Inflammatory cytokine and microRNA responses of primary human dendritic cells cultured with Helicobacter pylori strains

Primary human dendritic cells (DC) were used to explore the inflammatory effectors, including cytokines and microRNAs, regulated by Helicobacter pylori. In a 48 h ex-vivo co-culture system, both H. pylori B38 and B45 strains activated human DCs and promoted a strong inflammatory response characterized by the early production of pro-inflammatory TNFα and IL-6 cytokines, followed by IL-10, IL-1β, and IL-23 secretion. IL-23 was the only cytokine dependent on the cag pathogenicity island status of the bacterial strains. DC activation and cytokine production were accompanied by an early miR-146a upregulation followed by a strong miR-155 induction, which mainly controlled TNFα production. These results pave the way for further investigations into the nature of H. pylori antigens and the subsequently activated signaling pathways involved in the inflammatory response to H. pylori infection, the deregulation of which may likely contribute to gastric lymphomagenesis.


INTRODUCTION
Helicobacter pylori infection causes a chronic gastric mucosal inflammation, leading to peptic ulcer disease in 5-10% of the infected people, and to gastric adenocarcinoma and low-grade mucosa-associated lymphoid tissue (MALT) lymphoma in 1% of the cases. The pathogenesis of H. pylori infection has been linked to the strength of inflammation it promotes, which is correlated to the functionality of the cag pathogenicity island (PAI) in the bacteria (Censini et al., 1996). Gastric epithelial cells constitute the first line of defense against H. pylori; they produce interleukin (IL)-8, which promotes the recruitment of polynuclear cells. Immune cells including macrophages, dendritic cells (DC) and mucosa infiltrating lymphocytes take part in the innate and adaptative immune responses to the bacteria.
The pro-inflammatory properties of H. pylori strains have been mainly evaluated by measuring IL-8 production of the AGS gastric epithelial cell line, but they deserve to be investigated on immune cells due to their orchestrated pro-and anti-inflammatory cytokine production in response to pathogens. In vivo the professional antigen-presenting DC were found to be recruited into the gastric mucosa and, due to the emission of dendrites inserting themselves between epithelial cell tight junctions, they may be able to interact with H. pylori (Rescigno et al., 2008;Shiu and Blanchard, 2013). Their role in H. pylori-induced inflammatory response needs to be clarified.
Host defense against pathogens requires the induction of appropriate innate immune responses, as excessive or inappropriate activation of the immune system can be deleterious to the organism. Therefore, various immune regulators, including microRNAs (miRNA), also take part in the immune responses (Baltimore et al., 2008). MiRNA received considerable attention because of their implication in maintaining homeostasis in fundamental biological processes in non-pathological states, and their deregulation in pathological states (Sonkoly and Pivarcsi, 2009). Changes in miRNA expression in response to bacterial infection have been reported, including H. pylori infection in the gastric mucosa, in gastric epithelial cells and in immune cells (Zhang et al., 2008;Fassi Fehri et al., 2010;Belair et al., 2011;Matsushima et al., 2011).
In the present study, primary human DCs were used to explore the inflammatory effectors induced by H. pylori strains. Two fully sequenced H. pylori strains were included for this purpose, i.e., strains B38 (Thiberge et al., 2010) and B45 (Lehours et al., 2011) which are cagPAI negative and cagPAI positive, respectively. In parallel to cytokine production, miRNA changes induced by H. pylori were analyzed; they included measuring miR-146 and miR-155, to which specific immunomodulatory functions in H. pylori infection were assigned after performing loss of function experiments.

ETHICS STATEMENT
Written consent of hemochromatosis patients was obtained and approved by the French Ministry of Research and the French Aquitaine Limousin Blood Bank's (Bordeaux, France) ethics committee (approval number DC-2012DC- -1648.

In vitro GENERATION OF DCs
All tissue culture reagents were purchased at Invitrogen (Marly Le Roi, France). Peripheral blood mononuclear cells (PBMC) from hemochromatosis patients were isolated by centrifugation on a Ficoll gradient and captured using magnetic CD14 microbeads (Miltenyi Biotec, Paris, France), according to the manufacturer's protocol. To generate immature DCs, monocytes were grown for 7 days in the presence of GM-CSF (50 ng/ml) and IL-4 (25 ng/ml) in RPMI-1640 medium supplemented with 10% heatdecomplemented fetal calf serum, 2 mM of L-glutamine, and 50 μg/ml of vancomycin (Sandoz, Levallois Perret, France) at 37 • C in a 5% CO 2 atmosphere.

