Printer Friendly

Therapeutic potential of tolerogenic dendritic cells in IBD: from animal models to clinical application.

1. Introduction

The gut mucosa is continuously exposed to external food antigens and pathogens and to commensal flora microorganisms, mostly bacteria and fungi. This constant antigenic stimulation results in controlled inflammatory responses that are effectively suppressed by multiple nonimmune and immune factors. The intestinal immune system is capable of distinguishing between invasive organisms and harmless antigens. The host response to the intestinal microbiota can be categorized into three important categories: (1) the intestinal epithelium, which can efficiently modulate immune response by secreting inflammatory mediators, recruiting DCs and presenting antigens to T lymphocytes, (2) the innate immunity, including anatomical barriers, secretory molecules, and cellular components, that initiate the nonspecific immune response, and (3) the adaptive immunity, which is driven by B and T lymphocytes, responsible for antigen specific immune responses. This tight regulation, necessary to maintain intestinal homeostasis, is altered in IBD, resulting in uncontrolled immune responses to harmless microorganisms. Adaptive immunity is the most putative driver of tissue damage seen in IBD patients, although innate immune responses are definitively a prerequisite for the excessive activation of adaptive immunity [1]. Several studies have proposed that the inappropriate activation of DCs may contribute to the pathogenesis of IBD [2].

DCs are the most potent antigen-presenting cells linking innate and adaptive immune responses. Located in peripheral and lymphoid tissues, DCs are sentinels of the immune system recognizing and translating pathogenic or harmless signals into immunogenic or tolerogenic responses, respectively. DCs are especially well equipped to continuously sample these tissues for the presence of pathogenic microorganisms, and their detection relies on the recognition of conserved molecular structures, known as pathogen-associated-molecular-patterns (PAMPs) via pattern recognition receptors (PRRs). DCs orchestrate adaptive immune responses linking innate recognition of pathogens and driving and polarizing naive T cells activation. Due to their physiological properties and the availability of clinical grade reagents, DCs have been safely and successfully used in clinical trials aimed at stimulating an efficient immune response against tumors or infectious diseases [3, 4]. However, only a few recent studies have taken advantage of their specific tolerogenic properties to treat Type 1 diabetes [5] and rheumatoid arthritis patients [6]. Both studies have taken place in the last two years; thus, it is still too early to draw any conclusion in relation to their clinical efficacy. The majority of clinical studies to date have been carried out with ex vivo generated monocyte-derived DCs taking advantage of their plasticity. Several protocols to generate tol-DC have been described using different agents, including glucocorticoids such as dexamethasone [7, 8], mycophenolic acid [9], vitamin D3 (1a,25-dyhydroxyvitamin D3) [10], retinoic acid (RA), the combination of dexamethasone and vitamin D3 [11, 12], or rhIL-10 [13], which have been used to render DCs resistant to maturation. Therefore, ex vivo generated tol-DCs are considered as therapeutic vaccines to reestablish antigen-specific tolerance in autoimmune disorders. The aim of this review is to discuss DC subsets and their role in tolerance induction, preclinical studies in animal models of colitis, and our recent findings on tolDC generation and characterization in humans for clinical applications in Crohn's disease patients.

2. Human DC Subsets

Several subsets of circulating DCs have been defined in humans based on the lack of expression of typical lineage (CD3, CD19/CD20, CD14, and CD56) negative markers ([lin.sup.-]) and high levels of MHC class II (HLA-DR) positive cells [14]. Furthermore, a number of positive DC markers have been used to identify different DC subsets. Plasmacytoid DCs ([CD11c.sup.-]) are identified by the expression of BDCA-2 and BDCA-4 plus CD123, whereas myeloid DCs ([CD11c.sup.+]) can be further subdivided in BDCA-1 ([CD1c.sup.+]) and BDCA3 (CD141+) positive cells. Although evidence suggests the involvement of a particular DC subset in tolerance induction, it is now accepted that different DC subsets participate in immunity or tolerance showing functional maturation and plasticity depending on environmental signals received. However, recent advances have helped to associate the DC subsets to functional specialization. This functional specialization is linked to the different expression between DCs subsets of PRRs like toll-like receptors (TLR), C-type lectins, and the cytoplasmic NOD family proteins, as well as RIG-I and MDA-5 molecules. Whether this functional specialization is linked to different aspects of tolerance induction is an issue to be formally established.

