T-CELL RECEPTOR V-SEGMENT FREQUENCIES IN PERIPHERAL-BLOOD T-CELLS CORRELATE WITH HUMAN-LEUKOCYTE ANTIGEN TYPE

被引:182
作者
GULWANIAKOLKAR, B
POSNETT, DN
JANSON, CH
GRUNEWALD, J
WIGZELL, H
AKOLKAR, P
GREGERSEN, PK
SILVER, J
机构
[1] N SHORE UNIV HOSP,CORNELL UNIV MED COLL,DEPT MED,300 COMMUNITY DR,MANHASSET,NY 11030
[2] KAROLINSKA INST,DEPT IMMUNOL,S-10401 STOCKHOLM 60,SWEDEN
关键词
D O I
10.1084/jem.174.5.1139
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We compared T cell receptor (TCR) V-segment frequencies in human leukocyte antigen (HLA) identical siblings to sibling pairs who differ at one or both HLA haplotypes using four V-beta-specific and one V-alpha-specific monoclonal antibody. In every one of nine families HLA-identical sibs had the most similar patterns of V-segment frequencies in their peripheral blood, whereas totally mismatched sibs were, in general, the most dissimilar; HLA haploidentical sibs tended to be intermediate between the two groups. The degree of similarity among HLA-identical sibs was comparable to that observed among three pairs of identical twins suggesting that HLA is the major genetic component influencing TCR V-segment frequency. Consistent with this observation, it was found that the frequency of T cells expressing particular V-beta-segments was skewed towards either CD4+ or CD8+ cells indicating that T cells expressing some V-beta-genes may be positively selected primarily by class I or class II major histocompatibility complex proteins. Finally, it was observed that individuals who express the HLA class I specificity, B38, tend to express high levels of V-alpha-2.3+ cells among their CD8+ T cells. These observations represent definitive proof that human V-segment frequencies are profoundly influenced by the HLA complex.
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页码:1139 / 1146
页数:8
相关论文
共 24 条
  • [1] MAJOR HISTOCOMPATIBILITY COMPLEX HAPLOTYPE STUDIES IN ASHKENAZI JEWISH PATIENTS WITH PEMPHIGUS-VULGARIS
    AHMED, AR
    YUNIS, EJ
    KHATRI, K
    WAGNER, R
    NOTANI, G
    AWDEH, Z
    ALPER, CA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (19) : 7658 - 7662
  • [2] THE EFFECTS OF MHC GENE DOSAGE AND ALLELIC VARIATION ON T-CELL RECEPTOR SELECTION
    BERG, LJ
    FRANK, GD
    DAVIS, MM
    [J]. CELL, 1990, 60 (06) : 1043 - 1053
  • [3] IDIOTYPE-LIKE MOLECULES ON CELLS OF A HUMAN T-CELL LEUKEMIA
    BIGLER, RD
    FISHER, DE
    WANG, CY
    KAN, EAR
    KUNKEL, HG
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 158 (03) : 1000 - 1005
  • [4] POSITIVE SELECTION OF CD4+T CELLS MEDIATED BY MHC CLASS-II-BEARING STROMAL CELL IN THE THYMIC CORTEX
    BILL, J
    PALMER, E
    [J]. NATURE, 1989, 341 (6243) : 649 - 651
  • [5] THE MHC MOLECULE I-E IS NECESSARY BUT NOT SUFFICIENT FOR THE CLONAL DELETION OF V-BETA-11-BEARING T-CELLS
    BILL, J
    KANAGAWA, O
    WOODLAND, DL
    PALMER, E
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (04) : 1405 - 1419
  • [6] THE ROLE OF THE T-CELL RECEPTOR IN POSITIVE AND NEGATIVE SELECTION OF DEVELOPING T-CELLS
    BLACKMAN, M
    KAPPLER, J
    MARRACK, P
    [J]. SCIENCE, 1990, 248 (4961) : 1335 - 1341
  • [7] INFLUENCE OF THE MAJOR HISTOCOMPATIBILITY COMPLEX ON POSITIVE THYMIC SELECTION OF V-BETA-17A+ T-CELLS
    BLACKMAN, MA
    MARRACK, P
    KAPPLER, J
    [J]. SCIENCE, 1989, 244 (4901) : 214 - 217
  • [8] DELETION OF SELF-REACTIVE THYMOCYTES OCCURS AT A CD4+8+ PRECURSOR STAGE
    FOWLKES, BJ
    SCHWARTZ, RH
    PARDOLL, DM
    [J]. NATURE, 1988, 334 (6183) : 620 - 623
  • [9] BIASED EXPRESSION OF INDIVIDUAL T-CELL RECEPTOR V-GENE SEGMENTS IN CD4+ AND CD8+ HUMAN PERIPHERAL-BLOOD LYMPHOCYTES-T
    GRUNEWALD, J
    JANSON, CH
    WIGZELL, H
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (03) : 819 - 822
  • [10] JANSON CH, 1989, CANCER IMMUNOL IMMUN, V28, P225