Superantigen recognition by γδ T cells:: SEA recognition site for human Vγ2 T cell receptors

被引:46
作者
Morita, CT [1 ]
Li, HM
Lamphear, JG
Rich, RR
Fraser, JD
Mariuzza, RA
Lee, HK
机构
[1] Univ Iowa, Coll Med, Dept Internal Med, Div Rheumatol, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Med, Interdisciplinary Grp Immunol, Iowa City, IA 52242 USA
[3] Univ Maryland, Inst Biotechnol, Ctr Adv Res Biotechnol, Rockville, MD 20850 USA
[4] Baylor Coll Med, Dept Microbiol & Immunol, Houston, TX 77030 USA
[5] Emory Univ, Sch Med, Dept Med Microbiol & Immunol, Atlanta, GA 30322 USA
[6] Univ Auckland, Sch Med, Dept Mol Med, Auckland 1, New Zealand
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1074-7613(01)00113-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human gamma delta T cells expressing the V gamma 2V delta2 antigen receptors recognize nonpeptide prenyl pyrophosphate and alkylamine antigens. We find that they also recognize staphylococcal enterotoxin A superantigens in a manner distinct from the recognition of nonpeptide antigens. Using chimeric and mutant toxins, SEA amino acid residues 20-27 were shown to be required for gamma delta TCR recognition of SEA. Residues at 200-207 that are critical for specific alpha beta TCR recognition of SEA do not affect gamma delta TCR recognition. SEA residues 20-27 are located in an area contiguous with the binding site of V beta chains. This study defines a superantigen recognition site for a gamma delta T cell receptor and demonstrates the differences between V gamma 2V delta2(+) T cell recognition of superantigens and nonpeptide antigens.
引用
收藏
页码:331 / 344
页数:14
相关论文
共 84 条
[1]   T-LYMPHOCYTES WITH GAMMA-DELTA+ V-DELTA-2+ ANTIGEN RECEPTORS ARE PRESENT IN INCREASED PROPORTIONS IN A FRACTION OF PATIENTS WITH TUBERCULOSIS OR WITH SARCOIDOSIS [J].
BALBI, B ;
VALLE, MT ;
ODDERA, S ;
GIUNTI, D ;
MANCA, F ;
ROSSI, GA ;
ALLEGRA, L .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 148 (06) :1685-1690
[2]   LYMPHOCYTES BEARING THE GAMMA-DELTA T-CELL RECEPTOR IN ACUTE BRUCELLA-MELITENSIS INFECTION [J].
BERTOTTO, A ;
GERLI, R ;
SPINOZZI, F ;
MUSCAT, C ;
SCALISE, F ;
CASTELLUCCI, G ;
SPOSITO, M ;
CANDIO, F ;
VACCARO, R .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (05) :1177-1180
[3]   Direct ex vivo analysis of activated, fas-sensitive autoreactive T cells in human autoimmune disease [J].
Bieganowska, KD ;
Ausubel, LJ ;
Modabber, Y ;
Slovik, E ;
Messersmith, W ;
Hafler, DA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (09) :1585-1594
[4]   An innate view of gamma delta T cells [J].
Boismenu, R ;
Havran, WL .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) :57-63
[5]   MODULATION OF EPITHELIAL-CELL GROWTH BY INTRAEPITHELIAL GAMMA-DELTA T-CELLS [J].
BOISMENU, R ;
HAVRAN, WL .
SCIENCE, 1994, 266 (5188) :1253-1255
[6]  
Bukowski JF, 1998, J IMMUNOL, V161, P286
[7]  
BUKOWSKI JF, 1995, J IMMUNOL, V154, P998
[8]   Human γδ T cells recognize alkylamines derived from microbes, edible plants, and tea:: Implications for innate immunity [J].
Bukowski, JF ;
Morita, CT ;
Brenner, MB .
IMMUNITY, 1999, 11 (01) :57-65
[9]  
CALDWELL CW, 1995, AM J CLIN PATHOL, V103, P761
[10]   Major histocompatibility complex class I molecules modulate activation threshold and early signaling of T cell antigen receptor gamma/delta stimulated by nonpeptidic ligands [J].
Carena, I ;
Shamshiev, A ;
Donda, A ;
Colonna, M ;
DeLibero, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (10) :1769-1774