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Cytokine Profiles and Cell Proliferation Responses to Truncated ORF2 Protein in Iranian Patients Recovered from Hepatitis E Infection

Background. The aim of this study was to evaluate hepatitis E virus (HEV) specific cellular immune responses to truncated ORF2 protein in Iranian patients recovered from HEV infection. Information about HEV-specific immune responses could be useful in finding an effective way for development of HEV...

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Autores principales: Taherkhani, Reza, Farshadpour, Fatemeh, Makvandi, Manoochehr, Rajabi Memari, Hamid, Samarbafzadeh, Ali Reza, Sharifi, Nasrin, Naeimi, Behrouz, Tajbakhsh, Saeed, Akbarzadeh, Samad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586975/
https://www.ncbi.nlm.nih.gov/pubmed/26451149
http://dx.doi.org/10.1155/2015/523560
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author Taherkhani, Reza
Farshadpour, Fatemeh
Makvandi, Manoochehr
Rajabi Memari, Hamid
Samarbafzadeh, Ali Reza
Sharifi, Nasrin
Naeimi, Behrouz
Tajbakhsh, Saeed
Akbarzadeh, Samad
author_facet Taherkhani, Reza
Farshadpour, Fatemeh
Makvandi, Manoochehr
Rajabi Memari, Hamid
Samarbafzadeh, Ali Reza
Sharifi, Nasrin
Naeimi, Behrouz
Tajbakhsh, Saeed
Akbarzadeh, Samad
author_sort Taherkhani, Reza
collection PubMed
description Background. The aim of this study was to evaluate hepatitis E virus (HEV) specific cellular immune responses to truncated ORF2 protein in Iranian patients recovered from HEV infection. Information about HEV-specific immune responses could be useful in finding an effective way for development of HEV vaccine. Methods. A truncated form of HEV ORF2 protein containing amino acids 112-608 was used to stimulate peripheral blood mononuclear cells (PBMCs) separated from HEV-recovered and control groups. Finally, the levels of four cytokines, IFN-γ ELISPOT, and cell proliferative responses following stimulation with the truncated ORF2 protein were assessed in the both groups. Results. The truncated ORF2 protein was able to induce IFN-γ ELISPOT and cell proliferation responses and to produce significant amounts of IFN-γ and IL-12 cytokines, but low amounts of IL-10 and IL-4 cytokines in vitro. These responses were significantly higher in the recovered group compared to the control group. These results indicate the antigenic nature of the truncated ORF2 protein and production of T helper type 1 cytokines. Conclusion. The truncated ORF2 protein can effectively induce significant cellular immune responsesand can be introduced as a potential vaccine candidate. However, further studies are required to evaluate this protein in vivo.
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spelling pubmed-45869752015-10-08 Cytokine Profiles and Cell Proliferation Responses to Truncated ORF2 Protein in Iranian Patients Recovered from Hepatitis E Infection Taherkhani, Reza Farshadpour, Fatemeh Makvandi, Manoochehr Rajabi Memari, Hamid Samarbafzadeh, Ali Reza Sharifi, Nasrin Naeimi, Behrouz Tajbakhsh, Saeed Akbarzadeh, Samad J Trop Med Research Article Background. The aim of this study was to evaluate hepatitis E virus (HEV) specific cellular immune responses to truncated ORF2 protein in Iranian patients recovered from HEV infection. Information about HEV-specific immune responses could be useful in finding an effective way for development of HEV vaccine. Methods. A truncated form of HEV ORF2 protein containing amino acids 112-608 was used to stimulate peripheral blood mononuclear cells (PBMCs) separated from HEV-recovered and control groups. Finally, the levels of four cytokines, IFN-γ ELISPOT, and cell proliferative responses following stimulation with the truncated ORF2 protein were assessed in the both groups. Results. The truncated ORF2 protein was able to induce IFN-γ ELISPOT and cell proliferation responses and to produce significant amounts of IFN-γ and IL-12 cytokines, but low amounts of IL-10 and IL-4 cytokines in vitro. These responses were significantly higher in the recovered group compared to the control group. These results indicate the antigenic nature of the truncated ORF2 protein and production of T helper type 1 cytokines. Conclusion. The truncated ORF2 protein can effectively induce significant cellular immune responsesand can be introduced as a potential vaccine candidate. However, further studies are required to evaluate this protein in vivo. Hindawi Publishing Corporation 2015 2015-09-15 /pmc/articles/PMC4586975/ /pubmed/26451149 http://dx.doi.org/10.1155/2015/523560 Text en Copyright © 2015 Reza Taherkhani et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Taherkhani, Reza
Farshadpour, Fatemeh
Makvandi, Manoochehr
Rajabi Memari, Hamid
Samarbafzadeh, Ali Reza
Sharifi, Nasrin
Naeimi, Behrouz
Tajbakhsh, Saeed
Akbarzadeh, Samad
Cytokine Profiles and Cell Proliferation Responses to Truncated ORF2 Protein in Iranian Patients Recovered from Hepatitis E Infection
title Cytokine Profiles and Cell Proliferation Responses to Truncated ORF2 Protein in Iranian Patients Recovered from Hepatitis E Infection
title_full Cytokine Profiles and Cell Proliferation Responses to Truncated ORF2 Protein in Iranian Patients Recovered from Hepatitis E Infection
title_fullStr Cytokine Profiles and Cell Proliferation Responses to Truncated ORF2 Protein in Iranian Patients Recovered from Hepatitis E Infection
title_full_unstemmed Cytokine Profiles and Cell Proliferation Responses to Truncated ORF2 Protein in Iranian Patients Recovered from Hepatitis E Infection
title_short Cytokine Profiles and Cell Proliferation Responses to Truncated ORF2 Protein in Iranian Patients Recovered from Hepatitis E Infection
title_sort cytokine profiles and cell proliferation responses to truncated orf2 protein in iranian patients recovered from hepatitis e infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586975/
https://www.ncbi.nlm.nih.gov/pubmed/26451149
http://dx.doi.org/10.1155/2015/523560
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