CO-CULTURES OF IMMATURE DCs AND H. pylori STRAINS
Immature DCs were washed once in PBS and plated onto 24well plastic plates at a density of 5.10 5 cells per well in 1 ml of RPMI-1640 growth medium. Bacteria were recovered from the agar plates using a swab and resuspended in RPMI-1640 growth medium at an optical density of 0.6 at 600 nm, which corresponds to 3.10 7 CFU/ml. The bacteria were added to the DCs at the indicated multiplicity of infection (MOI) 1 and the cocultures were further incubated at 37 • C in a 5% CO2 atmosphere for 48 h.

DENDRITIC CELL APOPTOSIS
The occurrence of DC apoptosis was assessed using annexin V staining and propidium iodure incorporation. DCs were centrifuged at 2000 rpm for 10 min at 4 • C, washed once in cold PBS and resuspended in 25 μL of 0.01 M HEPES (pH 7.4), 0.14 M NaCl, and 0.25 mM CaCl 2 . The cells were labeled with 2.5 μL of anti-annexin V antibody (eBioscience) and 1 μL of propidium iodure (1 mg/mL) (Sigma Aldrich) for 15 min at 4 • C and analyzed by flow cytometry.

RNA EXTRACTION AND miRNA QUANTITATIVE RT-PCR
DCs were collected in Eppendorf tubes and pelleted by centrifugation at 2000 rpm for 5 min at room temperature. Total RNA was extracted from the DC pellet using a Trizol reagent (Invitrogen), according to manufacturer's instructions. RNA concentrations were determined by spectrophotometry (NanoDrop Technologies, Wilmington, DE, USA). RNA quality was determined on an Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA). For miRNA quantitations, 250 ng of total RNA were retrotranscribed using the miScript Reverse Transcription kit (Qiagen, Courtaboeuf, France) and qPCR was performed using a SYBr Green PCR kit and hsa-miR-155, hsa-miR-146a and SNOR25 specific primers (Qiagen), according to the manufacturer's instructions. The amplification profiles were measured on a Stratagene Mx3005P instrument (Life Technologies, Saint Aubin, France).

STATISTICAL ANALYSIS
Data were expressed as a ratio of fold induction compared to nonactivated DCs. For each experiment, all experimental conditions were tested three times and each experiment was conducted at least three times for each strain. Statistical analyses were done using the non-parametric Mann-Whitney test. A p-value of less than 0.05 was considered significant. All statistics were performed using SPSS 16.0F for Windows software (SPSS Inc., Chicago, IL, USA).

DENDRITIC CELL ACTIVATION BY H. pylori
The nature, the amount and the duration of the antigenic stimulation are important factors that can influence the inflammatory and molecular responses of DCs. Before infection, the immature DC phenotype (CD1a +, HLA-DR +, CD80 −, CD86 −, CD14 −, CD83−) was verified by flow cytometry (Figure A1).
H. pylori-activated DCs produced the same cytokines as LPSactivated DCs, both qualitatively and quantitatively, except for IL-10 (Figure 1). This potent anti-inflammatory molecule was found at a significantly higher level upon stimulation by both H. pylori B38 and B45 than by LPS. Moreover, compared to E. coli LPS, IL-10 production was significantly induced by H. pylori B38 strain as early as 6 h.
Analysis of cytokine production kinetics in H. pylori-activated DCs revealed the early, massive production of TNFα (Figure 1). TNFα reached its maximal level as early as 6 h in the presence of LPS or the bacteria, and remained quite stable thereafter. IL-6 was maximally stimulated by E. coli LPS as early as 6 h, and progressively with H. pylori (Figure 1).
There was generally no significant difference in the cytokine production between the two H. pylori strains, except for IL-23, a major cytokine involved in Th17 response, which was higher with B45 than with B38 (Figure 1). This difference could be attributed to the presence of the cagPAI in the B45 strain. To test this hypothesis, DCs were activated for 48 h by either H. pylori P12 strain or its isogenic cagPAI deletion mutant (Figure 1), and by 12 more H. pylori strains tested individually (6 cagPAI positive and 6 cagPAI negative) from our collection (Lehours et al., 2004a) (Figure 1). IL-23 secretion was significantly lower with the P12 mutant and the cagPAI negative strains than with the P12 wild type and the cagPAI positive strains confirming the positive influence of the cagPAI gene products on the secretion of this cytokine. IL-23 secretion started rather late following H. pylori infection, at 48 h