The gastrointestinal immune system is continuously exposed to potent stimuli from commensal bacteria and food. A specialized network of immune cells is organized in the mucosa in order to maintain immunologic tolerance. How DCs regulate immune response in the gut has been deeply investigated, and several DCs subsets and their function have been identified in mice. But whether these subsets are equivalent in humans needs to be further studied (reviewed by Mann et al. [15]). It is well known that DCs in the gut are generally hyporesponsive [16] and have the ability to imprint homing properties on T cells. Although defining cell markers to identify intestinal DCs is controversial, there are different strategies to identify human DCs in the mucosa. The most common one is by negative lineage of CD3, CD14, CD16, CD34, and expression of HLA-DR+. These cells are often mistaken as macrophages, and some authors prefer to differentiate both subsets by function and not by cell markers. Interestingly, CD103+ DCs have tolerogenic properties and share some functional aspects with murine CD103+ DCs. These "tolerogenic" DCs promote Treg differentiation [16] and produce RA [17] and indoleamine 2,3-dioxygenase (IDO) [18], molecules that can drive Tregs and are known to be involved in the induction of tolerance in the gut. The ability of CD103+ DCs to produce IL-10 and the lack of IL-12, together with the low expression of CD40, TLR2, and TLR4, make these cells suitable to be defined as the main regulators of immune tolerance in the intestinal tract. However, research in this area is very difficult and a lot more needs to be elucidated regarding human DC subsets and tolerance in the gut.

3. Mechanisms to Induce Tolerance

The functional properties of DCs are dependent on their maturation status. Due to the lack of expression of costimulatory molecules and MHCII, tol-DCs are able to induce T cell anergy, preventing T cell activation. It has been described that DCs suboptimal antigen presentation, combined with the expression of IDO or FasL (CD95L) leads to inhibition of T cell proliferation and T cell deletion [19] (Figure 1). The induction of Treg and Type 1 regulatory T cells (Tr1) by DCs is another mechanism to induce peripheral tolerance [20, 21]. The mechanisms by which DCs regulate immune responses, tolerance, and lamina propria homeostasis against commensal flora have not been fully elucidated. The immunosuppressive cytokine IL-10 is a crucial mediator of tolerance in the gut and it has a nonredundant role in limiting inflammatory responses in the intestine. IL-10 can act on a variety of immune cells and its secretion is certainly involved in Tregs and Tr1 induction as well as regulating the local inflammatory immune response via antigen-presenting cells [22-24]. Indeed, IL-10 is very important in maintaining intestinal homeostasis as revealed by the spontaneous chronic inflammatory disease (similar to Crohn's disease) that IL10 knockout mice develop. In addition, a severe form of Crohn's disease (with early-onsets of enterocolitis, involving hyperinflammatory immune responses in the intestine) in infants was associated with IL-10 receptor mutations in two unrelated consanguineous families [25]. IL-10 signaling directly suppresses Th17 and [Th17.sup.+][Th1.sup.+] cells in mice with established colitis [26]. All these features together make tol-DCs suitable to create an immunosuppressive environment that can potentially induce tolerance in the neighboring tissue.

