CD8+ T-cells: are they sufficient to prevent, contain or eradicate HIV-1 infection?

Scott A Brown, Julia L Hurwitz, Xiaoyan Zhan, Peter C Doherty, Karen S Slobod
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引用次数: 9

Abstract

The prevention of HIV-1 by vaccination has proven to be a formidable task. In an ongoing endeavor to end the HIV-1 pandemic, scientists seek vaccines that will elicit quantitatively and qualitatively robust B-cell and T-cell activities. Given that cytotoxic T-lymphocytes (CTL) play a substantial role in the immunological control of immunodeficiency virus infections, this review will focus on vaccines designed to elicit HIV-1-specific CTL. Vaccine approaches using various HIV-1 proteins or specific CTL determinants, partnered with diverse delivery systems and adjuvants will be discussed. Lessons from studies with other virus models (e.g. gamma herpes virus and influenza virus) will also be examined. Since CTL contribute to the success of vaccines in other model systems, an understanding of the strengths and possible limitations of these cells may be critical to future successes in the HIV-1 vaccine field.

CD8+ t细胞是否足以预防、控制或根除HIV-1感染?
通过接种疫苗预防HIV-1已被证明是一项艰巨的任务。在结束HIV-1大流行的持续努力中,科学家们寻求能够在数量和质量上引发强大的b细胞和t细胞活动的疫苗。鉴于细胞毒性t淋巴细胞(CTL)在免疫缺陷病毒感染的免疫控制中起着重要作用,本文将重点讨论设计用于诱导hiv -1特异性CTL的疫苗。将讨论使用各种HIV-1蛋白或特异性CTL决定因子的疫苗方法,以及不同的递送系统和佐剂。还将审查其他病毒模型(例如伽马疱疹病毒和流感病毒)研究的经验教训。由于CTL有助于其他模型系统中疫苗的成功,因此了解这些细胞的优势和可能的局限性可能对未来HIV-1疫苗领域的成功至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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