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增强T细胞反应的当前疫苗平台

Current Vaccine Platforms in Enhancing T-Cell Response.

作者信息

Ura Takehiro, Takeuchi Masaki, Kawagoe Tatsukata, Mizuki Nobuhisa, Okuda Kenji, Shimada Masaru

机构信息

Department of Ophthalmology and Visual Science, Graduate School of Medicine, Yokohama City University, Yokohama 236-0004, Japan.

Department of Ophthalmology and Visual Science, School of Medicine, St. Marianna University, Kawazaki 216-8511, Japan.

出版信息

Vaccines (Basel). 2022 Aug 21;10(8):1367. doi: 10.3390/vaccines10081367.

DOI:10.3390/vaccines10081367
PMID:36016254
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9413345/
Abstract

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.

摘要

T细胞介导的免疫诱导在疫苗开发中至关重要。最有效的疫苗可能会同时引发细胞免疫和体液免疫反应。疫苗的功效取决于抗原呈递细胞激活的T细胞。T细胞在疫苗的持续时间和交叉反应性方面也起着关键作用。此外,预先存在的T细胞免疫与传染病严重程度的降低有关。许多技术和递送平台已被设计用于诱导T细胞介导的疫苗免疫。通过控制动力学和靶向递送可增强疫苗的免疫原性。病毒载体是有吸引力的工具,能够使外源抗原在细胞内表达并诱导强大的免疫反应。然而,考虑到现有的抗载体免疫会损害疫苗功效,选择合适的病毒载体很有必要。mRNA疫苗具有快速和低成本生产的优势,并且首次作为COVID-19疫苗被批准用于临床。mRNA修饰和纳米材料封装有助于解决mRNA的不稳定性和翻译效率问题。本综述基于疫苗技术和递送平台总结了针对各种传染病的疫苗的T细胞反应,并讨论了这些前沿平台的未来发展方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d8f/9413345/912fd5ce0e45/vaccines-10-01367-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d8f/9413345/912fd5ce0e45/vaccines-10-01367-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d8f/9413345/912fd5ce0e45/vaccines-10-01367-g001.jpg

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