4. Plasmacytoid Dendritic Cells and Tolerance

Plasmacytoid DCs (pDC) appear to play an important role in the regulation of tolerance induction [27], transporting self-antigens from peripheral tissues in the thymus contributing to the inactivation of autoreactive T cells and induction of Tregs [28,29]. While present in tissues at very low numbers in the healthy steady-state, pDCs accumulate in lymphoid and nonlymphoid tissues under pathological or inflammatory conditions. In addition, the role of pDCs in controlling the intestinal homeostasis is largely unknown. Interestingly, liver and spleen pDCs express higher levels of NOD2 than conventional myeloid DCs (mDCs) and pDC are able to detect and respond to muramyl dipeptide (MDP). NOD2 ligation reduces IL-12, IL-6, and TNF-a production by pDC, in the presence or absence of either LPS or CpG stimulation [30] . Aberrant accumulation of pDCs in MLN and inflamed mucosa of IBD patients compared to controls has been shown [31]. Furthermore, highly purified pDCs from patients produced high levels of proinflammatory cytokines and showed an activated phenotype. However, IFN-[alpha] secretion induced by CpG-A was impaired in pDCs from IBD patients [31] . Another report showed that IBD patients lack circulating immature blood DCs (both DC subsets, myeloid, and plasmacytoid) during flares, which possibly migrate to the gut. An aberrant response to microbial surrogate stimuli suggests a disturbed interaction with commensals [32]. It has been recently shown that CCR9 expression in pDCs can home to the gut [33] and induce potent Treg responses that have a significant therapeutic effect in a model of intestinal Graft Versus Host Disease [34]. It is important to highlight that the clinical benefit of G-CSF therapy in Crohn's disease patients is thought to be related to its ability to induce IL-10-mediated regulatory functions, associated possibly with increased pDCs numbers in the inflamed gut [35]. However, a direct correlation between pDCs and the clinical benefit has not been established yet. Despite their reported role in the pathogenesis of certain autoimmune diseases, such as SLE or psoriasis, understanding pDC function in the pathogenesis of human diseases has just begun.

5. Role of Tol-DCs in IBD Animal Models

Experimental data generated in murine models of colitis are highly promising especially relating to the ability of tol-DCs to prevent, reverse, or ameliorate established colitis [12, 36, 37]. In a model of TNBS-induced colitis, which closely parallels the immune activation in Crohn's disease, injection of tol-DCs treated with Vasoactive Intestinal Peptide (VIP) [38] significantly ameliorated the clinical and histopathology severity of colitis in mice. An important aspect of this study was the route of administration of the DCs; the authors clearly show that by intraperitoneal administration DCs gain access to mesenteric lymph nodes, where the most important antigen presentation and activation of Th1/Th17 cells takes place [39]. In addition, different types of tol-DCs generated with a combination of dexamethasone plus vitamin D3 [12] or loaded with enterobacterial extract [36] were able to prevent the colitis induction. Several other animal models have revealed the therapeutic role of tol-DCs in preventing and ameliorating IBD in an antigen-specific way [37]. However, the current challenge is to bring this tol-DC therapy to the clinic for human patients. Several issues must be overcome such as the difference between IBD-induced animal models (reviewed by Neurath [40]) and the human disease, or the functional differences between mouse and human DCs. In summary, those promising results in rodents await to be translated into the human application.

6. Therapeutic Application of Tol-DCs in Crohn's Disease Patients

We have developed a protocol to produce tol-DCs under clinical grade conditions for the treatment of Crohn's disease patients (Figure 2) by conditioning monocyte-derived DC with dexamethasone at day 3, together with 24 hours maturation with a cytokine cocktail (IL-1[beta], IL-6, and TNF-[alpha]) plus [PGE.sub.2] [41]. Compared to mature and immature DCs, our tol-DCs produced higher levels of IL-10, even in response to gram-negative bacteria or synthetic LPS, with low or undetectable levels of IL-12p70, IL-23, or TNF-[alpha]. In addition, tol-DCs phenotype was consistently semimature with intermediate expression of costimulatory receptors (CD80 and CD86), low levels of CD83 and MHC class II, and the ability to inhibit T cell responses. It has been shown that DC activation with LPS or the clinical grade TLR4 ligand MPLA enhances tol-DCs migratory properties and antigen presentation capabilities [42]. Interestingly, even though the fact that isolated monocytes from Crohn's disease patients are in an enhanced proinflammatory environment [32], we showed that these cells from Crohn's disease patients can be educated towards tolerogenic phenotype. These results are in line with studies in other immune-based diseases like rheumatoid arthritis or multiple sclerosis [43, 44]. This is a key aspect for considering this DC-based treatment as a therapeutic option in IBD, because it might have occurred that genetic variants conferring susceptibility for Crohn's disease or the proinflammatory environment might alter the biology of DCs.

