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用于评估 PrEPVacc 疫苗试验中对 CN54gp140 和 AIDSVAX BE 的抗体反应的 ELISA 检测方法的优化和验证。

Optimization and validation of an ELISA assay for the determination of antibody responses to CN54gp140 and AIDSVAX BE for use in the Phase IIb PrEPVacc vaccine trial.

机构信息

MRC/UVRI and LSHTM Uganda Research Unit, Entebbe, Uganda.

Uganda Virus Research Institute, Entebbe, Uganda.

出版信息

PLoS One. 2022 Nov 3;17(11):e0275927. doi: 10.1371/journal.pone.0275927. eCollection 2022.

Abstract

PrEPVacc is an international, multi-centre, double-blind vaccine study comparing experimental combination vaccine regimens including DNA/AIDSVAX BE and DNA/CN54gp140 with placebo control. Simultaneously, daily oral PrEP is compared for efficacy against daily Truvada in the context of the current PrEP availability situation at the study sites. An important clinical trial outcome is the accurate measurement of in vivo antibody titer induced through vaccination. Here we report the validation of two ELISAs for CN54gp140 and AIDSVAX BE at Uganda Virus Research Institute that demonstrates precision, specificity, and robustness for assessing the reciprocal antibody end point titer in human serum. This is a critical endpoint for determining whether vaccination can provide any protection against HIV in populations at risk of acquiring HIV.

摘要

PrEPVacc 是一项国际性、多中心、双盲疫苗研究,旨在比较包括 DNA/AIDSVAX BE 和 DNA/CN54gp140 在内的实验性联合疫苗方案与安慰剂对照,同时比较每日口服 PrEP 与每日 Truvada 在研究地点目前 PrEP 可及性情况下的疗效。一个重要的临床试验结果是准确测量通过接种诱导的体内抗体滴度。在这里,我们报告了在乌干达病毒研究所对 CN54gp140 和 AIDSVAX BE 的两种 ELISA 的验证,证明了在评估人类血清中抗体效价终点的精确性、特异性和稳健性。这是确定疫苗接种是否可以为处于 HIV 感染风险中的人群提供任何 HIV 保护的关键终点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/add9/9632806/f3bde8597265/pone.0275927.g001.jpg

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