References
- Murphy, K., P. Travers, M. Walport, and C. Janeway. 2012. Janeway's immunobiology. Garland Science, New York. p. 466-468.
- Ciorba, M. A., T. E. Riehl, M. S. Rao, C. Moon, X. Ee, G. M. Nava, M. R. Walker, J. M. Marinshaw, T. S. Stappenbeck, and W. F. Stenson. 2012. Lactobacillus probiotic protects intestinal epithelium from radiation injury in a TLR-2/cyclo-oxygenase- 2-dependent manner. Gut 61: 829-838. https://doi.org/10.1136/gutjnl-2011-300367
- Fukuda, S., H. Toh, K. Hase, K. Oshima, Y. Nakanishi, K. Yoshimura, T. Tobe, J. M. Clarke, D. L. Topping, T. Suzuki, T. D. Taylor, K. Itoh, J. Kikuchi, H. Morita, M. Hattori, and H. Ohno. 2011. Bifidobacteria can protect from enteropathogenic infection through production of acetate. Nature 469: 543-547.
- Pickard, J. M., C. F. Maurice, M. A. Kinnebrew, M. C. Abt, D. Schenten, T. V. Golovkina, S. R. Bogatyrev, R. F. Ismagilov, E. G. Pamer, P. J. Turnbaugh, and A. V. Chervonsky. 2014. Rapid fucosylation of intestinal epithelium sustains host-commensal symbiosis in sickness. Nature 514: 638-641. https://doi.org/10.1038/nature13823
- Denning, T. L., B. A. Norris, O. Medina-Contreras, S. Manicassamy, D. Geem, R. Madan, C. L. Karp, and B. Pulendran. 2011. Functional specializations of intestinal dendritic cell and macrophage subsets that control Th17 and regulatory T cell responses are dependent on the T cell/APC ratio, source of mouse strain, and regional localization. J. Immunol. 187: 733-747. https://doi.org/10.4049/jimmunol.1002701
- Varol, C., A. Vallon-Eberhard, E. Elinav, T. Aychek, Y. Shapira, H. Luche, H. J. Fehling, W. D. Hardt, G. Shakhar, and S. Jung. 2009. Intestinal lamina propria dendritic cell subsets have different origin and functions. Immunity 31: 502-512. https://doi.org/10.1016/j.immuni.2009.06.025
-
Edelson, B. T., W. KC, R. Juang, M. Kohyama, L. A. Benoit, P. A. Klekotka, C. Moon, J. C. Albring, W. Ise, D. G. Michael, D. Bhattacharya, T. S. Stappenbeck, M. J. Holtzman, S. S. Sung, T. L. Murphy, K. Hildner, and K. M. Murphy. 2010. Peripheral
$CD103^+$ dendritic cells form a unified subset developmentally related to$CD8alpha^+$ conventional dendritic cells. J. Exp. Med. 207: 823-836. https://doi.org/10.1084/jem.20091627 - Forster, R., A. Schubel, D. Breitfeld, E. Kremmer, I. Renner-Muller, E. Wolf, and M. Lipp. 1999. CCR7 coordinates the primary immune response by establishing functional microenvironments in secondary lymphoid organs. Cell 99: 23-33. https://doi.org/10.1016/S0092-8674(00)80059-8
- Jang, M. H., N. Sougawa, T. Tanaka, T. Hirata, T. Hiroi, K. Tohya, Z. Guo, E. Umemoto, Y. Ebisuno, B. G. Yang, J. Y. Seoh, M. Lipp, H. Kiyono, and M. Miyasaka. 2006. CCR7 is critically important for migration of dendritic cells in intestinal lamina propria to mesenteric lymph nodes. J. Immunol. 176: 803-810. https://doi.org/10.4049/jimmunol.176.2.803
- Persson, E. K., E. Jaensson, and W. W. Agace. 2010. The diverse ontogeny and function of murine small intestinal dendritic cell/macrophage subsets. Immunobiology 215: 692-697. https://doi.org/10.1016/j.imbio.2010.05.013
- Helft, J., F. Ginhoux, M. Bogunovic, and M. Merad. 2010. Origin and functional heterogeneity of non-lymphoid tissue dendritic cells in mice. Immunol. Rev. 234: 55-75. https://doi.org/10.1111/j.0105-2896.2009.00885.x
