Cited by 24Gut microbiota and healthMultiple Sclerosis Research StudiesT-cell and B-cell Immunology

MAIT Cells and Microbiota in Multiple Sclerosis and Other Autoimmune Diseases

Open access
Mechelli, Rosella, Romano, Silvia, Romano, Carmela, Morena, Emanuele, Buscarinu, Maria Chiara, Bigi, Rachele, Bellucci, Gianmarco, Reniè, Roberta +3 more·2021·Microorganisms

Abstract

The functions of mucosal-associated invariant T (MAIT) cells in homeostatic conditions include the interaction with the microbiota and its products, the protection of body barriers, and the mounting of a tissue-repair response to injuries or infections. Dysfunction of MAIT cells and dysbiosis occur in common chronic diseases of inflammatory, metabolic, and tumor nature. This review is aimed at analyzing the changes of MAIT cells, as well as of the microbiota, in multiple sclerosis and other autoimmune disorders. Common features of dysbiosis in these conditions are the reduced richness of microbial species and the unbalance between pro-inflammatory and immune regulatory components of the gut microbiota. The literature concerning MAIT cells in these disorders is rather complex, and sometimes not consistent. In multiple sclerosis and other autoimmune conditions, several studies have been done, or are in progress, to find correlations between intestinal permeability, dysbiosis, MAIT cell responses, and clinical biomarkers in treated and treatment-naïve patients. The final aims are to explain what activates MAIT cells in diseases not primarily infective, which interactions with the microbiota are potentially pathogenic, and their dynamics related to disease course and disease-modifying treatments.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.3390/microorganisms9061132

Cites

9 of 9 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 104

  1. [1]Dusseaux M. Martin E. Serriari N. Péguillet I. Premel V. Louis D. Milder M. Le Bourhis L. Soudais C. Treiner E. Human MAIT cells are xenobiotic-resistant, tissue-targeted, CD161hi IL-17–secreting T cells Blood 2011 117 1250 1259 10.1182/blood-2010-08-303339 21084709 · DOI
  2. [2]Porcelli S. Yockey C.E. Brenner M.B. Balk S.P. Analysis of T cell antigen receptor (TCR) expression by human peripheral blood CD4-8- alpha/beta T cells demonstrates preferential use of several V beta genes and an invariant TCR alpha chain J. Exp. Med. 1993 178 1 16 10.1084/jem.178.1.1 8391057 PMC2191070 · DOI
  3. [3]Treiner E. Duban L. Bahram S. Radosavljevic M. Wanner V. Tilloy F. Affaticati P. Gilfillan S. Lantz O. Selection of evolutionarily conserved mucosal-associated invariant T cells by MR Nat. Cell Biol. 2003 422 164 169 10.1038/nature01433 12634786 · DOI · Paper page
  4. [4]Kjer-Nielsen L. Patel O. Corbett A.J. Le Nours J. Meehan B. Liu L. Bhati M. Chen Z. Kostenko L. Reantragoon R. MR1 presents microbial vitamin B metabolites to MAIT cells Nat. Cell Biol. 2012 491 717 723 10.1038/nature11605 23051753 · DOI · Paper page
  5. [5]Legoux F. Salou M. Lantz O. MAIT Cell Development and Functions: The Microbial Connection Immunology 2020 53 710 723 10.1016/j.immuni.2020.09.009 33053329 · DOI
  6. [6]Legoux F. Bellet D. Daviaud C. El Morr Y. Darbois A. Niort K. Procopio E. Salou M. Gilet J. Ryffel B. Microbial metabolites control the thymic development of mucosal-associated invariant T cells Science 2019 366 494 499 10.1126/science.aaw2719 31467190 · DOI · Paper page
  7. [7]Tilloy F. Treiner E. Park S.-H. Garcia C. Lemonnier F. De La Salle H. Bendelac A. Bonneville M. Lantz O. An Invariant T Cell Receptor α Chain Defines a Novel TAP-independent Major Histocompatibility Complex Class Ib–restricted α/β T Cell Subpopulation in Mammals J. Exp. Med. 1999 189 1907 1921 10.1084/jem.189.12.1907 10377186 PMC2192962 · DOI
