Wiehe Kevin, Nicely Nathan I, Lockwood Bradley, Kuraoka Masayuki, Anasti Kara, Arora Sabrina, Bowman Cindy M, Stolarchuk Christina, Parks Robert, Lloyd Krissey E, Xia Shi-Mao, Duffy Ryan, Shen Xiaoying, Kyratsous Christos A, Macdonald Lynn E, Murphy Andrew J, Scearce Richard M, Moody M Anthony, Alam S Munir, Verkoczy Laurent, Tomaras Georgia D, Kelsoe Garnett, Haynes Barton F
Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710;
Department of Medicine, Duke University School of Medicine, Durham, NC 27710.
J Immunol. 2017 Feb 1;198(3):1047-1055. doi: 10.4049/jimmunol.1601640. Epub 2016 Dec 23.
In the RV144 gp120 HIV vaccine trial, decreased transmission risk was correlated with Abs that reacted with a linear epitope at a lysine residue at position 169 (K169) in the HIV-1 envelope (Env) V2 region. The K169 V2 response was restricted to Abs bearing Vλ rearrangements that expressed aspartic acid/glutamic acid in CDR L2. The AE.A244 gp120 in AIDSVAX B/E also bound to the unmutated ancestor of a V2-glycan broadly neutralizing Ab, but this Ab type was not induced in the RV144 trial. In this study, we sought to determine whether immunodominance of the V2 linear epitope could be overcome in the absence of human Vλ rearrangements. We immunized IgH- and Igκ-humanized mice with the AE.A244 gp120 Env. In these mice, the V2 Ab response was focused on a linear epitope that did not include K169. V2 Abs were isolated that used the same human VH gene segment as an RV144 V2 Ab but paired with a mouse λ L chain. Structural characterization of one of these V2 Abs revealed how the linear V2 epitope could be engaged, despite the lack of aspartic acid/glutamic acid encoded in the mouse repertoire. Thus, despite the absence of the human Vλ locus in these humanized mice, the dominance of Vλ pairing with human VH for HIV-1 Env V2 recognition resulted in human VH pairing with mouse λ L chains instead of allowing otherwise subdominant V2-glycan broadly neutralizing Abs to develop.
在RV144 gp120 HIV疫苗试验中,传播风险降低与能与HIV-1包膜(Env)V2区第169位赖氨酸残基(K169)处的线性表位发生反应的抗体相关。K169 V2反应仅限于带有Vλ重排且在互补决定区L2中表达天冬氨酸/谷氨酸的抗体。AIDSVAX B/E中的AE.A244 gp120也与一种V2聚糖广泛中和抗体的未突变祖先结合,但在RV144试验中未诱导出这种抗体类型。在本研究中,我们试图确定在没有人类Vλ重排的情况下,V2线性表位的免疫优势是否能够被克服。我们用AE.A244 gp120 Env免疫IgH和Igκ人源化小鼠。在这些小鼠中,V2抗体反应集中在一个不包括K169的线性表位上。分离出的V2抗体使用了与RV144 V2抗体相同的人类VH基因片段,但与小鼠λ轻链配对。对其中一种V2抗体的结构表征揭示了尽管小鼠抗体库中没有编码天冬氨酸/谷氨酸,但线性V2表位是如何被结合的。因此,尽管这些人源化小鼠中没有人类Vλ基因座,但Vλ与人类VH配对对HIV-1 Env V2识别的优势导致人类VH与小鼠λ轻链配对,而不是让其他不占优势的V2聚糖广泛中和抗体得以产生。