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基于病毒样颗粒的 HIV-1 疫苗的设计理念。

Design Concepts of Virus-Like Particle-Based HIV-1 Vaccines.

机构信息

Microbiology Department, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.

EAVI2020 European AIDS Vaccine Initiative H2020 Research Programme, London, United Kingdom.

出版信息

Front Immunol. 2020 Sep 30;11:573157. doi: 10.3389/fimmu.2020.573157. eCollection 2020.

Abstract

Prophylactic vaccines remain the best approach for controlling the human immunodeficiency virus-1 (HIV-1) transmission. Despite the limited efficacy of the RV144 trial in Thailand, there is still no vaccine candidate that has been proven successful. Consequently, great efforts have been made to improve HIV-1 antigens design and discover delivery platforms for optimal immune elicitation. Owing to immunogenic, structural, and functional diversity, virus-like particles (VLPs) could act as efficient vaccine carriers to display HIV-1 immunogens and provide a variety of HIV-1 vaccine development strategies as well as prime-boost regimes. Here, we describe VLP-based HIV-1 vaccine candidates that have been enrolled in HIV-1 clinical trials and summarize current advances and challenges according to preclinical results obtained from five distinct strategies. This mini-review provides multiple perspectives to help in developing new generations of VLP-based HIV-1 vaccine candidates with better capacity to elicit specific anti-HIV immune responses.

摘要

预防性疫苗仍然是控制人类免疫缺陷病毒 1 型(HIV-1)传播的最佳方法。尽管泰国 RV144 试验的疗效有限,但仍没有一种疫苗候选药物被证明是成功的。因此,人们做出了巨大努力来改进 HIV-1 抗原设计,并发现了最佳免疫诱导的传递平台。由于免疫原性、结构和功能的多样性,病毒样颗粒(VLPs)可以作为有效的疫苗载体来展示 HIV-1 免疫原,并为各种 HIV-1 疫苗开发策略以及初次免疫-加强免疫方案提供支持。在这里,我们描述了已被纳入 HIV-1 临床试验的基于 VLP 的 HIV-1 疫苗候选物,并根据来自五种不同策略的临床前结果总结了当前的进展和挑战。本综述提供了多种视角,有助于开发新一代具有更强诱导特异性抗 HIV 免疫反应能力的基于 VLP 的 HIV-1 疫苗候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c95/7561392/181e4d81159f/fimmu-11-573157-g0001.jpg

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