Transduction Efficiency of Zika Virus E Protein Pseudotyped HIV-1
Zika virus
flavivirus
glioblastoma cell culture
gp41
human cerebrospinal fluid
lentiviral vector
pseudotypes
retroviral vector
transmembrane domain
Journal
Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829
Informations de publication
Date de publication:
17 Feb 2024
17 Feb 2024
Historique:
received:
11
01
2024
revised:
12
02
2024
accepted:
15
02
2024
medline:
24
2
2024
pubmed:
24
2
2024
entrez:
24
2
2024
Statut:
epublish
Résumé
The development of new tools against glioblastoma multiforme (GBM), the most aggressive and common cancer originating in the brain, remains of utmost importance. Lentiviral vectors (LVs) are among the tools of future concepts, and pseudotyping offers the possibility of tailoring LVs to efficiently transduce and inactivate GBM tumor cells. Zika virus (ZIKV) has a specificity for GBM cells, leaving healthy brain cells unharmed, which makes it a prime candidate for the development of LVs with a ZIKV coat. Here, primary GBM cell cultures were transduced with different LVs encased with ZIKV envelope variants. LVs were generated by using the pNL
Identifiants
pubmed: 38398205
pii: cancers16040814
doi: 10.3390/cancers16040814
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : ASKLEPIOS proresearch
ID : 4168, 4169, 4328
Organisme : Werner Otto Stiftung
ID : 6/95, 11/101