Remdesivir Influence on SARS-CoV-2 RNA Viral Load Kinetics in Nasopharyngeal Swab Specimens of COVID-19 Hospitalized Patients: A Real-Life Experience.

SARS-CoV-2 antiviral coronavirus cycle threshold nasopharyngeal swab remdesivir viral load

Journal

Microorganisms
ISSN: 2076-2607
Titre abrégé: Microorganisms
Pays: Switzerland
ID NLM: 101625893

Informations de publication

Date de publication:
25 Jan 2023
Historique:
received: 09 01 2023
revised: 21 01 2023
accepted: 22 01 2023
entrez: 25 2 2023
pubmed: 26 2 2023
medline: 26 2 2023
Statut: epublish

Résumé

There are still conflicting data on the virological effects of the SARS-CoV-2 direct antivirals used in clinical practice, in spite of the documented clinical efficacy. The aim of this monocentric retrospective study was to compare virologic and laboratory data of patients admitted due to SARS-CoV-2 infection from March to December 2020 treated with either remdesivir (R), a protease inhibitor (lopinavir or darunavir/ritonavir (PI)) or no direct antiviral drugs (NT). Viral load variation was indirectly assessed through PCR cycle threshold (Ct) values on the nasopharyngeal swab, analyzing the results from swabs obtained at ward admission and 7 (±2) days later. Overall, 253 patients were included: patients in the R group were significantly older, more frequently males with a significantly higher percentage of severe COVID-19, requiring more often intensive care admission, compared to the other groups. Ct variation over time did not differ amongst the three treatment groups and did not seem to be influenced by corticosteroid use, even after normalization of the treatment groups for disease severity. Non-survivors had lower Ct on admission and showed a significantly slower viral clearance compared to survivors. CD4 T-lymphocytes absolute count assessed at ward admission correlated with a reduced Ct variation over time. In conclusion, viral clearance appears to be slower in COVID-19 non-survivors, while it seems not to be influenced by the antiviral treatment received.

Identifiants

pubmed: 36838277
pii: microorganisms11020312
doi: 10.3390/microorganisms11020312
pmc: PMC9959460
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Gilead Sciences (United Kingdom)
ID : IN-IT-540-6233

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Auteurs

Laura Campogiani (L)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.
Infectious Disease Clinic, Policlinico Tor Vergata, 00133 Rome, Italy.

Marco Iannetta (M)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.
Infectious Disease Clinic, Policlinico Tor Vergata, 00133 Rome, Italy.

Andrea Di Lorenzo (A)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.
Infectious Disease Clinic, Policlinico Tor Vergata, 00133 Rome, Italy.

Marta Zordan (M)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.
Infectious Disease Clinic, Policlinico Tor Vergata, 00133 Rome, Italy.

Pier Giorgio Pace (PG)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.

Luigi Coppola (L)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.
Infectious Disease Clinic, Policlinico Tor Vergata, 00133 Rome, Italy.

Mirko Compagno (M)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.
Infectious Disease Clinic, Policlinico Tor Vergata, 00133 Rome, Italy.

Vincenzo Malagnino (V)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.
Infectious Disease Clinic, Policlinico Tor Vergata, 00133 Rome, Italy.

Elisabetta Teti (E)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.
Infectious Disease Clinic, Policlinico Tor Vergata, 00133 Rome, Italy.

Massimo Andreoni (M)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.
Infectious Disease Clinic, Policlinico Tor Vergata, 00133 Rome, Italy.

Loredana Sarmati (L)

Department of System Medicine, Tor Vergata University, 00133 Rome, Italy.
Infectious Disease Clinic, Policlinico Tor Vergata, 00133 Rome, Italy.

Classifications MeSH