Table 1.
HPV Particle Type | Method of Production | Particle and System Advantages | Particle and System Disadvantages |
---|---|---|---|
Native Virions | Organotypic raft culture system | Contains the full HPV capsid as well as full HPV genome Assembles and matures over a period of 10–20 days in tissue |
Expensive Slow production time |
Virus Like Particles (VLPs) | Transfection based system | Quick and inexpensive particle production | Codon modification of L1 and L2 is necessary for production Over-expression system Particles produced in non-relevant cell lines Particle assembly within 48 hours Maturation occurs overnight Deletion of in frame methionines upstream of the consensus methionine in L1 VLPs contain no genomes, which may alter particle structure |
Pseudovirions (PsVs) | Transfection based system | Quick and inexpensive particle production Ability to track cellular infectivity |
|
Quasivirions (QVs) | Transfection based system | Quick and inexpensive particle production Contains L1, L2, and a full HPV genome Closest to NVs—retains majority of cell surface exposed conformational epitopes |