2008
DOI: 10.1002/jgm.1284
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Novel recombinant adenovirus type 41 vector and its biological properties

Abstract: An Ad41 vector system was successfully constructed, which consisted of the backbone plasmid, shuttle plasmid and packaging cell line 293E12. This system can be utilized to generate genetically stable and acid-resistant recombinant Ad41 carrying any gene of interest.

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Cited by 23 publications
(23 citation statements)
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“…In contrast to the aggregation between pH 4.0 and 4.7, at pH 2.8, the virion hydrodynamic diameter was only 112 Ϯ 20 nm, suggesting minimal aggregation. This is consistent with studies showing that the enteric adenoviruses remain infective under the acidic conditions in the gut (49,50). A high positive -potential at low pH (Fig.…”
Section: Resultssupporting
confidence: 91%
“…In contrast to the aggregation between pH 4.0 and 4.7, at pH 2.8, the virion hydrodynamic diameter was only 112 Ϯ 20 nm, suggesting minimal aggregation. This is consistent with studies showing that the enteric adenoviruses remain infective under the acidic conditions in the gut (49,50). A high positive -potential at low pH (Fig.…”
Section: Resultssupporting
confidence: 91%
“…Wild-type HAdV-41, which originated from a fecal sample (NIVD103), has been described elsewhere [18]. pAd41-GFP, a plasmid that was constructed previously [18], contains the whole genome of HAdV-41 except the E1 region, which was replaced by a GFP gene.…”
Section: Methodsmentioning
confidence: 99%
“…pKAd41 was partially sequenced. The sequence information for the left end of the genome was combined with that of pAd41-GFP, which was sequenced previously [18], to generate the complete genome sequence (GenBank accession no. HM565136.3).…”
Section: Cloning Of the Hadv-41 Genome And Rescue Of The Virusmentioning
confidence: 99%
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“…Adenovirus is an ideal carrier [2]. This recombinant replication-defective adenovirus vector ( pAd/CMV/V5-DEST) could be used for gene therapy in tumors and has vast improvements compared with the previous generation of adenovirus vector [3]. There are lots of advantages to transfect with this vector both in vitro and in vivo, such as high transfection efficiency, low toxicity, weak immunogenicity, and long periods of gene product expression.…”
mentioning
confidence: 99%