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针对与MAIDS相关肿瘤以及感染LP - BM5 MAIDS缺陷逆转录病毒的小鼠细胞的细胞毒性T淋巴细胞。

Cytotoxic T lymphocytes directed against MAIDS-associated tumors and cells from mice infected by the LP-BM5 MAIDS defective retrovirus.

作者信息

Green W R, Crassi K M, Schwarz D A, Green K A

机构信息

Department of Microbiology, Dartmouth Medical School, Lebanon, New Hampshire 03756.

出版信息

Virology. 1994 Apr;200(1):292-6. doi: 10.1006/viro.1994.1189.

Abstract

The LP-BM5 retrovirus, a complex containing ecotropic helper, recombinant MCF, and defective retroviruses, causes an immunodeficiency-termed mouse AIDS (MAIDS). Many disease features of MAIDS resemble those of AIDS, including terminal B cell lymphomas. Previously we generated from MAIDS-susceptible C57BL/6 mice cytolytic T lymphocytes (CTL) specific for MAIDS-associated B cell lymphomas. Data of the present study (1) exclude MCF and establish a role for defective virus in generating C57BL/6 CTL to MAIDS-associated tumors by experiments involving in vitro stimulation with cells from LP-BM5, ecotropic, or ecotropic-rescued defective virus-infected mice and (2) confirm that such CTL are specific for tumors of MAIDS origin. Several approaches testing for direct involvement of defective virus or its gag-encoded polyprotein, however, did not provide evidence that MAIDS tumor-specific CTL were directed to structural virion proteins, suggesting the possibility that such CTL are specific for nonvirion antigens whose expression depends on the action of the defective genome in the MAIDS disease process.

摘要

LP-BM5逆转录病毒是一种包含嗜亲性辅助病毒、重组MCF病毒和缺陷型逆转录病毒的复合体,可引发一种名为小鼠艾滋病(MAIDS)的免疫缺陷疾病。MAIDS的许多疾病特征与艾滋病相似,包括晚期B细胞淋巴瘤。此前,我们从易患MAIDS的C57BL/6小鼠中培育出了对MAIDS相关B细胞淋巴瘤具有特异性的细胞毒性T淋巴细胞(CTL)。本研究的数据:(1)通过用来自LP-BM5、嗜亲性或嗜亲性拯救的缺陷型病毒感染小鼠的细胞进行体外刺激实验,排除了MCF病毒,并确定了缺陷型病毒在产生针对MAIDS相关肿瘤的C57BL/6 CTL中的作用;(2)证实了此类CTL对MAIDS起源的肿瘤具有特异性。然而,几种检测缺陷型病毒或其gag编码的多蛋白是否直接参与的方法,均未提供证据表明MAIDS肿瘤特异性CTL针对的是病毒体结构蛋白,这表明此类CTL可能针对的是非病毒体抗原,其表达取决于MAIDS疾病过程中缺陷基因组的作用。

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