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

Author:

Fumagalli Valeria12ORCID,Di Lucia Pietro12,Ravà Micol12,Marotta Davide12,Bono Elisa1,Grassi Stefano3,Donnici Lorena4ORCID,Cannalire Rolando5,Stefanelli Irina5ORCID,Ferraro Anastasia5,Esposito Francesca6ORCID,Pariani Elena7,Inverso Donato12ORCID,Montesano Camilla8,Delbue Serena9,Perlman Stanley1011ORCID,Tramontano Enzo6ORCID,De Francesco Raffaele412ORCID,Summa Vincenzo5ORCID,Guidotti Luca G12ORCID,Iannacone Matteo1213ORCID

Affiliation:

1. Division of Immunology, Transplantation, and Infectious Diseases IRCCS San Raffaele Scientific Institute Milan Italy

2. Vita‐Salute San Raffaele University Milan Italy

3. Pathology Unit IRCCS San Raffaele Scientific Institute Milan Italy

4. INGM ‐ Istituto Nazionale di Genetica Molecolare “Romeo ed Erica Invernizzi” Milan Italy

5. Department of Pharmacy, School of Medicine and Surgery University of Naples Federico II Naples Italy

6. Dipartimento di Scienze della Vita e dell'Ambiente Cittadella Universitaria di Monserrato Cagliari Italy

7. Department of Biomedical Sciences for Health University of Milan Milan Italy

8. Department of Chemistry La Sapienza University Rome Italy

9. Department of Biomedical, Surgical and Dental Sciences University of Milan Milan Italy

10. Department of Microbiology and Immunology University of Iowa Iowa City IA USA

11. Department of Pediatrics University of Iowa Iowa City IA USA

12. Department of Pharmacological and Biomolecular Sciences University of Milan Milan Italy

13. Experimental Imaging Center IRCCS San Raffaele Scientific Institute Milan Italy

Abstract

AbstractAlongside 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.

Funder

Ministero della Salute

Publisher

Springer Science and Business Media LLC

Subject

Molecular Medicine

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