Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Molecular and Cellular Biology Program, University of Washington, Seattle.
J Infect Dis. 2020 Jan 2;221(2):232-237. doi: 10.1093/infdis/jiz444.
Mother-to-child transmission of human immunodeficiency virus (HIV) occurs in the setting of maternal and passively acquired antibodies, providing a unique window into immune correlates of HIV risk. We compared plasma antibody binding to HIV antigens between 51 nontransmitting mother-infant pairs and 21 transmitting mother-infant pairs. Plasma antibody binding to a variety of gp41 ectodomain-containing antigens was associated with increased odds of transmission. Understanding the reasons why gp41 ectodomain-targeting antibodies are associated with transmission risk will be important in determining whether they can directly enhance infection or whether their presence reflects a redirecting of the humoral response away from targeting more protective epitopes.
母婴传播的人类免疫缺陷病毒(HIV)发生在母体和被动获得的抗体环境中,为 HIV 风险的免疫相关因素提供了一个独特的窗口。我们比较了 51 对非传播母婴对和 21 对传播母婴对的血浆抗体与 HIV 抗原的结合情况。与多种 gp41 胞外结构域包含抗原的血浆抗体结合与增加传播的几率有关。了解 gp41 胞外结构域靶向抗体与传播风险相关的原因,对于确定它们是否能直接增强感染,或者它们的存在是否反映了体液免疫反应从针对更具保护作用的表位转向,将是非常重要的。