T cell receptor repertoire usage in allotransplantation: An overview

被引:18
作者
Douillard, P [1 ]
Cuturi, MC [1 ]
Brouard, S [1 ]
Josien, R [1 ]
Soulillou, JP [1 ]
机构
[1] CHU Hotel Dieu, INSERM, ITERT, U437, F-44093 Nantes 01, France
关键词
D O I
10.1097/00007890-199910150-00001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lymphocytes express antigen receptors that allow the immune system to specifically recognize antigens, In transplantation, T cells play a critical role in the rejection process, and different protocols inhibiting T cell-mediated alloreactivity efficiently achieve prolongation of allograft survival. T cells can interact with alloantigens by two ways, either by the "indirect" pathway that correspond to the physiological mechanism of T cell immune recognition, or through the "direct" pathway where they recognize alloantigens directly on the surface of donor cells. If some T cells are specifically activated in allorecognition, one should be able to indirectly detect this "selection" by analyzing the T cell receptor usage that could be biased and reflect the preferential amplification of alloreactive lymphocyte subsets. Nevertheless compared with disease states such as cancer or autoimmunity the T cell receptor repertoire is still largely uncharacterized. We review the current results available on T cell repertoire usage in transplantation studies involving humans or various animal models. The T cell receptor repertoire involved in transplantation (restricted or unrestricted) and the features potentially common to alloimmune responses will be discussed.
引用
收藏
页码:913 / 921
页数:9
相关论文
共 99 条
  • [81] DIFFERENTIAL USAGE OF THE T-CELL RECEPTOR REPERTOIRE FOR ALLORECOGNITION OF HEART, LIVER, AND KIDNEY GRAFTS
    SHIRWAN, H
    CAJULIS, E
    MAKOWKA, L
    CRAMER, DV
    [J]. TRANSPLANTATION, 1995, 59 (12) : 1709 - 1714
  • [82] SHIRWAN H, 1993, J IMMUNOL, V151, P5228
  • [83] SHIRWAN H, 1993, TRANSPLANT P, V25, P2780
  • [84] SHIRWAN H, 1995, J IMMUNOL, V154, P1964
  • [85] INDIRECT PRESENTATION OF MHC ANTIGENS IN TRANSPLANTATION
    SHOSKES, DA
    WOOD, KJ
    [J]. IMMUNOLOGY TODAY, 1994, 15 (01): : 32 - 38
  • [86] Practical, biochemical and evolutionary implications of the discovery of HLA class I supermotifs
    Sidney, J
    Grey, HM
    Kubo, RT
    Sette, A
    [J]. IMMUNOLOGY TODAY, 1996, 17 (06): : 261 - 266
  • [87] GENETICS OF THE BLOOD-TRANSFUSION EFFECT ON HEART ALLOGRAFTS IN RATS
    SOULILLOU, JP
    BLANDIN, F
    GUNTHER, E
    LEMOINE, V
    [J]. TRANSPLANTATION, 1984, 38 (01) : 63 - 67
  • [88] IMMUNE REPERTOIRE OF GRAFT-INVADING T-CELLS
    SOULILLOU, JP
    BONNEVILLE, M
    MOISAN, JP
    VIE, H
    DEVILDER, MC
    HALLET, MM
    MOREAU, JF
    [J]. TRANSPLANT INTERNATIONAL, 1990, 3 (03) : 176 - 180
  • [89] IN-VIVO EXPANSION OF HLA-B35 ALLOREACTIVE T-CELLS SHARING HOMOLOGOUS T-CELL RECEPTORS - EVIDENCE FOR MAINTENANCE OF AN OLIGOCLONALLY DOMINATED ALLOSPECIFICITY BY PERSISTENT STIMULATION WITH AN AUTOLOGOUS MHC PEPTIDE COMPLEX
    STEINLE, A
    REINHARDT, C
    JANTZER, P
    SCHENDEL, DJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (02) : 503 - 513
  • [90] SOMATIC GENERATION OF ANTIBODY DIVERSITY
    TONEGAWA, S
    [J]. NATURE, 1983, 302 (5909) : 575 - 581