Canine Adenovirus Vectors: an Alternative for Adenovirus-Mediated Gene Transfer

Preclinical studies have shown that gene transfer following readministration of viral vectors is often inefficient due to the presence of neutralizing antibodies. Vectors derived from ubiquitous human adenoviruses may have limited clinical use because preexisting humoral and cellular immunity is fou...

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Podrobná bibliografie

Vydáno v:	J Virol
Hlavní autoři:	Kremer, Eric J., Boutin, Sylvie, Chillon, Miguel, Danos, Olivier
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	American Society for Microbiology (ASM) 2000
Témata:	Gene Therapy
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC111562/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10590140/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.74.1.505-512.2000
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