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实验性感染猕猴中针对负调控因子(nef)的抗体反应:与病毒血症、疾病进展以及针对病毒结构蛋白的血清转化的相关性。

Antibody response to the negative regulatory factor (nef) in experimentally infected macaques: correlation with viremia, disease progression, and seroconversion to structural viral proteins.

作者信息

Kirchhoff F, Voss G, Nick S, Stahl-Hennig C, Coulibaly C, Frank R, Jentsch K D, Hunsmann G

机构信息

German Primate Centre, Department of Virology and Immunology, Göttingen.

出版信息

Virology. 1991 Jul;183(1):267-72. doi: 10.1016/0042-6822(91)90139-3.

Abstract

The antibody response to structural and regulatory viral proteins was studied in 14 rhesus (Macaca mulatta) and 6 cynomolgus (Macaca fascicularis) macaques experimentally infected with HIV-2 or SIVMAC. To investigate the humoral antibody response to the negative regulatory factor (nef), the recombinant protein was expressed to high levels with recombinant vaccinia virus (VV). nef-specific antibodies were detected in 14 of 20 infected macaques (70%). In sera of all infected monkeys antibodies directed to the structural proteins gp120, p56, and p24 appeared 2 to 6 weeks postinfection. In contrast, the extent and the appearance of nef-specific antibodies during the course of infection varied considerably between individual animals. However, only in sera of four animals (20%) were nef-specific antibodies detectable as early as those against the core proteins p24 and p56. In SIVMAC-infected rhesus macaques at different clinical stages, the antibody response towards nef neither correlated with the development of viral latency nor to disease progression or viremia. Our data indicate that in macaques experimentally infected with SIV or HIV-2 antibody formation against nef is not a useful diagnostic marker either for early detection of viral infection or of disease progression.

摘要

在14只恒河猴(猕猴)和6只食蟹猴中研究了对HIV-2或SIVMAC进行实验性感染后针对病毒结构和调节蛋白的抗体反应。为了研究对负调节因子(nef)的体液抗体反应,用重组痘苗病毒(VV)将重组蛋白高效表达。在20只受感染的猕猴中有14只(70%)检测到了nef特异性抗体。在所有受感染猴子的血清中,针对结构蛋白gp120、p56和p24的抗体在感染后2至6周出现。相比之下,感染过程中nef特异性抗体的程度和出现时间在个体动物之间差异很大。然而,只有4只动物(20%)的血清中能像针对核心蛋白p24和p56那样早在感染后就检测到nef特异性抗体。在处于不同临床阶段的感染SIVMAC的恒河猴中,对nef的抗体反应既与病毒潜伏的发展无关,也与疾病进展或病毒血症无关。我们的数据表明,在实验性感染SIV或HIV-2的猕猴中,针对nef的抗体形成对于早期检测病毒感染或疾病进展都不是一个有用的诊断标志物。

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