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人类免疫缺陷病毒-1 疫苗设计:我们现在该往何处去?

Human immunodeficiency virus-1 vaccine design: where do we go now?

机构信息

Department Emerging Pathogens and Vaccines, The John Curtin School of Medical Research, The Australian National University, Canberra, Australian Capital Territory, Australia.

出版信息

Immunol Cell Biol. 2011 Mar;89(3):367-74. doi: 10.1038/icb.2010.118. Epub 2010 Oct 19.

Abstract

Numerous human immunodeficiency virus (HIV)-1 vaccines have been developed over the last three decades, but to date an effective HIV-1 vaccine that can be used for prophylactic or therapeutic purposes in humans has not been identified. The failures and limited successes of HIV-1 vaccines have highlighted the gaps in our knowledge with regard to fundamental immunity against HIV-1 and have provided insights for vaccine strategies that may be implemented for designing more effective HIV-1 vaccines in the future. Recent studies have shown that robust mucosal immunity, high avidity and polyfunctional T cells, and broadly neutralizing antibodies are important factors governing the induction of protective immunity against HIV-1. Furthermore, optimization of vaccine delivery methods for DNA or live viral vector-based vaccines, elucidating the immune responses of individuals who remain resistant to HIV-1 infections and also understanding the core immune responses mediating protection against simian immunodeficiency viruses (SIV) and HIV-1 in animal models following vaccination, are key aspects to be regarded for designing more effective HIV-1 vaccines in the future.

摘要

在过去的三十年中,已经开发了许多人类免疫缺陷病毒 (HIV)-1 疫苗,但迄今为止,尚未发现可用于预防或治疗人类的有效 HIV-1 疫苗。HIV-1 疫苗的失败和有限成功突出表明,我们对针对 HIV-1 的基本免疫的了解存在差距,并为疫苗策略提供了见解,这些策略可能会在未来用于设计更有效的 HIV-1 疫苗。最近的研究表明,强大的粘膜免疫、高亲和力和多功能 T 细胞以及广泛中和抗体是控制诱导针对 HIV-1 的保护性免疫的重要因素。此外,优化针对 DNA 或活病毒载体疫苗的疫苗接种方法、阐明对 HIV-1 感染仍具有抵抗力的个体的免疫反应,以及了解在接种疫苗后动物模型中针对猴免疫缺陷病毒 (SIV) 和 HIV-1 进行保护的核心免疫反应,都是未来设计更有效的 HIV-1 疫苗需要考虑的关键方面。

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