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从人外周血中分离出的携带γδ受体的细胞毒性T淋巴细胞的特异性

Specificity of gamma delta receptor-bearing cytotoxic T lymphocytes isolated from human peripheral blood.

作者信息

Bosnes V, Halvorsen R, Skaftadottir I, Gaudernack G, Thorsby E

机构信息

Institute of Transplantation Immunology, National Hospital, Oslo, Norway.

出版信息

Scand J Immunol. 1989 Jun;29(6):723-31. doi: 10.1111/j.1365-3083.1989.tb01177.x.

Abstract

T-cell receptor (TcR)-gamma delta-bearing lymphocytes were isolated from the peripheral blood of two healthy donors by immunomagnetic separation and subsequently cultured. The cell lines generated showed two distinct patterns of cytotoxicity. One TcR-gamma delta + cell line (HG.D) lysed K562 and U937 target cells, three TcR-gamma delta + cell lines lysed Daudi cells, and one TcR-gamma delta + cell line showed a shift from the former to the latter specificity during culture. Cold target inhibition experiments showed that the HG.D effector cells which were cytotoxic against U937 cells also lysed K562 cells. The cytotoxicity against Daudi cells was strongly inhibited by monoclonal antibodies (MoAb) against the CD3 complex, whereas the cytotoxicity of the HG.D cell line against K562 and U937 was unaffected by such antibodies. The cytotoxicity against Daudi cells was also strongly inhibited in the presence of anti-TcR-gamma delta MoAb. However, in two of the Daudi-specific cell lines, strong cytotoxicity against K562 cells was induced by anti-TcR-gamma delta MoAb. Anti-LFA-1 MoAb caused only a partial inhibition of cytotoxicity, while anti-CD2 and anti-TcR-alpha beta MoAb were found to have no effect. The results indicate that human gamma delta receptor-bearing T cells demonstrate a certain degree of target cell specificity, and that recognition of some target cells may be mediated through the TcR-gamma delta.

摘要

通过免疫磁珠分离法从两名健康供体的外周血中分离出携带γδ型T细胞受体(TcR)的淋巴细胞,随后进行培养。所产生的细胞系表现出两种不同的细胞毒性模式。一种TcR-γδ+细胞系(HG.D)可裂解K562和U937靶细胞,三种TcR-γδ+细胞系可裂解Daudi细胞,还有一种TcR-γδ+细胞系在培养过程中表现出从前者特异性向后者特异性的转变。冷靶抑制实验表明,对U937细胞具有细胞毒性的HG.D效应细胞也能裂解K562细胞。针对Daudi细胞的细胞毒性受到抗CD3复合物单克隆抗体(MoAb)的强烈抑制,而HG.D细胞系对K562和U937的细胞毒性不受此类抗体影响。抗TcR-γδ MoAb也能强烈抑制对Daudi细胞的细胞毒性。然而,在两种Daudi特异性细胞系中,抗TcR-γδ MoAb可诱导对K562细胞的强烈细胞毒性。抗LFA-1 MoAb仅部分抑制细胞毒性,而抗CD2和抗TcR-αβ MoAb则无作用。结果表明,人类携带γδ受体的T细胞表现出一定程度的靶细胞特异性,并且对某些靶细胞的识别可能通过TcR-γδ介导。

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