Evidence map›Paper›PMID 36946379›Full record

ArticleEMBO molecular medicine2023

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

Valeria Fumagalli, Pietro Di Lucia, Micol Ravà, Davide Marotta, Elisa Bono, Stefano Grassi, Lorena Donnici, Rolando Cannalire, Irina Stefanelli, Anastasia Ferraro and 11 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 25 citations in OpenAlex.

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  7. COVID-19 therapeutics.Clinical microbiology reviews · 2024
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 7 institutions in 2 countries.

Valeria FumagalliDivision of Immunology, Transplantation, and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID 0000-0003-2583-2498
Pietro Di LuciaDivision of Immunology, Transplantation, and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Micol RavàDivision of Immunology, Transplantation, and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Davide MarottaDivision of Immunology, Transplantation, and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Elisa BonoDivision of Immunology, Transplantation, and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Stefano GrassiPathology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Lorena DonniciINGM - Istituto Nazionale di Genetica Molecolare "Romeo ed Erica Invernizzi", Milan, Italy.ORCID 0000-0002-9153-9102
Rolando CannalireDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Irina StefanelliDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.ORCID 0000-0002-8861-4829
Anastasia FerraroDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Francesca EspositoDipartimento di Scienze della Vita e dell'Ambiente, Cittadella Universitaria di Monserrato, Cagliari, Italy.ORCID 0000-0001-9725-7977
Elena ParianiDepartment of Biomedical Sciences for Health, University of Milan, Milan, Italy.
Donato InversoDivision of Immunology, Transplantation, and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID 0000-0003-0987-3345
Camilla MontesanoDepartment of Chemistry, La Sapienza University, Rome, Italy.
Serena DelbueDepartment of Biomedical, Surgical and Dental Sciences, University of Milan, Milan, Italy.
Stanley PerlmanDepartment of Microbiology and Immunology, University of Iowa, Iowa City, IA, USA.ORCID 0000-0003-4213-2354
Enzo TramontanoDipartimento di Scienze della Vita e dell'Ambiente, Cittadella Universitaria di Monserrato, Cagliari, Italy.ORCID 0000-0002-4849-0980
Raffaele De FrancescoINGM - Istituto Nazionale di Genetica Molecolare "Romeo ed Erica Invernizzi", Milan, Italy.ORCID 0000-0001-8754-5123
Vincenzo SummaDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.ORCID 0000-0002-6288-2681
Luca G GuidottiDivision of Immunology, Transplantation, and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID 0000-0002-0205-2678
Matteo IannaconeDivision of Immunology, Transplantation, and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID 0000-0002-9370-2671
Vita-Salute San Raffaele University · ITUniversity of Naples Federico II · ITUniversity of Milan · ITUniversity of Cagliari · ITIstituto Nazionale Genetica Molecolare · ITSapienza University of Rome · ITUniversity of Iowa · US

Funding

SARS-CoV Proteins in Heterologous Viral InfectionP01AI060699 · NIAID · UNIVERSITY OF IOWA · PI PERLMAN, STANLEY · 2004 to 2021
$21.5M
Role of eicosanoids in pathogenic human CoV infectionsR01AI129269 · NIAID · UNIVERSITY OF IOWA · PI Stanley Perlman · 2016 to 2026
$4.7M
NIAID NIH HHS P01 AI060699NIAID NIH HHS R01 AI129269
6 · The paper itself

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.

Indexed as

Adaptive ImmunityAntiviral AgentsCOVID-19 Drug TreatmentLactamsAnimalsB-LymphocytesCOVID-19LeucineMemory T CellsMiceMice, Inbred C57BLNitrilesProlineSARS-CoV-2Antiviral AgentsLactamsLeucinenirmatrelvirNitrilesProlineadaptive immunityanimal modelsantiviral treatmentnirmatrelvirSARS-CoV-2

Identifiers

PMID36946379
PMCPMC10165354
OpenAlexW4353015399

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.