FIGURE 1 | Cytokine production in H. pylori -activated dendritic cells. (A)
Kinetics of TNFα, IL-6, and IL-10 secretion by E. coli LPS-or H. pylori-activated dendritic cells. DCs were either stimulated with E. coli LPS (100 ng/ml) or cocultivated with B38 H. pylori strain at MOI 1 for 6, 24, or 48 h. TNFα, IL-6, and IL-10 secretion in the culture supernantants was evaluated by flow cytometry (as described in Materials and Methods). The horizontal bar across the box indicates the median and the capped bars indicate the minimum and maximum data values of fold induction ratio vs. DCs alone obtained for 6 independent experiments corresponding to 6 different donors. These results are representative of the results obtained for H. pylori strain B45 for the same experiments. *for p < 0.05 and NS for p > 0.05 compared to E. coli LPS at the corresponding time-point. (B) Influence of the H. pylori cagPAI on the production of IL-23 by dendritic cells after H. pylori infection. (1) DCs were cocultured with B38 or B45 H. pylori strain at MOI 1 for 6, 24, or 48 h. IL-23 levels in culture supernatants were measured by ELISA. The horizontal bar across the box indicates the median and the capped bars indicate the minimum and maximum data values of fold induction ratio vs. non-activated DCs, for 6 independent experiments for each strain and for 6 different donors. *for p < 0.05 between the H. pylori strains B38 and B45 at the corresponding time-point. (2) DCs were cocultured for 48 h with H. pylori strain P12 and its isogenic cagPAI mutant (KO-P12) at MOI 1 or (3) with 12 ulcer-associated H. pylori strains tested individually (6 cagPAI positive and 6 cagPAI negative). IL-23 levels in culture supernatants were measured by ELISA. The horizontal bar across the box indicates the median and the capped bars indicate the minimum and maximum data values of fold induction ratio vs. non-activated DCs, for 3 independent experiments for each group of strains and for three different donors (*if p < 0.05).
for B38 and 24 h for B45 (Figure 1). Finally, both LPS-and H. pylori-mediated activation displayed similar patterns of progressive production of IL-1β, IL-8, and IL-12 over the time course ( Figure A4).
Kinetic analyses of miR-146 and miR-155 expression in DCs co-cultured with either the B38 or the B45 strain at MOI 1 showed that both miRNAs were upregulated as early as 6 h post-infection and increased progressively thereafter (Figure 2A). Whereas miR-146a reached 50% of its maximal stimulation as early as 6 h post-infection, miR-155 was dramatically upregulated between 6 and 24 h. Thus, at 48 h post-infection, miR-146 levels were increased by 5-10 fold over the basal level, and miR-155 by 100-200 fold. The statistical analysis of 13 independent experiments showed no significant difference between the B38 and B45 strains in their ability to upregulate the miRNAs, since miR146a expression was enhanced by 4.06 ± 0.47 and 4.8 ± 0.78 fold (p = 0.927), and miR-155 by 84.03 ± 15.87 and 99.17 ± 26.94 fold (p = 0.224), respectively. This suggests that the miRNA response of H. pylori-activated DC was independent of the strain's cagPAI status. miR-146a was upregulated more by the H. pylori strains than by LPS, contrary to miR-155, which reached the same intensity after LPS stimulation as after co-culture with either of the H. pylori strains (Figure 2A). At 48 h post-infection, miR-146a upregulation was positively correlated with a MOI up to 40, whereas miR-155 upregulation peaked at MOI 1-5 and decreased at higher ones ( Figure 2B). The global results indicate that miR-146a and miR-155 upregulations take part in the DC immune response to H. pylori, independently of their cagPAI status, with miR-146a upregulation preceding the massive miR-155 biosynthesis.
In order to investigate the importance of these miRNAs in the regulation of cytokine production upon infection, their mature forms were functionally inhibited using antisense oligonucleotides (or their scrambled controls), which were introduced into immature DCs using lipofectamin prior to the LPS or H. pylori challenge. Both miR-146a and miR-155 knockdown had little influence on the LPS-or H. pylori-mediated upregulation of DC surface activation markers, suggesting that neither one was required for this process (data not shown). Anti-miR-146 antisense oligonucleotides totally prevented LPS-or H. pyloritriggered miR-146 upregulation ( Figure 3A) and had no influence on the level of miR-155 induction, and vice versa, showing the efficiency of antisenses to inhibit miRNA expression, most likely by sequestering them. This also suggests that miR-146a and miR-155 expression may not be correlated in this cell system. Nevertheless, in response to H. pylori, two cytokines were clearly affected by this treatment (Figure 3B). First, in comparison to scrambled oligonucleotide-treated cells, TNFα production at 48 h was induced to a 50% greater extent in anti-miR-155-treated cells notably upon H. pylori infection, whereas it was weakly impaired (≤20%) by anti-miR-146. Second, anti-miR-146 treatment clearly impaired IL-10 production upon infection, whereas anti-miR-155 had no significant effect. miR-146a or miR-155 knockdown did not affect the cytokine response to LPS. This treatment did not alter IL-1β or IL-8 production and only weakly affected that of other cytokines after H. pylori challenge ( Figure A5).

