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Abstract
Aim:
Oncogenic
human papillomaviruses (HPV) cause various types of cancer, including
cervical cancer. The main protein of HPV is capsid, targeted in many vaccine
attempts. However, these vaccines do not cover enough high-risk HPV
serotypes. Therefore, a low-cost potential HPV vaccine to protect against all
serovars of the α-papillomaviruses family would be promising in the future.
Our study aimed to develop a therapeutic epitope vaccine for HPV using
bioinformatics methods.
Methodology:
Bioinformatics
approach was followed to analyze and identify potential T-cell and B-cell
dominant epitopes of HPV-66 L1 major capsid protein. Additionally, various
aspects of this protein were examined, including its physico-chemical
properties, and secondary and tertiary structures. These analyses helped us
to design an effective HPV infection therapeutic vaccine.
Results:
The
findings revealed that the L1 major capsid protein was unstable and
hydrophilic. The secondary structure of this protein composed 39% α- helices,
17.97% β sheets and 31.80% loops. Our study demonstrated 19 dominant epitopes
of HPV-66 L1 major capsid protein including 5 B-cell epitopes and 14 T-cell
epitopes (10 HTL epitopes, and 4 CTL epitopes) for a novel vaccine candidate.
Interpretation:
This
study provides a comprehensive biological information about the HPV-66 L1
major capsid protein, which will serve as a theoretical foundation for
developing a multi-epitope vaccine against HPV infection.
Key
words: B-cell
epitope, Cervical Cancer, Human papillomavirus, HPV66 L1 major capsid
protein, T-cell epitope
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