首页> 外文期刊>Virology >Effects of partially dismantling the CD4 binding site glycan fence of HIV-1 Envelope glycoprotein trimers on neutralizing antibody induction
【24h】

Effects of partially dismantling the CD4 binding site glycan fence of HIV-1 Envelope glycoprotein trimers on neutralizing antibody induction

机译:HIV-1包络糖蛋白三聚糖烯酮颗粒中和抗体诱导中和抗体诱导的CD4结合位点甘油栅栏的影响

获取原文
获取原文并翻译 | 示例
           

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,VLP轴承JR-FL菌株HIV-1包络三聚体通过利用197年的第197位的天然不存在的聚糖来引发效率中和抗体(NAB),在2/8只兔子(PLOS PATOG 11(5):E1004932)中。 绑定站点(CD4BS)。 在新的免疫免疫中,我们试图通过除去CD4BS的N362甘草来改善Nab反应。 所有4只兔子都开发了NAB。 一个针对我们以前的血清的N197糖粉孔。 两种血清依赖于N463甘草,再次表明CD4BS重叠。 异源提升似乎用N362甘油减少NAB冲突。 第四血清靶向N362甘油敏感表位。 VLP制造挑战阻止了我们免疫较大的兔子数量以赋予稳健的统计分析。 然而,趋势表明,靶向聚糖去除可以通过暴露新的表位来改善Nab诱导,并且可以使用理性异源升压来修饰Nab特异性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号