The Microbiota Determines Susceptibility to Experimental Autoimmune Uveoretinitis
Language English Country Egypt Media print-electronic
Document type Evaluation Study, Journal Article
Grant support
ETM/351
Chief Scientist Office - United Kingdom
PubMed
27294159
PubMed Central
PMC4886056
DOI
10.1155/2016/5065703
Knihovny.cz E-resources
- MeSH
- Adaptive Immunity MeSH
- Lymphocyte Activation MeSH
- Anti-Bacterial Agents pharmacology MeSH
- Autoantigens immunology MeSH
- Autoimmune Diseases chemically induced immunology microbiology MeSH
- Bacterial Load drug effects MeSH
- Germ-Free Life MeSH
- Interferon-gamma biosynthesis MeSH
- Interleukin-17 biosynthesis MeSH
- Macrophages immunology MeSH
- Microbiota * immunology MeSH
- Disease Models, Animal MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Eye immunology pathology MeSH
- Eye Proteins immunology MeSH
- Retinol-Binding Proteins immunology MeSH
- Flow Cytometry MeSH
- T-Lymphocytes, Regulatory immunology MeSH
- Retina immunology MeSH
- Retinitis chemically induced etiology immunology microbiology MeSH
- Uveitis chemically induced immunology microbiology MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Evaluation Study MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Autoantigens MeSH
- Interferon-gamma MeSH
- Interleukin-17 MeSH
- interstitial retinol-binding protein MeSH Browser
- Eye Proteins MeSH
- Retinol-Binding Proteins MeSH
The microbiota is a crucial modulator of the immune system. Here, we evaluated how its absence or reduction modifies the inflammatory response in the murine model of experimental autoimmune uveoretinitis (EAU). We induced EAU in germ-free (GF) or conventionally housed (CV) mice and in CV mice treated with a combination of broad-spectrum antibiotics either from the day of EAU induction or from one week prior to induction of disease. The severity of the inflammation was assessed by fundus biomicroscopy or by histology, including immunohistology. The immunophenotyping of T cells in local and distant lymph nodes was performed by flow cytometry. We found that GF mice and mice where the microbiota was reduced one week before EAU induction were protected from severe autoimmune inflammation. GF mice had lower numbers of infiltrating macrophages and significantly less T cell infiltration in the retina than CV mice with EAU. GF mice also had reduced numbers of IFN-γ and IL-17-producing T cells and increased numbers of regulatory T cells in the eye-draining lymph nodes. These data suggest that the presence of microbiota during autoantigen recognition regulates the inflammatory response by influencing the adaptive immune response.
See more in PubMed
Blank M., Barzilai O., Shoenfeld Y. Molecular mimicry and auto-immunity. Clinical Reviews in Allergy & Immunology. 2007;32(1):111–118. doi: 10.1007/s12016-007-0025-8. PubMed DOI
Saiga H., Shimada Y., Takeda K. Innate immune effectors in mycobacterial infection. Clinical and Developmental Immunology. 2011;2011:8. doi: 10.1155/2011/347594.347594 PubMed DOI PMC
Van Eden W., Wick G., Albani S., Cohen I. Stress, heat shock proteins, and autoimmunity: how immune responses to heat shock proteins are to be used for the control of chronic inflammatory diseases. Annals of the New York Academy of Sciences. 2007;1113:217–237. doi: 10.1196/annals.1391.020. PubMed DOI
Rothova A. Inflammatory cystoid macular edema. Current Opinion in Ophthalmology. 2007;18(6):487–492. doi: 10.1097/ICU.0b013e3282f03d2e. PubMed DOI