  8. [8]Honda K. Littman D.R. The microbiota in adaptive immune homeostasis and disease Nat. Cell Biol. 2016 535 75 84 10.1038/nature18848 27383982 · DOI · Paper page
  9. [10]Lin Q. Kuypers M. Philpott D.J. Mallevaey T. The dialogue between unconventional T cells and the microbiota Mucosal Immunol. 2020 13 867 876 10.1038/s41385-020-0326-2 32704035 · DOI
  10. [11]Schmaler M. Colone A. Spagnuolo J. Zimmermann M. Lepore M. Kalinichenko A. Bhatia S. Cottier F. Rutishauser T. Pavelka N. Modulation of bacterial metabolism by the microenvironment controls MAIT cell stimulation Mucosal Immunol. 2018 11 1060 1070 10.1038/s41385-018-0020-9 29743612 · DOI
  11. [12]Buscarinu M.C. Fornasiero A. Romano S. Ferraldeschi M. Mechelli R. Reniè R. Morena E. Romano C. Pellicciari G. Landi A.C. The Contribution of Gut Barrier Changes to Multiple Sclerosis Pathophysiology Front. Immunol. 2019 10 1916 10.3389/fimmu.2019.01916 31555257 PMC6724505 · DOI
  12. [14]Kadowaki A. Saga R. Lin Y. Sato W. Yamamura T. Gut microbiota-dependent CCR9+CD4+ T cells are altered in secondary progressive multiple sclerosis Brain 2019 142 916 931 10.1093/brain/awz012 30770703 PMC6439331 · DOI
  13. [15]Cekanaviciute E. Pröbstel A.-K. Thomann A. Runia T.F. Casaccia P. Sand I.K. Crabtree E. Singh S. Morrissey J. Barba P. Multiple Sclerosis-Associated Changes in the Composition and Immune Functions of Spore-Forming Bacteria mSystems 2018 3 e00083-18 10.1128/mSystems.00083-18 30417113 PMC6222044 · DOI
  14. [16]Saresella M. Marventano I. Barone M. La Rosa F. Piancone F. Mendozzi L. D’Arma A. Rossi V. Pugnetti L. Roda G. Alterations in Circulating Fatty Acid Are Associated with Gut Microbiota Dysbiosis and Inflammation in Multiple Sclerosis Front. Immunol. 2020 11 1390 10.3389/fimmu.2020.01390 32733460 PMC7358580 · DOI
  15. [17]Ling Z. Cheng Y. Yan X. Shao L. Liu X. Zhou D. Zhang L. Yu K. Zhao L. Alterations of the Fecal Microbiota in Chinese Patients with Multiple Sclerosis Front. Immunol. 2020 11 590783 10.3389/fimmu.2020.590783 33391265 PMC7772405 · DOI
  16. [18]Takewaki D. Suda W. Sato W. Takayasu L. Kumar N. Kimura K. Kaga N. Mizuno T. Miyake S. Hattori M. Alterations of the gut ecological and functional microenvironment in different stages of multiple sclerosis Proc. Natl. Acad. Sci. USA 2020 117 22402 22412 10.1073/pnas.2011703117 32839304 PMC7486801 · DOI
  17. [19]Reynders T. Devolder L. Valles-Colomer M. Van Remoortel A. Joossens M. De Keyser J. Nagels G. D’Hooghe M. Raes J. Gut microbiome variation is associated to Multiple Sclerosis phenotypic subtypes Ann. Clin. Transl. Neurol. 2020 7 406 419 10.1002/acn3.51004 32162850 PMC7187717 · DOI
  18. [20]Tankou S.K. Regev K. Healy B.C. Tjon E. Laghi L. Cox L.M. Kivisäkk P. Pierre I.V. Hrishikesh L. Gandhi R. A probiotic modulates the microbiome and immunity in multiple sclerosis Ann. Neurol. 2018 83 1147 1161 10.1002/ana.25244 29679417 PMC6181139 · DOI
  19. [21]Duscha A. Gisevius B. Hirschberg S. Yissachar N. Stangl G.I. Eilers E. Bader V. Haase S. Kaisler J. David C. Propionic Acid Shapes the Multiple Sclerosis Disease Course by an Immunomodulatory Mechanism Cell 2020 180 1067 1080 10.1016/j.cell.2020.02.035 32160527 · DOI
  20. [22]Berer K. Gerdes L.A. Cekanaviciute E. Jia X. Xiao L. Xia Z. Liu C. Klotz L. Stauffer U. Baranzini S.E. Gut microbiota from multiple sclerosis patients enables spontaneous autoimmune encephalomyelitis in mice Proc. Natl. Acad. Sci. USA 2017 114 10719 10724 10.1073/pnas.1711233114 28893994 PMC5635914 · DOI · Paper page
  21. [23]Liu S. Rezende R.M. Moreira T.G. Tankou S.K. Cox L.M. Wu M. Song A. Dhang F.H. Wei Z. Costamagna G. Oral Administration of miR-30d from Feces of MS Patients Suppresses MS-like Symptoms in Mice by Expanding Akkermansia muciniphila Cell Host Microbe 2019 26 779 794 10.1016/j.chom.2019.10.008 31784260 PMC6948921 · DOI
