg migration towards chemokines in vitro.
Results CCL20, CXCL1-3 and IL-8 concentrations were significantly increased in gastric biopsy samples from H pylori-infected patients. CCR6 (CCL20 receptor), CXCR1 and CXCR2 (IL-8 and CXCL1-3 receptors) were expressed by a higher proportion of peripheral blood Tregs in infected patients. Most gastric Tregs expressed these receptors. H pylori induced CCL20 production by gastric epithelial cells via cag pathogenicity island (cagPAI)-dependent NF-κB signalling. Foxp3+, but not Foxp3−, CD4 cells from infected mice migrated towards recombinant CCL20 in vitro.
Conclusions As well as increasing Treg numbers, H pylori infection induces a change in their characteristics. Expression of CCR6, CXCR1 and CXCR2 probably enables their migration towards CCL20 and IL-8 in the infected gastric mucosa. Such qualitative changes may also explain how H pylori protects against some extragastric inflammatory disorders.
- HELICOBACTER PYLORI
- T LYMPHOCYTES
- MUCOSAL IMMUNOLOGY
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Significance of this study
What is already known about this subject?
Helicobacter pylori infection is the major cause of peptic ulcer disease and gastric adenocarcinoma.
Individuals infected with H pylori have increased populations of immunosuppressive regulatory T cells (Tregs) in their gastric mucosa.
Those with an insufficient Treg response tend to have greater levels of inflammation in the gastric mucosa, and are more likely to develop peptic ulcer disease.
What are the new findings?
The concentration of the chemokine CCL20 is dramatically increased in the gastric mucosa of patients infected by H pylori and the vast majority of mucosal Tregs express its receptor CCR6.
Gastric biopsy samples from patients infected with cag+ strains contain higher concentrations of CCL20. CCL20 expression is induced in gastric epithelial cells in a cag type IV secretion system dependent manner.
Recombinant CCL20 induces the migration of Tregs in vitro, demonstrating its importance as a chemoattractant for these cells.
Homing receptor profiles of circulating Tregs differ between infected and uninfected patients. H pylori therefore imparts qualitative differences to these populations.
How might it impact on clinical practice in the foreseeable future?
This work indicates the importance of the CCL20–CCR6 axis in the recruitment of Tregs to the gastric mucosa. As this axis is also important in IBD, the study might contribute to the development of new treatments to suppress gastrointestinal inflammation.
Helicobacter pylori colonises the stomach in around half of the world's population.1 In most cases the infection is established during childhood and persists lifelong.2 This chronic infection leads to continuous low-level gastric inflammation, which is asymptomatic in most cases. However, some people develop more pronounced inflammation, which can lead to peptic ulcer disease (PUD) or gastric cancer.3 By understanding the factors which influence the inflammatory response to H pylori and gastric infiltration of immune cells, we may be able to identify those who are at increased risk of developing disease.
Proinflammatory chemokines and cytokines, such as interleukin 8 (IL-8), are secreted by gastric epithelial cells in response to H pylori infection, leading to immune cell recruitment.2 H pylori expresses virulence determinants, including the polymorphic vacuolating cytotoxin gene A (vacA) and the cag pathogenicity island (cagPAI), which influence disease risk.1 The cagPAI encodes a type IV secretion system (T4SS), which delivers the effector protein CagA and soluble bacterial cell wall components into host cells.4 Inflammatory signalling pathways are activated directly by CagA or through NOD1-recognition of cell wall components.5 ,6 The resulting cytokine production leads to increased mucosal infiltration of neutrophils, macrophages and proinflammatory T-helper subsets including Th1 and Th17 cells and an increased risk of PUD.5 ,7
One of the major modulators of inflammation is the subset of CD4 T cells known as regulatory T cells (Tregs). These cells suppress both innate and adaptive immune responses, and inhibit the activity of T-helper cells.8 Previously we showed that CD4+CD25hi cells are more abundant in the gastric mucosa of H pylori-infected patients, and that poor Treg responses are associated with PUD.9 Recruitment of Tregs to the gastric mucosa is important for controlling inflammation and pathology.9–12
We previously found that Tregs are also more abundant in the peripheral blood of H pylori-infected patients.13 This population of Tregs appears to have slightly different characteristics from those found in the gastric mucosa, in that not all peripheral blood CD4+CD25hi cells express FOXP3. We hypothesised that some peripheral blood Treg populations in infected patients are programmed for homing to the inflamed gastric mucosa.
