Brincidofovir inhibits polyomavirus infection

antiviral agents brain brincidofovir kidney polyomavirus

Journal

mBio
ISSN: 2150-7511
Titre abrégé: mBio
Pays: United States
ID NLM: 101519231

Informations de publication

Date de publication:
02 Jul 2024
Historique:
medline: 2 7 2024
pubmed: 2 7 2024
entrez: 2 7 2024
Statut: aheadofprint

Résumé

Polyomaviruses are species-specific DNA viruses that can cause disease in immunocompromised individuals. Despite their role as the causative agents for several diseases, there are no currently approved antivirals for treating polyomavirus infection. Brincidofovir (BCV) is an antiviral approved for the treatment of poxvirus infections and has shown activity against other double-stranded DNA viruses. In this study, we tested the efficacy of BCV against polyomavirus infection Widespread in the human population and able to persist asymptomatically for the life of an individual, polyomavirus infections cause a significant disease burden in the immunocompromised. Individuals undergoing immune suppression, such as kidney transplant patients or those treated for autoimmune diseases, are particularly at high risk for polyomavirus-associated diseases. Because no antiviral agent exists for treating polyomavirus infections, management of polyomavirus-associated diseases typically involves reducing or discontinuing immunomodulatory therapy. This can be perilous due to the risk of transplant rejection and the potential development of adverse immune reactions. Thus, there is a pressing need for the development of antivirals targeting polyomaviruses. Here, we investigate the effects of brincidofovir, an FDA-approved antiviral, on polyomavirus infection

Identifiants

pubmed: 38953354
doi: 10.1128/mbio.01049-24
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0104924

Subventions

Organisme : NINDS NIH HHS
ID : R35 NS127217
Pays : United States

Auteurs

Arrienne B Butic (AB)

Department of Microbiology and Immunology, Penn State College of Medicine, Hershey, Pennsylvania, USA.

Zoe E Katz (ZE)

Department of Microbiology and Immunology, Penn State College of Medicine, Hershey, Pennsylvania, USA.

Ge Jin (G)

Department of Microbiology and Immunology, Penn State College of Medicine, Hershey, Pennsylvania, USA.

Koji Fukushima (K)

SymBio Pharmaceuticals Limited, Toranomon, Minato, Tokyo, Japan.

Masatoshi Hazama (M)

SymBio Pharmaceuticals Limited, Toranomon, Minato, Tokyo, Japan.

Aron E Lukacher (AE)

Department of Microbiology and Immunology, Penn State College of Medicine, Hershey, Pennsylvania, USA.

Matthew D Lauver (MD)

Department of Microbiology and Immunology, Penn State College of Medicine, Hershey, Pennsylvania, USA.

Classifications MeSH