Xu Shiwei, Hudson Aaron, Janes Holly E, Tomaras Georgia D, Ackerman Margaret E
Quantitative Biomedical Sciences Program, Dartmouth College, Hanover, NH USA.
Biostatistics, Bioinformatics and Epidemiology Program, Vaccine and Infectious Disease Division, Fred Hutch Cancer Center, Seattle, WA, USA.
medRxiv. 2025 Sep 7:2025.09.03.25335025. doi: 10.1101/2025.09.03.25335025.
With a goal of unveiling mechanisms by which vaccines can provide protection against HIV-1 acquisition, several studies have explored correlates of risk of HIV-1 acquisition in HVTN 505, which was a phase IIb trial conducted to assess the safety and efficacy of a DNA plasmid and recombinant adenovirus serotype 5-vectored HIV vaccine regimen among individuals in the United States who were vulnerable to acquiring HIV. While this trial failed to meet its predetermined efficacy criteria, both immunological and virological correlates of reduced risk of acquisition have been reported, suggesting that at least some vaccine recipients were protected from some viruses. In this work, we describe application of a novel Positive-Unlabeled machine learning-based approach to infer protection status among vaccine recipients that did not acquire HIV, resulting in improved power to detect potential correlates of immunity. Having established the analytical robustness of protection status predictions using cross-validation and permutation testing strategies, we report increased confidence in previously identified correlates of risk, such as vaccine-elicited anti-HIV-1 Env glycoprotein IgG3 antibodies and antibody-dependent phagocytosis, and the new observation of an inverse correlation between inferred vaccine-mediated protection and virus-specific IgA responses. Though its biological validity is not established, this inference approach offers a new means to use case-control datasets to identify candidate markers of effective immune responses in the context of low vaccine efficacy.
为了揭示疫苗能够预防HIV-1感染的机制,多项研究探讨了HVTN 505中HIV-1感染风险的相关因素。HVTN 505是一项IIb期试验,旨在评估DNA质粒和重组腺病毒血清型5载体HIV疫苗方案在美国易感染HIV个体中的安全性和有效性。尽管该试验未达到预定的疗效标准,但已有关于感染风险降低的免疫和病毒学相关因素的报道,这表明至少一些疫苗接种者受到了某些病毒的保护。在这项工作中,我们描述了一种基于新型正无标记机器学习的方法在未感染HIV的疫苗接种者中推断保护状态的应用,从而提高了检测潜在免疫相关因素的能力。通过使用交叉验证和置换检验策略确定了保护状态预测的分析稳健性后,我们报告了对先前确定的风险相关因素(如疫苗诱导的抗HIV-1 Env糖蛋白IgG3抗体和抗体依赖性吞噬作用)的信心增强,以及推断的疫苗介导保护与病毒特异性IgA反应之间呈负相关的新观察结果。尽管其生物学有效性尚未确定,但这种推断方法提供了一种新手段,可在疫苗效力较低的情况下利用病例对照数据集来识别有效免疫反应的候选标志物。