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型特异性呼肠孤病毒抗血清阻断细胞毒性T细胞与靶细胞的相互作用:无包膜病毒的病毒血凝素与细胞表面相关的证据。

Type-specific reovirus antiserum blocks the cytotoxic T-cell-target cell interaction: evidence for the association of the viral hemagglutinin of a nonenveloped virus with the cell surface.

作者信息

Finberg R, Weiner H L, Burakoff S J, Fields B N

出版信息

Infect Immun. 1981 Feb;31(2):646-9. doi: 10.1128/iai.31.2.646-649.1981.

Abstract

It has previously been demonstrated that spleen cells from mice immunized with reovirus type 1 or 3 generate virus-specific cytotoxic T lymphocytes (CTL) after in vitro restimulation. Such cytotoxic T cells lyse H-2 identical targets that are infected with the appropriate reovirus type. Viral recombinants were used to demonstrate that the S1 gene is the predominant viral gene determining the specificity of the CTL. Reoviruses are nonenveloped, non-membrane-maturing viruses; therefore, it was important to determine whether viral products were being recognized by CTL on the surface of target cells. Antiserum blocking was utilized to investigate this issue. Using viral recombinants and antisera to reoviruses types 1 and 3, we were able to demonstrate that the major viral antigen recognized by the CTL on the target cell surface is the sigma 1 polypeptide encoded by the S1 genome segment. Thus, viral antigens on the target cell membrane seem to be important in the CTL response to a nonenveloped, non-membrane-maturing virus.

摘要

先前已经证明,用1型或3型呼肠孤病毒免疫的小鼠的脾细胞在体外再刺激后会产生病毒特异性细胞毒性T淋巴细胞(CTL)。这种细胞毒性T细胞会裂解被相应呼肠孤病毒类型感染的H-2相同靶细胞。病毒重组体被用于证明S1基因是决定CTL特异性的主要病毒基因。呼肠孤病毒是无包膜、非膜成熟病毒;因此,确定CTL是否在靶细胞表面识别病毒产物很重要。利用抗血清阻断来研究这个问题。使用病毒重组体和针对1型和3型呼肠孤病毒的抗血清,我们能够证明CTL在靶细胞表面识别的主要病毒抗原是由S1基因组片段编码的σ1多肽。因此,靶细胞膜上的病毒抗原在对无包膜、非膜成熟病毒的CTL反应中似乎很重要。

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