The chemokines CCL2, CCL4, CCL5, CCL22 and CXCL8 are known to play a role in the migration of Tregs into inflamed or tumour tissues.14–16 Others, including CCL2-5, CCL20 CCL22, CXCL1-3, CXCL8 and CXCL10 are upregulated in the H pylori-infected gastric mucosa,5 ,17–20 and expression of chemokine receptors and other adhesion molecules by immune cells is also increased.10 ,21 ,22 Our first step was to narrow down this array of homing molecules and receptors to those that might be important in Treg migration to the H pylori-infected gastric mucosa.
We began this study by quantifying chemokines in gastric biopsy lysates and found that IL-8, CCL20 and CXCL1-3 concentrations were the most upregulated in biopsy samples from infected compared with uninfected patients. We then went on to screen peripheral blood Tregs for a panel of homing receptors. We identified altered profiles of the chemokine receptors CCR6, CXCR1 and CXCR2 on Tregs from infected patients. Next, we defined the signalling pathways involved in H pylori-mediated induction of CCL20 expression by gastric epithelial cell lines. Finally, we showed that Tregs from infected mice can migrate towards CCL20 in vitro. These findings show that Tregs can be recruited by the gastric mucosal chemokine response to H pylori. This mechanism of Treg recruitment may be important for controlling inflammation and reducing cancer risk among people infected with H pylori.
Materials and methods
Reagents and chemicals were obtained from Sigma-Aldrich (Poole, UK) and fluorochrome-conjugated antibodies were obtained from BioLegend (San Diego, USA), unless otherwise stated.
Participants and clinical materials
Samples were donated by 180 patients (aged 18–86 years) undergoing routine upper gastrointestinal endoscopy at Queen's Medical Centre, Nottingham, UK (collected 2002–2012) after approval by the Nottingham Research Ethics Committee 2 from an unselected patient group, for whom H pylori status could be confirmed and the appropriate clinical materials were available. Patients presented with a variety of indications, most commonly dyspepsia, but were otherwise healthy. None of the patients were regularly taking non-steroidal anti-inflammatory drugs or other immunomodulatory drugs in the preceding 4 weeks, or antibiotics or proton pump inhibitor drugs during the preceding 2 weeks.
Blood samples and a series of eight gastric antral biopsy samples were collected with informed written consent.9 Complete sets of blood and biopsy samples were not available for all subjects. H pylori status was determined by rapid biopsy urease test, bacterial culture and histology. H pylori isolates were cagA genotyped as previously described.23 Clinical endoscopy observations were recorded. Uninfected donors had no gastric inflammation or disease.
Chemokine concentrations were measured by Luminex (see online supplementary methods) in antral gastric biopsy samples from 84 H pylori-infected donors (31 duodenal ulcer, 5 gastric ulcer, 48 without ulceration) and 39 uninfected donors and normalised for total protein.24 These groups were 52% and 46% male, respectively; mean ages 53.5 and 54.0 years.
Cell isolation and analysis by flow cytometry
Samples from 35 H pylori-infected donors (10 duodenal ulcer, 1 gastric ulcer, 24 without ulceration) and 46 uninfected donors were analysed by flow cytometry. These groups were 64% and 52% male, respectively; mean ages 51.0 and 53.6 years.
Six gastric biopsy samples were collected into culture medium (RPMI 1640/10% fetal calf serum/100 U/mL penicillin G/100 μg/mL streptomycin sulfate), rubbed through a sterile disposable 100 μm cell strainer (BD Biosciences, Oxford, UK), washed and resuspended at 1×106/mL.9 Peripheral blood mononuclear cells (PBMCs) were purified by density gradient centrifugation using Histopaque-1077 and resuspended at 1×106/mL.