7. Lack of Crohn's Disease Associated Antigen

DC-based therapies are envisaged to inhibit antigen-specific T cell responses, and the appropriated antigen selection to load DCs is under intensive research. Although humoral response against antigens derived from microbiota has been described in Crohn's disease patients, for example, elevations in anti-Saccharomyces cerevisiae antibodies (ASCA) in 4960% of cases [45], no T lymphocyte Crohn's disease-specific antigen has been properly identified. Although the disease is associated with a high inflammatory component, mainly corresponding to Th1 and Th17 T cells [38, 39], the antigenic specificity of these cells remains to be investigated. Interestingly, commensal-specific T cell responses are detected during mouse model of intestinal inflammation with Toxoplasma gondii infection [46, 47]. It is tempting to speculate that commensal specific T cells may represent an important component of the IBD, although much remains to be understood about this issue. In animal models, Yamanishi et al. [37] identified a specific protein, carbonic anhydrase I (CA I), specifically involved in the IBD pathogenesis. Interestingly, the authors demonstrate the role of CA I loaded tol-DCs in preventing the induction of colitis via Tregs. Pedersen et al. administered DCs pulsed with enterobacterial extract to suppress development of colitis [36]. However, other authors have demonstrated tolerance induction in colitis model without antigens [12, 38]. This mechanism would involve the generation of DCs secreting regulatory cytokines (TGF-[beta] and IL-10) and expressing inhibitory receptors that might overcome the necessity of a known antigen. This "transtolerance" may result in the generation of a specific regulatory response helping to restore the mucosal homeostasis.

8. Summary

DCs are powerful therapeutic tools to modify the immune response and restore the immune tolerance in Crohn's disease patients and other autoimmune diseases. An alternative to manipulate the different subsets of intestinal DC function is the in vitro generation of tol-DCs. Methods to obtain these cells in sufficient amounts have been developed. Tol-DCs may represent a new therapeutic strategy for Crohn's disease, where the alterations of the finely tuned balance between the immune system and the microflora result in disease. Several reports have indicated the therapeutic effect of tol-DCs in inhibiting IBD induction in animal models. These results highlight the importance of DCs in the intestinal homeostasis control and open new avenues for an innovative therapeutic indication for human patients.

Conflict of Interests

The authors declare no existing financial conflict of interests. 10.1155/2013/789814


[1] A. L. Hart, H. O. Al-Hassi, R. J. Rigby et al., "Characteristics of intestinal dendritic cells in inflammatory bowel diseases," Gastroenterology, vol. 129, no. 1, pp. 50-65, 2005.

[2] J. L. Coombes and F. Powrie, "Dendritic cells in intestinal immune regulation," Nature Reviews Immunology, vol. 8, no. 6, pp. 435-446, 2008.

[3] C. G. Figdor, I. J. de Vries, W. J. Lesterhuis, and C. J. Melief, "Dendritic cell immunotherapy: mapping the way," Nature Medicine, vol. 10, no. 5, pp. 475-480, 2004.

[4] R. M. Steinman and J. Banchereau, "Taking dendritic cells into medicine," Nature, vol. 449, no. 7161, pp. 419-426, 2007.

[5] N. Giannoukakis, B. Phillips, D. Finegold, J. Harnaha, and M. Trucco, "Phase I (safety) study of autologous tolerogenic dendritic cells in type 1 diabetic patients," Diabetes Care, vol. 34, no. 9, pp. 2026-2032, 2011.

[6] C. M. Hilkens and J. D. Isaacs, "Tolerogenic dendritic cell therapy for rheumatoid arthritis: where are we now?" Clinical & Experimental Immunology, vol. 172, pp. 148-157, 2013.

[7] L. Piemonti, P. Monti, P. Allavena et al., "Glucocorticoids affect human dendritic cell differentiation and maturation," Journal of Immunology, vol. 162, no. 11, pp. 6473-6481, 1999.

