Clinical Validation of a Novel T-cell Receptor Sequencing Assay for Identification of Recent or Prior SARS-CoV-2 Infection

التفاصيل البيبلوغرافية
العنوان: Clinical Validation of a Novel T-cell Receptor Sequencing Assay for Identification of Recent or Prior SARS-CoV-2 Infection
المؤلفون: Thomas Manley, Rachel M. Gittelman, Lance Baldo, Hans Nesse, Sudeb C. Dalai, Ian M. Kaplan, Caroline Taromino, John Alsobrook, Megan Herndon, Kipp Akers, Tera Eerkes, Emily Svejnoha, Sarah Duffy, Pam Witte, Jia Qadeer, Jennifer N. Dines, Thomas M. Snyder, Pashmi Vaney, Lynell Skewis, Anthony Monteforte, Cristina Wolf, Sally Howard
بيانات النشر: Cold Spring Harbor Laboratory, 2021.
سنة النشر: 2021
مصطلحات موضوعية: Immune system, Coronavirus disease 2019 (COVID-19), business.industry, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), T-cell receptor, Immunology, Medicine, Symptom onset, business, Pathogen, Whole blood, Serology
الوصف: BackgroundWhile diagnostic, therapeutic, and vaccine development in the COVID-19 pandemic has proceeded at unprecedented speed and scale, critical gaps remain in our understanding of the immune response to SARS-CoV-2. Current diagnostic strategies, including serology, have numerous limitations in addressing these gaps. Here we describe clinical performance of T- Detect™ COVID, the first reported assay to determine recent or prior SARS-CoV-2 infection based on T-cell receptor (TCR) sequencing and immune repertoire profiling from whole blood samples.MethodsMethods for high-throughput immunosequencing of the TCRβ gene from blood specimens have been described1. We developed a statistical classifier showing high specificity for identifying prior SARS-CoV-2 infection2, utilizing >4,000 SARS-CoV-2-associated TCR sequences from 784 cases and 2,447 controls across 5 independent cohorts. The T-Detect COVID Assay comprises immunosequencing and classifier application to yield a qualitative positive or negative result. Several retrospective and prospective cohorts were enrolled to assess assay performance including primary and secondary Positive Percent Agreement (PPA; N=205, N=77); primary and secondary Negative Percent Agreement (NPA; N=87, N=79); PPA compared to serology (N=55); and pathogen cross-reactivity (N=38).ResultsT-Detect COVID demonstrated high PPA in subjects with prior PCR-confirmed SARS-CoV-2 infection (97.1% 15+ days from diagnosis; 94.5% 15+ days from symptom onset), high NPA (∼100%) in presumed or confirmed SARS-CoV-2 negative cases, equivalent or higher PPA than two commercial EUA serology tests, and no evidence of pathogen cross-reactivity.ConclusionT-Detect COVID is a novel T-cell immunosequencing assay demonstrating high clinical performance to identify recent or prior SARS-CoV-2 infection from standard blood samples. This assay can provide critical insights on the SARS-CoV-2 immune response, with potential implications for clinical management, risk stratification, surveillance, assessing protective immunity, and understanding long-term sequelae.
DOI: 10.1101/2021.01.06.21249345
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d2fa83119b2e6922525c69a98284343d
https://doi.org/10.1101/2021.01.06.21249345
Rights: OPEN
رقم الانضمام: edsair.doi...........d2fa83119b2e6922525c69a98284343d
قاعدة البيانات: OpenAIRE
الوصف
DOI:10.1101/2021.01.06.21249345