Suttorp-Schulten M. S. A., Jager M. J., Kijlstra A. Recent developments in the treatment of posterior uveitis. Ocular Immunology and Inflammation. 1996;4(4):207–217. doi: 10.3109/09273949609079654. PubMed DOI
Pawate S., Sriram S. The role of infections in the pathogenesis and course of multiple sclerosis. Annals of Indian Academy of Neurology. 2010;13(2):80–86. doi: 10.4103/0972-2327.64622. PubMed DOI PMC
Caspi R. R., Roberge F. G., Chan C.-C., et al. A new model of autoimmune disease. Experimental autoimmune uveoretinitis induced in mice with two different retinal antigens. The Journal of Immunology. 1988;140(5):1490–1495. PubMed
Biswas A., Wilmanski J., Forsman H., et al. Negative regulation of Toll-like receptor signaling plays an essential role in homeostasis of the intestine. European Journal of Immunology. 2011;41(1):182–194. doi: 10.1002/eji.201040479. PubMed DOI PMC
Hrncir T., Stepankova R., Kozakova H., Hudcovic T., Tlaskalova-Hogenova H. Gut microbiota and lipopolysaccharide content of the diet influence development of regulatory T cells: studies in germ-free mice. BMC Immunology. 2008;9, article 65 doi: 10.1186/1471-2172-9-65. PubMed DOI PMC
Tlaskalová-Hogenová H., Stěpánková R., Kozáková H., et al. The role of gut microbiota (commensal bacteria) and the mucosal barrier in the pathogenesis of inflammatory and autoimmune diseases and cancer: contribution of germ-free and gnotobiotic animal models of human diseases. Cellular & Molecular Immunology. 2011;8(2):110–120. doi: 10.1038/cmi.2010.67. PubMed DOI PMC
Berer K., Mues M., Koutrolos M., et al. Commensal microbiota and myelin autoantigen cooperate to trigger autoimmune demyelination. Nature. 2011;479(7374):538–541. doi: 10.1038/nature10554. PubMed DOI
Garrett W. S., Gallini C. A., Yatsunenko T., et al. Enterobacteriaceae act in concert with the gut microbiota to induce spontaneous and maternally transmitted colitis. Cell Host & Microbe. 2010;8(3):292–300. doi: 10.1016/j.chom.2010.08.004. PubMed DOI PMC
Wu H.-J., Ivanov I. I., Darce J., et al. Gut-residing segmented filamentous bacteria drive autoimmune arthritis via T helper 17 cells. Immunity. 2010;32(6):815–827. doi: 10.1016/j.immuni.2010.06.001. PubMed DOI PMC
Lee Y. K., Menezes J. S., Umesaki Y., Mazmanian S. K. Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis. Proceedings of the National Academy of Sciences of the United States of America. 2011;108(supplement 1):4615–4622. doi: 10.1073/pnas.1000082107. PubMed DOI PMC
Denou E., Lolmède K., Garidou L., et al. Defective NOD2 peptidoglycan sensing promotes diet-induced inflammation, dysbiosis, and insulin resistance. EMBO Molecular Medicine. 2015;7(3):259–274. doi: 10.15252/emmm.201404169. PubMed DOI PMC
Markle J. G. M., Frank D. N., Mortin-Toth S., et al. Sex differences in the gut microbiome drive hormone-dependent regulation of autoimmunity. Science. 2013;339(6123):1084–1088. doi: 10.1126/science.1233521. PubMed DOI
Wen L., Ley R. E., Volchkov P. Y., et al. Innate immunity and intestinal microbiota in the development of Type 1 diabetes. Nature. 2008;455(7216):1109–1113. doi: 10.1038/nature07336. PubMed DOI PMC
Caspi R. R., Horai R., Zárate-Bladés C., et al. Activation of autoreactive T cells by endogenous commensal microflora provokes spontaneous autoimmunity in the immunologically privileged eye. Investigative Ophthalmology & Visual Science. 2014;55(13):4600–4600.
Nakamura Y., Metea C., Gruner H., et al. Altering the gut microbiota ameliorates experimental autoimmune uveitis. Investigative Ophthalmology & Visual Science. 2014;55(13):2497–2497.