Extracellular staining using anti-CD4-phycoerythrin (PE)-Texas Red (ECD; Beckman Coulter, High Wycombe, UK) and anti-CD25-PE-cyanin 7 (Pc7) with anti-CD127-PE, anti-CD62L-PE (eBioscience, San Diego, USA), anti-integrin αE-PE (eBioscience), anti-CCR10-PE, anti-CXCR1-PE or anti-intergrin β7-PE (eBioscience) and anti-CCR6-Alexa Fluor 647 (A647), anti-CCR7-A647, anti-CCR9-A647 or anti-CXCR2-A647 was carried out before cells were fixed in 0.5% formaldehyde. FOXP3 Perm buffer set (BioLegend) permeabilised cells were stained with anti-FOXP3-Alexa Fluor 488 (A488). Data on 200 000 events were acquired using a Beckman Coulter Cytomics FC500 and analysed with Weasel V.3.0, using appropriate isotype controls.
Cell lines and bacterial strains
The human gastric epithelial MKN28 and AGS (ATCC CRL-1739) cell lines were maintained in RPMI 1640 and nutrient mixture F12 Ham medium, respectively, supplemented with 10% heat inactivated fetal calf serum and 2 mM L-glutamine (Invitrogen) at 37°C in a 5% CO2 humidified atmosphere.
H pylori strains were cultured on Blood Agar Base No 2 containing 5% (vol/vol) horse blood (Oxoid, Cambridge, UK) at 37°C under microaerobic conditions. cagPAI+ H pylori strains 60190, 84183,25 26695, B128 7.13 and the cagPAI− strains SS126 and Tx30a25 were used, along with isogenic mutants deficient in vacA (60190ΔvacA, 84183ΔvacA), cagA (60190ΔcagA, 84183ΔcagA) and cagE (60190ΔcagE, 84183ΔcagE). A slt (HP0645) deletion mutant (26695Δslt) and 26695 parental strain were kindly donated by Dr Richard Ferrero, Monash University, Victoria, Australia.6
In vitro culture experiments
24-Well culture plates were seeded with 5×104 cells/well 24 h before experiments. An H pylori suspension was added to a multiplicity of infection (MOI) of five bacteria for each epithelial cell, and cultures were incubated for a further 24 h. MOIs were confirmed by viable cell counts. Cell culture supernatants were aliquoted and frozen at −80°C.
Human CCL20/MIP-3α ELISA (R&D Systems, Abingdon, UK) and Human IL-8 CytoSet ELISA (Invitrogen, Paisley, UK) kits were used, with a standard curve on each plate.
Inhibitor studies and siRNA transfections
Epithelial cells were treated with chemical inhibitors or siRNA duplexes as previously described.27 Specific chemical inhibitors—U0126 (10 μM; MEK1 inhibitor), SP600125 (10 μM; c-Jun-N-terminal kinase (JNK) inhibitor), SB203586 (10 μM; p38 inhibitor) and 6-amino-4-(4-phenoxyphenylethylamino) quinazoline (1 μM; NF-κB activation inhibitor)—were added to the cells for 1 h before and throughout 24 h infection. Control cells were treated with 50 ng/mL of recombinant tumour necrosis factor α (TNFα) (PeproTech, Rocky Hill, USA) to activate NF-κB.9
Validated siRNA duplexes targeting NFKB1, RELA and mitogen-activated protein kinase 1 (MAPK1) mRNA using HiPerfect transfection regent (QIAGEN, Hilden, Germany) were added to the cells 48 h before 24 h infection. Control cells received HiPerfect only, non-silencing AllStars Hs Negative Control siRNA or AllStars Hs Cell Death Control siRNA. Gene knockdowns were confirmed by western blotting using NF-κB p50 (Cell Signalling Technology Inc, Massachusetts, USA), NF-κB p65 (Merck Millipore, Darmstadt, Germany), extracellular signal-regulated kinase (ERK) (Santa Cruz Biotechnology, Santa Cruz, USA) and anti-actin antibodies.
