Technology Bundle ID
NCI-E-298-2016

Efficient Cell-Free Production of Papillomavirus Gene Transfer Vectors

Applications
Co-Inventors
John Schiller (NCI)
Development Status
Pre-clinical (in vivo)
ICs

Papillomavirus pseudoviruses that comprise the L1/L2 capsid proteins can package a wide variety of non-viral DNA plasmids and deliver the packaged genetic material to cells. This function makes them attractive candidates as targeted gene delivery vehicles. Current methods for the efficient production of papillomavirus pseudoviruses require the use of 293TT cells.  One key drawback to this production method is SV40 T antigen gene contamination introduced by the 293TT cells.  Because T antigen is a known oncoprotein, pseudoviruses generated using this methodology are unsuitable for clinical applications.  A second drawback is that intracellular production precludes production of toxin gene-transducing pseudovirions.  A third drawback is that intracellular production cannot be used to generate mRNA transducing vectors.

Scientists at the NCI have developed a novel, chemically defined, cell-free, papillomavirus-based vector production system that allows the incorporation of purified plasmid DNA (pseudogenome) or mRNA into high-titer papillomavirus L1/L2 capsids without the use of 293TT cells.  Titers as high as 1011 infectious units/mg of L1 were generated. Pseudoviruses were infectious both in vitro and in vivo, and should be compatible with good manufacturing practice (GMP) requirements.

Commercial Applications
  • GMP production of papillomavirus-based gene delivery vectors
  • Vaccine applications 
  • Cancer therapeutic applications 
  • Clinical evaluation of IVP vectors as agents for intravaginal vaccination or cancer treatment
Competitive Advantages
  • More suitable for clinical applications compared to standard production methods
  • Enables the generation of papillomavirus pseudovirions that can transduce cytotoxic genes
  • GMP-grade papillomavirus pseudovirus production
  • Chemically defined, cell-free, papillomavirus-based vector production system
  • Allows the incorporation of purified plasmid DNA (pseudogenome) or mRNA into high-titer papillomavirus L1/L2 capsids without the use of 293TT cells
  • High titer papillomavirus production methods (titers as high as 1011 infectious units/mg of L1)
  • Infectious both in vitro and in vivo
  • Overcomes the T antigen contamination issues found in current methods for production of papillomavirus based pseudoviruses

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