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在体外可中和原发性人类免疫缺陷病毒1型的人源抗体,在体内模型中并不能提供保护作用。

Human antibodies that neutralize primary human immunodeficiency virus type 1 in vitro do not provide protection in an in vivo model.

作者信息

Schutten M, Tenner-Racz K, Racz P, van Bekkum D W, Osterhaus A D

机构信息

Erasmus University Rotterdam, Department of Virology, The Netherlands.

出版信息

J Gen Virol. 1996 Aug;77 ( Pt 8):1667-75. doi: 10.1099/0022-1317-77-8-1667.

Abstract

Recently, conflicting data have been published about the ability of antibodies which efficiently neutralize T cell-adapted human immunodeficiency virus type 1 (HIV-1) strains to neutralize primary HIV-1 strains in vitro and in vivo. Here we present data indicating that such antibodies fail to neutralize primary HIV-1 strains in vivo. To this end, a newly developed chimeric human-to-mouse model was used, in which several aspects of primary HIV-1 infection are mimicked. Poly- and monoclonal antibodies protected the grafted human cells, in a dose-dependent way, from infection with T cell-adapted HIV-1 in this system. A human monoclonal antibody specific for the CD4 binding domain that efficiently neutralizes HIV-1 IIIB in vitro did not protect the human graft from HIV-1 IIIB infection. None of the antibodies provided protection in the in vivo model against infection with primary HIV-1 strains, although they were able to neutralize these same strains in vitro.

摘要

最近,关于能够有效中和T细胞适应性1型人类免疫缺陷病毒(HIV-1)毒株的抗体在体外和体内中和原发性HIV-1毒株的能力,已发表了相互矛盾的数据。在此,我们展示的数据表明,此类抗体在体内无法中和原发性HIV-1毒株。为此,使用了一种新开发的人源化小鼠嵌合模型,该模型模拟了原发性HIV-1感染的几个方面。在这个系统中,多克隆抗体和单克隆抗体以剂量依赖的方式保护移植的人类细胞免受T细胞适应性HIV-1感染。一种对CD4结合域具有特异性的人单克隆抗体,在体外能有效中和HIV-1 IIIB,但不能保护人类移植物免受HIV-1 IIIB感染。尽管这些抗体在体外能够中和原发性HIV-1毒株,但在体内模型中没有一种抗体能提供针对原发性HIV-1毒株感染的保护作用。

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