Horai R., Zárate-Bladés C. R., Dillenburg-Pilla P., et al. Microbiota-dependent activation of an autoreactive T cell receptor provokes autoimmunity in an immunologically privileged site. Immunity. 2015;43(2):343–353. doi: 10.1016/j.immuni.2015.07.014. PubMed DOI PMC
Tubo N. J., Pagán A. J., Taylor J. J., et al. Single naive CD4+ T cells from a diverse repertoire produce different effector cell types during infection. Cell. 2013;153(4):785–796. doi: 10.1016/j.cell.2013.04.007. PubMed DOI PMC
Stoppelkamp S., Reid D. M., Yeoh J., et al. Murine pattern recognition receptor dectin-1 is essential in the development of experimental autoimmune uveoretinitis. Molecular Immunology. 2015;67(2, part B):398–406. doi: 10.1016/j.molimm.2015.07.002. PubMed DOI
Avichezer D., Silver P. B., Chan C.-C., Wiggert B., Caspi R. R. Identification of a new epitope of human IRBP that induces autoimmune uveoretinitis in mice of the H-2b haplotype. Investigative Ophthalmology and Visual Science. 2000;41(1):127–131. PubMed
Broderick C., Hoek R. M., Forrester J. V., Liversidge J., Sedgwick J. D., Dick A. D. Constitutive retinal CD200 expression regulates resident microglia and activation state of inflammatory cells during experimental autoimmune uveoretinitis. American Journal of Pathology. 2002;161(5):1669–1677. doi: 10.1016/S0002-9440(10)64444-6. PubMed DOI PMC
Klimesova K., Kverka M., Zakostelska Z., et al. Altered gut microbiota promotes colitis-associated cancer in IL-1 receptor-associated kinase M-deficient mice. Inflammatory Bowel Diseases. 2013;19(6):1266–1277. doi: 10.1097/mib.0b013e318281330a. PubMed DOI PMC
Paques M., Guyomard J.-L., Simonutti M., et al. Panretinal, high-resolution color photography of the mouse fundus. Investigative Ophthalmology & Visual Science. 2007;48(6):2769–2774. doi: 10.1167/iovs.06-1099. PubMed DOI
Copland D. A., Wertheim M. S., Armitage W. J., Nicholson L. B., Raveney B. J. E., Dick A. D. The clinical time-course of experimental autoimmune uveoretinitis using topical endoscopic fundal imaging with histologic and cellular infiltrate correlation. Investigative Ophthalmology & Visual Science. 2008;49(12):5458–5465. doi: 10.1167/iovs.08-2348. PubMed DOI
Xu H., Koch P., Chen M., Lau A., Reid D. M., Forrester J. V. A clinical grading system for retinal inflammation in the chronic model of experimental autoimmune uveoretinitis using digital fundus images. Experimental Eye Research. 2008;87(4):319–326. doi: 10.1016/j.exer.2008.06.012. PubMed DOI
Thurau S. R., Chan C.-C., Nussenblatt R. B., Caspi R. R. Oral tolerance in a murine model of relapsing experimental autoimmune uveoretinitis (EAU): induction of protective tolerance in primed animals. Clinical & Experimental Immunology. 1997;109(2):370–376. doi: 10.1046/j.1365-2249.1997.4571356.x. PubMed DOI PMC
Dick A. D., Cheng Y. F., Liversidge J., Forrester J. V. Immunomodulation of experimental autoimmune uveoretinitis: a model of tolerance induction with retinal antigens. Eye. 1994;8(1):52–59. doi: 10.1038/eye.1994.10. PubMed DOI
Jones M., Cordell J. L., Beyers A. D., Tse A. G. D., Mason D. Y. Detection of T and B cells in many animal species using cross-reactive anti-peptide antibodies. Journal of Immunology. 1993;150(12):5429–5435. PubMed
Jiang H.-R., Hwenda L., Makinen K., Oetke C., Crocker P. R., Forrester J. V. Sialoadhesin promotes the inflammatory response in experimental autoimmune uveoretinitis. Journal of Immunology. 2006;177(4):2258–2264. doi: 10.4049/jimmunol.177.4.2258. PubMed DOI
Pagliari D., Piccirillo C. A., Larbi A., Cianci R. The interactions between innate immunity and microbiota in gastrointestinal diseases. Journal of Immunology Research. 2015;2015:3. doi: 10.1155/2015/898297.898297 PubMed DOI PMC
