Your browser doesn't support javascript.
loading
COVID-19 serology at population scale: SARS-CoV-2-specific antibody responses in saliva
Pranay R Randad; Nora Pisanic; Kate Kruczynski; Yukari C Manabe; David Thomas; Andrew Pekosz; Sabra Klein; Michael J Betenbaugh; William A Clarke; Oliver Laeyendecker; Patrizio P Caturegli; H Benjamin Larman; Barbara Detrick; Jessica K Fairley; Amy C Sherman; Nadine Rouphael; Srilatha Edupuganti; Douglas A Granger; Steve W Granger; Matthew Collins; Christopher D Heaney.
Afiliação
  • Pranay R Randad; Johns Hopkins Bloomberg School of Public Health
  • Nora Pisanic; Johns Hopkins Bloomberg School of Public Health
  • Kate Kruczynski; Johns Hopkins Bloomberg School of Public Health
  • Yukari C Manabe; Johns Hopkins University School of Medicine
  • David Thomas; Johns Hopkins School of Medicine
  • Andrew Pekosz; Johns Hopkins Bloomberg School of Public Health
  • Sabra Klein; Johns Hopkins Bloomberg School of Public Health
  • Michael J Betenbaugh; Johns Hopkins University
  • William A Clarke; Johns Hopkins School of Medicine
  • Oliver Laeyendecker; Johns Hopkins School of Medicine
  • Patrizio P Caturegli; Johns Hopkins School of Medicine
  • H Benjamin Larman; Johns Hopkins School of Medicine
  • Barbara Detrick; Johns Hopkins School of Medicine
  • Jessica K Fairley; Hubert Department of Global Health, Emory University Rollins School of Public Health
  • Amy C Sherman; The Hope Clinic of the Emory Vaccine Center, Emory University School of Medicine
  • Nadine Rouphael; The Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine
  • Srilatha Edupuganti; The Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine
  • Douglas A Granger; Institute for Interdisciplinary Salivary Bioscience Research, University of California Irvine
  • Steve W Granger; Salimetrics, LLC
  • Matthew Collins; The Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine
  • Christopher D Heaney; Johns Hopkins Bloomberg School of Public Health
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-20112300
Artigo de periódico
Um artigo publicado em periódico científico está disponível e provavelmente é baseado neste preprint, por meio do reconhecimento de similaridade realizado por uma máquina. A confirmação humana ainda está pendente.
Ver artigo de periódico
ABSTRACT
Non-invasive SARS-CoV-2 antibody testing is urgently needed to estimate the incidence and prevalence of SARS-CoV-2 infection at the general population level. Precise knowledge of population immunity could allow government bodies to make informed decisions about how and when to relax stay-at-home directives and to reopen the economy. We hypothesized that salivary antibodies to SARS-CoV-2 could serve as a non-invasive alternative to serological testing for widespread monitoring of SARS-CoV-2 infection throughout the population. We developed a multiplex SARS-CoV-2 antibody immunoassay based on Luminex technology and tested 167 saliva and 324 serum samples, including 134 and 118 negative saliva and serum samples, respectively, collected before the COVID-19 pandemic, and 33 saliva and 206 serum samples from participants with RT-PCR-confirmed SARS-CoV-2 infection. We evaluated the correlation of results obtained in saliva vs. serum and determined the sensitivity and specificity for each diagnostic media, stratified by antibody isotype, for detection of SARS-CoV-2 infection based on COVID-19 case designation for all specimens. Matched serum and saliva SARS-CoV-2 antigen-specific IgG responses were significantly correlated. Within the 10-plex SARS-CoV-2 panel, the salivary anti-nucleocapsid (N) protein IgG response resulted in the highest sensitivity for detecting prior SARS-CoV-2 infection (100% sensitivity at [≥]10 days post-SARS-CoV-2 symptom onset). The salivary anti-receptor binding domain (RBD) IgG response resulted in 100% specificity. Among individuals with SARS-CoV-2 infection confirmed with RT-PCR, the temporal kinetics of IgG, IgA, and IgM in saliva were consistent with those observed in serum. SARS-CoV-2 appears to trigger a humoral immune response resulting in the almost simultaneous rise of IgG, IgM and IgA levels both in serum and in saliva, mirroring responses consistent with the stimulation of existing, cross-reactive B cells. SARS-CoV-2 antibody testing in saliva can play a critically important role in large-scale "sero"-surveillance to address key public health priorities and guide policy and decision-making for COVID-19. 40-word summaryA multiplex immunoassay to detect SARS-CoV-2-specific antibodies in saliva performs with high diagnostic accuracy as early as ten days post-COVID-19 symptom onset. Highly sensitive and specific salivary COVID-19 antibody assays could advance broad immuno-surveillance goals in the USA and globally.
Licença
cc_by_nc_nd
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Diagnostic_studies / Experimental_studies / Observational_studies / Rct Idioma: En Ano de publicação: 2020 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Diagnostic_studies / Experimental_studies / Observational_studies / Rct Idioma: En Ano de publicação: 2020 Tipo de documento: Preprint
...