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Fighting an Epidemic in Political Context: Thirty-Five Years of HIV/AIDS Policy Making in the United States.在政治背景下抗击疫情:美国35年的艾滋病毒/艾滋病政策制定历程
Soc Hist Med. 2018 Dec 28;33(3):1001-1028. doi: 10.1093/shm/hky108. eCollection 2020 Aug.
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Structure and immunogenicity of a stabilized HIV-1 envelope trimer based on a group-M consensus sequence.基于群组 M 共识序列的稳定 HIV-1 包膜三聚体的结构和免疫原性。
Nat Commun. 2019 May 29;10(1):2355. doi: 10.1038/s41467-019-10262-5.
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An Asymmetric Opening of HIV-1 Envelope Mediates Antibody-Dependent Cellular Cytotoxicity.HIV-1 包膜的不对称开口介导抗体依赖的细胞细胞毒性。
Cell Host Microbe. 2019 Apr 10;25(4):578-587.e5. doi: 10.1016/j.chom.2019.03.002.
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Developability Assessment of Physicochemical Properties and Stability Profiles of HIV-1 BG505 SOSIP.664 and BG505 SOSIP.v4.1-GT1.1 gp140 Envelope Glycoprotein Trimers as Candidate Vaccine Antigens.HIV-1 BG505 SOSIP.664 和 BG505 SOSIP.v4.1-GT1.1 gp140 包膜糖蛋白三聚体作为候选疫苗抗原的理化性质和稳定性特征的可开发性评估。
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A Novel Vaccine Strategy Employing Serologically Different Chimpanzee Adenoviral Vectors for the Prevention of HIV-1 and HCV Coinfection.一种采用血清学不同的黑猩猩腺病毒载体的新型疫苗策略,用于预防 HIV-1 和 HCV 合并感染。
Front Immunol. 2019 Jan 18;9:3175. doi: 10.3389/fimmu.2018.03175. eCollection 2018.
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Structure-Based Vaccine Antigen Design.基于结构的疫苗抗原设计。
Annu Rev Med. 2019 Jan 27;70:91-104. doi: 10.1146/annurev-med-121217-094234.
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Poly(lactic acid) nanoparticles and cell-penetrating peptide potentiate mRNA-based vaccine expression in dendritic cells triggering their activation.聚乳酸纳米粒和穿膜肽增强树突状细胞中基于 mRNA 的疫苗表达,从而触发其激活。
Biomaterials. 2019 Mar;195:23-37. doi: 10.1016/j.biomaterials.2018.12.019. Epub 2018 Dec 21.
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Increased breadth of HIV-1 neutralization achieved by diverse antibody clones each with limited neutralization breadth.多种抗体克隆均可提高 HIV-1 中和广度,而每种克隆的中和广度有限。
PLoS One. 2018 Dec 19;13(12):e0209437. doi: 10.1371/journal.pone.0209437. eCollection 2018.
9
Efficient Induction of T Cells against Conserved HIV-1 Regions by Mosaic Vaccines Delivered as Self-Amplifying mRNA.通过自我扩增mRNA递送的嵌合疫苗有效诱导针对保守HIV-1区域的T细胞。
Mol Ther Methods Clin Dev. 2018 Oct 26;12:32-46. doi: 10.1016/j.omtm.2018.10.010. eCollection 2019 Mar 15.
10
Closing and Opening Holes in the Glycan Shield of HIV-1 Envelope Glycoprotein SOSIP Trimers Can Redirect the Neutralizing Antibody Response to the Newly Unmasked Epitopes.闭合和打开 HIV-1 包膜糖蛋白 SOSIP 三聚体糖盾上的孔,可以将中和抗体反应重新引导到新暴露的表位上。
J Virol. 2019 Feb 5;93(4). doi: 10.1128/JVI.01656-18. Print 2019 Feb 15.

HIV-1 疫苗设计的创新。

Innovations in HIV-1 Vaccine Design.

机构信息

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, USA.

Duke University School of Medicine and Duke Human Vaccine Institute, Durham, NC, USA.

出版信息

Clin Ther. 2020 Mar;42(3):499-514. doi: 10.1016/j.clinthera.2020.01.009. Epub 2020 Feb 5.

DOI:10.1016/j.clinthera.2020.01.009
PMID:32035643
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7102617/
Abstract

PURPOSE

The field of HIV-1 vaccinology has evolved during the last 30 years from the first viral vector HIV gene insert constructs to vaccination regimens using a myriad of strategies. These strategies now include germline-targeting, lineage-based, and structure-guided immunogen design. This narrative review outlines the historical context of HIV vaccinology and subsequently highlights the scientific discoveries during the last 6 years that promise to propel the field forward.

METHODS

We conducted a search of 2 electronic databases, PubMed and EMBASE, for experimental studies that involved new HIV immunogen designs between 2013 and 2019. During the title and abstract reviews, publications were excluded if they were written in language other than English and/or were a letter to the editor, a commentary, or a conference-only presentation. We then used ClinicalTrials.gov to identify completed and ongoing clinical trials using these strategies.

FINDINGS

The HIV vaccinology field has undergone periods of significant growth during the last 3 decades. Findings elucidated in preclinical studies have revealed the importance of the interaction between the cellular and humoral immune system. As a result, several new rationally designed vaccine strategies have been developed and explored in the last 6 years, including native-like envelope trimers, nanoparticle, and mRNA vaccine design strategies among others. Several of these strategies have shown enough promise in animal models to progress toward first-in-human Phase I clinical trials.

IMPLICATIONS

Rapid developments in preclinical and early-phase clinical studies suggest that a tolerable and effective HIV vaccine may be on the horizon.

摘要

目的

在过去的 30 年中,HIV-1 疫苗学领域从最初的病毒载体 HIV 基因插入构建物发展到使用多种策略的疫苗接种方案。这些策略现在包括种系靶向、谱系和结构导向的免疫原设计。本叙述性综述概述了 HIV 疫苗学的历史背景,随后强调了过去 6 年中有望推动该领域前进的科学发现。

方法

我们在 PubMed 和 EMBASE 这两个电子数据库中进行了搜索,以寻找涉及 2013 年至 2019 年间新型 HIV 免疫原设计的实验研究。在标题和摘要审查过程中,如果出版物是用英文以外的语言撰写的,或者是信件给编辑、评论或会议仅演示,则将其排除在外。然后,我们使用 ClinicalTrials.gov 来识别使用这些策略的已完成和正在进行的临床试验。

发现

在过去的 30 年中,HIV 疫苗学领域经历了几个重要的增长期。临床前研究的结果揭示了细胞和体液免疫系统相互作用的重要性。因此,在过去 6 年中,已经开发并探索了几种新的合理设计的疫苗策略,包括天然样包膜三聚体、纳米颗粒和 mRNA 疫苗设计策略等。这些策略中的几种在动物模型中表现出足够的前景,有望进入首次人体 I 期临床试验。

意义

临床前和早期临床研究的快速发展表明,一种可耐受且有效的 HIV 疫苗可能即将面世。