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人类镍反应性T细胞克隆的HLA限制性元件的特异性

Specificity of HLA restricting elements for human nickel reactive T cell clones.

作者信息

Emtestam L, Carlsson B, Marcusson J A, Wallin J, Möller E

机构信息

Department of Dermatology, Karolinska Institute, Huddinge Hospital, Stockholm, Sweden.

出版信息

Tissue Antigens. 1989 May;33(5):531-41. doi: 10.1111/j.1399-0039.1989.tb01704.x.

Abstract

In order to study the fine specificity of HLA class II restriction, we have established nickel specific T cell clones from a nickel allergic patient. Cells were cloned by limiting dilution after primary stimulation and selection of nickel specific blasts. Several clones were established which were all shown to carry the CD4 marker. All clones were shown to be completely blocked by monoclonal antibodies directed against DR antigens, but unaffected by antibodies against DQ or DP, thus demonstrating their DR specificity. For the study of HLA class II restriction, a panel of cell donors was carefully HLA typed by including the use of DRB and DQB cDNA probes. Specificity analysis, using allogeneic antigen presenting cells, revealed that the clones were either restricted to DR3- or DR4-like molecules, which is consistent with the fact that the donor was DR3, DR4 positive. However, the studies also revealed that the fine specificity of the DR3 and DR4 restriction could not be completely assessed by serological and genomic typing of panel cells. This indicates that cellularly defined HLA restriction elements recognized by T cells cannot be defined properly with available class II typing methods, and the results of these experiments documented the additional polymorphism of class II restriction elements. The clonal specificity analysis has shed further light on the biologically relevant level of DR polymorphism.

摘要

为了研究HLA II类分子限制的精细特异性,我们从一名对镍过敏的患者体内建立了镍特异性T细胞克隆。细胞在初次刺激和选择镍特异性母细胞后通过有限稀释法进行克隆。建立了几个克隆,所有克隆均显示携带CD4标记。所有克隆均被针对DR抗原的单克隆抗体完全阻断,但不受针对DQ或DP抗体的影响,从而证明了它们的DR特异性。为了研究HLA II类分子限制,通过使用DRB和DQB cDNA探针仔细对一组细胞供体进行了HLA分型。使用同种异体抗原呈递细胞进行的特异性分析表明,这些克隆要么受限于DR3样或DR4样分子,这与供体为DR3、DR4阳性的事实一致。然而,研究还表明,通过对一组细胞进行血清学和基因分型无法完全评估DR3和DR4限制的精细特异性。这表明,用现有的II类分型方法无法正确定义T细胞识别的细胞水平的HLA限制元件,这些实验结果证明了II类限制元件存在额外的多态性。克隆特异性分析进一步揭示了DR多态性在生物学上的相关水平。

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