In silico accelerated identification of structurally conserved CD8+ and CD4+ T-cell epitopes in high-risk HPV types
Primary approach to prevent cervical cancer includes the development of human papillomavirus (HPV) vaccines. Currently available HPV vaccines (Gardasil and Cervarix) predominantly consider HPV16 and HPV18 strains. However, due to ignorance of the other high-risk strains aside from HPV16 and HPV18 du...
Saved in:
| Main Authors: | , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
24 May 2012
|
| In: |
Infection, genetics and evolution
Year: 2012, Volume: 12, Issue: 7, Pages: 1513-1518 |
| ISSN: | 1567-7257 |
| DOI: | 10.1016/j.meegid.2012.02.022 |
| Online Access: | Verlag, Volltext: http://dx.doi.org/10.1016/j.meegid.2012.02.022 Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S1567134812001463 
|
| Author Notes: | Shishir K. Gupta, Mugdha Srivastava, Bashir A. Akhoon, Shailendra K. Gupta, Niels Grabe |
| Summary: | Primary approach to prevent cervical cancer includes the development of human papillomavirus (HPV) vaccines. Currently available HPV vaccines (Gardasil and Cervarix) predominantly consider HPV16 and HPV18 strains. However, due to ignorance of the other high-risk strains aside from HPV16 and HPV18 during vaccine development, the critical need is to synthesize a vaccine with possible protection against all the high-risk HPV types. One feasible approach is to design a vaccine containing conserved immunogenic peptides that represent the genotypic diversity of all the current and future high-risk HPV types. While the epitopes derived from sequentially conserved regions may undergo mutations, it is worthwhile to explore the structurally conserved regions as a new dimension for epitope prediction. In the present study, 81 structurally conserved peptides were predicted to have immune relevance as T-cell epitopes of all the reported high-risk HPV proteins studied. A small dataset of three epitopes was also recognized as potential vaccine candidates generating both CD8+ and CD4+ responses. |
|---|---|
| Item Description: | Gesehen am 16.08.2018 |
| Physical Description: | Online Resource |
| ISSN: | 1567-7257 |
| DOI: | 10.1016/j.meegid.2012.02.022 |