[8] D. Rozkova, R. Horvath, J. Bartunkova, and R. Spisek, "Gluco-corticoids severely impair differentiation and antigen presenting function of dendritic cells despite upregulation of Toll-like receptors," Clinical Immunology, vol. 120, no. 3, pp. 260-271, 2006.

[9] C. Lagaraine, R. Lemoine, C. Baron, H. Nivet, F. Velge-Roussel, and Y. Lebranchu, "Induction of human [CD4.sup.+] regulatory T cells by mycophenolic acid-treated dendritic cells," Journal of Leukocyte Biology, vol. 84, no. 4, pp. 1057-1064, 2008.

[10] G. Penna and L. Adorini, "1[alpha],25-dihydroxyvitamin D3 inhibits differentiation, maturation, activation, and survival of dendritic cells leading to impaired alloreactive T cell activation," Journal of Immunology, vol. 164, no. 5, pp. 2405-2411, 2000.

[11] M. Naranjo-Gomez, D. Ralch-Regue, C. Onate et al., "Comparative study of clinical grade human tolerogenic dendritic cells," Journal of Translational Medicine, vol. 9, p. 89, 2011.

[12] A. E. Pedersen, E. G. Schmidt, M. Gad, S. S. Poulsen, and M. H. Claesson, "Dexamethasone/1[alpha]-25-dihydroxyvitamin D3-treated dendritic cells suppress colitis in the SCID T-cell transfer model," Immunology, vol. 127, no. 3, pp. 354-364, 2009.

[13] M. A. Boks, J. R. Kager-Groenland, M. S. Haasjes, J. J. Zwaginga, S. M. van Ham, and A. ten Brinke, "IL-10-generated tolerogenic dendritic cells are optimal for functional regulatory T cell induction--a comparative study of human clinical-applicable DC," Clinical Immunology, vol. 142, no. 3, pp. 332-342, 2012.

[14] M. Collin, N. McGovern, and M. Haniffa, "Human dendritic cell subsets," Immunology, vol. 140, no. 1, pp. 22-30, 2013.

[15] E. R. Mann, J. D. Landy, D. Bernardo et al., "Intestinal dendritic cells: their role in intestinal inflammation, manipulation by the gut microbiota and differences between mice and men," Immunology Letters, vol. 150, pp. 30-40, 2013.

[16] J. L. Coombes, K. R. Siddiqui, C. V. Arancibia-Carcamo et al., "A functionally specialized population of mucosal [CD103.sup.+] DCs induces [Foxp3.sup.+] regulatory T cells via a TGF-[beta] -and retinoic acid-dependent mechanism," Journal of Experimental Medicine, vol. 204, no. 8, pp. 1757-1764, 2007.

[17] C. M. Sun, J. A. Hall, R. B. Blank et al., "Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid," Journal of Experimental Medicine, vol. 204, no. 8, pp. 1775-1785, 2007.

[18] G. Matteoli, E. Mazzini, I. D. Iliev et al., "Gut [CD103.sup.+] dendritic cells express indoleamine 2,3-dioxygenase which influences T regulatory/T effector cell balance and oral tolerance induction," Gut, vol. 59, no. 5, pp. 595-604, 2010.

[19] K. Mahnke, E. Schmitt, L. Bonifaz, A. H. Enk, and H. Jonuleit, "Immature, but not inactive: the tolerogenic function of immature dendritic cells," Immunology and Cell Biology, vol. 80, no. 5, pp. 477-483, 2002.

[20] N. Cools, P. Ponsaerts, V. F. van Tendeloo, and Z. N. Berneman, "Balancing between immunity and tolerance: an interplay between dendritic cells, regulatory T cells, and effector T cells," Journal of Leukocyte Biology, vol. 82, no. 6, pp. 1365-1374, 2007.

[21] S. Rutella and F. Locatelli, "Intestinal dendritic cells in the pathogenesis of inflammatory bowel disease," World Journal of Gastroenterology, vol. 17, no. 33, pp. 3761-3775, 2011.

[22] G. Perona-Wright, S. M. Anderton, S. E. Howie, and D. Gray, "IL-10 permits transient activation of dendritic cells to tolerize T cells and protect from central nervous system autoimmune disease," International Immunology, vol. 19, no. 9, pp. 1123-1134, 2007.