  22. [24]Cox L.M. Maghzi A.H. Liu S. Tankou S.K. Bs F.H.D. Bs V.W. Song A. Wasén C. Tauhid S. Chu R. Gut Microbiome in Progressive Multiple Sclerosis Ann. Neurol. 2021 89 1195 1211 10.1002/ana.26084 33876477 PMC8132291 · DOI
  23. [25]Mu Q. Tavella V.J. Kirby J.L. Cecere T.E. Chung M. Lee J. Li S. Ahmed S.A. Eden K. Allen I.C. Antibiotics ameliorate lupus-like symptoms in mice Sci. Rep. 2017 7 1 14 10.1038/s41598-017-14223-0 29057975 PMC5651817 · DOI
  24. [26]Mu Q. Zhang H. Liao X. Lin K. Liu H. Edwards M.R. Ahmed S.A. Yuan R. Li L. Cecere T.E. Control of lupus nephritis by changes of gut microbiota Microbiome 2017 5 1 12 10.1186/s40168-017-0300-8 28697806 PMC5505136 · DOI
  25. [27]Luo X.M. Edwards M.R. Mu Q. Yu Y. Vieson M.D. Reilly C.M. Ahmed S.A. Bankole A.A. Gut Microbiota in Human Systemic Lupus Erythematosus and a Mouse Model of Lupus Appl. Environ. Microbiol. 2017 84 15 10.1128/AEM.02288-17 PMC5795066 29196292 · DOI
  26. [28]Zhang X. Zhang D. Jia H. Feng Q. Wang D. Liang D. Wu X. Li J. Tang L. Li Y. The oral and gut microbiomes are perturbed in rheumatoid arthritis and partly normalized after treatment Nat. Med. 2015 21 895 905 10.1038/nm.3914 26214836 · DOI · Paper page
  27. [30]Tsigalou C. Stavropoulou E. Bezirtzoglou E. Current Insights in Microbiome Shifts in Sjogren’s Syndrome and Possible Therapeutic Interventions Front. Immunol. 2018 9 1106 10.3389/fimmu.2018.01106 29881381 PMC5976780 · DOI
  28. [31]Sheehan D. Moran C. Shanahan F. The microbiota in inflammatory bowel disease J. Gastroenterol. 2015 50 495 507 10.1007/s00535-015-1064-1 25808229 · DOI
  29. [32]Ma Y. Xu X. Li M. Cai J. Wei Q. Niu H. Gut microbiota promote the inflammatory response in the pathogenesis of systemic lupus erythematosus Mol. Med. 2019 25 1 16 10.1186/s10020-019-0102-5 31370803 PMC6676588 · DOI
  30. [33]Hevia A. Milani C. López P. Cuervo A. Arboleya S. Duranti S. Turroni F. González S. Suárez A. Gueimonde M. Intestinal Dysbiosis Associated with Systemic Lupus Erythematosus mBio 2014 5 e01548-14 10.1128/mBio.01548-14 25271284 PMC4196225 · DOI
  31. [35]Khorasani S. Mahmoudi M. Kalantari M.R. Arab F.L. Esmaeili S.-A. Mardani F. Tabasi N. Rastin M. Amelioration of regulatory T cells by Lactobacillus delbrueckii and Lactobacillus rhamnosus in pristane-induced lupus mice model J. Cell. Physiol. 2019 234 9778 9786 10.1002/jcp.27663 30370554 · DOI
  32. [36]Esmaeili S.-A. Mahmoudi M. Rezaieyazdi Z. Sahebari M. Tabasi N. Sahebkar A. Rastin M. Generation of tolerogenic dendritic cells usingLactobacillus rhamnosusandLactobacillus delbrueckiias tolerogenic probiotics J. Cell. Biochem. 2018 119 7865 7872 10.1002/jcb.27203 29943843 · DOI
  33. [37]Van der Meulen T.A. Harmsen H.J. Vila A.V. Kurilshikov A. Liefers S.C. Zhernakova A. Fu J. Wijmenga C. Weersma R.K. de Leeuw K. Shared gut, but distinct oral microbiota composition in primary Sjögren’s syndrome and systemic lupus erythematosus J. Autoimmun. 2019 97 77 87 10.1016/j.jaut.2018.10.009 30416033 · DOI
  34. [38]Greiling T.M. Dehner C. Chen X. Hughes K. Iñiguez A.J. Boccitto M. Ruiz D.Z. Renfroe S.C. Vieira S.M. Ruff W.E. Commensal orthologs of the human autoantigen Ro60 as triggers of autoimmunity in lupus Sci. Transl. Med. 2018 10 eaan2306 10.1126/scitranslmed.aan2306 29593104 PMC5918293 · DOI
  35. [39]Van Der Meulen T.A. Harmsen H.J.M. Bootsma H. Liefers S.C. Vila A.V. Zhernakova A. Fu J. Wijmenga C. Spijkervet F.K.L. Kroese F.G.M. Dysbiosis of the buccal mucosa microbiome in primary Sjögren’s syndrome patients Rheumatology 2018 57 2225 2234 10.1093/rheumatology/key215 30060225 · DOI
  36. [40]Van Der Meulen T.A. Harmsen H.J.M. Bootsma H. Liefers S.C. Vila A.V. Zhernakova A. Weersma R.K. Spijkervet F.K.L. Kroese F.G.M. Vissink A. Reduced salivary secretion contributes more to changes in the oral microbiome of patients with primary Sjögren’s syndrome than underlying disease Ann. Rheum. Dis. 2018 77 1542 1544 10.1136/annrheumdis-2018-213026 29572289 · DOI
