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Performance of three rapid antigen tests against the SARS-CoV-2 Omicron variant
Sanjat Kanjilal; Sujata Chalise; Adnan Shami Shah; Chi-An Cheng; Yasmeen Senussi; Rockib Uddin; Vamsi Thiriveedhi; Ha Eun Cho; Seamus Carroll; Jacob Lemieux; Sarah Turbett; David R. Walt.
Afiliação
  • Sanjat Kanjilal; Harvard Medical School & Harvard Pilgrim Healthcare Institute
  • Sujata Chalise; Brigham and Women's Hospital & Harvard Medical School
  • Adnan Shami Shah; Brigham and Women's Hospital & Harvard Medical School
  • Chi-An Cheng; Brigham and Women's Hospital & Harvard Medical School
  • Yasmeen Senussi; Brigham and Women's Hospital & Harvard Medical School
  • Rockib Uddin; Massachusetts General Hospital
  • Vamsi Thiriveedhi; Massachusetts General Hospital
  • Ha Eun Cho; Massachusetts General Hospital
  • Seamus Carroll; Massachusetts General Hospital
  • Jacob Lemieux; Massachusetts General Hospital
  • Sarah Turbett; Massachusetts General Hospital
  • David R. Walt; Brigham and Women's Hospital & Harvard Medical School
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22271142
ABSTRACT
Rapid antigen detection tests (RADTs) for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are now in widespread use in the United States. RADTs play an important role in maintaining an open society but require periodic reassessment to ensure test performance remains intact as the virus evolves. The nucleocapsid (N) protein is the target for the majority of RADTs and the SARS-CoV-2 Omicron variant has several N protein mutations that are previously uncharacterized. We sought to assess the impact of these mutations by testing 30 Omicron variant samples across a wide range of viral loads on three widely used RADTs the iHealth COVID-19 Antigen Rapid Test, the ACON Laboratories FlowFlex COVID-19 Antigen Home Test, and the Abbott BinaxNOW COVID-19 Antigen Card, using 30 Delta variant samples as a comparator. We found no change in the analytic sensitivity of all three RADTs for detection of Omicron versus Delta, but noted differences in performance between assays. No RADT was able to detect samples with a cycle threshold (Ct) value of [≥]27.5 for the envelope gene target on the Roche cobas RT-PCR assay. Epidemiologic studies are necessary to correlate these findings with their real-world performance.
Licença
cc_by_nc
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Estudo diagnóstico / Estudo observacional Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Estudo diagnóstico / Estudo observacional Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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