[23] M. Kuwana, J. Kaburaki, T. M. Wright, Y. Kawakami, and Y. Ikeda, "Induction of antigen-specific human [CD4.sup.+] T cell anergy by peripheral blood DC2 precursors," European Journal of Immunology, vol. 31, pp. 2547-2557, 2001.

[24] P Allavena, L. Piemonti, D. Longoni et al., "IL-10 prevents the differentiation of monocytes to dendritic cells but promotes their maturation to macrophages," European Journal of Immunology, vol. 28, pp. 359-369, 1998.

[25] E. O. Glocker, D. Kotlarz, K. Boztuget al., "Inflammatory bowel disease and mutations affecting the interleukin-10 receptor," The New England Journal of Medicine, vol. 361, no. 21, pp. 2033-2045, 2009.

[26] S. Huber, N. Gagliani, E. Esplugues et al., "Th17 cells express interleukin-10 receptor and are controlled by [Foxp3.sup.-] and [Foxp3.sup.+] regulatory [CD4.sup.+] T cells in an interleukin-10-dependent manner," Immunity, vol. 34, no. 4, pp. 554-565, 2011.

[27] B. M. Matta, A. Castellaneta, and A. W. Thomson, "Tolerogenic plasmacytoid DC," European Journal of Immunology, vol. 40, no. 10, pp. 2667-2676, 2010.

[28] E. Martln-Gayo, E. Sierra-Filardi, A. L. Corbl, and M. L. Toribio, "Plasmacytoid dendritic cells resident in human thymus drive natural Treg cell development," Blood, vol. 115, no. 26, pp. 53665375, 2010.

[29] S. Hanabuchi, N. Watanabe, Y.-H. Wang et al., "Human plasmacytoid predendritic cells activate NK cells through glucocorticoid-induced tumor necrosis factor receptor-ligand (GITRL)," Blood, vol. 107, no. 9, pp. 3617-3623, 2006.

[30] A. Castellaneta, T. L. Sumpter, L. Chen, D. Tokita, and A. W. Thomson, "NOD2 ligation subverts IFN-[alpha] production by liver plasmacytoid dendritic cells and inhibits their T cell allostimulatory activity via B7-H1 Up-regulation," Journal of Immunology, vol. 183, no. 11, pp. 6922-6932, 2009.

[31] D. C. Baumgart, D. Metzke, O. Guckelberger et al., "Aberrant plasmacytoid dendritic cell distribution and function in patients with Crohn's disease and ulcerative colitis," Clinical and Experimental Immunology, vol. 166, no. 1, pp. 46-54, 2011.

[32] D. C. Baumgart, D. Metzke, J. Schmitz et al., "Patients with active inflammatory bowel disease lack immature peripheral blood plasmacytoid and myeloid dendritic cells," Gut, vol. 54, no. 2, pp. 228-236, 2005.

[33] M. Wendland, N. Czeloth, N. Mach et al., "CCR9 is a homing receptor for plasmacytoid dendritic cells to the small intestine," Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 15, pp. 6347-6352, 2007

[34] H. Hadeiba, T. Sato, A. Habtezion, C. Oderup, J. Pan, and E. C. Butcher, "CCR9 expression defines tolerogenic plasmacytoid dendritic cells able to suppress acute graft-versus-host disease," Nature Immunology, vol. 9, no. 11, pp. 1253-1260, 2008.

[35] P J. Mannon, F. Leon, I. J. Fuss et al., "Successful granulocytecolony stimulating factor treatment of Crohn's disease is associated with the appearance of circulating interleukin-10producing T cells and increased lamina propria plasmacytoid dendritic cells," Clinical and Experimental Immunology, vol. 155, no. 3, pp. 447-456, 2009.