Animal experiments were approved by the University of Nottingham animal welfare and ethical review body, under UK Home Office Licence 40/3399. Foxp3-green fluorescent protein (GFP) C57/BL6 mice (JAX strain B6.Cg-Foxp3tm2(EGFP)Tch/J)28 were infected by oral gavage on three alternate days with doses of 1 × 109 H pylori strain B128 7.13 in 100 µL Isosensitest broth (Oxoid).11 After 3 weeks mice were humanely killed, their spleens were removed and rubbed through a sterile disposable 100 μm cell strainer. Cells were enriched using an EasySep Mouse CD4 T cell enrichment kit (StemCell Technologies, Vancouver, Canada), and sorted into GFP+ and GFP− populations using a MoFlo XDP flow cytometer (Beckman Coulter). Infection was confirmed using quantitative culture of stomach tissue homogenate, as described previously.29 The median colonisation density for the infected mice was 1.31×105 colony-forming units/g (range 0.625–3.88×105) and colonies were confirmed as H pylori by urease tests and Gram staining.
Migration assays were performed using 96-well Transwell plates with a 5.0 µm polycarbonate membrane (Corning Life Sciences, Corning, USA).30 Culture medium (150 μL) with or without 500 ng/mL of recombinant mouse CCL20 was placed in the lower chamber.31 Culture medium (100 μL) containing 1×105 cells was placed in the upper chamber. Each experiment was performed in triplicate. After 5 h, migrated cells in the lower chamber were counted. Migration index was calculated by dividing the number of migrated cells by the mean migration seen in the medium-only control wells.
Statistical analyses were carried out using Prism 6.00 (GraphPad Software, California, USA). A two-tailed p value ≤0.05 was taken as significant. In vivo data were displayed in box-and-whisker plots showing median, IQR and total range, and compared using Mann–Whitney U tests. In vitro data were described using means and SDs, and analysed using one-way analysis of variance with Dunnett's post hoc test for multiple comparisons.
CCL20, IL-8 and CXCL1-3 concentrations were greatly elevated in H pylori-infected gastric biopsy samples
We began by identifying chemokines which were the most upregulated during H pylori infection. The chemokine concentrations in gastric biopsy samples from infected and uninfected patients were measured using Luminex assays. Most were upregulated during infection; however, the greatest increases were in CCL20 (MIP-3α), CXCL1-3 (GROα, β and γ) and CXCL8 (IL-8). The median concentrations in biopsy samples from infected patients were 9.5-fold higher for CCL20 (p<0.0001) and 14.8-fold higher for IL-8 (p<0.0001) compared with those from uninfected patients (figure 1). The chemokines CXCL1-3 are >90% homologous and this kit could not distinguish between them; however, we observed that their combined median concentrations were 6.1-fold higher (p<0.0001) in infected patients. Other chemokines were increased by only 1.7–3.1-fold.
Peripheral blood Treg homing receptor profiles are altered in H pylori-infected patients
Having identified the chemokines most upregulated during infection, we examined homing receptor expression profiles on circulating Tregs and whether these were altered in infected patients. We hypothesised that differences in peripheral blood Treg homing receptor profiles in the infected patients might indicate receptors which contribute to Treg migration to the infected gastric mucosa.
PBMCs from 18 H pylori-infected and 20 uninfected patients were analysed using flow cytometry. Gating on lymphocytes from forward and side scatter plots, Tregs were defined as CD4+CD25hi events. The CD25hi gate was set corresponding to the position of CD127lo and FOXP3+ events (figure 2A,B). Using these gating criteria, the proportion of CD4+CD25hi events among the lymphocyte population was significantly higher in the H pylori-infected patients (p=0.02) (figure 2C).
