Moebius U, Herrmann F, Hercend T, Meuer S C
Abteilung Angewandte Immunologie, Deutsches Krebsforschungszentrum, Heidelberg, FRG.
J Clin Invest. 1991 May;87(5):1567-74. doi: 10.1172/JCI115170.
T cell clones were established from peripheral blood of a patient with severe aplastic anemia. 8 of 18 individual clonal T cell populations stably coexpressed CD4 and CD8 molecules, a phenotype characteristic for thymocytes and a minor subpopulation of circulating T lymphocytes. Analysis of T cell receptor genes revealed identical rearrangements of T cell receptor beta chain genes, suggesting clonality of these T cells. CD4+/CD8+ T cells clones were found to be efficiently cytotoxic towards autologous lymphoblasts. Autocytotoxicity could be blocked by a CD3 MAb, a MAb specific for monomorphic MHC class II determinants, and particularly, by an MHC-DP-specific MAb, suggesting specificity for autologous DP molecules. Perhaps more important, CD4+/CD8+ T cell clones inhibited differentiation of autologous progenitor enriched bone marrow cells in vitro by a direct cell-mediated mechanism. These data suggest that circulating cytotoxic CD4+/CD8+ T cell clones specific for autologous MHC-DP determinants may be involved in hematopoietic failure in some cases of aplastic anemia.
从一名重型再生障碍性贫血患者的外周血中建立了T细胞克隆。18个单个克隆T细胞群体中有8个稳定地共表达CD4和CD8分子,这是胸腺细胞和循环T淋巴细胞的一个小亚群的表型特征。T细胞受体基因分析显示T细胞受体β链基因存在相同的重排,表明这些T细胞具有克隆性。发现CD4+/CD8+ T细胞克隆对自体淋巴母细胞具有高效的细胞毒性。自体细胞毒性可被CD3单克隆抗体、一种针对单态性MHC II类决定簇的单克隆抗体,特别是一种针对MHC-DP的单克隆抗体所阻断,提示对自体DP分子具有特异性。也许更重要的是,CD4+/CD8+ T细胞克隆在体外通过直接的细胞介导机制抑制富含自体祖细胞的骨髓细胞的分化。这些数据表明,针对自体MHC-DP决定簇的循环细胞毒性CD4+/CD8+ T细胞克隆可能在某些再生障碍性贫血病例的造血功能衰竭中起作用。