Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; Department of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; Department of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; Department of Biomedical Research, National Jewish Health, 1400, Jackson St., Denver, CO 80206, USA.
Curr Opin Immunol. 2017 Aug;47:44-51. doi: 10.1016/j.coi.2017.06.005. Epub 2017 Jul 19.
Adjuvants have been deliberately added to vaccines since the 1920's when alum was discovered to boost antibody responses, leading to better protection. The first adjuvants were discovered by accident and were used in the safer but less immunogenic subunit vaccines, supposedly by providing an antigen depot to extend antigen presentation. Since that time, much has been discovered about how these adjuvants impact cells at the tissue site to activate innate immune responses, mobilize dendritic cells and drive adaptive immunity. New approaches to vaccine construction for infectious diseases that have so far not been well addressed by conventional vaccines often attempt to induce antibodies, polyfunctional CD4 T cells and CD8 CTLs. The discovery of pattern recognition receptors and ligands that drive desired T cell responses has led to development of novel adjuvant strategies using immunomodulatory agents to direct appropriate immune responses.
自 1920 年代发现明矾可以增强抗体反应,从而提供更好的保护以来,人们一直在疫苗中有意添加佐剂。最早的佐剂是偶然发现的,用于更安全但免疫原性较低的亚单位疫苗,据称是通过提供抗原储存库来延长抗原呈递。从那时起,人们发现了很多关于这些佐剂如何在组织部位影响细胞以激活先天免疫反应、动员树突状细胞并驱动适应性免疫的知识。针对传染病的新型疫苗构建方法,通常试图诱导抗体、多功能 CD4 T 细胞和 CD8 CTL,但传统疫苗对此尚未很好地解决。模式识别受体和配体的发现,这些受体和配体可以驱动所需的 T 细胞反应,这导致了使用免疫调节剂来指导适当免疫反应的新型佐剂策略的发展。
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