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Effects of Partially Dismantling the CD4 Binding Site Glycan Fence of HIV-1 Envelope Glycoprotein Trimers on Neutralizing Antibody Induction

机译:HIV-1包膜糖蛋白三聚体的部分拆除CD4结合位点糖栅对中和抗体诱导的影响

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摘要

Previously, VLPs bearing JR-FL strain HIV-1 Envelope trimers elicited potent neutralizing antibodies (nAbs) in 2/8 rabbits (PLoS Pathog 11(5): e1004932) by taking advantage of a naturally absent glycan at position 197 that borders the CD4 binding site (CD4bs). In new immunizations, we attempted to improve nAb responses by removing the N362 glycan that also lines the CD4bs. All 4 rabbits developed nAbs. One targeted the N197 glycan hole like our previous sera. Two sera depended on the N463 glycan, again suggesting CD4bs overlap. Heterologous boosts appeared to reduce nAb clashes with the N362 glycan. The fourth serum targeted a N362 glycan-sensitive epitope. VLP manufacture challenges prevented us from immunizing larger rabbit numbers to empower a robust statistical analysis. Nevertheless, trends suggest that targeted glycan removal may improve nAb induction by exposing new epitopes and that it may be possible to modify nAb specificity using rational heterologous boosts.
机译:以前,携带JR-FL毒株HIV-1包膜三聚体的VLP通过利用与CD4接界的197位天然不存在的聚糖,在2/8只兔子中诱导了有效的中和抗体(nAbs)(PLoS Pathog 11(5):e1004932)。结合位点(CD4bs)。在新的免疫接种中,我们试图通过去除也排列CD4bs的N362聚糖来改善nAb反应。所有4只兔均产生nAb。一个像我们以前的血清一样针对N197聚糖孔。两个血清依赖于N463聚糖,再次表明CD4b重叠。异源增强似乎减少了与N362聚糖的nAb冲突。第四种血清靶向N362聚糖敏感表位。 VLP制造方面的挑战使我们无法对更大数量的兔子进行免疫以进行可靠的统计分析。然而,趋势表明靶向的聚糖去除可以通过暴露新的表位来改善nAb诱导,并且可能可以使用合理的异源增强来修饰nAb特异性。

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