Regression of papillomas induced by cottontail rabbit papillomavirus is associated with infiltration of CD8+ cells and persistence of viral DNA after regression

R Selvakumar, A Schmitt, T Iftner, R Ahmed… - Journal of …, 1997 - Am Soc Microbiol
R Selvakumar, A Schmitt, T Iftner, R Ahmed, FO Wettstein
Journal of virology, 1997Am Soc Microbiol
Cottontail rabbit papillomavirus (CRPV) is a highly oncogenic papillomavirus and has been
successfully used as a model to develop protective vaccines against papillomaviruses.
Papillomas induced by the virus may spontaneously regress, suggesting that CRPV can
also serve as a model to develop therapeutic vaccines. As a first step toward this goal, we
have analyzed immunologic and viral aspects associated with papilloma regression and
have identified several features unique to regression. Immunohistochemical staining of …
Cottontail rabbit papillomavirus (CRPV) is a highly oncogenic papillomavirus and has been successfully used as a model to develop protective vaccines against papillomaviruses. Papillomas induced by the virus may spontaneously regress, suggesting that CRPV can also serve as a model to develop therapeutic vaccines. As a first step toward this goal, we have analyzed immunologic and viral aspects associated with papilloma regression and have identified several features unique to regression. Immunohistochemical staining of biopsies from growing and regressing papillomas and from sites after complete regression showed infiltration of CD8+ cells into the basal and suprabasal layers of the epidermis only during active regression. In situ hybridizations with mRNA-specific probes were strongly positive for E6 and E7 mRNAs during regression, but no late mRNA was present. Viral DNA was detected by in situ hybridization during regression but not after regression. However, analysis by PCR revealed persistence of viral DNA for several months at the majority of regression sites. The results suggest that stimulation of a strong CD8+ response to virus-infected cells is important for an effective therapeutic vaccine and that special attention should be given to the suppression of latent infection.
American Society for Microbiology