Your browser doesn't support javascript.
loading
Host response-based screening to identify undiagnosed cases of COVID-19and expand testing capacity
Nagarjuna R. Cheemarla; Anderson F. Brito; Joseph R. Fauver; Tara Alpert; Chantal B.F. Vogels; Saad B. Omer; Albert Ko; Nathan D. Grubaugh; Marie L. Landry; Ellen F. Foxman.
Afiliación
  • Nagarjuna R. Cheemarla; Yale School of Medicine
  • Anderson F. Brito; Yale School of Public Health
  • Joseph R. Fauver; Yale School of Public Health
  • Tara Alpert; Yale School of Public Health
  • Chantal B.F. Vogels; Yale School of Public Health
  • Saad B. Omer; Yale Institute of Global Health
  • Albert Ko; Yale University School of Public Health
  • Nathan D. Grubaugh; Yale School of Public Health
  • Marie L. Landry; Yale School of Medicine
  • Ellen F. Foxman; Yale School of Medicine
Preprint en En | PREPRINT-MEDRXIV | ID: ppmedrxiv-20109306
ABSTRACT
The COVID-19 pandemic has created unprecedented challenges in diagnostic testing. At the beginning of the epidemic, a confluence of factors resulted in delayed deployment of PCR-based diagnostic tests, resulting in lack of testing of individuals with symptoms of the disease. Although these tests are now more widely available, it is estimated that a three- to ten-fold increase in testing capacity will be required to ensure adequate surveillance as communities reopen1. In response to these challenges, we evaluated potential roles of host response-based screening in the diagnosis of COVID-19. Previous work from our group showed that the nasopharyngeal (NP) level of CXCL10, a protein produced as part of the host response to viral infection, is a sensitive predictor of respiratory virus infection across a wide spectrum of viruses2. Here, we show that NP CXCL10 is elevated during SARS-CoV-2 infection and use a CXCL10-based screening strategy to identify four undiagnosed cases of COVID-19 in Connecticut in early March. In a second set of samples tested at the Yale New Haven Hospital, we show that NP CXCL10 had excellent performance as a rule-out test (NPV 0.99, 95% C.I. 0.985-0.997). Our results demonstrate how biomarker-based screening could be used to leverage existing PCR testing capacity to rapidly enable widespread testing for COVID-19. One Sentence SummaryWe describe a host-response based screening strategy to identify undiagnosed cases of COVID-19 and to expand capacity for PCR-based testing.
Licencia
cc_no
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Diagnostic_studies / Experimental_studies / Prognostic_studies Idioma: En Año: 2020 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Diagnostic_studies / Experimental_studies / Prognostic_studies Idioma: En Año: 2020 Tipo del documento: Preprint