病毒学
中和抗体
非人灵长类
抗体
人类免疫缺陷病毒(HIV)
艾滋病疫苗
启动(农业)
生物
免疫学
医学
疫苗试验
进化生物学
植物
发芽
作者
Jon M. Steichen,Ivy Phung,Eugenia Salcedo,Gabriel Ozorowski,Jordan R. Willis,Sabyasachi Baboo,Alessia Liguori,Christopher A. Cottrell,Jonathan L. Torres,Patrick Madden,Krystal Manyuan,Henry J. Sutton,Jeong Hyun Lee,Oleksandr Kalyuzhniy,Joel D. Allen,Oscar L. Rodriguez,Yumiko Adachi,Tina-Marie Mullen,Erik Georgeson,Michael Kubitz
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2024-05-16
卷期号:384 (6697)
被引量:16
标识
DOI:10.1126/science.adj8321
摘要
Germline-targeting immunogens hold promise for initiating the induction of broadly neutralizing antibodies (bnAbs) to HIV and other pathogens. However, antibody-antigen recognition is typically dominated by heavy chain complementarity determining region 3 (HCDR3) interactions, and vaccine priming of HCDR3-dominant bnAbs by germline-targeting immunogens has not been demonstrated in humans or outbred animals. In this work, immunization with N332-GT5, an HIV envelope trimer designed to target precursors of the HCDR3-dominant bnAb BG18, primed bnAb-precursor B cells in eight of eight rhesus macaques to substantial frequencies and with diverse lineages in germinal center and memory B cells. We confirmed bnAb-mimicking, HCDR3-dominant, trimer-binding interactions with cryo-electron microscopy. Our results demonstrate proof of principle for HCDR3-dominant bnAb-precursor priming in outbred animals and suggest that N332-GT5 holds promise for the induction of similar responses in humans.
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