DISCUSSION
In this manuscript, we aimed at analyzing the initial steps of the immune response to H. pylori strains. We therefore developed an ex vivo co-culture cell system, in which we showed that H. pylori strains were able to activate primary human DCs and promote strong proinflammatory cytokine and miRNA responses. Although most of the observed effects were independent of the H. pylori cagPAI status, the cagPAI positive strain specifically upregulated IL-23, most likely to orientate DCs to promote a Th17 response. Numerous articles have been published on the interaction between H. pylori and DCs, however, with a huge heterogeneity in the bacterial strains, MOI and experimental conditions (viable/sonicated/paraformaldehyde-treated bacteria) (Guiney et al., 2003;Hafsi et al., 2004;Kranzer et al., 2004Kranzer et al., , 2005Kao et al., 2006;Mitchell et al., 2007;Rad et al., 2009;Andres et al., 2010;Kao et al., 2010;Fehlings et al., 2012). Our data were obtained using primary human DCs from several donors. All experiments were repeated with at least three different donors in order to ensure the reliability of the results. Significant productions of several cytokines (TNFα, IL-1β, IL-6, IL-8, IL-10, IL-12, and IL-23) were observed in H. pylori-activated DCs, TNFα and

FIGURE 3 | Effect of miR-146a and miR-155 loss of function in H. pylori -induced miRNA levels and TNFα and IL-10 production. (A)
Changes in miR-146a and mir-155 relative levels in DCs transfected with anti-miRNA oligonucleotides: DCs were transfected with 100 nM of miRNA-antisense (anti-miR-146a or anti-miR-155) or scrambled oligonucleotides before being challenged with B38 or B45 H. pylori strains at MOI 1 for 48 h. RTqPCR data are presented as the fold induction ratio (mean + standard deviation of triplicates) in activated DCs and are representative of one experiment out of 4.*if p < 0.05 compared to miRNA levels obtained on activated DCs treated with scrambled oligonucleotides. (B) TNFα and IL-10 production in activated DCs transfected by either anti-miR146a or anti-miR155 oligonucleotides: DCs were transfected as in (A) and activated with E. coli LPS (100 ng/ml) or H. pylori B38 or B45 strains at MOI 1 for 48 h. TNFα and IL-10 production was evaluated by flow cytometry. The horizontal bar across the box indicates the median and the capped bars indicate the minimum and maximum data values of fold induction ratio compared to scrambled oligonucleotide-treated cells for 4 independent experiments corresponding to 4 different donors (*if p < 0.05).
IL-6 being produced at the highest levels. In vivo, TNFα contributes to monocyte maturation after recruitment, whereas IL-6 supports the transition between the early stages of the infection and the sustained mononuclear influx into the infected gastric mucosa. Early production of TNFα and IL-6 upon LPS stimulation reflects the intrinsic property of E. coli LPS to trigger TLR4 signaling pathways, a property that is not shared by H. pylori LPS (Rad et al., 2009). Delayed secretion of TNFα and IL-6 by H. pylori-activated DCs as compared to LPS-activated ones may depend on bacterial DNA and RNA recognition by endosomal TLR9 and TLR8, respectively (Rad et al., 2009), a later process when compared to the recognition of pathogen associated-motifs by surface TLRs. At later time points (24 and 48 h), a switch in the inflammatory response occurred with an accumulation over time of IL-6, IL-10, IL-23, and IL-1β, without any significant induction of TGFβ. The late IL-10 and IL-12 production by H. pylori-activated DCs may coincide in vivo with their homing in lymph nodes (Kranzer et al., 2004). IL-10 was secreted at a higher level after DC activation by H. pylori than by E. coli LPS, in accordance with recent data, which showed that H. pylori interactions with both TLR2 and the lectin DC-SIGN contributed to an antiinflammatory environment via the release of IL-10 (Rad et al., 2009;Fehlings et al., 2012). IL-12, which plays a role in the differentiation of naive T cells toward Th1 cells (Pellicano et al., 2007), was the least produced cytokine upon DC activation. In the present study, the high IL-10 and TNFα levels secreted by activated DCs could be responsible for the