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Promising Cytomegalovirus-Based Vaccine Vector Induces Robust CD8(+) T-Cell Response

Vaccination has had great success in combating diseases, especially infectious diseases. However, traditional vaccination strategies are ineffective for several life-threatening diseases, including acquired immunodeficiency syndrome (AIDS), tuberculosis, malaria, and cancer. Viral vaccine vectors re...

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Detalles Bibliográficos
Autores principales: Liu, Jian, Jaijyan, Dabbu Kumar, Tang, Qiyi, Zhu, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770317/
https://www.ncbi.nlm.nih.gov/pubmed/31510028
http://dx.doi.org/10.3390/ijms20184457
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author Liu, Jian
Jaijyan, Dabbu Kumar
Tang, Qiyi
Zhu, Hua
author_facet Liu, Jian
Jaijyan, Dabbu Kumar
Tang, Qiyi
Zhu, Hua
author_sort Liu, Jian
collection PubMed
description Vaccination has had great success in combating diseases, especially infectious diseases. However, traditional vaccination strategies are ineffective for several life-threatening diseases, including acquired immunodeficiency syndrome (AIDS), tuberculosis, malaria, and cancer. Viral vaccine vectors represent a promising strategy because they can efficiently deliver foreign genes and enhance antigen presentation in vivo. However, several limitations, including pre-existing immunity and packaging capacity, block the application of viral vectors. Cytomegalovirus (CMV) has been demonstrated as a new type of viral vector with additional advantages. CMV could systematically elicit and maintain high frequencies of effector memory T cells through the “memory inflation” mechanism. Studies have shown that CMV can be genetically modified to induce distinct patterns of CD8(+) T-cell responses, while some unconventional CD8(+) T-cell responses are rarely induced through conventional vaccine strategies. CMV has been used as a vaccine vector to deliver many disease-specific antigens, and the efficacy of these vaccines was tested in different animal models. Promising results demonstrated that the robust and unconventional T-cell responses elicited by the CMV-based vaccine vector are essential to control these diseases. These accumulated data and evidence strongly suggest that a CMV-based vaccine vector represents a promising approach to develop novel prophylactic and therapeutic vaccines against some epidemic pathogens and tumors.
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spelling pubmed-67703172019-10-30 Promising Cytomegalovirus-Based Vaccine Vector Induces Robust CD8(+) T-Cell Response Liu, Jian Jaijyan, Dabbu Kumar Tang, Qiyi Zhu, Hua Int J Mol Sci Review Vaccination has had great success in combating diseases, especially infectious diseases. However, traditional vaccination strategies are ineffective for several life-threatening diseases, including acquired immunodeficiency syndrome (AIDS), tuberculosis, malaria, and cancer. Viral vaccine vectors represent a promising strategy because they can efficiently deliver foreign genes and enhance antigen presentation in vivo. However, several limitations, including pre-existing immunity and packaging capacity, block the application of viral vectors. Cytomegalovirus (CMV) has been demonstrated as a new type of viral vector with additional advantages. CMV could systematically elicit and maintain high frequencies of effector memory T cells through the “memory inflation” mechanism. Studies have shown that CMV can be genetically modified to induce distinct patterns of CD8(+) T-cell responses, while some unconventional CD8(+) T-cell responses are rarely induced through conventional vaccine strategies. CMV has been used as a vaccine vector to deliver many disease-specific antigens, and the efficacy of these vaccines was tested in different animal models. Promising results demonstrated that the robust and unconventional T-cell responses elicited by the CMV-based vaccine vector are essential to control these diseases. These accumulated data and evidence strongly suggest that a CMV-based vaccine vector represents a promising approach to develop novel prophylactic and therapeutic vaccines against some epidemic pathogens and tumors. MDPI 2019-09-10 /pmc/articles/PMC6770317/ /pubmed/31510028 http://dx.doi.org/10.3390/ijms20184457 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Liu, Jian
Jaijyan, Dabbu Kumar
Tang, Qiyi
Zhu, Hua
Promising Cytomegalovirus-Based Vaccine Vector Induces Robust CD8(+) T-Cell Response
title Promising Cytomegalovirus-Based Vaccine Vector Induces Robust CD8(+) T-Cell Response
title_full Promising Cytomegalovirus-Based Vaccine Vector Induces Robust CD8(+) T-Cell Response
title_fullStr Promising Cytomegalovirus-Based Vaccine Vector Induces Robust CD8(+) T-Cell Response
title_full_unstemmed Promising Cytomegalovirus-Based Vaccine Vector Induces Robust CD8(+) T-Cell Response
title_short Promising Cytomegalovirus-Based Vaccine Vector Induces Robust CD8(+) T-Cell Response
title_sort promising cytomegalovirus-based vaccine vector induces robust cd8(+) t-cell response
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770317/
https://www.ncbi.nlm.nih.gov/pubmed/31510028
http://dx.doi.org/10.3390/ijms20184457
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