MAIT cells in immune-mediated tissue injury and repair

被引:3
作者
Waterhoelter, Alex [1 ,2 ,3 ]
Wunderlich, Malte [1 ,2 ,3 ]
Turner, Jan-Eric [1 ,2 ,3 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Dept Med 3, Hamburg, Germany
[2] Univ Med Ctr Hamburg Eppendorf, Hamburg Ctr Translat Immunol, Hamburg, Germany
[3] Univ Med Ctr Hamburg Eppendorf, Hamburg Ctr Kidney Hlth HCKH, Hamburg, Germany
关键词
Autoimmunity; Chronic inflammation; MAIT cells; Tissue repair; INVARIANT T-CELLS; INDUCED COLITIS; INNATE; ACTIVATION; DISEASE; INVOLVEMENT; DEFICIENCY; EVOLUTION; CHILDREN; SIGNALS;
D O I
10.1002/eji.202350483
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mucosal-associated invariant T (MAIT) cells are T cells that express a semi-invariant alpha beta T-cell receptor (TCR), recognizing non-peptide antigens, such as microbial-derived vitamin B2 metabolites, presented by the nonpolymorphic MHC class I related-1 molecule. Like NKT cells and gamma delta T cells, MAIT cells belong to the group of innate-like T cells that combine properties of the innate and adaptive immune systems. They account for up to 10% of the blood T-cell population in humans and are particularly abundant at mucosal sites. Beyond the emerging role of MAIT cells in antibacterial and antiviral defenses, increasing evidence suggests additional functions in noninfectious settings, including immune-mediated inflammatory diseases and tissue repair. Here, we discuss recent advances in the understanding of MAIT cell functions in sterile tissue inflammation, with a particular focus on autoimmunity, chronic inflammatory diseases, and tissue repair. MAIT cells have dual functions in immune-mediated tissue injury and repair. Depending on the context, MAIT cells can exacerbate inflammation and tissue injury by producing pro-inflammatory cytokines and cytotoxic molecules or mediate tissue protection by regulating other immune cell subsets and secreting tissue repair factors.image
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页数:11
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共 120 条
  • [11] Persistent deficiency of mucosal-associated invariant T cells during dermatomyositis
    Cassius, Charles
    Branchtein, Mylene
    Battistella, Maxime
    Amode, Reyhan
    Lepelletier, Clemence
    Jachiet, Marie
    de Masson, Adele
    Frumholtz, Laure
    Chasset, Francois
    Amoura, Zahir
    Mathian, Alexis
    Samri, Assia
    Monfort, Jean-Benoit
    Bachmeyer, Claude
    Bengoufa, Djaouida
    Cordoliani, Florence
    Bagot, Martine
    Bensussan, Armand
    Bouaziz, Jean-David
    Le Buanec, Helene
    [J]. RHEUMATOLOGY, 2020, 59 (09) : 2282 - 2286
  • [12] Development of Asthma in Inner-City Children: Possible Roles of MAIT Cells and Variation in the Home Environment
    Chandra, Shilpi
    Wingender, Gerhard
    Greenbaum, Jason A.
    Khurana, Archana
    Gholami, Amin M.
    Ganesan, Anusha-Preethi
    Rosenbach, Michael
    Jaffee, Katy
    Gern, James E.
    Wood, Robert
    O'Connor, George
    Sandel, Megan
    Kattan, Meyer
    Bacharier, Leonard
    Togias, Alkis
    Horner, Anthony A.
    Kronenberg, Mitchell
    [J]. JOURNAL OF IMMUNOLOGY, 2018, 200 (06) : 1995 - 2003
  • [13] Single-cell RNA sequencing of immune cells in patients with acute gout
    Chang, Jan-Gowth
    Tu, Siang-Jyun
    Huang, Chung-Ming
    Chen, Yu-Chia
    Chiang, Hui-Shan
    Lee, Ya-Ting
    Yen, Ju-Chen
    Lin, Chia-Li
    Chung, Chin-Chun
    Liu, Ta-Chih
    Chang, Ya-Sian
    [J]. SCIENTIFIC REPORTS, 2022, 12 (01)
  • [14] Mucosal-associated invariant T-cell activation and accumulation after in vivo infection depends on microbial riboflavin synthesis and co-stimulatory signals
    Chen, Z.
    Wang, H.
    D'Souza, C.
    Sun, S.
    Kostenko, L.
    Eckle, S. B. G.
    Meehan, B. S.
    Jackson, D. C.
    Strugnell, R. A.
    Cao, H.
    Wang, N.
    Fairlie, D. P.
    Liu, L.
    Godfrey, D. I.
    Rossjohn, J.
    McCluskey, J.
    Corbett, A. J.
    [J]. MUCOSAL IMMUNOLOGY, 2017, 10 (01) : 58 - 68
  • [15] CXCL12-CXCR4-Mediated Chemotaxis Supports Accumulation of Mucosal-Associated Invariant T Cells Into the Liver of Patients With PBC
    Chen, Zhilei
    Liu, Suying
    He, Chengmei
    Sun, Jinlei
    Wang, Li
    Chen, Hua
    Zhang, Fengchun
    [J]. FRONTIERS IN IMMUNOLOGY, 2021, 12
  • [16] Activation status of mucosal-associated invariant T cells reflects disease activity and pathology of systemic lupus erythematosus
    Chiba, Asako
    Tamura, Naoto
    Yoshikiyo, Kazunori
    Murayama, Goh
    Kitagaichi, Mie
    Yamaji, Ken
    Takasaki, Yoshinari
    Miyake, Sachiko
    [J]. ARTHRITIS RESEARCH & THERAPY, 2017, 19
  • [17] Mucosal-associated invariant T cells promote inflammation and exacerbate disease in murine models of arthritis
    Chiba, Asako
    Tajima, Ryohsuke
    Tomi, Chiharu
    Miyazaki, Yusei
    Yamamura, Takashi
    Miyake, Sachiko
    [J]. ARTHRITIS AND RHEUMATISM, 2012, 64 (01): : 153 - 161
  • [18] Genomics and the Multifactorial Nature of Human Autoimmune Disease
    Cho, Judy H.
    Gregersen, Peter K.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (17) : 1612 - 1623
  • [19] Altered distribution and enhanced osteoclastogenesis of mucosal-associated invariant T cells in gouty arthritis
    Cho, Young-Nan
    Jeong, Hae-Seong
    Park, Ki-Jeong
    Kim, Hyung-Seok
    Kim, Eun-Hee
    Jin, Hye-Mi
    Jung, Hyun-Ju
    Ju, Jae Kyun
    Choi, Sung-Eun
    Kang, Ji-Hyoun
    Park, Dong-Jin
    Kim, Tae-Jong
    Lee, Shin-Seok
    Kee, Seung-Jung
    Park, Yong-Wook
    [J]. RHEUMATOLOGY, 2020, 59 (08) : 2124 - 2134
  • [20] Mucosal-Associated Invariant T Cell Deficiency in Systemic Lupus Erythematosus
    Cho, Young-Nan
    Kee, Seung-Jung
    Kim, Tae-Jong
    Jin, Hye Mi
    Kim, Moon-Ju
    Jung, Hyun-Ju
    Park, Ki-Jeong
    Lee, Sung-Ji
    Lee, Shin-Seok
    Kwon, Yong-Soo
    Kee, Hae Jin
    Kim, Nacksung
    Park, Yong-Wook
    [J]. JOURNAL OF IMMUNOLOGY, 2014, 193 (08) : 3891 - 3901