CD1 and MR1 recognition by human γδ T cells

被引:5
|
作者
Van Rhijn, Ildiko [1 ,2 ,3 ]
Le Nours, Jerome [4 ,5 ,6 ]
机构
[1] Brigham & Womens Hosp, Div Rheumatol Inflammat & Immun, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Univ Utrecht, Fac Vet Med, Dept Infect Dis & Immunol, Yalelaan 1, NL-3584 CL Utrecht, Netherlands
[4] Monash Univ, Biomed Discovery Inst, Infect & Immun Program, Clayton, Vic 3800, Australia
[5] Monash Univ, Biomed Discovery Inst, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
[6] Monash Univ, Australian Res Council Ctr Excellence Adv Mol Ima, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会; 美国国家卫生研究院;
关键词
CD1; glycoproteins; MR1; molecule; MHC-like molecules; gamma delta T cells; ANTIGEN RECEPTOR GENES; PERIPHERAL-BLOOD; COMPLEX; STRESS; BINDS; IDENTIFICATION; REPERTOIRE; DIVERSITY; MOLECULES; EXPANSION;
D O I
10.1016/j.molimm.2020.12.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The two main T cell lineages, alpha beta and gamma delta T cells, play a central role in immunity. Unlike alpha beta T cells that recognize antigens bound to the Major Histocompatibility Complex (MHC) or MHC class I-like antigen-presenting molecules, the ligands for gamma delta T cell receptors (TCRs) are much more diverse. However, it is now clear that gamma delta TCRs can also recognize MHC class I-like molecules, including CD1b, CD1c, CD1d and the MHC class I-related protein 1 (MR1). Yet, our understanding at the molecular level of gamma delta T cell immunity to CD1 and MR1 is still very limited. Here, we discuss new molecular paradigms underpinning gamma delta TCRs recognition of antigens, antigen-presenting molecules or both. The recent discovery of recognition of MR1 by a gamma delta TCR at a position located underneath the antigen display platform reinforces the view that gamma delta TCRs can approach their ligands from many directions, unlike alpha beta TCRs that bind MHC, CD1 and MR1 targets in an aligned, end to end fashion.
引用
收藏
页码:95 / 100
页数:6
相关论文
共 50 条
  • [31] The CD1 family and T cell recognition of lipid antigens
    Dutronc, Y
    Porcelli, SA
    TISSUE ANTIGENS, 2002, 60 (05): : 337 - 353
  • [32] T lymphocyte recognition of human group 1 CD1 molecules: Implications for innate and acquired immunity
    Sugita, M
    Brenner, MB
    SEMINARS IN IMMUNOLOGY, 2000, 12 (06) : 511 - 516
  • [33] CD1 RECOGNITION BY MOUSE NK1(+) T-LYMPHOCYTES
    BENDELAC, A
    LANTZ, O
    QUIMBY, ME
    YEWDELL, JW
    BENNINK, JR
    BRUTKIEWICZ, RR
    SCIENCE, 1995, 268 (5212) : 863 - 865
  • [34] Bacteria, mucosal-associated invariant T cells and MR1
    Chua, Wei-Jen
    Hansen, Ted H.
    IMMUNOLOGY AND CELL BIOLOGY, 2010, 88 (08): : 767 - 769
  • [35] CD1 and CD1-restricted T cells in infections with intracellular bacteria
    Schaible, UE
    Kaufmann, SHE
    TRENDS IN MICROBIOLOGY, 2000, 8 (09) : 419 - 425
  • [36] Presentation of glycolipid antigens by mouse and human CD1 molecules to NK T cells
    Naidenko, O
    Kronenberg, M
    10TH INTERNATIONAL CONGRESS ON IMMUNOLOGY, VOLS 1 AND 2, 1998, : 273 - 278
  • [37] T-cell recognition of glycolipids presented by CD1 proteins
    Young, DC
    Moody, DB
    GLYCOBIOLOGY, 2006, 16 (07) : 103R - 112R
  • [38] Functionally diverse human T cells recognize non-microbial antigens presented by MR1
    Lepore, Marco
    Kalinichenko, Artem
    Calogero, Salvatore
    Kumar, Pavanish
    Paleja, Bhairav
    Schmaler, Mathias
    Narang, Vipin
    Zolezzi, Francesca
    Poidinger, Michael
    Mori, Lucia
    De Libero, Gennaro
    ELIFE, 2017, 6
  • [39] MR1 discovery
    Keiichiro Hashimoto
    Immunogenetics, 2016, 68 : 491 - 498
  • [40] CD1 presentation of microbial nonpeptide antigens to T cells
    Jullien, D
    Stenger, S
    Ernst, WA
    Modlin, RL
    JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (12): : S29 - S32