  37. [41]Alam J. Lee A. Lee J. Kwon D.I. Park H.K. Park J.-H. Jeon S. Baek K. Lee J. Park S.-H. Dysbiotic oral microbiota and infected salivary glands in Sjögren’s syndrome PLoS ONE 2020 15 e0230667 10.1371/journal.pone.0230667 32208441 PMC7092996 · DOI
  38. [42]Rusthen S. Kristoffersen A.K. Young A. Galtung H.K. Petrovski B.É. Palm Ø. Enersen M. Jensen J.L. Dysbiotic salivary microbiota in dry mouth and primary Sjögren’s syndrome patients PLoS ONE 2019 14 e0218319 10.1371/journal.pone.0218319 31211815 PMC6581286 · DOI
  39. [44]Kamal Y. Kandil M. Eissa M. Yousef R. Elsaadany B. Probiotics as a prophylaxis to prevent oral candidiasis in patients with Sjogren’s syndrome: A double-blinded, placebo-controlled, randomized trial Rheumatol. Int. 2020 40 873 879 10.1007/s00296-020-04558-9 32219478 · DOI
  40. [45]Choi S.H. Oh J.W. Ryu J.S. Kim H.M. Im S.-H. Kim K.P. Kim M.K. IRT5 Probiotics Changes Immune Modulatory Protein Expression in the Extraorbital Lacrimal Glands of an Autoimmune Dry Eye Mouse Model Investig. Opthalmol. Vis. Sci. 2020 61 42 10.1167/iovs.61.3.42 32232342 PMC7401425 · DOI
  41. [46]Kishikawa T. Maeda Y. Nii T. Motooka D. Matsumoto Y. Matsushita M. Matsuoka H. Yoshimura M. Kawada S. Teshigawara S. Metagenome-wide association study of gut microbiome revealed novel aetiology of rheumatoid arthritis in the Japanese population Ann. Rheum. Dis. 2019 79 103 111 10.1136/annrheumdis-2019-215743 31699813 PMC6937407 · DOI
  42. [47]Scher J.U. Sczesnak A. Longman R.S. Segata N. Ubeda C. Bielski C. Rostron T. Cerundolo V. Pamer E.G. Abramson S.B. Expansion of intestinal Prevotella copri correlates with enhanced susceptibility to arthritis eLife 2013 2 e01202 10.7554/eLife.01202 24192039 PMC3816614 · DOI · Paper page
  43. [48]Alpizar-Rodriguez D. Lesker T.R. Gronow A. Gilbert B. Raemy E. Lamacchia C. Gabay C. Finckh A. Strowig T. Prevotella copri in individuals at risk for rheumatoid arthritis Ann. Rheum. Dis. 2019 78 590 593 10.1136/annrheumdis-2018-214514 30760471 · DOI · Paper page
  44. [49]Liu X. Zou Q. Zeng B. Fang Y. Wei H. Analysis of Fecal Lactobacillus Community Structure in Patients with Early Rheumatoid Arthritis Curr. Microbiol. 2013 67 170 176 10.1007/s00284-013-0338-1 23483307 · DOI
  45. [51]Vaghef-Mehrabany E. Alipour B. Homayouni-Rad A. Sharif S.-K. Asghari-Jafarabadi M. Zavvari S. Probiotic supplementation improves inflammatory status in patients with rheumatoid arthritis Nutrients 2014 30 430 435 10.1016/j.nut.2013.09.007 24355439 · DOI
  46. [52]Zamani B. Golkar H.R. Farshbaf S. Emadi-Baygi M. Tajabadi-Ebrahimi M. Jafari P. Akhavan R. Taghizadeh M. Memarzadeh M.R. Asemi Z. Clinical and metabolic response to probiotic supplementation in patients with rheumatoid arthritis: A randomized, double-blind, placebo-controlled trial Int. J. Rheum. Dis. 2016 19 869 879 10.1111/1756-185X.12888 27135916 · DOI
  47. [53]Hatakka K. Martio J. Korpela M. Herranen M. Poussa T. Laasanen T. Saxelin M. Vapaatalo H. Moilanen E. Korpela R. Effects of probiotic therapy on the activity and activation of mild rheumatoid arthritis—A pilot study Scand. J. Rheumatol. 2003 32 211 215 10.1080/03009740310003695 14626627 · DOI
  48. [54]Pineda M.D.L.A. Thompson S.F. Summers K. De Leon F. Pope J. Reid G. A randomized, double-blinded, placebo-controlled pilot study of probiotics in active rheumatoid arthritis Med. Sci. Monit. 2011 17 CR347 CR354 10.12659/msm.881808 21629190 PMC3539551 · DOI
  49. [55]De Goffau M.C. Fuentes S. Bogert B.V.D. Honkanen H. De Vos W.M. Welling G.W. Hyoty H. Harmsen H.J.M. Aberrant gut microbiota composition at the onset of type 1 diabetes in young children Diabetology 2014 57 1569 1577 10.1007/s00125-014-3274-0 24930037 · DOI
