A
vaccine comprising human papillomavirus type 16 (HPV16) L2, E6 and E7 in a single tandem fusion
protein (termed TA-CIN) has the potential advantages of both broad cross-protection against HPV transmission through induction of L2
antibodies able to cross neutralize different HPV types and of
therapy by stimulating T cell responses targeting HPV16 early
proteins. However, patients vaccinated with TA-CIN alone develop weak HPV
neutralizing antibody and E6/E7-specific T cell responses. Here we test TA-CIN formulated along with the adjuvant
GPI-0100, a semi-synthetic
quillaja saponin analog that was developed to promote both humoral and cellular immune responses. Subcutaneous administration to mice of TA-CIN (20 microg) with 50microg
GPI-0100, three times at biweekly intervals, elicited high titer HPV16 neutralizing serum antibody, robust neutralizing titers for other HPV16-related types, including HPV31 and HPV58, and neutralized to a lesser extent other genital mucosatropic papillomaviruses like HPV18, HPV45, HPV6 and HPV11. Notably, vaccination with TA-CIN in
GPI-0100 protected mice from cutaneous HPV16 challenge as effectively as HPV16 L1 VLP without adjuvant. Formulation of TA-CIN with
GPI-0100 enhanced the production of E7-specific,
interferon gamma producing CD8(+) T cell precursors by 20-fold. Vaccination with TA-CIN in
GPI-0100 also completely prevented
tumor growth after challenge with 5x10(4) HPV16-transformed TC-1
tumor cells, whereas vaccination with TA-CIN alone delayed
tumor growth. Furthermore, three monthly vaccinations with 125 microg of TA-CIN and 1000 microg
GPI-0100 were well tolerated by pigtail macaques and induced both HPV16 E6/E7-specific T cell responses and serum
antibodies that neutralized all HPV types tested.