Hone David M, DeVico Anthony L, Fouts Timothy R, Onyabe David Y, Agwale Simon M, Wambebe Charles O, Blattner William A, Gallo Robert C, Lewis George K
Divisions of Basic Science and Vaccine Research, Institute of Human Virology, University of Maryland Biotechnology Institute, Baltimore, Maryland 21201, USA.
J Hum Virol. 2002 Jan-Feb;5(1):17-23.
The antigenic diversity, rapid genetic integration into host cell DNA, and immune evasion tactics of human immunodeficiency virus type 1 (HIV-1) create formidable obstacles to the development of an effective vaccine against it. In spite of this, the advent of conformationally constrained HIV-1 Env and gp120 immunogens has made it feasible to formulate HIV-1 vaccines that induce broadly cross-reactive neutralizing antibodies and afford protection through humoral mechanisms. This paper reviews recent advances made by the authors toward the development of an HIV-1 vaccine that elicits such antibodies in both the mucosal and systemic immune compartments.
1型人类免疫缺陷病毒(HIV-1)的抗原多样性、迅速整合到宿主细胞DNA中的能力以及免疫逃逸策略,为开发针对它的有效疫苗造成了巨大障碍。尽管如此,构象受限的HIV-1包膜糖蛋白(Env)和糖蛋白120(gp120)免疫原的出现,使得制备能诱导广泛交叉反应性中和抗体并通过体液机制提供保护的HIV-1疫苗成为可能。本文综述了作者们在开发一种能在黏膜和全身免疫区室中引发此类抗体的HIV-1疫苗方面取得的最新进展。