PBMCs were then analysed for a panel of homing receptors using flow cytometry (figure 3). The proportion of CD4+CD25hi events expressing each homing receptor varied widely (figure 3C). When examining cells from all patients together, a median of 94% of the CD4+CD25hi events expressed CD62L, 57% were CCR6+ and 34% CCR10+. Less than 10% expressed CCR7, CCR9, CXCR1, CXCR2 or integrins αE and β7. Some receptors varied according to H pylori status. Compared with uninfected patients, a significantly higher proportion of CD4+CD25hi events from infected patients were CCR6+ (medians: 46.7% and 63.2% respectively, p=0.034), CXCR1+ (medians: 0.7% and 9.8%, p=0.040) and CXCR2+ medians: 0.2% and 4.0%, p=0.040). Given these results we concentrated further investigations on the role of CCR6 (CCL20 receptor), CXCR1 and CXCR2 (IL-8 and CXCL1-3 receptors).
Most gastric mucosal Tregs express CCR6 and many express IL-8 receptors
We next examined if CCR6, CXCR1 and CXCR2 were also present on gastric Tregs. Gastric biopsy lymphocytes from 18 infected and 26 uninfected patients were stained for CCR6, CXCR1 and CXCR2 and analysed using flow cytometry (figure 3D). Over 90% of the CD4+CD25hi events from gastric biopsy samples expressed CCR6, regardless of H pylori status. The proportions of CD4+CD25hi cells expressing CXCR1 and CXCR2 were also higher in the gastric biopsy samples than the PBMCs (72.6% and 57.8%, respectively), but there was no significant difference between the infected and uninfected patients. The total number of CD4+CD25hi and CD4+CD25hiCCR6+ events in biopsies from each patient was calculated (figure 3E). As previously described the number of CD4+CD25hi events was increased in infected patients (median 4921) compared with uninfected patients (median 1025; p=0.014). Biopsy samples from H pylori-infected patients also contained significantly increased numbers of CD4+CD25hiCCR6+ events (medians 837.5 and 4754, respectively; p=0.021). These results show that Tregs in the gastric compartment are enriched for those expressing CCR6, CXCR1 and CXCR2, and suggest that they may direct Treg homing to the mucosa.
H pylori-induced CCL20 and IL-8 expression by gastric epithelial cell lines is cagT4SS dependent
Next, we used two human gastric epithelial cell lines to examine the role of H pylori virulence factors in inducing the CCL20 response in vitro. We also examined IL-8 which, unlike CXCL1-3, is a T cell chemoattractant, and has been shown to be predominantly induced by the cagT4SS.6 Our biopsy data suggest that CCL20 induction may also be dependent on the cagT4SS; therefore IL-8 responses were measured as a control. MKN28 and AGS cells were infected with H pylori at a MOI of five bacteria per cell for 24 h before assaying CCL20 and IL-8 production. Compared with uninfected AGS cells, CCL20 concentrations were significantly increased by co-culture with strains 60190 (3.8-fold, p=0.005), 84183 (7.5-fold, p<0.001), 26695 (11.2-fold p<0.0001) and B128 (3.3-fold, p=0.011) (figure 4A). These strains all have an intact cagPAI and express the active s1/m1 form of VacA. In contrast, Tx30a (cagPAI-negative, s2/m2 vacA) and SS1 (defective cagPAI, s2/m2 vacA) did not significantly stimulate CCL20 production above the level of uninfected controls, but induced low-level IL-8 expression (figure 4B).
Cell lines were then co-cultured with isogenic mutants derived from multiple parental stains of H pylori, null for candidate cagPAI genes and vacA. Their effects on CCL20 and IL-8 were similar, but more pronounced in MKN28 than AGS cells (figure 4). The ΔcagA mutants induced less CCL20 than their wild-type parental strains but this was only significant for MKN28 cells (60190ΔcagA:1.4-fold lower, p=0.039; 84183ΔcagA: 1.5-fold, p=0.022). However, deletion of the cagE gene, resulting in a disabled T4SS, led to CCL20 concentrations similar to those of uninfected controls for both cell lines (compared with wild-type for AGS cells, 60190ΔcagE: 9.9-fold lower, p=0.031; 84183ΔcagE: 3.3-fold lower, p=0.001). Disruption of vacA did not alter the levels of CCL20 production. These data suggest that the cagT4SS is necessary for H pylori-induction of CCL20, but this is only partially dependent on CagA delivery.
