Multiply deleted [E1, polymerase-, and pTP-] adenovirus vector persists despite deletion of the preterminal protein

J Gene Med. Jul-Aug 2000;2(4):250-9. doi: 10.1002/1521-2254(200007/08)2:4<250::AID-JGM113>3.0.CO;2-3.

Abstract

Background: The inherent limitations of [E1-]Ad vectors as gene therapy vehicles suggest that further modifications may improve their overall performance profiles. However, Ad vector modifications can have untoward effects on their basic biology, e.g., some helper-virus dependent Ad vectors have been found to be unstable without the presence of preterminal protein (pTP) activities. Despite this concern, we generated a new class of helper-virus independent Ad vector that was multiply deleted for the E1, polymerase, and pTP genes, and investigated the ramifications of these deletions upon several vector performance parameters.

Methods: The construction and propagation of an [E1-, polymerase-, pTP-]Ad vector was achieved with the use of trans-complementing cells co-expressing the Ad E1, polymerase and pTP genes.

Results: High titer production of the [E1-, polymerase-, pTP-]Ad vector was successfully accomplished via conventional Ad purification techniques. This unique class of Ad vector was capable of long-term gene transfer in vivo (despite lacking pTP functions) that was concomitant with a significantly decreased hepatic toxicity.

Conclusions: Previous studies had suggested that Ad genome persistence in vivo may be dependent upon the presence of low level vector genome replication and/or pTP functions. Our results suggest that [E1-, polymerase-, pTP-]Ad vectors can overcome these barriers. The further benefits afforded by the use of this class of Ad vector (increased cloning capacity, high level growth, decreased propensity to generate replication competent Ad (RCA), decreased toxicity) suggests that they will be highly beneficial for use in several aspects of human gene therapy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenoviridae / genetics*
  • Adenovirus E1 Proteins / genetics
  • Animals
  • Cell Line
  • DNA-Directed DNA Polymerase / genetics
  • Gene Deletion*
  • Gene Transfer Techniques*
  • Genetic Vectors
  • Genome, Viral*
  • Helper Viruses / genetics
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Mice, SCID
  • Phosphoproteins / genetics*
  • Protein Precursors / genetics*
  • Transduction, Genetic
  • Viral Proteins / genetics*

Substances

  • Adenovirus E1 Proteins
  • Phosphoproteins
  • Protein Precursors
  • Viral Proteins
  • pTP protein, adenovirus
  • DNA-Directed DNA Polymerase