接种疫苗
病毒学
抗体
中和抗体
医学
人类免疫缺陷病毒(HIV)
疫苗试验
免疫学
信使核糖核酸
生物
基因
遗传学
作者
K. Rachael Parks,Zoe Moodie,Mary Allen,Catherine Yen,Briana D. Furch,Kellie J. MacPhee,Gabriel Ozorowski,Jack Heptinstall,William O. Hahn,Zi-Han Zheng,Huiyin Lu,Shannon Grant,Elize Domin,Michael O. Duff,Aaron Seese,Constanza Marini-Macouzet,Lamar Ballweber-Fleming,Wen-Hsin Lee,Christopher A. Cottrell,Alessia Liguori
标识
DOI:10.1126/scitranslmed.ady6831
摘要
mRNA technology might accelerate development of an urgently needed preventive human immunodeficiency virus (HIV) vaccine. We evaluated the safety and immunogenicity of three mRNA-encoded envelope trimers, including two doses of soluble and membrane-anchored forms, in a randomized, open-label, phase 1 clinical trial. Vaccines were generally well tolerated, although 6.5% (7 of 108) of participants developed urticaria, a higher proportion than seen with other mRNA vaccines. mRNA-encoded trimers induced strong envelope-specific B and T cell responses. Immunization with membrane-anchored trimers, intended to obscure epitopes at the trimer base targeted by nonneutralizing antibodies, reduced the frequency of base-binding serum antibodies in comparison with soluble trimers. Three immunizations elicited autologous tier 2 serum neutralizing antibodies in 80% of vaccinees receiving the membrane-anchored trimers, in contrast to only 4% receiving the soluble trimer. Thus, with demonstration of more favorable safety, mRNA-encoded membrane-anchored HIV envelope trimers represent a promising platform for HIV vaccine clinical development.
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