Virologic and Immunologic Characterization of Coronavirus Disease 2019 Recrudescence After Nirmatrelvir/Ritonavir Treatment
- PMID: 35723411
- PMCID: PMC9278181
- DOI: 10.1093/cid/ciac496
Virologic and Immunologic Characterization of Coronavirus Disease 2019 Recrudescence After Nirmatrelvir/Ritonavir Treatment
Abstract
We isolated a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) BA.2 variant from a person with coronavirus disease 2019 recrudescence after nirmatrelvir/ritonavir treatment. Antiviral sensitivity and neutralizing antibody testing were performed with both parental SARS-CoV-2 and multiple variants of concern. We found that neither nirmatrelvir resistance nor absence of neutralizing immunity was a likely cause of the recrudescence.
Keywords: COVID-19; COVID-19 recrudescence; Omicron; nirmatrelvir; treatment rebound.
© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Conflict of interest statement
Potential conflicts of interest. A. F. C. has received contract payments from Nurix Therapeutics and has options in Covicept Therapeutics. D. M. S. has served as a consultant for Bayer Healthcare, Kiadis Pharmaceuticals, and Signant Health, and has equity stake in Vx Biosciences, Model Medicines, Linear Therapies, and FluxErgy. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
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Virologic and Immunologic Characterization of COVID-19 Recrudescence after Nirmatrelvir/Ritonavir Treatment.Res Sq [Preprint]. 2022 May 18:rs.3.rs-1662783. doi: 10.21203/rs.3.rs-1662783/v1. Res Sq. 2022. Update in: Clin Infect Dis. 2023 Feb 8;76(3):e530-e532. doi: 10.1093/cid/ciac496. PMID: 35611335 Free PMC article. Updated. Preprint.
References
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- US Food and Drug Administration, Center for Drug Evaluation and Research. Emergency use authorization (EUA) for Paxlovid (nirmatrelvir tablets copackaged with ritonavir tablets). 2021. Available at: https://www.fda.gov/media/155194/download. Accessed 31 May 2022.
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