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细胞毒性T淋巴细胞多表位DNA质粒(EP HIV-1090)疫苗在健康的、未感染1型人类免疫缺陷病毒(HIV-1)的成年人中的安全性和免疫原性。

Safety and immunogenicity of cytotoxic T-lymphocyte poly-epitope, DNA plasmid (EP HIV-1090) vaccine in healthy, human immunodeficiency virus type 1 (HIV-1)-uninfected adults.

作者信息

Gorse Geoffrey J, Baden Lindsey R, Wecker Margaret, Newman Mark J, Ferrari Guido, Weinhold Kent J, Livingston Brian D, Villafana Tonya L, Li Hongli, Noonan Elizabeth, Russell Nina D

机构信息

Department of Veterans Affairs Medical Center and Saint Louis University, St. Louis, MO 63104, United States.

出版信息

Vaccine. 2008 Jan 10;26(2):215-23. doi: 10.1016/j.vaccine.2007.10.061. Epub 2007 Nov 20.

Abstract

We evaluated EP HIV-1090 vaccine, a DNA plasmid encoding 21 cytotoxic T-lymphocyte (CTL) epitopes of human immunodeficiency virus type 1 (HIV-1) and the pan-DR helper T-lymphocyte epitope (PADRE), in a dose escalation, randomized, double-blinded, placebo-controlled Phase 1 trial. Vaccine, at 0.5, 2.0, or 4.0mg doses, or placebo was injected four times over 6 months. Forty-two healthy, HIV-1-uninfected adults were enrolled. Using an interferon-gamma ELISPOT assay, a response to PADRE was detected in one vaccine recipient. Three vaccine recipients raised anti-HIV-1 CD8+ CTL measured by chromium-release assay. The vaccine was safe and well-tolerated, but only weakly immunogenic.

摘要

我们在一项剂量递增、随机、双盲、安慰剂对照的1期试验中评估了EP HIV-1090疫苗,这是一种编码1型人类免疫缺陷病毒(HIV-1)的21个细胞毒性T淋巴细胞(CTL)表位和泛DR辅助性T淋巴细胞表位(PADRE)的DNA质粒。疫苗以0.5、2.0或4.0mg剂量,或安慰剂在6个月内注射4次。招募了42名健康的、未感染HIV-1的成年人。使用干扰素-γ ELISPOT检测法,在一名疫苗接种者中检测到对PADRE的反应。通过铬释放试验测量,三名疫苗接种者产生了抗HIV-1 CD8+ CTL。该疫苗安全且耐受性良好,但免疫原性较弱。

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