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Tailored Immunogens Direct Affinity Maturation toward HIV Neutralizing Antibodies

机译:针对HIV中和抗体的量身定制的免疫原直接亲和力成熟

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Induction of broadly neutralizing antibodies (bnAbs) is a primary goal of HIV vaccine development. VRC01-class bnAbs are important vaccine leads because their precursor B cells targeted by an engineered priming immunogen are relatively common among humans. This priming immunogen has demonstrated the ability to initiate a bnAb response in animal models, but recall and maturation toward bnAb development has not been shown. Here, we report the development of boosting immunogens designed to guide the genetic and functional maturation of previously primed VRC01-class precursors. Boosting a transgenic mouse model expressing germline VRC01 heavy chains produced broad neutralization of near-native isolates (N276A) and weak neutralization of fully native HIV. Functional and genetic characteristics indicate that the boosted mAbs are consistent with partially mature VRC01-class antibodies and place them on a maturation trajectory that leads toward mature VRC01-class bnAbs. The results show how reductionist sequential immunization can guide maturation of HIV bnAb responses.
机译:诱导广泛中和的抗体(bnAbs)是HIV疫苗开发的主要目标。 VRC01级bnAb是重要的疫苗领先产品,因为它们被工程化的启动免疫原靶向的前体B细胞在人类中相对较常见。这种致敏免疫原已证明能够在动物模型中引发bnAb应答,但尚未显示出对bnAb发育的回忆和成熟。在这里,我们报告了增强免疫原的发展,旨在指导先前引发的VRC01类前体的遗传和功能成熟。促进表达种系VRC01重链的转基因小鼠模型,可产生中和近乎纯的分离物(N276A)的广泛中和作用,以及完全天然HIV的弱中和作用。功能和遗传特征表明,增强的mAb与部分成熟的VRC01类抗体一致,并将其置于导致成熟VRC01类bnAb的成熟轨迹上。结果表明,还原剂序贯免疫法如何指导HIV bnAb反应的成熟。

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