T-CELLS WITH 2 FUNCTIONAL ANTIGEN-SPECIFIC RECEPTORS

被引:111
作者
HARDARDOTTIR, F
BARON, JL
JANEWAY, CA
机构
[1] YALE UNIV,SCH MED,IMMUNOBIOL SECT,NEW HAVEN,CT 06510
[2] HOWARD HUGHES MED INST,NEW HAVEN,CT 06510
关键词
D O I
10.1073/pnas.92.2.354
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although the clonal selection theory states that lymphocytes should bear only a single specificity of receptor, there is much evidence that some T cells, at least, bear two receptors, Here, we have used mice transgenic for genes encoding an autoreactive T-cell receptor (TCR) to examine the specificity of T cells bearing two functional TCRs, We find that T cells developing in mice that do not express the major histocompatibility complex (MHC) molecule recognized as self by the transgene-encoded TCR express both this TCR and a second TCR that is specific for the MHC molecules of the strain in which it arose, Thus, these T cells have two TCRs, each specific for a distinct antigen bound to a distinct MHC molecule, In contrast, when raised in mice bearing the MHC for which the receptor is specific, T cells develop that express the transgene-encoded TCR almost exclusively, Such mice are highly susceptible to autoimmune disease. Our data suggest that on most T cells bearing two TCRs, only one is specific for peptides bound to self-MHC molecules and, thus, that expression of two TCRs does not usually confer reactivity to two unrelated antigens.
引用
收藏
页码:354 / 358
页数:5
相关论文
共 17 条
[1]  
BARON J, 1994, THESIS YALE U NEW HA
[2]   SURFACE EXPRESSION OF ALPHA-4 INTEGRIN BY CD4 T-CELLS IS REQUIRED FOR THEIR ENTRY INTO BRAIN PARENCHYMA [J].
BARON, JL ;
MADRI, JA ;
RUDDLE, NH ;
HASHIM, G ;
JANEWAY, CA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (01) :57-68
[3]   ANTIGEN MHC-SPECIFIC T-CELLS ARE PREFERENTIALLY EXPORTED FROM THE THYMUS IN THE PRESENCE OF THEIR MHC LIGAND [J].
BERG, LJ ;
PULLEN, AM ;
FAZEKAS DE ST GROTH, B ;
MATHIS, D ;
BENOIST, C ;
DAVIS, MM .
CELL, 1989, 58 (06) :1035-1046
[4]   EXCLUSION AND INCLUSION OF ALPHA-T-CELL AND BETA-T-CELL RECEPTOR ALLELES [J].
BORGULYA, P ;
KISHI, H ;
UEMATSU, Y ;
VONBOEHMER, H .
CELL, 1992, 69 (03) :529-537
[5]   TRANSGENIC MICE THAT EXPRESS A MYELIN BASIC PROTEIN-SPECIFIC T-CELL RECEPTOR DEVELOP SPONTANEOUS AUTOIMMUNITY [J].
GOVERMAN, J ;
WOODS, A ;
LARSON, L ;
WEINER, LP ;
HOOD, L ;
ZALLER, DM .
CELL, 1993, 72 (04) :551-560
[6]   EXPRESSION OF 2 ALPHA-CHAINS ON THE SURFACE OF T-CELLS IN T-CELL RECEPTOR TRANSGENIC MICE [J].
HEATH, WR ;
MILLER, JFAP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) :1807-1811
[7]   THE CYTOPLASMIC TAIL OF THE T-CELL RECEPTOR ZETA-CHAIN IS DISPENSABLE FOR ANTIGEN-MEDIATED T-CELL ACTIVATION [J].
HERMANS, MHA ;
MALISSEN, B .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (09) :2257-2262
[8]   AN MHC INTERACTION SITE MAPS TO THE AMINO-TERMINAL HALF OF THE T-CELL RECEPTOR ALPHA-CHAIN VARIABLE DOMAIN [J].
HONG, SC ;
CHELOUCHE, A ;
LIN, RH ;
SHAYWITZ, D ;
BRAUNSTEIN, NS ;
GLIMCHER, L ;
JANEWAY, CA .
CELL, 1992, 69 (06) :999-1009
[9]   ANTIGEN RECOGNITION BY CLONED CYTO-TOXIC LYMPHOCYTES-T FOLLOWS RULES PREDICTED BY THE ALTERED-SELF HYPOTHESIS [J].
HUNIG, TR ;
BEVAN, MJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 155 (01) :111-125
[10]  
KAYE J, 1984, J EXP MED, V159, P1397, DOI 10.1084/jem.159.5.1397