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人类白细胞抗原-DC抗原可作为人类细胞毒性T淋巴细胞的识别元件。

HLA-DC antigens can serve as recognition elements for human cytotoxic T lymphocytes.

作者信息

Spits H, Borst J, Giphart M, Coligan J, Terhorst C, De Vries J E

出版信息

Eur J Immunol. 1984 Apr;14(4):299-304. doi: 10.1002/eji.1830140404.

DOI:10.1002/eji.1830140404
PMID:6609821
Abstract

The specificity of four cytotoxic T lymphocyte (CTL) clones which recognize class II major histocompatibility complex (MHC) antigens was analyzed. All clones recognized antigens associated with the serologically defined HLA-DRw6 specificity. The activity of two of these clones, JR-2-2 and JR-2-10, could be inhibited by a monoclonal antibody Q 5/13 specific for a monomorphic determinant present on HLA-DR. In contrast, the activity of the two other CTL clones, JR-2-19 and JR-2-26, was not blocked by Q 5/13, but by a new monoclonal reagent, SPV-L3. This latter monoclonal antibody precipitated a two-chain structure of 28 kDa and 33 kDa and reacts with a monomorphic determinant. The molecular weight of the polypeptides precipitated with SPV-L3 was slightly less than those precipitated with a HLA-DR-specific monoclonal reagent. In addition two-dimensional gel electrophoresis showed that the antigen precipitated by SPV-L3 differed in charge from those precipitated with the anti-HLA-DR antibody. These results indicate that SPV-L3 recognizes a class II MHC product different from HLA-DR. This observation was confirmed by partial amino acid sequence analysis of the two chains which revealed that the molecule precipitated by SPV-L3 is homologous to HLA-DC/DS molecules. Therefore this report provides the first evidence that human cytotoxic T cells can recognize HLA-DC/DS antigens.

摘要

分析了四个识别Ⅱ类主要组织相容性复合体(MHC)抗原的细胞毒性T淋巴细胞(CTL)克隆的特异性。所有克隆均识别与血清学定义的HLA-DRw6特异性相关的抗原。其中两个克隆JR-2-2和JR-2-10的活性可被对HLA-DR上存在的单态决定簇特异的单克隆抗体Q 5/13抑制。相反,另外两个CTL克隆JR-2-19和JR-2-26的活性不受Q 5/13的阻断,而是被一种新的单克隆试剂SPV-L3阻断。后一种单克隆抗体沉淀出28 kDa和33 kDa的双链结构,并与一个单态决定簇反应。用SPV-L3沉淀的多肽的分子量略小于用HLA-DR特异性单克隆试剂沉淀的多肽。此外,二维凝胶电泳显示,SPV-L3沉淀的抗原在电荷上与抗HLA-DR抗体沉淀的抗原有差异。这些结果表明,SPV-L3识别一种不同于HLA-DR的Ⅱ类MHC产物。对两条链的部分氨基酸序列分析证实了这一观察结果,该分析表明,SPV-L3沉淀的分子与HLA-DC/DS分子同源。因此,本报告首次提供了人类细胞毒性T细胞可识别HLA-DC/DS抗原的证据。

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