Case report: Clearance of longstanding, immune-deficiency-associated, vaccine-derived polio virus infection following remdesivir therapy for chronic SARS-CoV-2 infection.

CVID - common variable immunodeficiency disorders immune deficiency associated vaccine derived poliovirus (iVDPV) polio primary immune deficiencies (PID) remdesivir vaccine derived poliovirus

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2023
Historique:
received: 01 01 2023
accepted: 07 02 2023
entrez: 20 3 2023
pubmed: 21 3 2023
medline: 22 3 2023
Statut: epublish

Résumé

The global polio eradication campaign has had remarkable success in reducing wild-type poliovirus infection, largely built upon the live attenuated Sabin oral poliovirus vaccine. Whilst rare, vaccine poliovirus strains may cause infection and subsequently revert to a neurovirulent type, termed vaccine-derived poliovirus (VDPV). Persistent, vaccine derived infection may occur in an immunocompromised host (iVDPV), where it is a recognised complication following receipt of the Sabin vaccine. This has significant implications for the global polio eradication campaign and there is currently no agreed global strategy to manage such patients.Here we describe a case of a 50-year-old man with common variable immune deficiency, persistently infected with a neurovirulent vaccine-derived type 2 poliovirus following vaccination in childhood. iVDPV infection had proven resistant to multiple prior attempts at treatment with human breast milk, ribavirin and oral administration of a normal human pooled immunoglobulin product. His iVDPV infection subsequently resolved after 12 days treatment with remdesivir, an adenosine analogue prodrug that is an inhibitor of viral RNA-dependent RNA polymerase, administered as treatment for a prolonged, moderate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. iVDPV from the patient, isolated prior to treatment, was subsequently demonstrated to be sensitive to remdesivir in vitro. Based on the observations made in this case, and the mechanistic rationale for use with iVDPV, there is strong justification for further clinical studies of remdesivir treatment as a potentially curative intervention in patients with iVDPV infection.

Identifiants

pubmed: 36936936
doi: 10.3389/fimmu.2023.1135834
pmc: PMC10022663
doi:

Substances chimiques

Poliovirus Vaccine, Oral 0
remdesivir 3QKI37EEHE

Types de publication

Case Reports Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1135834

Informations de copyright

Copyright © 2023 Bermingham, Canning, Wilton, Kidd, Klapsa, Majumdar, Sooriyakumar, Martin and Huissoon.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

William Hywel Bermingham (WH)

Department of Immunology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

Benjamin Canning (B)

Department of Virology, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.

Thomas Wilton (T)

Division of Vaccines, National Institute for Biological Standards and Control, Medicines and Healthcare Products Regulatory Agency, Potters Bar, United Kingdom.

Michael Kidd (M)

Public Health Laboratory, UK Health Security Agency, Birmingham, United Kingdom.

Dimitra Klapsa (D)

Division of Vaccines, National Institute for Biological Standards and Control, Medicines and Healthcare Products Regulatory Agency, Potters Bar, United Kingdom.

Manasi Majumdar (M)

Division of Vaccines, National Institute for Biological Standards and Control, Medicines and Healthcare Products Regulatory Agency, Potters Bar, United Kingdom.

Kavitha Sooriyakumar (K)

Department of Immunology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

Javier Martin (J)

Division of Vaccines, National Institute for Biological Standards and Control, Medicines and Healthcare Products Regulatory Agency, Potters Bar, United Kingdom.

Aarnoud P Huissoon (AP)

Department of Immunology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

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Classifications MeSH