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自然发生的鼠白血病病毒诱导的白血病抗原:它们与粗病毒及其他鼠白血病病毒抗原的关系。

Antigens of leukemias induced by naturally occurring murine leukemia virus: their relation to the antigens of gross virus and other murine leukemia viruses.

作者信息

Geering G, Old L J, Boyse E A

出版信息

J Exp Med. 1966 Oct 1;124(4):753-72. doi: 10.1084/jem.124.4.753.

Abstract

Leukemias can be induced in W/Fu inbred rats by neonatal inoculation of normal thymus cells of C58 mice. These leukemias are not transplantable to C58 mice or to adult W/Fu rats, but they can be kept in passage in W/Fu rats aged 0 to 7 days. Adult W/Fu rats inoculated repeatedly with these isogenic leukemias produce cytotoxic and precipitating antibodies. These antisera are of particular value in the analysis of the antigens of leukemia cells and of leukemia viruses because their mode of preparation precludes the formation of antibody against any normal constituents of the cell. Analysis based on the cytotoxic test indicates the presence of 2 distinct cell surface antigens in leukemias induced by Passage A Gross virus or occurring spontaneously in mice of high-incidence strains. All leukemias and other tissues known to contain G (Gross) leukemia antigen have both determinants, but certain leukemias of low-incidence strains have only 1 of them and so were previously classified G-. Immunoprecipitation with these antisera reveals the presence of a cellular antigen common to G+ cells and absent from G- cells; the same antigen can be demonstrated in ether-treated Gross virus, but not in intact virus. This antigen is present also in ether-treated preparations of the Friend, Moloney, and Rauscher leukemia viruses, but not in Bittner (mammary tumor) virus. Thus it may be regarded as a group-specific antigen of murine leukemia viruses, in contrast to the type-specific cellular antigens demonstrable by the cytotoxic test. Four additional antigens associated with leukemias induced by wild-type Gross virus have been demonstrated by immunoprecipitation, but their relation to viral and cellular antigens has not been determined.

摘要

通过给新生的W/Fu近交系大鼠接种C58小鼠的正常胸腺细胞,可诱发白血病。这些白血病不能移植到C58小鼠或成年W/Fu大鼠体内,但可在0至7日龄的W/Fu大鼠中传代保存。反复接种这些同基因白血病的成年W/Fu大鼠会产生细胞毒性和沉淀抗体。这些抗血清在分析白血病细胞和白血病病毒的抗原方面具有特殊价值,因为其制备方式可防止形成针对细胞任何正常成分的抗体。基于细胞毒性试验的分析表明,由A株格罗斯病毒诱发或在高发病率品系小鼠中自发产生的白血病中存在两种不同的细胞表面抗原。所有已知含有G(格罗斯)白血病抗原的白血病和其他组织都有这两种决定簇,但某些低发病率品系的白血病只有其中一种,因此以前被归类为G-。用这些抗血清进行免疫沉淀显示,存在一种G+细胞共有的细胞抗原,而G-细胞中不存在这种抗原;在经乙醚处理的格罗斯病毒中也可证明存在相同的抗原,但完整病毒中没有。这种抗原在经乙醚处理的Friend、莫洛尼和劳舍尔白血病病毒制剂中也存在,但在比特纳(乳腺肿瘤)病毒中不存在。因此,与通过细胞毒性试验可证明的型特异性细胞抗原相比,它可被视为鼠白血病病毒的一种群特异性抗原。通过免疫沉淀还证明了与野生型格罗斯病毒诱发的白血病相关的另外四种抗原,但它们与病毒和细胞抗原的关系尚未确定。

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Some further data on cytotoxic isoantibodies in the mouse.关于小鼠细胞毒性同种抗体的一些进一步数据。
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