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自组装两亲性嵌段共聚物作为免疫治疗的双重递药系统。

Self-assembled amphiphilic copolymers as dual delivery system for immunotherapy.

机构信息

Aix Marseille Univ, CNRS, Institut de Chimie Radicalaire, Marseille, France.

Université Lyon 1, CNRS, UMR 5305, Biologie Tissulaire et Ingénierie Thérapeutique, IBCP, 69367 Lyon, France.

出版信息

Eur J Pharm Biopharm. 2019 Sep;142:232-239. doi: 10.1016/j.ejpb.2019.06.022. Epub 2019 Jun 20.

Abstract

Subunit vaccines using recombinant antigens appear as the privileged vaccination technology for safety reasons but still require the development of carriers/adjuvants ensuring optimal immunogenicity and efficacy. Micelles from self-assembled amphiphilic copolymers have recently emerged as highly relevant and promising candidates owing to their ease of preparation, low size (entering in lymphatic capillaries for reaching lymph nodes), size/surface tunability and chemical versatility enabling introduction of stimuli (e.g. pH) responsive features and biofunctionalization with dedicated molecules. In particular, research efforts have increasingly focused on dendritic cells (DCs) targeting and activation by co-delivering (with antigen) ligands of pattern recognition receptors (PRRs, e.g. toll-like receptors). Such strategy has appeared as one of the most effective for eliciting CD 8+ T-cell response, which is crucial in the eradication of tumors and numerous infectious diseases. In this short review, we highlight the recent advances in such micelle-based carriers in subunit vaccination and how their precise engineering can be a strong asset for guiding and controlling immune responses.

摘要

基于重组抗原的亚单位疫苗因其安全性而成为首选的疫苗技术,但仍需要开发载体/佐剂以确保最佳的免疫原性和疗效。最近,自组装两亲性共聚物形成的胶束因其易于制备、粒径小(进入淋巴管以到达淋巴结)、粒径/表面可调节性以及化学多功能性而成为极具潜力的候选物,可引入响应刺激(例如 pH)的特性并通过专用分子进行生物功能化。特别是,研究工作越来越集中在通过共递(与抗原)模式识别受体(PRR,例如 Toll 样受体)配体来靶向和激活树突状细胞(DC)上。这种策略已被证明是引发 CD8+T 细胞反应的最有效方法之一,对于消除肿瘤和许多传染病至关重要。在这篇简短的综述中,我们强调了基于胶束的载体在亚单位疫苗接种中的最新进展,以及它们的精确工程设计如何成为指导和控制免疫反应的有力手段。

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