[Immunosorption of individual HIV proteins and virions].

Iu M Lopukhin, V V Pavlenko, D V Kulaev, T K Liukova, D D Petrunin, E V Karamov, I A Rudneva
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引用次数: 0

Abstract

Immunosorbents specifically binding native (gp160, gp120, gp41) and recombinant env proteins and HIV-I virions were synthesized on the basis of Sepharose 4B and Silica with immobilized ligands such as gamma-fraction of rabbit antiserum to HIV-I proteins and purified antibodies to env proteins of HIV-I. The possibility was shown of selective extraction of HIV-I virions and individual HIV proteins both in vitro and in vivo. The titer of virus antigens (in ELISA) after perfusion via an immunosorbent of patterns with a high content of virions and HIV-I proteins was 8 times as low as the starting titer (after perfusion via the control sorbent it was 2-fold decreased). Extracorporeal immunosorption in animals after intravenous injection of recombinant env protein permitted the latter's titer to be 5 times lower. After perfusion via the control sorbent the titer dropped by at least 20% as compared with the starting titer. The possibility of using immunosorption in multimodality therapy of AIDS is under discussion.

[单个HIV蛋白和病毒粒子的免疫吸附]。
以Sepharose 4B和Silica为基础,以兔抗血清γ -部分为固定配体,合成了特异性结合天然(gp160、gp120、gp41)和重组env蛋白和HIV-I病毒粒子的免疫吸附剂和纯化的HIV-I env蛋白抗体。在体外和体内均可选择性地提取HIV- i病毒粒子和单个HIV蛋白。通过高病毒粒子和HIV-I蛋白含量的免疫吸附剂灌注后的病毒抗原滴度(ELISA)比起始滴度低8倍(通过对照吸附剂灌注后降低2倍)。动物静脉注射重组env蛋白后的体外免疫吸附使后者的滴度降低了5倍。通过对照吸附剂灌注后,滴度与起始滴度相比至少下降了20%。在艾滋病的多模式治疗中使用免疫吸收的可能性正在讨论中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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