...
首页> 外文期刊>MBio >Recognition Patterns of the C1/C2 Epitopes Involved in Fc-Mediated Response in HIV-1 Natural Infection and the RV114 Vaccine Trial
【24h】

Recognition Patterns of the C1/C2 Epitopes Involved in Fc-Mediated Response in HIV-1 Natural Infection and the RV114 Vaccine Trial

机译:C1 / C2表位的识别模式参与了HIV-1天然感染的FC介导的反应和RV114疫苗试验

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Antibodies (Abs) specific for CD4-induced envelope (Env) epitopes within constant region 1 and 2 (C1/C2) were induced in the RV144 vaccine trial, where antibody-dependent cellular cytotoxicity (ADCC) correlated with reduced risk of HIV-1 infection. We combined X-ray crystallography and fluorescence resonance energy transfer-fluorescence correlation spectroscopy to describe the molecular basis for epitopes of seven RV144 Abs and compared them to A32 and C11, C1/C2 Abs induced in HIV infection. Our data indicate that most vaccine Abs recognize the 7-stranded β-sandwich of gp120, a unique hybrid epitope bridging A32 and C11 binding sites. Although primarily directed at the 7-stranded β-sandwich, some accommodate the gp120 N terminus in C11-bound 8-stranded conformation and therefore recognize a broader range of CD4-triggered Env conformations. Our data also suggest that Abs of RV144 and RV305, the RV144 follow-up study, although likely initially induced by the ALVAC-HIV prime encoding full-length gp120, matured through boosting with truncated AIDSVAX gp120 variants.
机译:在RV144疫苗试验中诱导恒定区域1和2(C1 / C2)内的CD4诱导的封套(ENV)表位的抗体(ABS),其中依赖于依赖于抗体依赖性细胞细胞毒性(ADCC),与HIV-1的风险降低相关感染。我们组合X射线晶体学和荧光共振能量转移 - 荧光相关光谱,描述七个RV144 ABS表位的分子基础,并将其与HIV感染诱导的A32和C11,C1 / C2 ABS进行比较。我们的数据表明,大多数疫苗ABS识别GP120的7链β - 夹层,杂交表位桥接A32和C11结合位点。尽管主要针对7链β-夹层,但是一些在C11结合的8链构象中容纳GP120 N末端,因此识别更广泛的CD4触发的ENV构象。我们的数据还表明,RV144和RV305的ABS,RV144的后续研究虽然可能最初由编码全长GP120的ALVAC-HIV PRIME诱导,但通过截断的AIDVAX GP120变体升压成熟。

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