Nirmatrelvir treatment of SARS-CoV-2-infected mice blunts antiviral adaptive immune responses

EMBO Mol Med. 2023 May 8;15(5):e17580. doi: 10.15252/emmm.202317580. Epub 2023 Mar 22.

Abstract

Alongside vaccines, antiviral drugs are becoming an integral part of our response to the SARS-CoV-2 pandemic. Nirmatrelvir-an orally available inhibitor of the 3-chymotrypsin-like cysteine protease-has been shown to reduce the risk of progression to severe COVID-19. However, the impact of nirmatrelvir treatment on the development of SARS-CoV-2-specific adaptive immune responses is unknown. Here, by using mouse models of SARS-CoV-2 infection, we show that nirmatrelvir administration blunts the development of SARS-CoV-2-specific antibody and T cell responses. Accordingly, upon secondary challenge, nirmatrelvir-treated mice recruited significantly fewer memory T and B cells to the infected lungs and mediastinal lymph nodes, respectively. Together, the data highlight a potential negative impact of nirmatrelvir treatment with important implications for clinical management and might help explain the virological and/or symptomatic relapse after treatment completion reported in some individuals.

Keywords: SARS-CoV-2; adaptive immunity; animal models; antiviral treatment; nirmatrelvir.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptive Immunity* / drug effects
  • Animals
  • Antiviral Agents* / administration & dosage
  • B-Lymphocytes / immunology
  • COVID-19 / immunology
  • COVID-19 Drug Treatment*
  • Lactams* / administration & dosage
  • Memory T Cells / immunology
  • Mice
  • Mice, Inbred C57BL
  • SARS-CoV-2

Substances

  • nirmatrelvir
  • Antiviral Agents
  • Lactams