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来自膀胱移行细胞癌(TCC)患者的具有选择性特异性的MHC非限制性细胞毒性T细胞克隆。

MHC nonrestricted cytotoxic T cell clones with selective specificity from patients with transitional cell carcinoma (TCC) of the urinary bladder.

作者信息

Hansson Y, Vargas-Cortes M, Paulie S, Perlmann P

机构信息

Department of Immunology, University of Stockholm, Sweden.

出版信息

Cancer Immunol Immunother. 1988;27(3):205-12. doi: 10.1007/BF00205441.

Abstract

Lymphocytes from patients with transitional cell carcinoma (TCC) of the urinary bladder are more cytotoxic to bladder tumor cells than to a variety of control cells. This disease-related cytotoxicity has previously been shown to involve several mechanisms and different types of effector cells. To analyze further the nature of the effector cells operative in this system, peripheral blood lymphocytes from eight TCC patients were stimulated in vitro with TCC extract and cultured in the presence of interleukin 2 and allogeneic feeder cells. When tested for cytotoxicity in vitro on a target cell panel including both adherent and nonadherent cell lines, the lymphocytes killed a broad spectrum of targets in a major histocompatibility complex (MHC)-unrestricted fashion. When cloned by limiting dilution, clones were obtained which displayed a more restricted pattern of target cell killing. Some of the clones were highly but not exclusively selective for TCC-derived target cells. Phenotypically, these cells resembled mature T cells of CTL-type (CD8+/CD4-). They also expressed the CD3/5 T cell antigen receptor complex but target cell killing was not MHC-restricted. The results of various inhibition experiments suggested that the CD3/TCR complex was involved in the cytotoxicity exhibited by these effector cells. However, its precise role in target cell recognition and the identification of the tumor cell structures recognised by the effector cells require further studies.

摘要

膀胱癌移行细胞癌(TCC)患者的淋巴细胞对膀胱肿瘤细胞的细胞毒性比对多种对照细胞更强。先前已表明,这种与疾病相关的细胞毒性涉及多种机制和不同类型的效应细胞。为了进一步分析该系统中起作用的效应细胞的性质,用TCC提取物体外刺激8名TCC患者的外周血淋巴细胞,并在白细胞介素2和同种异体饲养细胞存在的情况下进行培养。当在包括贴壁和非贴壁细胞系的靶细胞板上进行体外细胞毒性测试时,淋巴细胞以主要组织相容性复合体(MHC)非限制性方式杀死了广泛的靶细胞。通过有限稀释克隆时,获得了显示出更受限的靶细胞杀伤模式的克隆。一些克隆对TCC衍生的靶细胞具有高度但并非唯一的选择性。从表型上看,这些细胞类似于CTL型(CD8 + / CD4-)的成熟T细胞。它们还表达CD3 / 5 T细胞抗原受体复合物,但靶细胞杀伤不受MHC限制。各种抑制实验的结果表明,CD3 / TCR复合物参与了这些效应细胞表现出的细胞毒性。然而,其在靶细胞识别中的精确作用以及效应细胞识别的肿瘤细胞结构的鉴定需要进一步研究。

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本文引用的文献

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