A novel HPV prophylactic peptide vaccine, designed by immunoinformatics and structural vaccinology approaches

Manica Negahdaripour1, Mahboobeh Eslami2, Navid Nezafat2

  • 1Department of Pharmaceutical Biotechnology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran; Pharmaceutical Sciences Research Center, Shiraz University of Medical Science, Shiraz, Iran.

Insights

A novel peptide vaccine was computationally designed for human papillomavirus (HPV) prophylaxis, targeting cervical cancer. This vaccine candidate incorporates L2 protein epitopes and immune-stimulating adjuvants to elicit robust humoral and cellular responses.

Area of Science:

  • Immunology
  • Vaccinology
  • Computational Biology

Background:

  • Cervical cancer, caused by human papillomavirus (HPV), is a significant global health concern for women.
  • Existing HPV vaccines face challenges including cost and limited type coverage, necessitating new prophylactic vaccine development.
  • Epitope-based vaccines, while promising, often exhibit low immunogenicity, a hurdle that adjuvants may address.

Purpose of the Study:

  • To design a novel peptide vaccine candidate for human papillomavirus (HPV) prophylaxis against cervical cancer using immunoinformatics and computational approaches.
  • To enhance vaccine immunogenicity by incorporating immunodominant L2 epitopes and potent immune-stimulating adjuvants.

Main Methods:

  • Utilized immunoinformatics and computational tools to select and assemble HPV 16 L2 epitopes and universal T-helper epitopes.
  • Integrated TLR agonists (Flagellin, TLR4 agonist) and PADRE/TpD to enhance immune response induction.
  • Evaluated physicochemical, structural, and immunological properties; performed molecular modeling, refinement, validation, docking, and molecular dynamics studies.

Main Results:

  • A novel peptide construct was designed by linking HPV 16 L2 epitopes (aa 10-36, 65-89) with adjuvants like Flagellin and universal T-helper epitopes.
  • Computational analyses confirmed favorable physicochemical and structural properties, including a stable 3D structure.
  • Molecular docking and dynamics simulations indicated stable interactions between the designed vaccine and TLR5.

Conclusions:

  • A potential vaccine candidate for HPV prophylaxis was successfully designed with promising immunological and physicochemical characteristics.
  • The designed vaccine is anticipated to induce both humoral and cellular immune responses crucial for protection against HPV infection and cervical cancer.