首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Human cytotoxic T-lymphocyte recognition of an HLA-A3 gene product expressed on murine L cells: the only human gene product required on the target cells for lysis is the class I heavy chain.
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Human cytotoxic T-lymphocyte recognition of an HLA-A3 gene product expressed on murine L cells: the only human gene product required on the target cells for lysis is the class I heavy chain.

机译:鼠L细胞上表达的HLA-A3基因产物的人细胞毒性T淋巴细胞识别:靶细胞裂解所需的唯一人基因产物是I类重链。

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摘要

To dissect the molecular basis for T-cell recognition of class I major histocompatibility complex antigens, we have examined the ability of human cytotoxic T lymphocytes (CTL) to recognize murine L cells transformed with a human class I gene. Three transformed L-cell lines were generated that expressed the human HLA-A3 gene from donor E1 at levels comparable to those of the endogenous L-cell H-2Kk molecules. CTL were generated in secondary and tertiary mixed lymphocyte culture against the HLA-A3 subtype of donor E1 by culturing irradiated E1 peripheral blood lymphocytes with the peripheral blood lymphocytes of responder donor M3 (M3 shares all defined class I antigens with E1 but expresses a different HLA-A3 subtype). Each of the HLA-A3-transformed L cells was lysed by M3 anti-E1 CTL in a short-term 51Cr release assay and this recognition was blocked by a monoclonal anti-HLA-A3 antibody. Antibodies specific for the human T8 and LFA-1 molecules on the CTL effectors (but absent from the transformed targets) also blocked lysis of each of the HLA-A3 transformed L-cell targets. Antibodies to other T-cell molecules failed to block lysis. The present results demonstrate that human CTL can recognize human class I molecules on targets that do not express any other human gene product and further suggest that effector T-cell molecules T8 and LFA-1 are functionally involved in this recognition process.
机译:为了剖析T细胞识别I类主要组织相容性复合抗原的分子基础,我们检查了人类细胞毒性T淋巴细胞(CTL)识别由人类I类基因转化的鼠L细胞的能力。产生了三种转化的L细胞系,它们以与内源L细胞H-2Kk分子相当的水平表达了来自供体E1的人HLA-A3基因。 CTL是通过将放射的E1外周血淋巴细胞与响应者供体M3的外周血淋巴细胞一起培养而在针对供体E1的HLA-A3亚型的二级和三级混合淋巴细胞培养中产生的(M3与E1共享所有已定义的I类抗原,但表达不同的HLA -A3亚型)。在短期51Cr释放试验中,M3抗E1 CTL裂解了每个HLA-A3转化的L细胞,并且这种识别被单克隆抗HLA-A3抗体阻断。对CTL效应子上的人T8和LFA-1分子具有特异性的抗体(但不存在于转化的靶标中)也阻断了每个HLA-A3转化的L细胞靶标的裂解。其他T细胞分子的抗体未能阻止裂解。本结果证明人CTL可以识别不表达任何其他人基因产物的靶标上的人I类分子,并且进一步表明效应T细胞分子T8和LFA-1在功能上参与了该识别过程。

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