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Identification and validation of immunogenic potential of India specific HPV-16 variant constructs: In-silico & in-vivo insight to vaccine development

Cervical cancer is one of the most common gynecological cancers in the world but in India, it is the top most cancer among women. Persistent infection with high-risk human papillomaviruses (HR-HPVs) is the most important risk factor. The sequence variation(s) in the most common HR-HPV i.e. HPV type...

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Autores principales: Kumar, Anoop, Hussain, Showket, Sharma, Gagan, Mehrotra, Ravi, Gissmann, Lutz, Das, Bhudev C., Bharadwaj, Mausumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623767/
https://www.ncbi.nlm.nih.gov/pubmed/26507515
http://dx.doi.org/10.1038/srep15751
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author Kumar, Anoop
Hussain, Showket
Sharma, Gagan
Mehrotra, Ravi
Gissmann, Lutz
Das, Bhudev C.
Bharadwaj, Mausumi
author_facet Kumar, Anoop
Hussain, Showket
Sharma, Gagan
Mehrotra, Ravi
Gissmann, Lutz
Das, Bhudev C.
Bharadwaj, Mausumi
author_sort Kumar, Anoop
collection PubMed
description Cervical cancer is one of the most common gynecological cancers in the world but in India, it is the top most cancer among women. Persistent infection with high-risk human papillomaviruses (HR-HPVs) is the most important risk factor. The sequence variation(s) in the most common HR-HPV i.e. HPV type 16 leads to altered biological functions with possible clinical significance in the different geographical locations. Sixteen major variants (V1-V16) in full length L1 gene of HPV-16 were identified following analysis of 250 prospectively collected cervical cancer tissue biopsies and their effect on immunogenicity was studied. The effect of these major variations on the epitopes were predicted by in silico methods and the immunogenicity of variants and respective reference DNA vaccine constructs were evaluated by administration of prepared DNA vaccine constructs in female BALB/c mice to evaluate antibody titer. In the present study, L500F (V16) variation showed a significant ~2.7 fold (p < 0.002) increase in antibody titer, whereas T379P (V8) showed ~0.4 fold (p < 0.328) decrease after final injection. These results showed a promising roadmap for the development of DNA based vaccine and for the generation of effective response, though there is a need to study more prevalent variants of HPV in the Indian population.
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spelling pubmed-46237672015-11-03 Identification and validation of immunogenic potential of India specific HPV-16 variant constructs: In-silico & in-vivo insight to vaccine development Kumar, Anoop Hussain, Showket Sharma, Gagan Mehrotra, Ravi Gissmann, Lutz Das, Bhudev C. Bharadwaj, Mausumi Sci Rep Article Cervical cancer is one of the most common gynecological cancers in the world but in India, it is the top most cancer among women. Persistent infection with high-risk human papillomaviruses (HR-HPVs) is the most important risk factor. The sequence variation(s) in the most common HR-HPV i.e. HPV type 16 leads to altered biological functions with possible clinical significance in the different geographical locations. Sixteen major variants (V1-V16) in full length L1 gene of HPV-16 were identified following analysis of 250 prospectively collected cervical cancer tissue biopsies and their effect on immunogenicity was studied. The effect of these major variations on the epitopes were predicted by in silico methods and the immunogenicity of variants and respective reference DNA vaccine constructs were evaluated by administration of prepared DNA vaccine constructs in female BALB/c mice to evaluate antibody titer. In the present study, L500F (V16) variation showed a significant ~2.7 fold (p < 0.002) increase in antibody titer, whereas T379P (V8) showed ~0.4 fold (p < 0.328) decrease after final injection. These results showed a promising roadmap for the development of DNA based vaccine and for the generation of effective response, though there is a need to study more prevalent variants of HPV in the Indian population. Nature Publishing Group 2015-10-28 /pmc/articles/PMC4623767/ /pubmed/26507515 http://dx.doi.org/10.1038/srep15751 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kumar, Anoop
Hussain, Showket
Sharma, Gagan
Mehrotra, Ravi
Gissmann, Lutz
Das, Bhudev C.
Bharadwaj, Mausumi
Identification and validation of immunogenic potential of India specific HPV-16 variant constructs: In-silico & in-vivo insight to vaccine development
title Identification and validation of immunogenic potential of India specific HPV-16 variant constructs: In-silico & in-vivo insight to vaccine development
title_full Identification and validation of immunogenic potential of India specific HPV-16 variant constructs: In-silico & in-vivo insight to vaccine development
title_fullStr Identification and validation of immunogenic potential of India specific HPV-16 variant constructs: In-silico & in-vivo insight to vaccine development
title_full_unstemmed Identification and validation of immunogenic potential of India specific HPV-16 variant constructs: In-silico & in-vivo insight to vaccine development
title_short Identification and validation of immunogenic potential of India specific HPV-16 variant constructs: In-silico & in-vivo insight to vaccine development
title_sort identification and validation of immunogenic potential of india specific hpv-16 variant constructs: in-silico & in-vivo insight to vaccine development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623767/
https://www.ncbi.nlm.nih.gov/pubmed/26507515
http://dx.doi.org/10.1038/srep15751
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