  50. [56]De Goffau M.C. Luopajärvi K. Knip M. Ilonen J. Ruohtula T. Härkönen T. Orivuori L. Hakala S. Welling G.W. Harmsen H.J. Fecal Microbiota Composition Differs between Children With -Cell Autoimmunity and Those Without Diabetes 2013 62 1238 1244 10.2337/db12-0526 23274889 PMC3609581 · DOI
  51. [57]Kostic A.D. Gevers D. Siljander H. Vatanen T. Hyoty H. Hämäläinen A.-M. Peet A. Tillmann V. Pöhö P. Mattila I. The Dynamics of the Human Infant Gut Microbiome in Development and in Progression toward Type 1 Diabetes Cell Host Microbe 2015 17 260 273 10.1016/j.chom.2015.01.001 25662751 PMC4689191 · DOI
  52. [58]Jia L. Shan K. Pan L.-L. Feng N. Lv Z. Sun Y. Lingling J. Wu C. Zhang H. Chen W. Clostridium butyricum CGMCC0313.1 Protects against Autoimmune Diabetes by Modulating Intestinal Immune Homeostasis and Inducing Pancreatic Regulatory T Cells Front. Immunol. 2017 8 1345 10.3389/fimmu.2017.01345 29097999 PMC5654235 · DOI
  53. [59]Hu Y. Jin P. Peng J. Zhang X. Wong F.S. Wen L. Different immunological responses to early-life antibiotic exposure affecting autoimmune diabetes development in NOD mice J. Autoimmun. 2016 72 47 56 10.1016/j.jaut.2016.05.001 27178773 PMC4958594 · DOI
  54. [60]Peng J. Narasimhan S. Marchesi J.R. Benson A. Wong F.S. Wen L. Long term effect of gut microbiota transfer on diabetes development J. Autoimmun. 2014 53 85 94 10.1016/j.jaut.2014.03.005 24767831 PMC4361177 · DOI
  55. [61]Marietta E.V. Gomez A.M. Yeoman C. Tilahun A.Y. Clark C.R. Luckey D.H. Murray J.A. White B.A. Kudva Y.C. Rajagopalan G. Low Incidence of Spontaneous Type 1 Diabetes in Non-Obese Diabetic Mice Raised on Gluten-Free Diets Is Associated with Changes in the Intestinal Microbiome PLoS ONE 2013 8 e78687 10.1371/journal.pone.0078687 24236037 PMC3827256 · DOI
  56. [62]Nishida A. Inoue R. Inatomi O. Bamba S. Naito Y. Andoh A. Gut microbiota in the pathogenesis of inflammatory bowel disease Clin. J. Gastroenterol. 2018 11 1 10 10.1007/s12328-017-0813-5 29285689 · DOI
  57. [63]Lopez-Siles M. Duncan S.H. Garcia-Gil L.J. Martinez-Medina M. Faecalibacterium prausnitzii: From microbiology to diagnostics and prognostics ISME J. 2017 11 841 852 10.1038/ismej.2016.176 28045459 PMC5364359 · DOI
  58. [64]Lopez-Siles M. Martinez-Medina M. Surís-Valls R. Aldeguer X. Sabat-Mir M. Duncan S.H. Flint H.J. Garcia-Gil L.J. Changes in the Abundance of Faecalibacterium prausnitzii Phylogroups I and II in the Intestinal Mucosa of Inflammatory Bowel Disease and Patients with Colorectal Cancer Inflamm. Bowel Dis. 2016 22 28 41 10.1097/MIB.0000000000000590 26595550 · DOI · Paper page
  59. [65]Peterson D.A. Frank D.N. Pace N.R. Gordon J.I. Metagenomic Approaches for Defining the Pathogenesis of Inflammatory Bowel Diseases Cell Host Microbe 2008 3 417 427 10.1016/j.chom.2008.05.001 18541218 PMC2872787 · DOI · Paper page
  60. [66]Ahmed I. Roy B.C. Khan S.A. Septer S. Umar S. Microbiome, Metabolome and Inflammatory Bowel Disease Microorganisms 2016 4 20 10.3390/microorganisms4020020 PMC5029486 27681914 · DOI
  61. [67]Annibali V. Ristori G. Angelini D.F. Serafini B. Mechelli R. Cannoni S. Romano S. Paolillo A. Abderrahim H. Diamantini A. CD161highCD8+T cells bear pathogenetic potential in multiple sclerosis Brain 2011 134 542 554 10.1093/brain/awq354 21216829 · DOI
  62. [68]Friese M.A. Fugger L. Pathogenic CD8+T cells in multiple sclerosis Ann. Neurol. 2009 66 132 141 10.1002/ana.21744 19743458 · DOI
  63. [69]Sawcer S. Hellenthal G. Pirinen M. Spencer C.C.A. Patsopoulos N.A. Moutsianas L. Dilthey A. Su Z. Freeman C. Hunt S.E. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Nature 2011 476 214 219 10.1038/nature10251 21833088 PMC3182531 · DOI · Paper page
  64. [71]Miyazaki Y. Miyake S. Chiba A. Lantz O. Yamamura T. Mucosal-associated invariant T cells regulate Th1 response in multiple sclerosis Int. Immunol. 2011 23 529 535 10.1093/intimm/dxr047 21712423 · DOI
