Long-term T cell immune reconstitution in 2 SCID patients after BMT

被引:7
作者
Godthelp, BC
van Tol, MJD
Vossen, JM
van den Elsen, PJ
机构
[1] Leiden Univ, Med Ctr, Dept Immunohematol & Blood Bank, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Pediat, NL-2300 RC Leiden, Netherlands
关键词
D O I
10.1016/S0198-8859(98)00013-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To evaluate the long-term reconstitution of the T cell immune repertoire in recipients of an allogeneic Bone Marrow Transplantation (allo-BMT), we have analyzed the T cell receptor (TCR) repertoire in the periphery and the T cell response against tetanus toroid in two T-B+ Severe Combined Immunodeficiency Disease (SCID) patients more than 11 years after HLA haploidentical allo-BMT. Our studies demonstrate that in the periphery of allo-BMT recipients, on the basis of TCR V-gene segment usage, the T cell immune repertoire long after allo-BMT is diverse, as is that of the donor. However, when donor and allo-BMT recipient were compared, differences were noted in the TCR Complementarity Determining Region 3 (CDR3) size distributions and in the T cell response against tetanus toroid. In particular, the tetanus toroid specific T cell clones differed in their use of HLA restriction elements, and expressed different T cell receptors. Moreover, we have uncovered donor-type tetanus toroid specific T cell clones which were established from allo-BMT recipient derived peripheral blood lymphocytes and were found to be restricted by the nonshared recipient allele. This observation suggests a role for recipient-mediated T cell selection processes, in the thymus or at extra-thymic sites. (C) American Society for Histocompatibility and Immunogenetics, 1998. Published by Elsevier Science Inc.
引用
收藏
页码:225 / 238
页数:14
相关论文
共 60 条
  • [1] ALKOLAR PN, 1993, J IMMUNOL, V150, P2761
  • [2] Arden Bernhard, 1995, Immunogenetics, V42, P455
  • [3] Oligoclonality of CD8+ T cells in health and disease: Aging, infection, or immune regulation?
    Batliwalla, F
    Monteiro, J
    Serrano, D
    Gregersen, PK
    [J]. HUMAN IMMUNOLOGY, 1996, 48 (1-2) : 68 - 76
  • [4] PREFERENTIAL V-BETA-GENE USAGE AND LACK OF JUNCTIONAL SEQUENCE CONSERVATION AMONG HUMAN T-CELL RECEPTORS SPECIFIC FOR A TETANUS TOXIN DERIVED PEPTIDE - EVIDENCE FOR A DOMINANT ROLE OF A GERMLINE-ENCODED V-REGION IN ANTIGEN MAJOR HISTOCOMPATIBILITY COMPLEX RECOGNITION
    BOITEL, B
    ERMONVAL, M
    PANINABORDIGNON, P
    MARIUZZA, RA
    LANZAVECCHIA, A
    ACUTO, O
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (03) : 765 - 777
  • [5] CONSERVED NUCLEOTIDE-SEQUENCES AT THE 5' END OF T-CELL RECEPTOR VARIABLE GENES FACILITATE POLYMERASE CHAIN-REACTION AMPLIFICATION
    BROEREN, CPM
    VERJANS, GMGM
    VANEDEN, W
    KUSTERS, JG
    LENSTRA, JA
    LOGTENBERG, T
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (03) : 569 - 575
  • [6] BUCKLEY RH, 1986, J IMMUNOL, V136, P2398
  • [7] OPTIMAL CONDITIONS FOR DIRECTLY SEQUENCING DOUBLE-STRANDED PCR PRODUCTS WITH SEQUENASE
    CASANOVA, JL
    PANNETIER, C
    JAULIN, C
    KOURILSKY, P
    [J]. NUCLEIC ACIDS RESEARCH, 1990, 18 (13) : 4028 - 4028
  • [8] THE OUTLINE STRUCTURE OF THE T-CELL ALPHA-BETA-RECEPTOR
    CHOTHIA, C
    BOSWELL, DR
    LESK, AM
    [J]. EMBO JOURNAL, 1988, 7 (12) : 3745 - 3755
  • [9] T-CELL RECEPTOR VARIABLE BETA-GENES SHOW DIFFERENTIAL EXPRESSION IN CD4 AND CD8 T-CELLS
    DAVEY, MP
    MEYER, MM
    MUNKIRS, DD
    BABCOCK, D
    BRAUN, MP
    HAYDEN, JB
    BAKKE, AC
    [J]. HUMAN IMMUNOLOGY, 1991, 32 (03) : 194 - 202
  • [10] EUROPEAN EXPERIENCE OF BONE-MARROW TRANSPLANTATION FOR SEVERE COMBINED IMMUNODEFICIENCY
    FISCHER, A
    LANDAIS, P
    FRIEDRICH, W
    MORGAN, G
    GERRITSEN, B
    FASTH, A
    PORTA, F
    GRISCELLI, C
    GOLDMAN, SF
    LEVINSKY, R
    VOSSEN, J
    [J]. LANCET, 1990, 336 (8719) : 850 - 854