low IL-12 secretion due to their ability to inhibit its production (Langenkamp et al., 2000). In addition, IL-23 was the only cytokine dependent on the strain's cagPAI status. This result is still a matter of debate. Indeed several papers show that cagPAI could influence in vitro IL-23 release by DCs (Khamri et al., 2009;Tanaka et al., 2010). However, others argue that cagPAI does not regulate cytokine production in DCs cocultured with H. pylori (Kao et al., 2010;Horvath et al., 2012). Previous data from experiments on human gastric biopsies infected with H. pylori indicate that myeloid DCs co-localize with IL-23 and IL-17-producing, infiltrating lymphocytes (Khamri et al., 2010); one could therefore hypothesize that the H. pylori B45 strain may be able to induce a Th17 response, likely mediated by the cagPAI status. As IL-23 also plays an important role in sustaining Th17 responses in addition to acting on lymphoid cells to induce IL-17 (Shi et al., 2010;Hitzler et al., 2013), signaling pathways involved in this phenomenon deserve further investigation.
In parallel to the cytokine response profile, miR-155 and miR-146a were co-upregulated most intensely and invariably in activated DCs, independently of the cagPAI status of the bacterial strain. These two miRNA were previously expressed at high levels in H. pylori-infected gastric mucosa Lario et al., 2012). Our results clearly show that the extent of their upregulation as well as their kinetics and MOI-dependence did not evolve in parallel with the time-course of H. pylori-activated DCs. MiR-146 upregulation takes part in the early immune program activated in DCs by H. pylori, as it reached 50% of its maximal 10 fold stimulation as early as 6 h post-infection, while miR-155 was induced at a striking rate 24 h post-infection, reaching 200 fold the stimulated levels at 48 h. The massive induction of miR-155 in DCs over the time-course of their activation by both LPS and H. pylori is consistent with previous findings (O'Connell et al., 2007;Tili et al., 2007;Martinez-Nunez et al., 2009). Indeed, miR-155 can be induced by pathogen-associated ligands via TLR-, NF-κB-, and MyD 88-dependent pathways or by several cytokines such as IL-1β (Ceppi et al., 2009) and TNFα (Tili et al., 2007) which are both likely to sustain the high miR-155 biosynthesis induced in LPS-stimulated or H. pylori-infected DCs. An alternative miR-155 activation by bacterial peptidoglycan sensing via the cytoplasmic NOD2 receptor has been reported (Schulte et al., 2013), which may participate to the massive miR-155 induction. Contrary to miR-146, miR-155 was induced via a biphasic profile according to the MOI, suggesting that at a high MOI, the increasing level of some inflammatory cytokines might negatively regulate miR-155 expression. As the antiinflammatory cytokine IL-10 was found to inhibit LPS-induced miR-155 upregulation without affecting miR-146a (McCoy et al., 2010), it is likely that H. pylori-stimulated IL-10 production is responsible for the decreased miR-155 upregulation at high MOIs.
The role of miR-146 and miR-155 in the innate immune responses was deduced from the identification of their respective targets. As miR-146a targets and silences TNF-receptorassociated factor and IL-1β receptor-associated kinase mRNAs, which are key adapter molecules in the TLR/ NFκB pathway, the role of miR-146a upregulation in response to pathogens was shown to moderate TLR-triggering of the NFκB pathway via a negative feedback loop, thus avoiding overproduction of proinflammatory IL-1β and TNFα cytokines (Taganov et al., 2006;Nahid et al., 2009;Lu et al., 2010). A similar immune regulatory function was assigned to miR-155 which targets several gene transcripts of the NF-κB pathway (FADD, Ripk1, IKK, and NIK), as well as the immune cell transcription factor PU, Src homology 2 domain-containing inositol-5-phosphatase (SHIP) and CCAAT enhancer-binding protein beta (C/EBPbeta) (Rodriguez et al., 2007;Tili et al., 2007;Costinean et al., 2009;Schulte et al., 2013). In addition, miR-155 also stabilizes the TNFα mRNA (Tili et al., 2007;Semaan et al., 2011), suggesting that simultaneous anti-and pro-inflammatory effects of miR-155 most likely contribute to the