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针对由格罗斯、弗里德或劳舍尔白血病病毒诱导的同基因肿瘤的H-2限制性T杀伤细胞的病毒特异性。

Viral specificity of H-2-restricted T killer cells directed against syngeneic tumors induced by Gross, Friend, or Rauscher leukemia virus.

作者信息

Plata F, Lilly F

出版信息

J Exp Med. 1979 Nov 1;150(5):1174-86. doi: 10.1084/jem.150.5.1174.

Abstract

Cytolytic T lymphocytes (CTL) were generated against murine tumors induced by Gross, Friend, or Rauscher leukemia virus (LV) in syngeneic mixed leukocyte-tumor cell cultures. Analogous to the patterns of specificity observed with antibodies to LV-induced cell surface antigens, CTL could be classified into two major groups of specificity. Tumor cells induced by Friend, Moloney, or Rauscher virus and positive for the FMR antigen were killed by syngeneic CTL immune to any one of these three LV; the same CTL, however, were incapable of killing syngeneic tumor cells induced by Gross LV. The converse was true for Gross LV-specific CTL: these CTL were specific for syngeneic tumor cells expressing the Gross virus-associated cell-surface antigen (GCSA), and not the FMR antigen. The H-2 specificities of the two groups of LV-immune CTL were also compared, because in both cases, CTL were restricted in their killing activity to H-2-identical tumor target cells. When CTL from single strains of mice were generated against syngeneic FMR- or GCSA-positive tumor cells, differences were observed with respect both to the requirement for the expression of compatible H-2K or H-2D specificities, and to the intensity of the CTL response in congenic mice of the H-2b, H-2d, and H-2k haplotypes.

摘要

在同基因混合白细胞-肿瘤细胞培养物中,产生了针对由格罗斯、弗里德或劳舍尔白血病病毒(LV)诱导的小鼠肿瘤的细胞毒性T淋巴细胞(CTL)。与针对LV诱导的细胞表面抗原的抗体所观察到的特异性模式类似,CTL可分为两个主要的特异性组。由弗里德、莫洛尼或劳舍尔病毒诱导且FMR抗原呈阳性的肿瘤细胞,可被对这三种LV中的任何一种具有免疫性的同基因CTL杀死;然而,相同的CTL无法杀死由格罗斯LV诱导的同基因肿瘤细胞。对于格罗斯LV特异性CTL来说情况则相反:这些CTL对表达格罗斯病毒相关细胞表面抗原(GCSA)而非FMR抗原的同基因肿瘤细胞具有特异性。还比较了两组LV免疫CTL的H-2特异性,因为在这两种情况下,CTL的杀伤活性都局限于H-2相同的肿瘤靶细胞。当从小鼠的单个品系中产生针对同基因FMR或GCSA阳性肿瘤细胞的CTL时,在对兼容的H-2K或H-2D特异性表达的需求以及H-2b、H-2d和H-2k单倍型的同源小鼠中CTL反应的强度方面都观察到了差异。

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