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Current Vaccine Platforms in Enhancing T-Cell Response

The induction of T cell-mediated immunity is crucial in vaccine development. The most effective vaccine is likely to employ both cellular and humoral immune responses. The efficacy of a vaccine depends on T cells activated by antigen-presenting cells. T cells also play a critical role in the duratio...

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Autores principales: Ura, Takehiro, Takeuchi, Masaki, Kawagoe, Tatsukata, Mizuki, Nobuhisa, Okuda, Kenji, Shimada, Masaru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413345/
https://www.ncbi.nlm.nih.gov/pubmed/36016254
http://dx.doi.org/10.3390/vaccines10081367
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author Ura, Takehiro
Takeuchi, Masaki
Kawagoe, Tatsukata
Mizuki, Nobuhisa
Okuda, Kenji
Shimada, Masaru
author_facet Ura, Takehiro
Takeuchi, Masaki
Kawagoe, Tatsukata
Mizuki, Nobuhisa
Okuda, Kenji
Shimada, Masaru
author_sort Ura, Takehiro
collection PubMed
description The induction of T cell-mediated immunity is crucial in vaccine development. The most effective vaccine is likely to employ both cellular and humoral immune responses. The efficacy of a vaccine depends on T cells activated by antigen-presenting cells. T cells also play a critical role in the duration and cross-reactivity of vaccines. Moreover, pre-existing T-cell immunity is associated with a decreased severity of infectious diseases. Many technical and delivery platforms have been designed to induce T cell-mediated vaccine immunity. The immunogenicity of vaccines is enhanced by controlling the kinetics and targeted delivery. Viral vectors are attractive tools that enable the intracellular expression of foreign antigens and induce robust immunity. However, it is necessary to select an appropriate viral vector considering the existing anti-vector immunity that impairs vaccine efficacy. mRNA vaccines have the advantage of rapid and low-cost manufacturing and have been approved for clinical use as COVID-19 vaccines for the first time. mRNA modification and nanomaterial encapsulation can help address mRNA instability and translation efficacy. This review summarizes the T cell responses of vaccines against various infectious diseases based on vaccine technologies and delivery platforms and discusses the future directions of these cutting-edge platforms.
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spelling pubmed-94133452022-08-27 Current Vaccine Platforms in Enhancing T-Cell Response Ura, Takehiro Takeuchi, Masaki Kawagoe, Tatsukata Mizuki, Nobuhisa Okuda, Kenji Shimada, Masaru Vaccines (Basel) Review The induction of T cell-mediated immunity is crucial in vaccine development. The most effective vaccine is likely to employ both cellular and humoral immune responses. The efficacy of a vaccine depends on T cells activated by antigen-presenting cells. T cells also play a critical role in the duration and cross-reactivity of vaccines. Moreover, pre-existing T-cell immunity is associated with a decreased severity of infectious diseases. Many technical and delivery platforms have been designed to induce T cell-mediated vaccine immunity. The immunogenicity of vaccines is enhanced by controlling the kinetics and targeted delivery. Viral vectors are attractive tools that enable the intracellular expression of foreign antigens and induce robust immunity. However, it is necessary to select an appropriate viral vector considering the existing anti-vector immunity that impairs vaccine efficacy. mRNA vaccines have the advantage of rapid and low-cost manufacturing and have been approved for clinical use as COVID-19 vaccines for the first time. mRNA modification and nanomaterial encapsulation can help address mRNA instability and translation efficacy. This review summarizes the T cell responses of vaccines against various infectious diseases based on vaccine technologies and delivery platforms and discusses the future directions of these cutting-edge platforms. MDPI 2022-08-21 /pmc/articles/PMC9413345/ /pubmed/36016254 http://dx.doi.org/10.3390/vaccines10081367 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ura, Takehiro
Takeuchi, Masaki
Kawagoe, Tatsukata
Mizuki, Nobuhisa
Okuda, Kenji
Shimada, Masaru
Current Vaccine Platforms in Enhancing T-Cell Response
title Current Vaccine Platforms in Enhancing T-Cell Response
title_full Current Vaccine Platforms in Enhancing T-Cell Response
title_fullStr Current Vaccine Platforms in Enhancing T-Cell Response
title_full_unstemmed Current Vaccine Platforms in Enhancing T-Cell Response
title_short Current Vaccine Platforms in Enhancing T-Cell Response
title_sort current vaccine platforms in enhancing t-cell response
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413345/
https://www.ncbi.nlm.nih.gov/pubmed/36016254
http://dx.doi.org/10.3390/vaccines10081367
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