Suppr超能文献

监测 Sotrovimab 水平作为对 SARS-CoV-2 疫苗无反应的肾移植受者的暴露前预防。

Monitoring of Sotrovimab-Levels as Pre-Exposure Prophylaxis in Kidney Transplant Recipients Not Responding to SARS-CoV-2 Vaccines.

机构信息

Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, 1090 Vienna, Austria.

Center of Virology, Medical University of Vienna, 1090 Vienna, Austria.

出版信息

Viruses. 2023 Jul 26;15(8):1624. doi: 10.3390/v15081624.

Abstract

Sotrovimab, a monoclonal antibody against SARS-CoV-2, is used as a pre-exposition prophylaxis (PrEP) against COVID-19, but monitoring strategies using routine test systems have not been defined. Twenty kidney transplant recipients without antibodies after vaccination received 500 mg Sotrovimab. Antibody levels were quantified over eight weeks using live-virus neutralization (BA1 and BA2), antibody binding assays (TrimericS, Elecsys, QuantiVAC) and surrogate virus neutralization tests (sVNTs; TECOmedical, cPass and NeutraLISA). Sotrovimab neutralized both Omicron subvariants (BA1 NT titer 90 (+-50) > BA2 NT titer 33 (+-15) one hour post infusion). Sotrovimab was measurable on all used immunoassays, although a prior 1:100 dilution was necessary for Elecsys due to a presumed prozone effect. The best correlation with live-virus neutralization titers was found for QuantiVAC and TrimericS, with a respective R of 0.65/0.59 and 0.76/0.57 against BA1/BA2. Elecsys showed an R of 0.56/0.54 for BA1/BA2, respectively. sVNT values increased after infusion but had only a poor correlation with live-virus neutralization titers (TECOmedical and cPass) or did not reach positivity thresholds (NeutraLISA). Antibody measurements by the used immunoassays showed differences in antibody levels and only a limited correlation with neutralization capacity. We do not recommend sVNTs for monitoring SARS-CoV-2 neutralization by Sotrovimab.

摘要

索特罗维单抗是一种针对 SARS-CoV-2 的单克隆抗体,被用作 COVID-19 的暴露前预防(PrEP),但尚未确定使用常规检测系统的监测策略。20 名接种疫苗后未产生抗体的肾移植受者接受了 500 毫克索特罗维单抗。使用活病毒中和(BA1 和 BA2)、抗体结合测定(TrimericS、Elecsys、QuantiVAC)和替代病毒中和试验(sVNTs;TECOmedical、cPass 和 NeutraLISA)在八周内定量检测抗体水平。索特罗维单抗中和了奥密克戎亚变种(BA1 NT 滴度 90(+-50)> BA2 NT 滴度 33(+-15)输注后一小时)。索特罗维单抗可在所有使用的免疫测定中检测到,尽管由于假定的前区效应,Elecsys 需要进行 1:100 的稀释。与活病毒中和滴度的最佳相关性是 QuantiVAC 和 TrimericS,BA1/BA2 的 R 分别为 0.65/0.59 和 0.76/0.57。Elecsys 分别为 BA1/BA2 的 R 为 0.56/0.54。输注后 sVNT 值增加,但与活病毒中和滴度相关性较差(TECOmedical 和 cPass)或未达到阳性阈值(NeutraLISA)。使用的免疫测定中的抗体测量显示了抗体水平的差异,与中和能力的相关性有限。我们不建议使用 sVNTs 监测索特罗维单抗对 SARS-CoV-2 的中和作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c533/10459887/58887e09231e/viruses-15-01624-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验