The cagPAI also induces IL-8 via peptidoglycan activation of NOD1. To determine if this mechanism is also important in CCL20 induction, cells were cultured with an slt null mutant (26695Δslt). This mutant has comparable growth rates to its parental strain, but produces up to 40% less cell wall disaccharide tripeptide owing to a defect in the slt-encoded lytic transglycosylase.6 ,32 The 26695Δslt mutant stimulated 9.9-fold (p<0.0001) and 19.1-fold (p=0.0004) lower CCL20 concentrations than the wild-type by MKN28 and AGS cells respectively (figure 4A,C). A similar decrease in IL-8 was also seen, in line with previous reports.6 ,25 These results show that CCL20 expression is induced by H pylori in a cagT4SS-dependent manner, largely via CagA-independent signalling. In agreement with this, gastric biopsy samples from patients infected with cagA+ strains contained higher CCL20 concentrations (p=0.021) than those infected with a cagA− strain (see online supplementary figure S1).
The NF-κB and MAPK1-pathways are important in H pylori-induced CCL20 expression
We investigated the role of NF-κB and the ERK, p38 and JNK MAP kinase signalling pathways, known to be activated by the cagT4SS.4 MKN28 cells were cultured with H pylori strain 60190 in the presence of specific drug inhibitors for each pathway and the effects on CCL20 and IL-8 production were assessed (figure 5). NF-κB and MEK1 inhibitors significantly reduced induction of CCL20 compared with untreated control wells (10-fold, p=0.0001 and sixfold, p=0.0005, respectively), whereas the effect of the p38 inhibitor did not reach statistical significance. JNK inhibition appeared to increase CCL20 expression (1.9-fold, p=0.0001). Uninfected cells were treated with recombinant TNFα as a positive control activator of NF-κB, which increased CCL20 expression (threefold, p=0.018). The treatments had very similar effects on IL-8 expression. These results confirm the importance of NF-κB and suggest the MAPK1 pathways may also have a significant role in H pylori-induction of CCL20.
To investigate these mechanisms more precisely, MKN28 cells were treated with siRNA duplexes to silence expression of NFKB1 (which encodes the NF-κBp50 subunit), RELA (NF-κBp65) and MAPK1 for 48 h before infection with 60190 H pylori (figure 6A,B). In agreement with the previous data, greatly reduced CCL20 concentrations were seen in infected cells where RELA (11-fold, p<0.001) and MAPK1 (108-fold, p<0.001) expression was knocked down (figure 6B). These duplexes had similar effects on IL-8 expression (figure 6C), suggesting that IL-8 and CCL20 are induced by the same pathways.
Mouse Tregs migrate towards CCL20
To investigate whether CCL20 is a chemoattractant for Tregs, we used Foxp3-GFP transgenic mice as this provides the most reliable means of Treg cell purification. Mice were infected with the cagPAI+ H pylori strain B128, and killed 3 weeks later. As expected there were higher frequencies of CD4+Foxp3+ events in gastric mucosa of infected mice (medians of 0.44% of CD3+ events for uninfected and 1.75% for infected, p=0.002). GFP+ and GFP− CD4+ splenocytes were isolated from infected mice (figure 7A). Flow cytometry analysis showed that 9.5% of the GFP+ Foxp3+ population expressed CCR6, compared with only 0.71% of the GFP− Foxp3− cells (figure 7B). Migration of these populations towards 500 ng/mL recombinant murine CCL20 (rCCL20) was assessed using an in vitro transwell assay (figure 7C). Foxp3− cells did not migrate; however, the Foxp3+ population showed significant migration (p=0.006). This is probably due to the increased proportion of CCR6+ events amongst Foxp3+ cells.