fine-tuning of the TNF-mediated inflammation. We assessed the role of miR-146 and miR-155 in the DC cytokine response to H. pylori using specific antisenses to each miRNA, which inhibit their silencing function by competition with their binding sites on mRNA targets. Thus, the most noticeable effect of miR-155 loss of function in our cell system was an enhanced TNFα production by H. pylori, an effect consistent with the immunomodulatory role assigned to miR-155 upregulation in response to microbial stimuli (O'Connell et al., 2007;Rodriguez et al., 2007;Ceppi et al., 2009;Martinez-Nunez et al., 2009). Enhanced TNFα response to H. pylori in the absence of miR-155 may also be facilitated by the downregulation of miR-125b which we observed in our microarray (Table 1), and which directly targets TNFα (Tili et al., 2007). In our miR-146 loss of function experiment, no cytokine response was markedly altered with the exception of IL-10. The impaired production of this anti-inflammatory cytokine in response to H. pylori is concordant with the previously established immunomodulatory role of miR-146 upon infection, but it was not accompanied by an enhanced production of inflammatory cytokines in anti-miR-146-treated cells as expected. A possible explanation for the decreased IL-10 response to H. pylori in the absence of miR-146 could be that miR-146 loss of function unmasks the regulatory effects of other miRNAs: for instance, let-7e, which directly targets IL-10 (Schulte et al., 2011) was upregulated in H. pylori-activated DCs (Table 1) and may subsequently negatively regulate IL-10. The differences in the effects of miR-146 and miR-155 knockdown, which stress the prominent role of miR-155 in H. pylori-activated DCs, could be related to different functional specializations of these two seemingly co-induced miRNAs, as recently reported in LPSstimulated murine macrophages (Schulte et al., 2013); miR-146 responded to sub-inflammatory stimuli to prevent TLR activation, and miR-155 responded to pro-inflammatory stimuli as a global limiter of the inflammatory response. Our experimental conditions established a TNFα-filled, pro-inflammatory environment in cultured DCs, and thus preferentially elicited miR-155 functions.
miR-146a and miR-155 expressions may be of special interest in H. pylori-mediated immune pathologies, because they are associated with NFκB activation, a pathway strongly activated during H. pylori infection and in H. pylori-driven MALT lymphoma. High expression of miR-146a was associated with chronic inflammatory diseases (Sonkoly and Pivarcsi, 2009) and miR-155 represents an important element in B cell lymphoma development (Costinean et al., 2006), indicating that alterations in the fine-tuning of innate immune responses by miRNAs may contribute to inflammatory disorders. Other miRNAs, which are differentially regulated in H. pylori-activated DCs, deserve further investigation; among them, miR-187, which was strongly upregulated in the H. pylori-activated DCs, could control IL-10-driven anti-inflammatory responses (Rossato et al., 2012).
In conclusion, the co-culture cell system presented here allowed the identification of pro-and anti-inflammatory effectors in response to H. pylori and revealed the influence of the cagPAI on the immune responses. These important findings pave the way for further investigations on the nature of H. pylori antigens and the subsequently activated signaling pathways involved in the inflammatory response to H. pylori infection.

FIGURE A5 | Effect of miR-146a or miR-155 loss of function on
H. pylori -induced IL-23, IL-6, IL-12, IL-1β and IL-8 production. DCs were transfected with 100 nM of miRNA-antisense (anti-miR-146a or anti-miR-155) or scrambled oligonucleotides before being challenged with B38 or B45 H. pylori strains at MOI 1 for 48 h. IL-6 secretion was evaluated by flow cytometry, whereas IL-1β, IL-8, IL-12, and IL-23 production were assessed by ELISA. The horizontal bar across the box indicates the median and the capped bars indicate the minimum and maximum data values of fold induction ratio compared to scrambled oligonucleotide-treated cells, for 4 independent experiments corresponding to 4 different donors (*if p < 0.05).