A polyvalent DNA prime with matched polyvalent protein/GLA-SE boost regimen elicited the most robust and broad IgG and IgG3 V1V2 binding antibody and CD4+ T cell responses among 13 HIV vaccine trials.

IF 7.5 2区 医学 Q1 IMMUNOLOGY
Emerging Microbes & Infections Pub Date : 2025-12-01 Epub Date: 2025-04-07 DOI:10.1080/22221751.2025.2485317
Zoe Moodie, Shuying Sue Li, Elena E Giorgi, LaTonya D Williams, One Dintwe, Lindsay N Carpp, Shiyu Chen, Kelly E Seaton, Sheetal S Sawant, Lu Zhang, Jack Heptinstall, Shuying Liu, Nicole Grunenberg, Frank Tomaka, Supachai Rerks-Ngarm, Punnee Pitisuttithum, Sorachai Nitayaphan, Julie A Ake, Sandhya Vasan, Giuseppe Pantaleo, Ian Frank, Lindsey R Baden, Paul A Goepfert, Michael Keefer, Mike Chirenje, Mina C Hosseinipour, Kathryn Mngadi, Fatima Laher, Nigel Garrett, Linda-Gail Bekker, Stephen De Rosa, Erica Andersen-Nissen, James G Kublin, Shan Lu, Peter B Gilbert, Glenda E Gray, Lawrence Corey, M Juliana McElrath, Georgia D Tomaras
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引用次数: 0

Abstract

Developing an effective HIV vaccine is a momentous challenge. An exceptionally wide range of candidate HIV vaccines have been tested, yet many were poorly immunogenic, and of the select few that advanced into efficacy trials, only one demonstrated any efficacy. Here we report the results of the largest-scale cross-protocol immunogenicity comparison to date: 13 HIV vaccine trials (including 36 vaccine regimens) conducted across nine countries worldwide, strengthened by standardized trial designs, validated assays in centralized laboratories, and harmonized immunogenicity endpoints - providing an objective approach to identify the HIV vaccine candidate(s) with the best immunogenicity. A polyvalent DNA prime + protein boost regimen (HVTN 124) including Env immunogens of four subtypes, matched between prime and boost, achieved the best anti-V1V2 antibody responses by a large margin and also induced high CD4+ T-cell responses - two key immune responses implicated in HIV vaccine protection. Our results provide strong support to test this promising HIV vaccine design in more advanced phase clinical trials and will also guide the future design of additional HIV vaccines.Trial registration: ClinicalTrials.gov identifier: NCT01799954..Trial registration: ClinicalTrials.gov identifier: NCT02109354..Trial registration: ClinicalTrials.gov identifier: NCT02404311..Trial registration: ClinicalTrials.gov identifier: NCT02207920..Trial registration: ClinicalTrials.gov identifier: NCT02296541..Trial registration: ClinicalTrials.gov identifier: NCT03284710..Trial registration: ClinicalTrials.gov identifier: NCT02915016..Trial registration: ClinicalTrials.gov identifier: NCT02997969..Trial registration: ClinicalTrials.gov identifier: NCT03122223..Trial registration: ClinicalTrials.gov identifier: NCT03409276..Trial registration: ClinicalTrials.gov identifier: NCT02968849..Trial registration: ClinicalTrials.gov identifier: NCT03060629..Trial registration: ClinicalTrials.gov identifier: NCT00223080..

在13项HIV疫苗试验中,多价DNA引物与匹配的多价蛋白/GLA-SE增强方案引发了最强大和广泛的IgG和IgG3 V1V2结合抗体和CD4+ T细胞反应。
研制有效的艾滋病毒疫苗是一项重大挑战。已经测试了非常广泛的候选艾滋病毒疫苗,但许多疫苗的免疫原性很差,在进入疗效试验的少数几个疫苗中,只有一种显示出任何疗效。在此,我们报告了迄今为止最大规模的跨方案免疫原性比较的结果:在全球9个国家进行的13项HIV疫苗试验(包括36种疫苗方案),通过标准化试验设计、集中实验室验证的分析和统一的免疫原性终点来加强,提供了一种确定具有最佳免疫原性的HIV候选疫苗的客观方法。多价DNA引物+蛋白增强方案(HVTN 124)包括四种亚型的Env免疫原,在引物和增强之间匹配,获得了最佳的抗v1v2抗体应答,并且还诱导了高CD4+ t细胞应答-两种与HIV疫苗保护相关的关键免疫应答。我们的研究结果为在更先进的临床试验中测试这种有希望的HIV疫苗设计提供了强有力的支持,也将指导未来设计更多的HIV疫苗。试验注册:ClinicalTrials.gov标识符:NCT01799954。试验注册:ClinicalTrials.gov标识符:NCT02109354。试验注册:ClinicalTrials.gov标识符:NCT02404311。试验注册:ClinicalTrials.gov标识符:NCT02207920。试验注册:ClinicalTrials.gov标识符:NCT02296541。试验注册:ClinicalTrials.gov标识符:NCT03284710。试验注册:ClinicalTrials.gov标识符:NCT02915016。试验注册:ClinicalTrials.gov标识符:NCT02997969。试验注册:ClinicalTrials.gov标识符:NCT03122223。试验注册:ClinicalTrials.gov标识符:NCT03409276。试验注册:ClinicalTrials.gov标识符:NCT02968849。试验注册:ClinicalTrials.gov标识符:NCT03060629。试验注册:ClinicalTrials.gov标识符:NCT00223080。
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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来源期刊
Emerging Microbes & Infections
Emerging Microbes & Infections IMMUNOLOGY-MICROBIOLOGY
CiteScore
26.20
自引率
2.30%
发文量
276
审稿时长
20 weeks
期刊介绍: Emerging Microbes & Infections is a peer-reviewed, open-access journal dedicated to publishing research at the intersection of emerging immunology and microbiology viruses. The journal's mission is to share information on microbes and infections, particularly those gaining significance in both biological and clinical realms due to increased pathogenic frequency. Emerging Microbes & Infections is committed to bridging the scientific gap between developed and developing countries. This journal addresses topics of critical biological and clinical importance, including but not limited to: - Epidemic surveillance - Clinical manifestations - Diagnosis and management - Cellular and molecular pathogenesis - Innate and acquired immune responses between emerging microbes and their hosts - Drug discovery - Vaccine development research Emerging Microbes & Infections invites submissions of original research articles, review articles, letters, and commentaries, fostering a platform for the dissemination of impactful research in the field.
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