清脆的
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
抗体
计算生物学
病毒学
2019-20冠状病毒爆发
生物
2019年冠状病毒病(COVID-19)
医学
免疫学
疾病
传染病(医学专业)
遗传学
病理
基因
爆发
作者
Yanan Tang,Turun Song,Gao L,Saifu Yin,Ming Ma,Yun Tan,Lijuan Wu,Yang Yang,Yanqun Wang,Tao Lin,Feng Li
标识
DOI:10.1038/s41467-022-32371-4
摘要
Abstract CRISPR diagnostics are powerful tools for detecting nucleic acids but are generally not deployable for the detection of clinically important proteins. Here, we report an u ltrasensitive CRISPR-based antibody detection (UCAD) assay that translates the detection of anti-SARS-CoV-2 antibodies into CRISPR-based nucleic acid detection in a homogeneous solution and is 10,000 times more sensitive than the classic immunoassays. Clinical validation using serum samples collected from the general population (n = 197), demonstrates that UCAD has 100% sensitivity and 98.5% specificity. With ultrahigh sensitivity, UCAD enables the quantitative analysis of serum anti-SARS-CoV-2 levels in vaccinated kidney transplant recipients who are shown to produce “undetectable” anti-SARS-CoV-2 using standard immunoassay. Because of the high sensitivity and simplicity, we anticipate that, upon further clinical validation against large cohorts of clinical samples, UCAD will find wide applications for clinical uses in both centralized laboratories and point-of-care settings.
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