[36] A. E. Pedersen, M. Gad, N. N. Kristensen, C. Haase, C. H. Nielsen, and M. H. Claesson, "Tolerogenic dendritic cells pulsed with enterobacterial extract suppress development of colitis in the severe combined immunodeficiency transfer model," Immunology, vol. 121, no. 4, pp. 526-532, 2007

[37] H. Yamanishi, H. Murakami, Y. Ikeda et al., "Regulatory dendritic cells pulsed with carbonic anhydrase I protect mice from colitis induced by [CD4.sup.+][CD25.sup.-] T cells," Journal of Immunology, vol. 188, no. 5, pp. 2164-2172, 2012.

[38] E. Gonzalez-Rey and M. Delgado, "Therapeutic treatment of experimental colitis with regulatory dendritic cells generated with vasoactive intestinal peptide," Gastroenterology, vol. 131, no. 6, pp. 1799-1811, 2006.

[39] A. Sakuraba, T. Sato, N. Kamada, M. Kitazume, A. Sugita, and T. Hibi, "Th1/Th17 immune response is induced by mesenteric lymph node dendritic cells in crohn's disease," Gastroenterology, vol. 137, no. 5, pp. 1736-1745, 2009.

[40] M. F. Neurath, "Animal models of inflammatory bowel diseases: illuminating the pathogenesis of colitis, ileitis and cancer," Digestive Diseases, vol. 30, supplement 1, pp. 91-94, 2012.

[41] R. Cabezon, E. Ricart, C. Espana, J. Panes, and D. Benitez-Ribas, "Gram-negative enterobacteria induce tolerogenic maturation in dexamethasone conditioned dendritic cells," PLoS One, vol. 7, Article ID e52456, 2012.

[42] A. E. Anderson, D. J. Swan, B. L. Sayers et al., "LPS activation is required for migratory activity and antigen presentation by tolerogenic dendritic cells," Journal of Leukocyte Biology, vol. 85, no. 2, pp. 243-250, 2009.

[43] D. Raich-Regue, L. Grau-Lopez, M. Naranjo-Gomez et al., "Stable antigen-specific T-cell hyporesponsiveness induced by tolerogenic dendritic cells from multiple sclerosis patients," European Journal of Immunology, vol. 42, no. 3, pp. 771-782, 2012.

[44] R. A. Harry, A. E. Anderson, J. D. Isaacs, and C. M. Hilkens, "Generation and characterisation of therapeutic tolerogenic dendritic cells for rheumatoid arthritis," Annals of the Rheumatic Diseases, vol. 69, no. 11, pp. 2042-2050, 2010.

[45] S. Vermeire and P Rutgeerts, "Antibody responses in crohn's disease," Gastroenterology, vol. 126, no. 2, pp. 601-604, 2004.

[46] T. W. Hand, L. M. Dos Santos, N. Bouladoux et al., "Acute gastrointestinal infection induces long-lived microbiota-specific T cell responses," Science, vol. 337, pp. 1553-1556, 2012.

[47] Y. Belkaid, N. Bouladoux, and T. W. Hand, "Effector and memory T cell responses to commensal bacteria," Trends in Immunology, vol. 34, pp. 299-306, 2013.

Raquel Cabezon (1) and Daniel Benitez-Ribas (2)

(1) Fundacio Clinic, Hospital Clinic i Provincial and Centre Esther Koplowitz, 08036 Barcelona, Spain

(2) Department of Experimental Gastroenterology, Centro de Investigation Biomedica en Red de Enfermedades Hepaticasy Digestivas (CIBERehd), Hospital Clinic i Provincial and Centre Esther Koplowitz, Carrer Rosello 149-153, 08036 Barcelona, Spain

Correspondence should be addressed to Daniel Benitez-Ribas;

Received 26 July 2013; Accepted 27 September 2013

Academic Editor: Lenin Pavon
COPYRIGHT 2013 Hindawi Limited
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2013 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Author:Cabezon, Raquel; Benitez-Ribas, Daniel
Publication:Journal of Immunology Research
Date:Jan 1, 2013
Previous Article:New insights into the role of the immune microenvironment in breast carcinoma.
Next Article:Sleep loss as a factor to induce cellular and molecular inflammatory variations.

Terms of use | Privacy policy | Copyright © 2022 Farlex, Inc. | Feedback | For webmasters |