HIV-1 Vpr Functions in Primary CD4

CD4+ T cells G2 arrest HIV-1 Nef Vif Vpr Vpu accessory viral proteins inflammation interferon response pathogenesis restriction factors

Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
09 Mar 2024
Historique:
received: 31 01 2024
revised: 05 03 2024
accepted: 05 03 2024
medline: 28 3 2024
pubmed: 28 3 2024
entrez: 28 3 2024
Statut: epublish

Résumé

HIV-1 encodes four accesory proteins in addition to its structural and regulatory genes. Uniquely amongst them, Vpr is abundantly present within virions, meaning it is poised to exert various biological effects on the host cell upon delivery. In this way, Vpr contributes towards the establishment of a successful infection, as evidenced by the extent to which HIV-1 depends on this factor to achieve full pathogenicity in vivo. Although HIV infects various cell types in the host organism, CD4

Identifiants

pubmed: 38543785
pii: v16030420
doi: 10.3390/v16030420
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : SCHI1073/7-2

Auteurs

Carlos Alberto Vanegas-Torres (CA)

Institute for Medical Virology and Epidemiology of Viral Diseases, University Hospital Tuebingen, 72076 Tuebingen, Germany.

Michael Schindler (M)

Institute for Medical Virology and Epidemiology of Viral Diseases, University Hospital Tuebingen, 72076 Tuebingen, Germany.

Classifications MeSH