Permissible and immunogenic HLA-A mismatches: Cytotoxic T-cell precursor frequencies reflect graft survival data

被引:12
作者
Roelen, DL
Stobbe, I
Young, NT
van Bree, SPMJ
Doxiadis, IIN
Oudshoorn, M
Morris, PJ
Wood, KJ
Claas, FHJ
机构
[1] Leiden Univ, Ctr Med, Dept Immunohaematol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Ctr Med, Blood Bank, NL-2300 RC Leiden, Netherlands
[3] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg, Oxford OX3 9DU, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
HLA; transplantation; cytotoxic T lymphocytes; permissible; immunogenic;
D O I
10.1016/S0198-8859(01)00263-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Analysis of the in vivo immunogenicity of single HLA mismatches, in the context of a patient's own human leukocyte antigen (HLA) phenotype, has been used to define permissible and immunogenic HLA mismatches, Kidney graft survival in the case of permissible mismatches was similar to that of completely HLA matched combinations, whereas immunogenic mismatches lead to a significantly poorer graft survival. The present study rested whether such permissible and immunogenic HLA mismatches are reflected in the in vitro cytotoxic T-lymphocyte (CTL) allorepertoire. Limiting dilution experiments were performed to analyze the number of precursor CTL directed against individual HLA class I antigens. In general, the frequency of CTLp directed against permissible HLA-A antigens (n = 70, mean frequency 27 CTLp I, per million peripheral blood lymphocytes [PBL]) was found to be significantly lower compared with the CTLp directed against immunogenic HLA-A antigens (n = 73, mean frequency 59 CTLp per million PBL). The difference was found both in healthy individuals and a population of renal transplant candidates. These results were confirmed by a retrospective analysis of CTLp frequencies performed between partly mismatched unrelated bone marrow donors and their potential recipients. In conclusion, on the population level the permissible and immunogenic HLA-A mismatches are indeed reflected in the CTL allorepertoire. However, due to the big overlap of the CTLp frequencies in these populations, the permissible or immunogenic nature of a mismatch for a particular patient should be determined on an individual basis. Human Immunology 62, 661-667 (2001). (C) American Society for Histocompatibility and Immunogenetics, 2001. Published by Elsevier Science Inc.
引用
收藏
页码:661 / 667
页数:7
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