Diversity of γδ T-cell antigens

被引:86
作者
Born, Willi K. [1 ,2 ]
Aydintug, M. Kemal [1 ]
O'Brien, Rebecca L. [1 ,2 ]
机构
[1] Natl Jewish Hlth, Integrated Dept Immunol, Denver, CO 80206 USA
[2] Univ Colorado Denver, Aurora, CO USA
关键词
antigen recognition; ligand; T-cell receptor; gamma delta T cells; MYCOBACTERIUM-TUBERCULOSIS; PERIPHERAL-BLOOD; IMMUNE-RESPONSES; ALPHA-BETA; (E)-4-HYDROXY-3-METHYL-BUT-2-ENYL PYROPHOSPHATE; LISTERIA-MONOCYTOGENES; RECEPTOR GENES; HUMAN-MEMORY; RECOGNITION; SPECIFICITY;
D O I
10.1038/cmi.2012.45
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the last two decades, it has become clear that gamma delta T cells recognize a diverse array of antigens including self and foreign, large and small, and peptidic and non-peptidic molecules. In this respect, gamma delta antigens as a whole resemble more the antigens recognized by antibodies than those recognized by alpha beta T cells. Because of this antigenic diversity, no single mechanism-such as the major histocompatibility complex (MHC) restriction of alpha beta T cells-is likely to provide a basis for all observed T-cell antigen receptor (TCR)-dependent gamma delta T-cell responses. Furthermore, available evidence suggests that many individual gamma delta T cells are poly-specific, probably using different modes of ligand recognition in their responses to unrelated antigens. While posing a unique challenge in the maintenance of self-tolerance, this broad reactivity pattern might enable multiple overlapping uses of gamma delta T-cell populations, and thus generate a more efficient immune response. Cellular & Molecular Immunology (2013) 10, 13-20; doi:10.1038/cmi.2012.45; published online 22 October 2012
引用
收藏
页码:13 / 20
页数:8
相关论文
共 112 条
[61]  
KIM HT, 1995, J IMMUNOL, V154, P1614
[62]  
KOZBOR D, 1990, J IMMUNOL, V144, P3677
[63]   HUMAN TCR-GAMMA+/DELTA+, CD8+ LYMPHOCYTE-T RECOGNIZE TETANUS TOXOID IN AN MHC-RESTRICTED FASHION [J].
KOZBOR, D ;
TRINCHIERI, G ;
MONOS, DS ;
ISOBE, M ;
RUSSO, G ;
HANEY, JA ;
ZMIJEWSKI, C ;
CROCE, CM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (05) :1847-1851
[64]   γ/δ T-cell stimulation by pamidronate [J].
Kunzmann, V ;
Bauer, E ;
Wilhelm, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (09) :737-738
[65]   CD4+CD25+ Treg cells inhibit human memory γδ T cells to produce IFN-γ in response to M tuberculosis antigen ESAT-6 [J].
Li, Li ;
Wu, Chang-You .
BLOOD, 2008, 111 (12) :5629-5636
[66]   Human memory but not nave γδ T cells from TST-positive individuals respond to M tuberculosis antigen Reply [J].
Li, Li ;
Wu, Chang-You .
BLOOD, 2008, 112 (12) :4777-4777
[67]   STRUCTURE AND SPECIFICITY OF A CLASS-II MHC ALLOREACTIVE GAMMA-DELTA-T-CELL RECEPTOR HETERODIMER [J].
MATIS, LA ;
FRY, AM ;
CRON, RQ ;
COTTERMAN, MM ;
DICK, RF ;
BLUESTONE, JA .
SCIENCE, 1989, 245 (4919) :746-749
[68]   MAJOR HISTOCOMPATIBILITY COMPLEX-LINKED SPECIFICITY OF GAMMA-DELTA-RECEPTOR-BEARING LYMPHOCYTES-T [J].
MATIS, LA ;
CRON, R ;
BLUESTONE, JA .
NATURE, 1987, 330 (6145) :262-264
[69]   β2-glycoprotein I and oxidative inflammation in early atherogenesis: A progression from innate to adaptive immunity? [J].
Matsuura, Eiji ;
Lopez, Luis R. ;
Shoenfeld, Yehuda ;
Ames, Paul R. J. .
AUTOIMMUNITY REVIEWS, 2012, 12 (02) :241-249
[70]   Analysis of immune responses directed toward a recombinant early secretory antigenic target six-kilodalton protein-culture filtrate protein 10 fusion protein in Mycobacterium bovis-infected cattle [J].
Maue, AC ;
Waters, WR ;
Davis, WC ;
Palmer, MV ;
Minion, FC ;
Estes, DM .
INFECTION AND IMMUNITY, 2005, 73 (10) :6659-6667