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H-2 限制性水疱性口炎病毒特异性细胞毒性 T 细胞的靶抗原。

Target antigens for H-2-restricted vesicular stomatitis virus-specific cytotoxic T cells.

作者信息

Zinkernagel R M, Althage A, Holland J

出版信息

J Immunol. 1978 Aug;121(2):744-8.

PMID:210232
Abstract

Cytotoxic thymus-derived lymphocytes from mice infected with vesicular stomatitis virus (VSV) are H-2 restricted and virus specific for the Indiana and New Jersey strains of VSV. VSV-Indiana-immune T cells can lyse target cells infected with the temperature sensitive (ts) mutant ts 045 about 30 times better when target cell infection occurs at the permissive rather than the non-permissive temperature. Since this mutant fails to express the glycoprotein at the cell surface when grown at the nonpermissive temperature, our results support the view that the viral glycoprotein is involved in defining the major target antigen for VSV-specific T cells. However, the tl 17 mutant that expresses a mutant glycoprotein at the cell surface was lysed, suggesting that the expressed mutated glycoprotein can cross-react with Indiana wild-type glycoprotein. Targets infected at the nonpermissive temperature with VSV ts G31 (mutant in the matrix protein) are still susceptible to T cell-mediated lysis but at a lower level of sensitivity. These results are compatible with the interpretation that for VSV-specific T cell lysis of infected target cells, the viral glycoprotein is a major target antigen and must be expressed, and that the matrix protein plays a lesser role, probably by indirectly influencing glycoprotein configuration at the cell surface.

摘要

感染水疱性口炎病毒(VSV)的小鼠的细胞毒性胸腺来源淋巴细胞受H-2限制,且对VSV的印第安纳株和新泽西株具有病毒特异性。当靶细胞感染发生在允许温度而非非允许温度时,VSV-印第安纳免疫T细胞对感染温度敏感(ts)突变体ts 045的靶细胞的裂解能力要强约30倍。由于该突变体在非允许温度下生长时无法在细胞表面表达糖蛋白,我们的结果支持以下观点:病毒糖蛋白参与确定VSV特异性T细胞的主要靶抗原。然而,在细胞表面表达突变糖蛋白的tl 17突变体被裂解,这表明表达的突变糖蛋白可与印第安纳野生型糖蛋白发生交叉反应。在非允许温度下用VSV ts G31(基质蛋白突变体)感染的靶细胞仍然易受T细胞介导的裂解,但敏感性较低。这些结果与以下解释相符:对于感染的靶细胞的VSV特异性T细胞裂解,病毒糖蛋白是主要靶抗原且必须表达,而基质蛋白起的作用较小,可能是通过间接影响细胞表面的糖蛋白构型。

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