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佐剂增强树突状细胞的交叉呈递:更有效的疫苗的关键?

Adjuvants Enhancing Cross-Presentation by Dendritic Cells: The Key to More Effective Vaccines?

机构信息

Radiotherapy and OncoImmunology Laboratory, Department of Radiation Oncology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands.

Department of Anesthesiology, Pain and Palliative Medicine, Radboud University Medical Center, Nijmegen, Netherlands.

出版信息

Front Immunol. 2018 Dec 13;9:2874. doi: 10.3389/fimmu.2018.02874. eCollection 2018.

DOI:10.3389/fimmu.2018.02874
PMID:30619259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6300500/
Abstract

Over the last decades, vaccine development has advanced significantly in pursuing higher safety with less side effects. However, this is often accompanied by a reduction in vaccine immunogenicity and an increased dependency on adjuvants to enhance vaccine potency. Especially for diseases like cancer, it is important that therapeutic vaccines contain adjuvants that promote strong T cell responses. An important mode of action for such adjuvants is to prolong antigen exposure to dendritic cells (DCs) and to induce their maturation. These mature DCs are extremely effective in the activation of antigen-specific T cells, which is a pre-requisite for induction of potent and long-lasting cellular immunity. For the activation of CD8 cytotoxic T cell responses, however, the exogenous vaccine antigens need to gain access to the endogenous MHCI presentation pathway of DCs, a process referred to as antigen cross-presentation. In this review, we will focus on recent insights in clinically relevant vaccine adjuvants that impact DC cross-presentation efficiency, including aluminum-based nanoparticles, saponin-based adjuvants, and Toll-like receptor ligands. Furthermore, we will discuss the importance of adjuvant combinations and highlight new developments in cancer vaccines. Understanding the mode of action of adjuvants in general and on antigen cross-presentation in DCs in particular will be important for the design of novel adjuvants as part of vaccines able to induce strong cellular immunity.

摘要

在过去的几十年中,疫苗的开发在追求更高的安全性和更少的副作用方面取得了显著进展。然而,这通常伴随着疫苗免疫原性的降低和对佐剂的依赖增加,以增强疫苗效力。特别是对于癌症等疾病,治疗性疫苗中含有佐剂来促进强烈的 T 细胞反应非常重要。此类佐剂的一个重要作用模式是延长抗原暴露于树突状细胞(DC)的时间,并诱导其成熟。这些成熟的 DC 非常有效地激活抗原特异性 T 细胞,这是诱导有效和持久细胞免疫的前提。然而,对于 CD8 细胞毒性 T 细胞反应的激活,外源性疫苗抗原需要进入 DC 的内源性 MHC I 呈递途径,这一过程称为抗原交叉呈递。在这篇综述中,我们将重点介绍影响 DC 交叉呈递效率的临床相关疫苗佐剂的最新进展,包括基于铝的纳米粒子、皂苷佐剂和 Toll 样受体配体。此外,我们还将讨论佐剂组合的重要性,并强调癌症疫苗的新进展。了解佐剂的作用模式以及佐剂对 DC 中抗原交叉呈递的影响对于设计能够诱导强烈细胞免疫的新型佐剂作为疫苗的一部分非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c038/6300500/88c2ff78afd5/fimmu-09-02874-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c038/6300500/88c2ff78afd5/fimmu-09-02874-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c038/6300500/88c2ff78afd5/fimmu-09-02874-g0001.jpg

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