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非洲猪瘟病毒特异性细胞毒性T淋巴细胞识别32千道尔顿即刻早期蛋白(vp32)。

African swine fever virus-specific cytotoxic T lymphocytes recognize the 32 kDa immediate early protein (vp32).

作者信息

Alonso F, Domínguez J, Viñuela E, Revilla Y

机构信息

Centro de Investigación en Sanidad Animal, INIA, Madrid, Spain.

出版信息

Virus Res. 1997 Jun;49(2):123-30. doi: 10.1016/s0168-1702(97)01459-7.

Abstract

African swine fever (ASF) virus-specific cytotoxic T lymphocyte (CTL) activity has been studied in a model in which SLA inbred minipigs were experimentally infected with an attenuated isolate of the virus. The CTL assays were performed using alveolar macrophages as target cells. The specific lysis is mediated by purified CD8+ lymphocytes but not by CD4+ cells and can be blocked by incubation with anti-SLA class I monoclonal antibodies. The purified CD8+ population produced high levels of interferon-gamma after ASF virus stimulation. In an attempt to define the viral proteins recognized by CTL, target cells infected with a recombinant vaccinia virus (VV) expressing the ASF virus p32, an immediate early protein during ASF virus replication, were recognized and lysed by CTL. This assay may be useful for VV recombinant screening in order to identify other potential target ASF virus proteins.

摘要

在一个用SLA近交小型猪经实验感染病毒减毒株的模型中,对非洲猪瘟(ASF)病毒特异性细胞毒性T淋巴细胞(CTL)活性进行了研究。CTL检测以肺泡巨噬细胞作为靶细胞。特异性裂解由纯化的CD8 +淋巴细胞介导,而非CD4 +细胞,并且可以通过与抗SLA I类单克隆抗体孵育来阻断。纯化的CD8 +群体在ASF病毒刺激后产生高水平的干扰素-γ。为了确定CTL识别的病毒蛋白,表达ASF病毒p32(ASF病毒复制过程中的一种立即早期蛋白)的重组痘苗病毒(VV)感染的靶细胞被CTL识别并裂解。该检测方法可能有助于VV重组体筛选,以鉴定其他潜在的ASF病毒靶蛋白。

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