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
Department of Veterans Affairs Medical Center and Saint Louis University, St. Louis, MO 63104, United States.
Vaccine. 2008 Jan 10;26(2):215-23. doi: 10.1016/j.vaccine.2007.10.061. Epub 2007 Nov 20.
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.
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。