Devico Anthony L, Fouts Timothy R, Shata Mohamed T, Kamin-Lewis Roberta, Lewis George K, Hone David M
Division of Vaccine Research, Institute of Human Virology, University of Maryland Biotechnology Institute, 725 W. Lombard Street, Baltimore, MD 21201, USA.
Vaccine. 2002 May 6;20(15):1968-74. doi: 10.1016/s0264-410x(02)00080-4.
Given the increasing incidence of HIV-1 infection world-wide, an affordable, effective vaccine is probably the only way that this virus will be contained. Accordingly, our group is developing an oral prime-boost strategy with the primary goal of eliciting broadly neutralizing antibodies against HIV-1 to provide sterilizing immunity for this virus. Our secondary goal is to elicit broadly cross-reactive anti-viral CD8(+) T cells by this strategy to blunt any breakthrough infections that occur after vaccination of individuals who fail to develop sterilizing immunity. This article describes our progress in the use of the live attenuated intracellular bacteria, Salmonella and Shigella, as oral delivery vehicles for DNA vaccines and the development of conformationally constrained HIV-1 Env immunogens that elicit broadly neutralizing antibodies.
鉴于全球范围内HIV-1感染发病率不断上升,一种价格可承受、有效的疫苗可能是控制这种病毒的唯一途径。因此,我们团队正在开发一种口服初免-加强策略,其主要目标是诱导产生针对HIV-1的广泛中和抗体,为该病毒提供无菌免疫。我们的次要目标是通过该策略诱导产生广泛交叉反应的抗病毒CD8(+) T细胞,以抑制在未能产生无菌免疫的个体接种疫苗后发生的任何突破性感染。本文描述了我们在使用减毒活细胞内细菌(沙门氏菌和志贺氏菌)作为DNA疫苗的口服递送载体以及开发能诱导广泛中和抗体的构象受限HIV-1 Env免疫原方面取得的进展。