  65. [72]Croxford J.L. Miyake S. Huang Y.-Y. Shimamura M. Yamamura T. Invariant Vα19i T cells regulate autoimmune inflammation Nat. Immunol. 2006 7 987 994 10.1038/ni1370 16878136 · DOI
  66. [73]Salou M. Nicol B. Garcia A. Baron D. Michel L. Elong-Ngono A. Hulin P. Nedellec S. Jacq-Foucher M. Le Frère F. Neuropathologic, phenotypic and functional analyses of Mucosal Associated Invariant T cells in Multiple Sclerosis Clin. Immunol. 2016 166–167 1 11 10.1016/j.clim.2016.03.014 27050759 · DOI · Paper page
  67. [74]Willing A. Leach O.A. Ufer F. Attfield K.E. Steinbach K. Kursawe N. Piedavent M. Friese M.A. CD8+MAIT cells infiltrate into the CNS and alterations in their blood frequencies correlate with IL-18 serum levels in multiple sclerosis Eur. J. Immunol. 2014 44 3119 3128 10.1002/eji.201344160 25043505 · DOI
  68. [75]Held K. Bhonsle-Deeng L. Siewert K. Sato W. Beltrán E. Schmidt S. Rühl G. Ng J.K. Engerer P. Moser M. αβ T-cell receptors from multiple sclerosis brain lesions show MAIT cell–related features Neurol. Neuroimmunol. Neuroinflammation 2015 2 e107 10.1212/NXI.0000000000000107 PMC4426681 25977934 · DOI
  69. [76]Willing A. Jäger J. Reinhardt S. Kursawe N. Friese M.A. Production of IL-17 by MAIT Cells Is Increased in Multiple Sclerosis and Is Associated with IL-7 Receptor Expression J. Immunol. 2018 200 974 982 10.4049/jimmunol.1701213 29298833 · DOI
  70. [77]Mexhitaj I. Nyirenda M.H. Li R. O’Mahony J. Rezk A. Rozenberg A. Moore C.S. Johnson T. Sadovnick D. Collins D.L. Abnormal effector and regulatory T cell subsets in paediatric-onset multiple sclerosis Brain 2019 142 617 632 10.1093/brain/awz017 30759186 PMC6391601 · DOI
  71. [78]Contentti E.C. Farez M.F. Correale J. Mucosal-Associated Invariant T Cell Features and TCR Repertoire Characteristics During the Course of Multiple Sclerosis Front. Immunol. 2019 10 2690 10.3389/fimmu.2019.02690 31824489 PMC6880779 · DOI
  72. [79]Abrahamsson S.V. Angelini D.F. Dubinsky A.N. Morel E. Oh U. Jones J.L. Carassiti D. Reynolds R. Salvetti M. Calabresi P.A. Non-myeloablative autologous haematopoietic stem cell transplantation expands regulatory cells and depletes IL-17 producing mucosal-associated invariant T cells in multiple sclerosis Brain 2013 136 2888 2903 10.1093/brain/awt182 23864273 PMC3754461 · DOI
  73. [80]Moore J.J. Massey J.C. Ford C.D. Khoo M.L. Zaunders J.J. Hendrawan K. Barnett Y. Barnett M.H. Kyle K.A. Zivadinov R. Prospective phase II clinical trial of autologous haematopoietic stem cell transplant for treatment refractory multiple sclerosis J. Neurol. Neurosurg. Psychiatry 2019 90 514 521 10.1136/jnnp-2018-319446 30538138 · DOI
  74. [81]Longbrake E.E. Cantoni C. Chahin S. Cignarella F. Cross A.H. Piccio L. Dimethyl fumarate induces changes in B- and T-lymphocyte function independent of the effects on absolute lymphocyte count Mult. Scler. J. 2018 24 728 738 10.1177/1352458517707069 28480794 PMC5665729 · DOI
  75. [82]Hedström A.K. Smoking and its interaction with genetics in MS etiology Mult. Scler. J. 2019 25 180 186 10.1177/1352458518801727 30251921 · DOI
  76. [83]Ammitzbøll C. Börnsen L. Christensen J.R. Ratzer R. Nielsen B.R. Søndergaard H.B. von Essen M. Sellebjerg F. Smoking reduces circulating CD26 hi CD161 hi MAIT cells in healthy individuals and patients with multiple sclerosis J. Leukoc. Biol. 2017 101 1211 1220 10.1189/jlb.3A0616-267R 28179539 · DOI
  77. [84]Ammitzbøll C. von Essen M.R. Chow H.H. McWilliam O. Hansen R.H. Sellebjerg F. MAIT cell subtypes in multiple sclerosis J. Neuroimmunol. 2020 339 577117 10.1016/j.jneuroim.2019.577117 31812897 · DOI · Paper page