- Bogunovic, M., F. Ginhoux, J. Helft, L. Shang, D. Hashimoto, M. Greter, K. Liu, C. Jakubzick, M. A. Ingersoll, M. Leboeuf, E. R. Stanley, M. Nussenzweig, S. A. Lira, G. J. Randolph, and M. Merad. 2009. Origin of the lamina propria dendritic cell network. Immunity 31: 513-525. https://doi.org/10.1016/j.immuni.2009.08.010
- Tezuka, H., Y. Abe, M. Iwata, H. Takeuchi, H. Ishikawa, M. Matsushita, T. Shiohara, S. Akira, and T. Ohteki. 2007. Regulation of IgA production by naturally occurring TNF/iNOS-producing dendritic cells. Nature 448: 929-933. https://doi.org/10.1038/nature06033
- Mucida, D., N. Kutchukhidze, A. Erazo, M. Russo, J. J. Lafaille, and M. A. Curotto de Lafaille. 2005. Oral tolerance in the absence of naturally occurring Tregs. J. Clin. Invest. 115: 1923-1933. https://doi.org/10.1172/JCI24487
-
McDole, J. R., L. W. Wheeler, K. G. McDonald, B. Wang, V. Konjufca, K. A. Knoop, R. D. Newberry, and M. J. Miller. 2012. Goblet cells deliver luminal antigen to
$CD103^+$ dendritic cells in the small intestine Nature 483: 345-349. https://doi.org/10.1038/nature10863 -
Farache, J., I. Koren, I. Milo, I. Gurevich, K. W. Kim, E. Zigmond, G. C. Furtado, S. A. Lira, and G. Shakhar. 2013. Luminal bacteria recruit
$CD103^+$ dendritic cells into the intestinal epithelium to sample bacterial antigens for presentation. Immunity 38: 581-595. https://doi.org/10.1016/j.immuni.2013.01.009 -
Coombes, J. L., K. R. Siddiqui, C. V. rancibia-Carcamo, J. Hall, C. M. Sun, Y. Belkaid, and F. Powrie. 2007. A functionally specialized population of mucosal
$CD103^+$ DCs induces$Foxp3^+$ regulatory T cells via a TGF-beta and retinoic acid-dependent mechanism. J. Exp. Med. 204: 1757-1764. https://doi.org/10.1084/jem.20070590 - Sun, C. M., J. A. Hall, R. B. Blank, N. Bouladoux, M. Oukka, J. R. Mora, and Y. Belkaid. 2007. Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 Treg cells via retinoic acid. J. Exp. Med. 204: 1775-1785. https://doi.org/10.1084/jem.20070602
- Mucida, D., Y. Park, G. Kim, O. Turovskaya, I. Scott, M. Kronenberg, and H. Cheroutre. 2007. Reciprocal TH17 and regulatory T cell differentiation mediated by retinoic acid. Science 317: 256-260. https://doi.org/10.1126/science.1145697
- Denning, T. L., Y. C. Wang, S. R. Patel, I. R. Williams, and B. Pulendran. 2007. Lamina propria macrophages and dendritic cells differentially induce regulatory and interleukin 17-producing T cell responses. Nat. Immunol. 8: 1086-1094. https://doi.org/10.1038/ni1511
-
Hadis, U., B. Wahl, O. Schulz, M. Hardtke-Wolenski, A. Schippers, N. Wagner, W. Muller, T. Sparwasser, R. Forster, and O. Pabst. 2011. Intestinal tolerance requires gut homing and expansion of
$Foxp3^+$ regulatory T cells in the lamina propria. Immunity 34: 37-246. - Niess, J. H., S. Brand, X. Gu, L. Landsman, S. Jung, B. A. McCormick, J. M. Vyas, M. Boes, H. L. Ploegh, J. G. Fox, D. R. Littman, and H. C. Reinecker. 2005. CX3CR1-mediated dendritic cell access to the intestinal lumen and bacterial clearance. Science 307: 254-258. https://doi.org/10.1126/science.1102901