We found that Tregs in human gastric biopsy samples are predominantly CCR6+, which allows them to respond to cagT4SS-induced CCL20 expression during H pylori infection.
This paper provides a number of new findings. For the first time we have described changes in the profiles of chemokine receptors expressed by circulating Tregs from H pylori-infected patients compared with uninfected patients. The association between H pylori and increased proportions of CCR6+, CXCR1+ and CXCR2+ Tregs in the bloodstream allowed us to target these receptors and their chemokine ligands in subsequent experiments. Previous work has concentrated on characterising the expression of homing receptors on gastric T cells during H pylori-induced disease.19–21 Indeed, we found that Tregs isolated from the gastric mucosa are predominantly CCR6+. However, characterising the peripheral Treg response to infection provides two advantages: first, obtaining blood samples from patients is less invasive than endoscopy, giving greater potential for larger study groups; and second, more Tregs can be recovered, allowing more detailed characterisation using multiple markers.
The intriguing finding that more CD4+CD25hicells express CCR6 in the peripheral blood of H pylori-infected patients led us to investigate its ligand, CCL20. We demonstrated that CCL20 levels were increased in the gastric mucosa of H pylori-infected patients, in keeping with previous findings.20 ,33 However, we also showed for the first time that CCL20 concentrations were increased in the infected gastric mucosa by a similar degree to the widely studied chemokine IL-8, and CCL20 levels were much higher. The other chemokines were almost all present at higher concentrations in infected tissue, but their levels were increased threefold at most. This highlights the importance of CCL20 in the mucosal response to H pylori. The high basal levels of CCL20 in the gastric mucosa goes some way to explain why, even in uninfected patients, most gastric Tregs express CCR6. Surprisingly, almost all Tregs isolated from the gastric mucosa expressed CCR6. However, the number of Tregs infiltrating the gastric mucosa is significantly increased in H pylori infection9 and here we show that the number of CCR6+ Tregs in the gastric mucosa of H pylori infected patients is also significantly increased.
We built on previous co-culture experiments which showed that CCL20 mRNA levels in gastric epithelial cell lines were reduced in response to a cagPAI-deficient strain,33 to demonstrate for the first time that peptidoglycan components delivered by the cag T4SS are the major inducers of CCL20 production in gastric epithelial cell lines. A number of different transcription factor binding sites have been described in the CCL20 gene promoter region, including sites for activator protein 1 (AP-1) and NF-κB.34 MEK and NF-κB signalling have been linked to CCL20 induction in response to proinflammatory stimuli in other cell types, including colonic epithelial cells.35 We show that in gastric epithelial cells H pylori peptidoglycan components activate ERK and NF-κB signalling, thus inducing CCL20 in a similar way to that already described for IL-8.6 Previously, the p38 pathway was shown to be important in activation of IL-8 production in response to H pylori peptidoglycan.36 Our data confirm that IL-8 is significantly reduced in cells treated with a p38 inhibitor. However, although we observed that inhibiting the p38 pathway led to a consistent reduction in CCL20 production across the three independent experiments performed, this did not reach statistical significance when all data were combined. Therefore, ERK and NF-κB signalling (and possibly also p38) mediate the induction of CCL20 in response to H pylori peptidoglycan via the cagT4SS, In support of these findings, we observed the highest mucosal CCL20 concentrations in patients infected with a cagA+ strain of H pylori.