  78. [85]Acquaviva M. Bassani C. Sarno N. Costa G.D. Romeo M. Sangalli F. Colombo B. Moiola L. Martinelli V. Comi G. Loss of Circulating CD8+ CD161high T Cells in Primary Progressive Multiple Sclerosis Front. Immunol. 2019 10 1922 10.3389/fimmu.2019.01922 31474991 PMC6702304 · DOI
  79. [86]Chiba A. Murayama G. Miyake S. Mucosal-Associated Invariant T Cells in Autoimmune Diseases Front. Immunol. 2018 9 1333 10.3389/fimmu.2018.01333 29942318 PMC6004381 · DOI
  80. [87]Cho Y.-N. Kee S.-J. Kim T.-J. Jin H.M. Kim M.-J. Jung H.-J. Park K.-J. Lee S.-J. Lee S.-S. Kwon Y.-S. Mucosal-Associated Invariant T Cell Deficiency in Systemic Lupus Erythematosus J. Immunol. 2014 193 3891 3901 10.4049/jimmunol.1302701 25225673 · DOI
  81. [88]Chiba A. Tamura N. Yoshikiyo K. Murayama G. Kitagaichi M. Yamaji K. Takasaki Y. Miyake S. Activation status of mucosal-associated invariant T cells reflects disease activity and pathology of systemic lupus erythematosus Arthritis Res. 2017 19 1 10 10.1186/s13075-017-1257-5 PMC5348792 28288675 · DOI
  82. [89]Koppejan H. Jansen D.T.S.L. Hameetman M. Thomas R. Toes R.E.M. Van Gaalen F.A. Altered composition and phenotype of mucosal-associated invariant T cells in early untreated rheumatoid arthritis Arthritis Res. 2019 21 1 7 10.1186/s13075-018-1799-1 PMC6321723 30611306 · DOI
  83. [90]Wang J.J. Macardle C. Weedon H. Beroukas D. Banovic T. Mucosal-associated invariant T cells are reduced and functionally immature in the peripheral blood of primary Sjögren’s syndrome patients Eur. J. Immunol. 2016 46 2444 2453 10.1002/eji.201646300 27461134 · DOI
  84. [91]Guggino G. Di Liberto D. Pizzo M.L. Saieva L. Alessandro R. Dieli F. Triolo G. Ciccia F. IL-17 polarization of MAIT cells is derived from the activation of two different pathways Eur. J. Immunol. 2017 47 2002 2003 10.1002/eji.201747140 28815578 · DOI
  85. [92]Rouxel O. Da Silva J. Beaudoin L. Nel I. Tard C. Cagninacci L. Kiaf B. Oshima M. Diedisheim M. Salou M. Cytotoxic and regulatory roles of mucosal-associated invariant T cells in type 1 diabetes Nat. Immunol. 2017 18 1321 1331 10.1038/ni.3854 28991267 PMC6025738 · DOI
  86. [93]Kuric E. Krogvold L. Hanssen K.F. Dahl-Jørgensen K. Skog O. Korsgren O. No Evidence for Presence of Mucosal-Associated Invariant T Cells in the Insulitic Lesions in Patients Recently Diagnosed with Type 1 Diabetes Am. J. Pathol. 2018 188 1744 1748 10.1016/j.ajpath.2018.04.009 29803829 · DOI
  87. [94]Serriari N.-E. Eoche M. LaMotte L. Lion J. Fumery M. Marcelo P. Chatelain D. Barre A. Nguyen-Khac E. Lantz O. Innate mucosal-associated invariant T (MAIT) cells are activated in inflammatory bowel diseases Clin. Exp. Immunol. 2014 176 266 274 10.1111/cei.12277 24450998 PMC3992039 · DOI
  88. [95]Hiejima E. Kawai T. Nakase H. Tsuruyama T. Morimoto T. Yasumi T. Taga T. Kanegane H. Hori M. Ohmori K. Reduced Numbers and Proapoptotic Features of Mucosal-associated Invariant T Cells as a Characteristic Finding in Patients with Inflammatory Bowel Disease Inflamm. Bowel Dis. 2015 21 1529 1540 10.1097/MIB.0000000000000397 25946569 · DOI
  89. [96]Tominaga K. Yamagiwa S. Setsu T. Kimura N. Honda H. Kamimura H. Honda Y. Takamura M. Yokoyama J. Suzuki K. Possible involvement of mucosal-associated invariant T cells in the progression of inflammatory bowel diseases Biomed. Res. 2017 38 111 121 10.2220/biomedres.38.111 28442662 · DOI
  90. [97]Hinks T.S.C. Mucosal-associated invariant T cells in autoimmunity, immune-mediated diseases and airways disease Immunology 2016 148 1 12 10.1111/imm.12582 26778581 PMC4819138 · DOI
  91. [98]Lisnevskaia L. Murphy G. Isenberg D. Systemic lupus erythematosus Lancet 2014 384 1878 1888 10.1016/S0140-6736(14)60128-8 24881804 · DOI · Paper page
  92. [99]Smolen J.S. Aletaha D. McInnes I.B. Rheumatoid arthritis Lancet 2016 388 2023 2038 10.1016/S0140-6736(16)30173-8 27156434 · DOI
