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被病毒特异性细胞毒性T淋巴细胞识别的痘苗感染细胞的靶抗原。

Target antigen of vaccinia-infected cells recognized by virus-specific cytotoxic T lymphocytes.

作者信息

Oie M, Ichihashi Y

出版信息

Microbiol Immunol. 1981;25(4):361-75. doi: 10.1111/j.1348-0421.1981.tb00038.x.

Abstract

A vaccinia-specific target antigen for recognition of anti-vaccinia cytotoxic T lymphocytes (CTL) was found to be formed on the surface of infected cells through two distinct processes. In the first phase, the expression of the target antigen was dependent on the dose of inoculated virus, without specific protein synthesis. The target antigen seems to be produced by virus-cell fusion. In the second phase, the expression of the target antigen was accompanied by synthesis of an early protein. In spite of the difference in their mode of expression, the first-phase and the second-phase target antigens were cross-reactive in cytotoxicity inhibition assays. Cowpox virus, CPR Cl strain, brought about a lower response than vaccinia virus, IHD-J strain, in both sensitization of CTL and formation of CTL-susceptible cells at both the first and the second phase. The cross-reactive, but inefficient, recognition of anti-vaccinia CTL for cowpox-infected cells suggested a slight difference in the target antigens of the two viruses. Attempts to identify the target antigen were then made by comparing the polypeptide composition of vaccinia virus, cowpox virus, and their recombinants. SDS-PAGE analysis of trypsin-activated viruses revealed 44K (cowpox)/45K (vaccinia) polypeptides which corresponded to the difference in target cell formation. Trypsinization of the viruses also increased the ability of the virus to induce the production of CTL-susceptible target cells.

摘要

一种用于识别抗痘苗细胞毒性T淋巴细胞(CTL)的痘苗特异性靶抗原,被发现是通过两个不同过程在受感染细胞表面形成的。在第一阶段,靶抗原的表达依赖于接种病毒的剂量,无需特定蛋白质合成。靶抗原似乎是由病毒-细胞融合产生的。在第二阶段,靶抗原的表达伴随着一种早期蛋白质的合成。尽管它们的表达模式不同,但在细胞毒性抑制试验中,第一阶段和第二阶段的靶抗原具有交叉反应性。在CTL致敏以及第一阶段和第二阶段CTL敏感细胞形成方面,牛痘病毒CPR Cl株比痘苗病毒IHD-J株引起的反应更低。抗痘苗CTL对牛痘感染细胞的交叉反应但低效的识别表明这两种病毒的靶抗原存在细微差异。随后通过比较痘苗病毒、牛痘病毒及其重组体的多肽组成来尝试鉴定靶抗原。对胰蛋白酶激活的病毒进行SDS-PAGE分析,发现了44K(牛痘)/45K(痘苗)多肽,这与靶细胞形成的差异相对应。对病毒进行胰蛋白酶处理也增强了病毒诱导产生CTL敏感靶细胞的能力。

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