免疫原性
接种疫苗
病毒学
表位
抗体
第41页
中和抗体
医学
病毒包膜
三聚体
免疫学
信使核糖核酸
化学
基因
生物化学
二聚体
有机化学
作者
K. Rachael Parks,Zoe Moodie,Mary Allen,Catherine Yen,Briana D. Furch,Kellie J. MacPhee,Gabriel Ozorowski,Jack Heptinstall,William O. Hahn,Zihan 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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