Human mucosal-associated invariant T (MAIT) cells possess capacity for B cell help

被引:66
|
作者
Bennett, Michael S. [1 ,3 ]
Trivedi, Shubhanshi [1 ]
Iyer, Anita S. [1 ]
Hale, J. Scott [2 ]
Leung, Daniel T. [1 ,2 ]
机构
[1] Univ Utah, Sch Med, Div Infect Dis, Dept Internal Med, Salt Lake City, UT 84132 USA
[2] Univ Utah, Sch Med, Dept Pathol, Div Microbiol & Immunol, Salt Lake City, UT 84132 USA
[3] ARUP Labs, ARUP Inst Clin & Expt Pathol, Salt Lake City, UT USA
基金
美国国家卫生研究院;
关键词
plasmablast; B cell help; MR-1; antibody; RECEPTOR HETEROGENEITY; IMMUNE-RESPONSES; ACTIVATION; MR1; PROLIFERATION; MECHANISM; ANTIGENS; INNATE; GAMMA;
D O I
10.1189/jlb.4A0317-116R
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human MAIT cells have the capacity to provide help to B cells through induction of plasmablast differentiation and antibody production. Mucosal-associated invariant T (MAIT) cells are an innate-like T cell subset, restricted by the nonclassic MHC class I-related protein MR1 and enriched at mucosal sites. Human studies have shown an association between MAIT cells and pathogen-specific antibody responses. In this study, we investigate the effect of human MAIT cells on B cells ex vivo. We found that supernatants from microbe- or cytokine-stimulated MAIT cells, when added to purified autologous B cells, increase frequencies of plasmablasts and promote IgA, IgG, and IgM production. We found effects to be mostly MR1-dependent and that the increases in plasmablasts are likely a result of increased differentiation from memory B cells. Furthermore, microbe-activated MAIT cell supernatant contains multiple cytokines known to stimulate B cells, including IL-6, -10, and -21. This study thus provides the first direct evidence of a newly identified role of MAIT cells in providing help to B cells.
引用
收藏
页码:1261 / 1269
页数:9
相关论文
共 50 条
  • [31] MUCOSAL-ASSOCIATED INVARIANT T (MAIT) CELL REGULATION NETWORKS IN ANTI-TUMOR IMMUNITY
    Ruf, Benjamin
    Catania, Vanessa
    Kedei, Noemi
    Wabitsch, Simon
    Ma, Chi
    Diggs, Laurence
    Zhang, Qianfei
    Heinrich, Bernd
    Subramanyam, Varun
    Cui, Linda
    Sakai, Shunsuke
    Oh, Sangmi
    Stovroff, Merrill
    Barry, Clifton, III
    Barber, Daniel
    Kroemer, Alexander
    Korangy, Firouzeh
    Greten, Tim
    JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2021, 9 : A721 - A721
  • [32] Brain and kidney tumors are differentially infiltrated by subsets of mucosal-associated invariant T (MAIT) cells
    Illes, Z.
    Peterfalvi, A.
    Gomori, E.
    Magyarlaki, T.
    Pal, J.
    Szereday, L.
    JOURNAL OF NEURAL TRANSMISSION, 2007, 114 (07) : CXXXII - CXXXII
  • [33] Mucosal-Associated Invariant T (MAIT) Cell Frequency is Preserved in Pediatric Heart Transplant Recipients
    Loh, L.
    Gapin, L.
    Abbott, J.
    Nakano, S. J.
    JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2023, 42 (04): : S475 - S475
  • [34] Bifidobacteria and Mucosal-Associated Invariant T (MAIT) Cells: A New Approach to Colorectal Cancer Prevention?
    Bozkurt, Huseyin Sancar
    Quigley, Eamonn M. M.
    GASTROINTESTINAL DISORDERS, 2019, 1 (02): : 266 - 272
  • [35] Mucosal-Associated Invariant T (MAIT) Cells As a Potential Therapeutic Target for Systemic Lupus Erythematosus
    Murayama, Goh
    Chiba, Asako
    Nomura, Atsushi
    Amano, Hirofumi
    Yamaji, Ken
    Tamura, Naoto
    Miyake, Sachiko
    ARTHRITIS & RHEUMATOLOGY, 2018, 70
  • [36] Mucosal-associated invariant T cells in Giant Cell Arteritis
    Ghesquiere, Thibault
    Ciudad, Marion
    Ramon, Andre
    Greigert, Helene
    Gerard, Claire
    Cladiere, Claudie
    Thebault, Marine
    Genet, Coraline
    Devilliers, Herve
    Maurier, Francois
    Ornetti, Paul
    Quipourt, Valerie
    Gabrielle, Pierre-Henry
    Creuzot-Garcher, Catherine
    Tarris, Georges
    Martin, Laurent
    Soudry-Faure, Agnes
    Saas, Philippe
    Audia, Sylvain
    Bonnotte, Bernard
    Samson, Maxime
    JOURNAL OF AUTOIMMUNITY, 2021, 121
  • [37] Profibrogenic functions of mucosal-associated invariant T (MAIT) cells during chronic liver injury
    Hegde, Pushpa
    Weiss, Emmanuel
    Ferrere, Gladys
    Gupta, Abhishak
    Kiaf, Badr
    Wan, Jinghong
    Paradis, Valerie
    Moreau, Richard
    Lehuen, Agnes
    Lotersztajn, Sophie
    HEPATOLOGY, 2016, 64 : 99A - 100A
  • [38] Mucosal-associated invariant T cells and disease
    Toubal, Amine
    Nel, Isabelle
    Lotersztajn, Sophie
    Lehuen, Agnes
    NATURE REVIEWS IMMUNOLOGY, 2019, 19 (10) : 643 - 657
  • [39] Mucosal-associated invariant T cells and disease
    Amine Toubal
    Isabelle Nel
    Sophie Lotersztajn
    Agnès Lehuen
    Nature Reviews Immunology, 2019, 19 : 643 - 657
  • [40] Development of mucosal-associated invariant T cells
    Koay, Hui-Fern
    Godfrey, Dale I.
    Pellicci, Daniel G.
    IMMUNOLOGY AND CELL BIOLOGY, 2018, 96 (06): : 598 - 606