- Mazzini, E., L. Massimiliano, G. Penna, and M. Rescigno. 2014. Oral tolerance can be established via gap junction transfer of fed antigens from CX3CR1(+) macrophages to CD103(+) dendritic cells. Immunity 40: 248-261. https://doi.org/10.1016/j.immuni.2013.12.012
- Chang, S. Y., J. H. Song, B. Guleng, C. A. Cotoner, S. Arihiro, Y. Zhao, H. S. Chiang, M. O'Keeffe, G. Liao, C. L. Karp, M. N. Kweon, A. H. Sharpe, A. Bhan, C. Terhorst, and H. C. Reinecker. 2013. Circulatory antigen processing by mucosal dendritic cells controls CD8(+) T cell activation. Immunity 38: 153-165. https://doi.org/10.1016/j.immuni.2012.09.018
- Longman, R. S., G. E. Diehl, D. A. Victorio, J. R. Huh, C. Galan, E. R. Miraldi, A. Swaminath, R. Bonneau, E. J. Scherl, and D. R. Littman. 2014. CX(3)CR1(+) mononuclear phagocytes support colitis-associated innate lymphoid cell production of IL-22. J. Exp. Med. 211: 1571-1583. https://doi.org/10.1084/jem.20140678
- Dasgupta, S., D. Erturk-Hasdemir, J. Ochoa-Reparaz, H. C. Reinecker, and D. L. Kasper. 2014. Plasmacytoid dendritic cells mediate anti-inflammatory responses to a gut commensal molecule via both innate and adaptive mechanisms. Cell Host Microbe 15: 413-423. https://doi.org/10.1016/j.chom.2014.03.006
- Lee, S. E., X. Li, J. C. Kim, J. Lee, J. M. Gonzalez-Navajas, S. H. Hong, I. K. Park, J. H. Rhee, and E. Raz. 2012. Type I interferons maintain Foxp3 expression and T-regulatory cell functions under inflammatory conditions in mice. Gastroenterology 143: 145-154. https://doi.org/10.1053/j.gastro.2012.03.042
- Kole, A., J. He, A. Rivollier, D. D. Silveira, K. Kitamura, K. J. Maloy, and B. L. Kelsall. 2013. Type I IFNs regulate effector and regulatory T cell accumulation and anti-inflammatory cytokine production during T cell-mediated colitis. J. Immunol. 191: 2771-2779. https://doi.org/10.4049/jimmunol.1301093
-
Schulz, O., E. Jaensson, E. K. Persson, X. Liu, T. Worbs, W. W. Agace, and O. Pabst. 2009. Intestinal
$CD103^+$ , but not$CX3CR1^+$ , antigen sampling cells migrate in lymph and serve classical dendritic cell functions. J. Exp. Med. 206: 3101-3114. https://doi.org/10.1084/jem.20091925 -
Jaensson, E., H. Uronen-Hansson, O. Pabst, B. Eksteen, J. Tian, J. L. Coombes, P. L. Berg, T. Davidsson, F. Powrie, B. Johansson-Lindbom, and W. W. Agace. 2008. Small intestinal
$CD103^+$ dendritic cells display unique functional properties that are conserved between mice and humans. J. Exp. Med. 205: 2139-2149. https://doi.org/10.1084/jem.20080414 - Ivanov, I. I., K. Atarashi, N. Manel, E. L. Brodie, T. Shima, U. Karaoz, D. Wei, K. C. Goldfarb, C. A. Santee, S. V. Lynch, T. Tanoue, A. Imaoka, K. Itoh, K. Takeda, Y. Umesaki, K. Honda, and D. R. Littman. 2009. Induction of intestinal Th17 cells by segmented filamentous bacteria. Cell 139: 485-498. https://doi.org/10.1016/j.cell.2009.09.033
- Goto, Y., C. Panea, G. Nakato, A. Cebula, C. Lee, M. G. Diez, T. M. Laufer, L. Ignatowicz, and I. I. Ivanov. 2014. Segmented filamentous bacteria antigens presented by intestinal dendritic cells drive mucosal Th17 cell differentiation. Immunity 40: 594-607. https://doi.org/10.1016/j.immuni.2014.03.005