  93. [100]Jubair W.K. Hendrickson J.D. Severs E.L. Schulz H.M. Adhikari S. Ir D. Pagan J.D. Anthony R.M. Robertson C.E. Frank D.N. Modulation of Inflammatory Arthritis in Mice by Gut Microbiota Through Mucosal Inflammation and Autoantibody Generation Arthritis Rheumatol. 2018 70 1220 1233 10.1002/art.40490 29534332 PMC6105374 · DOI
  94. [101]Liu X. Zeng B. Zhang J. Li W. Mou F. Wang H. Zou Q. Zhong B. Wu L. Wei H. Role of the Gut Microbiome in Modulating Arthritis Progression in Mice Sci. Rep. 2016 6 30594 10.1038/srep30594 27481047 PMC4969881 · DOI
  95. [102]Ma Q. Xing C. Long W. Wang H.Y. Liu Q. Wang R.-F. Impact of microbiota on central nervous system and neurological diseases: The gut-brain axis J. Neuroinflammation 2019 16 1 14 10.1186/s12974-019-1434-3 30823925 PMC6397457 · DOI
  96. [103]Shahane A. Patel R. The epidemiology of Sjögren’s syndrome Clin. Epidemiol. 2014 6 247 255 10.2147/CLEP.S47399 25114590 PMC4122257 · DOI
  97. [104]Qin B. Wang J. Yang Z. Yang M. Ma N. Huang F. Zhong R. Epidemiology of primary Sjögren’s syndrome: A systematic review and meta-analysis Ann. Rheum. Dis. 2014 74 1983 1989 10.1136/annrheumdis-2014-205375 24938285 · DOI
  98. [105]Lehuen A. Diana J. Zaccone P. Cooke A. Immune cell crosstalk in type 1 diabetes Nat. Rev. Immunol. 2010 10 501 513 10.1038/nri2787 20577267 · DOI
  99. [106]Ju J.K. Cho Y.-N. Park K.-J. Kwak H.D. Jin H.-M. Park S.-Y. Kim H.S. Kee S.-J. Park Y.-W. Activation, Deficiency, and Reduced IFN-γ Production of Mucosal-Associated Invariant T Cells in Patients with Inflammatory Bowel Disease J. Innate Immun. 2020 12 422 434 10.1159/000507931 32535589 PMC7506267 · DOI
  100. [107]Deng J. Yu X.-Q. Wang P.-H. Inflammasome activation and Th17 responses Mol. Immunol. 2019 107 142 164 10.1016/j.molimm.2018.12.024 30739833 · DOI
  101. [108]Dixon B.R.E.A. Hossain R. Patel R.V. Algood H.M.S. Th17 Cells in Helicobacter pylori Infection: A Dichotomy of Help and Harm Infect. Immun. 2019 87 10.1128/IAI.00363-19 PMC6803329 31427446 · DOI
  102. [109]Yan J. Allen S. McDonald E. Das I. Mak J.Y.W. Liu L. Fairlie D.P. Meehan B.S. Chen Z. Corbett A.J. MAIT Cells Promote Tumor Initiation, Growth, and Metastases via Tumor MR Cancer Discov. 2020 10 124 141 10.1158/2159-8290.CD-19-0569 31826876 · DOI
  103. [110]Ochoa-Repáraz J. Mielcarz D.W. Ditrio L.E. Burroughs A.R. Foureau D.M. Haque-Begum S. Kasper L.H. Role of Gut Commensal Microflora in the Development of Experimental Autoimmune Encephalomyelitis J. Immunol. 2009 183 6041 6050 10.4049/jimmunol.0900747 19841183 · DOI · Paper page
  104. [111]Lee Y.K. Menezes J.S. Umesaki Y. Mazmanian S.K. Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis Proc. Natl. Acad. Sci. USA 2011 108 4615 4622 10.1073/pnas.1000082107 20660719 PMC3063590 · DOI · Paper page

Cited by

Sorted by citations

Authors
Mechelli, R., Romano, S., Romano, C., Morena, E., Buscarinu, M. C., Bigi, R., Bellucci, G., Reniè, R., Pellicciari, G., Salvetti, M., & Ristori, G.
Affiliations
  • San Raffaele University of Rome (IT)
  • Sapienza University of Rome (IT)
  • Istituto Neurologico Mediterraneo (IT)
  • Fondazione Santa Lucia (IT)
Corresponding author
Salvetti, Marco
Venue
Microorganisms
Publisher
MDPI AG
Published
2021-05-24
Volume
9
Issue
6
Pages
1132
ISSN
2076-2607 (ISSN-L)
OpenAlex
W3164954225
Cited by
24
References
9
Citations by year
2025: 4 · 2024: 3 · 2023: 9 · 2022: 3 · 2021: 5
FWCI
0.52
Type
journal article
Language
en
Open access
Locations
  • Microorganisms (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • IRIS Research product catalog (Sapienza University of Rome) (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
Keywords
mucosal-associated invariant T cells, gut microbiota, dysbiosis, multiple sclerosis, autoimmune disease, intestinal permeability, disease-modifying therapy, biomarkers, tissue repair

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review