Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue N., D3-100, Seattle, WA 98109, USA.
Immunity. 2010 Oct 29;33(4):542-54. doi: 10.1016/j.immuni.2010.09.011.
Recent findings have brought optimism that development of a successful human immunodeficiency virus type-1 (HIV-1) vaccine lies within reach. Studies of early events in HIV-1 infection have revealed when and where HIV-1 is potentially vulnerable to vaccine-targeted immune responses. With technical advances in human antibody production, clues about how antibodies recognize HIV-1 envelope proteins have uncovered new targets for immunogen design. A recent vaccine regimen has shown modest efficacy against HIV-1 acquisition. However, inducing long-term T and B cell memory and coping with HIV-1 diversity remain high priorities. Mediators of innate immunity may play pivotal roles in blocking infection and shaping immunity; vaccine strategies to capture these activities are under investigation. Challenges remain in integrating basic, preclinical and clinical research to improve predictions of types of immunity associated with vaccine efficacy, to apply these insights to immunogen design, and to accelerate evaluation of vaccine efficacy in persons at-risk for infection.
最近的研究结果带来了希望,即成功开发人类免疫缺陷病毒 1 型 (HIV-1) 疫苗已指日可待。对 HIV-1 感染早期事件的研究揭示了 HIV-1 在何时何地容易受到疫苗靶向免疫反应的影响。随着人类抗体产生技术的进步,有关抗体如何识别 HIV-1 包膜蛋白的线索揭示了免疫原设计的新靶标。最近的疫苗方案显示出对 HIV-1 获得性感染的适度疗效。然而,诱导长期 T 和 B 细胞记忆并应对 HIV-1 多样性仍然是重中之重。先天免疫介质可能在阻断感染和塑造免疫方面发挥关键作用;正在研究捕捉这些活动的疫苗策略。在整合基础、临床前和临床研究以提高对与疫苗疗效相关的免疫类型的预测、将这些见解应用于免疫原设计以及加速对感染风险人群中疫苗疗效的评估方面,仍然存在挑战。