- Yang, Y., M. B. Torchinsky, M. Gobert, H. Xiong, M. Xu, J. L. Linehan, F. Alonzo, C. Ng, A. Chen, X. Lin, A. Sczesnak, J. J. Liao, V. J. Torres, M. K. Jenkins, J. J. Lafaille, and D. R. Littman. 2014. Focused specificity of intestinal TH17 cells towards commensal bacterial antigens. Nature 510: 152-156. https://doi.org/10.1038/nature13279
- Persson, E. K., H. Uronen-Hansson, M. Semmrich, A. Rivollier, K. Hagerbrand, J. Marsal, S. Gudjonsson, U. Hakansson, B. Reizis, K. Kotarsky, and W. W. Agace. 2013. IRF4 transcription-factor-dependent CD103(+)CD11b(+) dendritic cells drive mucosal T helper 17 cell differentiation. Immunity 38: 958-969. https://doi.org/10.1016/j.immuni.2013.03.009
- Kinnebrew, M. A., C. G. Buffie, G. E. Diehl, L. A. Zenewicz, I. Leiner, T. M. Hohl, R. A. Flavell, D. R. Littman, and E. G. Pamer. 2012. Interleukin 23 production by intestinal CD103(+)CD11b(+) dendritic cells in response to bacterial flagellin enhances mucosal innate immune defense. Immunity 36: 276-287. https://doi.org/10.1016/j.immuni.2011.12.011
- Uematsu, S., K. Fujimoto, M. H. Jang, B. G. Yang, Y. J. Jung, M. Nishiyama, S. Sato, T. Tsujimura, M. Yamamoto, Y. Yokota, H. Kiyono, M. Miyasaka, K. J. Ishii, and S. Akira. 2008. Regulation of humoral and cellular gut immunity by lamina propria dendritic cells expressing Toll-like receptor 5. Nat. Immunol. 9: 769-776. https://doi.org/10.1038/ni.1622
-
Fujimoto, K., T. Karuppuchamy, N. Takemura, M. Shimohigoshi, T. Machida, Y. Haseda, T. Aoshi, K. J. Ishii, S. Akira, and S. Uematsu. 2011. A new subset of
$CD103^+$ $CD8alpha^+$ dendritic cells in the small intestine expresses TLR3, TLR7, and TLR9 and induces Th1 response and CTL activity. J. Immunol. 186: 6287-6295. https://doi.org/10.4049/jimmunol.1004036 - Lecuyer, E., S. Rakotobe, H. Lengline-Garnier, C. Lebreton, M. Picard, C. Juste, R. Fritzen, G. Eberl, K. D. McCoy, A. J. Macpherson, C. A. Reynaud, N. Cerf-Bensussan, and V. Gaboriau-Routhiau. 2014. Segmented filamentous bacterium uses secondary and tertiary lymphoid tissues to induce gut IgA and specific T helper 17 cell responses. Immunity 40: 608-620. https://doi.org/10.1016/j.immuni.2014.03.009
- Palm, N. W., M. R. de Zoete, T. W. Cullen, N. A. Barry, J. Stefanowski, L. Hao, P. H. Degnan, J. Hu, I. Peter, W. Zhang, E. Ruggiero, J. H. Cho, A. L. Goodman, and R. A. Flavell. 2014. Immunoglobulin A coating identifies colitogenic bacteria in inflammatory bowel disease. Cell 158: 1000-1010. https://doi.org/10.1016/j.cell.2014.08.006
- Tezuka, H., Y. Abe, J. Asano, T. Sato, J. Liu, M. Iwata, and T. Ohteki. 2011. Prominent role for plasmacytoid dendritic cells in mucosal T cell-independent IgA induction. Immunity 34: 247-257. https://doi.org/10.1016/j.immuni.2011.02.002
- Molenaar, R., M. Knippenberg, G. Goverse, B. J. Olivier, A. F. de Vos, T. O'Toole, and R. E. Mebius. 2011. Expression of retinaldehyde dehydrogenase enzymes in mucosal dendritic cells and gut-draining lymph node stromal cells is controlled by dietary vitamin A. J. Immunol. 186: 1934-1942. https://doi.org/10.4049/jimmunol.1001672
- Mora, J. R., M. Iwata, B. Eksteen, S. Y. Song, T. Junt, B. Senman, K. L. Otipoby, A. Yokota, H. Takeuchi, P. Ricciardi-Castagnoli, K. Rajewsky, D. H. Adams, and U. H. von Andrian. 2006. Generation of gut-homing IgA-secreting B cells by intestinal dendritic cells. Science 314: 1157-1160. https://doi.org/10.1126/science.1132742
