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采用DNA初免和重组gp140蛋白加强免疫方案在小鼠和猕猴中诱导HIV-1 B亚型和AE亚型特异性中和抗体

Induction of HIV-1 subtype B and AE-specific neutralizing antibodies in mice and macaques with DNA prime and recombinant gp140 protein boost regimens.

作者信息

Center Rob J, Wheatley Adam K, Campbell Shahan M, Gaeguta Adriana J, Peut Viv, Alcantara Sheilajen, Siebentritt Carly, Kent Stephen J, Purcell Damian F J

机构信息

Department of Microbiology and Immunology, University of Melbourne, Parkville, 3010 VIC, Australia.

出版信息

Vaccine. 2009 Nov 5;27(47):6605-12. doi: 10.1016/j.vaccine.2009.08.016. Epub 2009 Aug 25.

Abstract

We developed highly expressing clade B and AE DNA and envelope protein (Env) vaccines for evaluation in mice and macaques as DNA prime/protein boost regimens. High levels of Env-specific antibodies were induced in mice, albeit with limited neutralizing activity in vitro. A combined clade B and AE regimen induced high titer Env-specific antibody in two pigtail macaques that neutralized several strains of HIV-1. However, upon mucosal challenge with SHIV(SF162P3) no protection from infection was observed. Although the vaccines tested provide a platform for inducing robust humoral immunity, further refinements to broaden coverage against divergent strains and induce mucosal immunity are needed.

摘要

我们开发了高表达的B亚型和AE亚型DNA及包膜蛋白(Env)疫苗,用于在小鼠和猕猴中作为DNA初免/蛋白加强方案进行评估。在小鼠中诱导出了高水平的Env特异性抗体,尽管体外中和活性有限。B亚型和AE亚型联合方案在两只食蟹猕猴中诱导出了高滴度的Env特异性抗体,该抗体可中和多种HIV-1毒株。然而,在用SHIV(SF162P3)进行黏膜攻击后,未观察到对感染的保护作用。尽管所测试的疫苗提供了一个诱导强大体液免疫的平台,但仍需要进一步改进以扩大对不同毒株的覆盖范围并诱导黏膜免疫。

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