Our results suggest that bacterial strains better equipped to interact with their host, such as those with an intact cagT4SS, may more strongly influence the immunoregulatory response. In support of this, we previously showed that patients infected with cagPAI+ H pylori strains had higher levels of IL10 mRNA and increased infiltration of CD4+CD25hi cells in their gastric mucosa.9 These data may appear to be in conflict with the evidence that PUD is more common among individuals infected with cagPAI+ strains.1 Kido et al37 have suggested that the cagT4SS has a dual role in H pylori infection, acting to both promote and suppress gastritis. Using mouse models, they showed that infection, particularly with a CagA+ H pylori strain, was important for inducing the migration of T cells (primed by either CagA+ or CagA− infections) into the gastric mucosa, resulting in gastritis. Conversely, adoptive transfer of T cells first primed by a CagA+ infection led to an accumulation of Tregs in the gastric mucosa of recipient mice and gastritis was attenuated; this did not occur with T cells primed by CagA− H pylori. Their conclusion that the cagT4SS is extremely important for the induction of a protective Treg response is also supported by our findings. In patients infected with a cagPAI+ strain, high cytokine expression leads to gastritis, and we propose that the effect of the cagT4SS on Treg migration becomes more important for controlling this inflammation. Ulcers probably result when there is a deficiency in this process.
Treg migration patterns contribute to the tight control of their anti-inflammatory effects and can be altered during an ongoing response, to target immune suppression.22 ,38 ,39 The altered human Treg homing receptor profiles seen here may be important in controlling the inflammatory response to H pylori. Tregs reduce inflammation to avoid excess damage to the host and, in H pylori infection, inflammation drives disease. Looking at Treg homing might help to identify patients at risk of developing more extensive disease. CCR6 is also expressed by a number of other cell types including dendritic cells and B lymphocytes,40 which also play important roles in the host response to H pylori infection. CCR6 is highly expressed on the proinflammatory Th17 cell type.30 The balance between Th17 and Treg cells is thought to be important in determining the severity of H pylori-mediated gastric inflammation.41 Both Th17 and Tregs preferentially localise to mucosal surfaces through CCL20 signalling, and the CCL20–CCR6 axis is currently the subject of a great deal of research in IBD.42 ,43 Similar to our findings, CCL20 expression is elevated in the IBD mucosa, and protection from colitis has been shown to be mediated by CCR6+ Tregs.44 ,45 There is growing evidence that H pylori infection is negatively associated with IBD,46 ,47 but if this is the case the mechanism remains unclear. Induction of CCR6+ Tregs by H pylori may result in their migration towards CCL20 expressed in the stomach and the intestine to modulate inflammation. Future work therefore needs to elucidate the role of the CCL20–CCR6 axis in the H pylori-infected gastric mucosa, and its possible influence on IBD.
In summary, we showed that increased proportions of Tregs express the chemokine receptors CCR6, CXCR1 and CXCR2 in the peripheral blood of H pylori-infected individuals. However, the majority of gastric Tregs express CCR6. In gastric biopsy samples CCL20, the only chemokine recognised by CCR6, is increased in response to H pylori and is more abundant than IL-8. CCL20 expression is induced in gastric epithelial cells in a cagT4SS-dependent manner by H pylori via the NF-κB and MAPK pathways. Recombinant CCL20 induces migration of purified mouse Tregs. We are now developing mouse model assays to further characterise the role of the CCL20–CCR6 axis in Treg cell homing in vivo.
We are grateful to Dr Adrian Robins, Mrs Nina Lane and Miss Nicola Croxall for their kind assistance with flow cytometry techniques.
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Correction notice Open Access license has been updated since published Online First.
Contributors KR, KWC and JCA conceived and planned the study. KWC, DPL, RJMI, ES and HS carried out the experimental work. KWC, DPL, RJMI, JCA and KR analysed the data. The manuscript was prepared by KWC and KR, and reviewed and approved by all authors.
Funding This article presents independent research supported by the Medical Research Council—project grant G0601170, Strategic Skills Award Supplement to a doctoral training grant studentship for KWC (G1000401) and clinical research training fellowships for RJMI (G1000311) and ES (G0701377). It was also supported in part by the National Institute for Health Research (NIHR), through the NIHR Biomedical Research Unit in Gastrointestinal and Liver Diseases at Nottingham University Hospitals NHS Trust and the University of Nottingham. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health.
Competing interests None.
Patient consent Obtained.
Ethics approval Nottingham research ethics committee 2.
Provenance and peer review Not commissioned; externally peer reviewed.
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