- Chang, S. Y., H. R. Cha, O. Igarashi, P. D. Rennert, A. Kissenpfennig, B. Malissen, M. Nanno, H. Kiyono, and M. N. Kweon. 2008. Cutting edge: Langerin+ dendritic cells in the mesenteric lymph node set the stage for skin and gut immune system cross-talk. J. Immunol. 180: 4361-4365. https://doi.org/10.4049/jimmunol.180.7.4361
- Iwata, M., A. Hirakiyama, Y. Eshima, H. Kagechika, C. Kato, and S. Y. Song. 2004. Retinoic acid imprints gut-homing specificity on T cells. Immunity 21: 527-538. https://doi.org/10.1016/j.immuni.2004.08.011
- Chang, S. Y., H. R. Cha, J. H. Chang, H. J. Ko, H. Yang, B. Malissen, M. Iwata, and M. N. Kweon. 2010. Lack of retinoic acid leads to increased langerin-expressing dendritic cells in gut-associated lymphoid tissues. Gastroenterology 138: 1468-1478, e6. https://doi.org/10.1053/j.gastro.2009.11.006
- Chang, S. Y., and M. N. Kweon. 2010. Langerin-expressing dendritic cells in gut-associated lymphoid tissues. Immunol. Rev. 234: 233-246. https://doi.org/10.1111/j.0105-2896.2009.00878.x
- Sutherland, D. B., and S. Fagarasan. 2014.Gut reactions: Eosinophils add another string to their bow. Immunity 40: 455-457. https://doi.org/10.1016/j.immuni.2014.04.003
- Chu, V. T., A. Beller, S. Rausch, J. Strandmark, M. Zanker, O. Arbach, A. Kruglov, and C. Berek. 2014. Eosinophils promote generation and maintenance of immunoglobulin-A-expressing plasma cells and contribute to gut immune homeostasis. Immunity 40: 582-593. https://doi.org/10.1016/j.immuni.2014.02.014
- Chu, D. K., R. Jimenez-Saiz, C. P. Verschoor, T. D. Walker, S. Goncharova, A. Llop-Guevara, P. Shen, M. E. Gordon, N. G. Barra, J. D. Bassett, J. Kong, R. Fattouh, K. D. McCoy, D. M. Bowdish, J. S. Erjefalt, O. Pabst, A. A. Humbles, R. Kolbeck, S. Waserman, and M. Jordana. 2014. Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo. J. Exp. Med. 211: 1657-1672. https://doi.org/10.1084/jem.20131800
- Atarashi, K., T. Tanoue, T. Shima, A. Imaoka, T. Kuwahara, Y. Momose, G. Cheng, S. Yamasaki, T. Saito, Y. Ohba, T. Taniguchi, K. Takeda, S. Hori, I. I. Ivanov, Y. Umesaki, K. Itoh, and K. Honda. 2011. Induction of colonic regulatory T cells by indigenous Clostridium species. Science 331: 337-341. https://doi.org/10.1126/science.1198469
- Atarashi, K., T. Tanoue, K. Oshima, W. Suda, Y. Nagano, H. Nishikawa, S. Fukuda, T. Saito, S. Narushima, K. Hase, S. Kim, J. V. Fritz, P. Wilmes, S. Ueha, K. Matsushima, H. Ohno, B. Olle, S. Sakaguchi, T. Taniguchi, H. Morita, M. Hattori, and K. Honda. 2013. Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota. Nature 500: 232-236. https://doi.org/10.1038/nature12331
- Benson, M. J., K. Pino-Lagos, M. Rosemblatt, and R. J. Noelle. 2007. All-trans retinoic acid mediates enhanced Treg cell growth, differentiation, and gut homing in the face of high levels of co-stimulation1. J. Exp. Med. 204: 1765-1774. https://doi.org/10.1084/jem.20070719
- Mora, J. R., M. R. Bono, N. Manjunath, W. Weninger, L. L. Cavanagh, M. Rosemblatt, and U. H. Von Andrian. 2003. Selective imprinting of gut-homing T cells by Peyer's patch dendritic cells. Nature 424: 88-93. https://doi.org/10.1038/nature01726
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