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Human papillomavirus type 16 L2-E7-E6 fusion protein (HPV16 L2-E7-E6 fusion protein)

Target
HPV16 L2-E7-E6 fusion protein
Molecular classification
Other (engineered fusion protein), Viral antigen (composed of viral structural and non-structural proteins), Vaccine antigen
01

Overview

The human papillomavirus type 16 L2-E7-E6 fusion protein, also known as TA-CIN, is a recombinant protein vaccine candidate that fuses three HPV16 antigens: L2 (minor capsid protein), E6, and E7 (oncoproteins involved in cell transformation and viral persistence). The L2 region enables the induction of broadly cross-neutralizing antibodies against HPV, while the E6 and E7 regions serve as targets for T-cell-mediated responses, providing both prophylactic and therapeutic potential. This fusion protein is not naturally occurring but is engineered to maximize immunogenicity for both the prevention and treatment of HPV16-associated cancers, especially cervical and other anogenital cancers. Studies in mice, macaques, and humans show induction of both antibody and T cell responses, cross-protection against multiple HPV genotypes, and potential to block infection and eliminate HPV-transformed cells. Safety and tolerability in early-phase clinical trials are promising, but further validation is necessary for clinical use.

Other names
TA-CINHPV16 L2E7E6 fusion proteinHPV16 L2-E6-E7 fusion protein
02

Mechanism of action

Induction of virus-neutralizing antibodies (against L2 domain) Induction of cytotoxic T cell responses (against E6 and E7 oncoproteins) Combined prophylactic and therapeutic effect: prevention of new infection and clearance of infected or transformed cells

03

Biological functions

Stimulates humoral immune response (L2 component induces neutralizing antibodies)Stimulates cell-mediated immune response (E6/E7 components induce T cell responses)Induces both prophylactic and therapeutic immunity against HPV16 and related HPV types
04

Disease associations

Infection (prevention of HPV infection)Cancer (immunotherapy of HPV-driven malignancies such as cervical cancer)
05

Safety considerations

Phase I studies report good tolerability in humans and animal modelsNo serious adverse events noted in clinical trials; however, longer-term and larger studies needed for full safety assessment
06

Interacting drugs

TA-CIN

3 more in the full profile.

07

Biomarkers

Titers of neutralizing antibodies to L2 or HPV16T cell responses to E6/E7 antigens (measured by IFN-γ ELISPOT or similar assays)

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