McChesney M, Tanneau F, Regnault A, Sansonetti P, Montagnier L, Kieny M P, Rivière Y
Département de Médecine, Institut Pasteur, Paris, France.
Eur J Immunol. 1990 Jan;20(1):215-20. doi: 10.1002/eji.1830200131.
A heterogenous population of envelope glycoprotein-specific cytotoxic effector cells are found in the peripheral blood of individuals infected with HIV-1, and in many cases env-specific lysis is not restricted by MHC molecules and is not blocked by antibody to CD3 (Rivière, Y. et al., J. Virol. 1989, 63:2270). In order to detect env-specific cytotoxic T lymphocytes (CTL) in fresh peripheral blood mononuclear cells of HIV-1-infected donors, a mutant env gene with deletion of the amino-terminal signal sequence was inserted into vaccinia virus. This deletion of the amino-terminal signal sequence was inserted into vaccinia virus. This deletion results in synthesis of an envelope protein that is not glycosylated and not expressed at the surface of infected cells. Target cells infected with this recombinant vaccinia virus are not lysed by antibody-mediated cellular cytotoxicity, but they are recognized by secondary CTL. Comparing lysis of target cells expressing gp160 of HIV-1 and the signal peptide deletion mutant, primary env-specific CTL were detected in some individuals infected with HIV-1.
在感染HIV-1的个体外周血中发现了一群异质性的包膜糖蛋白特异性细胞毒性效应细胞,在许多情况下,env特异性裂解不受MHC分子限制,也不被抗CD3抗体阻断(Rivière, Y.等人,《病毒学杂志》,1989年,63:2270)。为了在感染HIV-1的供体的新鲜外周血单个核细胞中检测env特异性细胞毒性T淋巴细胞(CTL),将一个缺失氨基末端信号序列的env突变基因插入痘苗病毒。这个氨基末端信号序列的缺失被插入到痘苗病毒中。这种缺失导致合成一种未糖基化且不在感染细胞表面表达的包膜蛋白。感染这种重组痘苗病毒的靶细胞不会被抗体介导的细胞毒性裂解,但它们会被二级CTL识别。通过比较表达HIV-1 gp160的靶细胞和信号肽缺失突变体的裂解情况,在一些感染HIV-1的个体中检测到了初级env特异性CTL。