Pagliari D., Urgesi R., Frosali S., et al. The interaction among microbiota, immunity, and genetic and dietary factors is the condicio sine qua non celiac disease can develop. Journal of Immunology Research. 2015;2015:10. doi: 10.1155/2015/123653.123653 PubMed DOI PMC
Kverka M., Tlaskalova-Hogenova H. Two faces of microbiota in inflammatory and autoimmune diseases: triggers and drugs. APMIS. 2013;121(5):403–421. doi: 10.1111/apm.12007. PubMed DOI
Bonamichi-Santos R., Aun M. V., Agondi R. C., Kalil J., Giavina-Bianchi P. Microbiome and asthma: what have experimental models already taught us? Journal of Immunology Research. 2015;2015:8. doi: 10.1155/2015/614758.614758 PubMed DOI PMC
Nelson M. H., Diven M. A., Huff L. W., Paulos C. M. Harnessing the microbiome to enhance cancer immunotherapy. Journal of Immunology Research. 2015;2015:12. doi: 10.1155/2015/368736.368736 PubMed DOI PMC
Giorgetti G., Brandimarte G., Fabiocchi F., et al. Interactions between innate immunity, microbiota, and probiotics. Journal of Immunology Research. 2015;2015:7. doi: 10.1155/2015/501361.501361 PubMed DOI PMC
Honda K., Littman D. R. The microbiome in infectious disease and inflammation. Annual Review of Immunology. 2012;30(1):759–795. doi: 10.1146/annurev-immunol-020711-074937. PubMed DOI PMC
Hansen C. H. F., Nielsen D. S., Kverka M., et al. Patterns of early gut colonization shape future immune responses of the host. PLoS ONE. 2012;7(3) doi: 10.1371/journal.pone.0034043.e34043 PubMed DOI PMC
Hudcovic T., Štěpánková R., Cebra J., Tlaskalová-Hogenová H. The role of microflora in the development of intestinal inflammation: acute and chronic colitis induced by dextran sulfate in germ-free and conventionally reared immunocompetent and immunodeficient mice. Folia Microbiologica. 2001;46(6):565–572. doi: 10.1007/bf02818004. PubMed DOI
Řeháková Z., Čapková J., Štěpánková R., et al. Germ-free mice do not develop ankylosing enthesopathy, a spontaneous joint disease. Human Immunology. 2000;61(6):555–558. doi: 10.1016/S0198-8859(00)00122-1. PubMed DOI
Forrester J. V., Xu H., Kuffová L., Dick A. D., McMenamin P. G. Dendritic cell physiology and function in the eye. Immunological Reviews. 2010;234(1):282–304. doi: 10.1111/j.0105-2896.2009.00873.x. PubMed DOI
Preisova J. Treatment of sympathetic ophthalmia with penicillin. Ceskoslovenská Oftalmologie. 1952;8(3):151–157. PubMed
Grove D. I., Mahmoud A. A. F., Warren K. S. Suppression of cell-mediated immunity by metronidazole. International Archives of Allergy and Applied Immunology. 1977;54(5):422–427. doi: 10.1159/000231857. PubMed DOI
Furusawa Y., Obata Y., Fukuda S., et al. Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells. Nature. 2013;504(7480):446–450. doi: 10.1038/nature12721. PubMed DOI
Martín R., Chain F., Miquel S., et al. The commensal bacterium Faecalibacterium prausnitzii is protective in DNBS-induced chronic moderate and severe colitis models. Inflammatory Bowel Diseases. 2014;20(3):417–430. doi: 10.1097/01.mib.0000440815.76627.64. PubMed DOI
Dong Q., Brulc J. M., Iovieno A., et al. Diversity of bacteria at healthy human conjunctiva. Investigative Ophthalmology & Visual Science. 2011;52(8):5408–5413. doi: 10.1167/iovs.10-6939. PubMed DOI PMC
Lee E. J., Brown B. R., Vance E. E., et al. Mincle activation and the Syk/Card9 signaling axis are central to the development of autoimmune disease of the eye. The Journal of Immunology. 2016;196(7):3148–3158. doi: 10.4049/jimmunol.1502355. PubMed DOI PMC
Contribution of Infectious Agents to the Development of Celiac Disease
Immune Privilege: The Microbiome and Uveitis
Crucial Role of Microbiota in Experimental Psoriasis Revealed by a Gnotobiotic Mouse Model