Nanoparticle-neutrophils interactions for autoimmune regulation

IF 15.2 1区 医学 Q1 PHARMACOLOGY & PHARMACY Advanced drug delivery reviews Pub Date : 2024-04-23 DOI:10.1016/j.addr.2024.115316
Daniel Kupor , Michael L. Felder , Shivanie Kodikalla , Xueqi Chu , Omolola Eniola-Adefeso
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Abstract

Neutrophils play an essential role as ‘first responders’ in the immune response, necessitating many immune-modulating capabilities. Chronic, unresolved inflammation is heavily implicated in the progression and tissue-degrading effects of autoimmune disease. Neutrophils modulate disease pathogenesis by interacting with the inflammatory and autoreactive cells through effector functions, including signaling, degranulation, and neutrophil extracellular traps (NETs) release. Since the current gold standard systemic glucocorticoid administration has many drawbacks and side effects, targeting neutrophils in autoimmunity provides a new approach to developing therapeutics. Nanoparticles enable targeting of specific cell types and controlled release of a loaded drug cargo. Thus, leveraging nanoparticle properties and interactions with neutrophils provides an exciting new direction toward novel therapies for autoimmune diseases. Additionally, recent work has utilized neutrophil properties to design novel targeted particles for delivery into previously inaccessible areas. Here, we outline nanoparticle-based strategies to modulate neutrophil activity in autoimmunity, including various nanoparticle formulations and neutrophil-derived targeting.

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纳米粒子与中性粒细胞相互作用,促进自身免疫调节
中性粒细胞在免疫反应中扮演着 "第一反应者 "的重要角色,需要许多免疫调节能力。慢性、未解决的炎症与自身免疫性疾病的发展和组织退化效应有很大关系。中性粒细胞通过信号传导、脱颗粒和中性粒细胞胞外捕获物(NETs)释放等效应功能与炎症细胞和自体反应细胞相互作用,从而调节疾病的发病机制。由于目前金标准的全身性糖皮质激素用药存在许多缺点和副作用,因此针对自身免疫中的中性粒细胞开发治疗药物提供了一种新方法。纳米颗粒可靶向特定细胞类型并控制药物的释放。因此,利用纳米粒子的特性以及与中性粒细胞的相互作用,为自身免疫疾病的新型疗法提供了一个令人兴奋的新方向。此外,最近的研究还利用中性粒细胞的特性设计了新型靶向颗粒,可将药物输送到以前无法进入的区域。在此,我们概述了在自身免疫疾病中调节中性粒细胞活性的基于纳米颗粒的策略,包括各种纳米颗粒配方和中性粒细胞衍生靶向。
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来源期刊
CiteScore
28.10
自引率
5.00%
发文量
294
审稿时长
15.1 weeks
期刊介绍: The aim of the Journal is to provide a forum for the critical analysis of advanced drug and gene delivery systems and their applications in human and veterinary medicine. The Journal has a broad scope, covering the key issues for effective drug and gene delivery, from administration to site-specific delivery. In general, the Journal publishes review articles in a Theme Issue format. Each Theme Issue provides a comprehensive and critical examination of current and emerging research on the design and development of advanced drug and gene delivery systems and their application to experimental and clinical therapeutics. The goal is to illustrate the pivotal role of a multidisciplinary approach to modern drug delivery, encompassing the application of sound biological and physicochemical principles to the engineering of drug delivery systems to meet the therapeutic need at hand. Importantly the Editorial Team of ADDR asks that the authors effectively window the extensive volume of literature, pick the important contributions and explain their importance, produce a forward looking identification of the challenges facing the field and produce a Conclusions section with expert recommendations to address the issues.
期刊最新文献
Editorial Board Preface: RNA delivery technologies: From concept toward the clinic Delivery and kinetics of immersion optical clearing agents in tissues: Optical imaging from ex vivo to in vivo Extracellular vesicles versus lipid nanoparticles for the delivery of nucleic acids Corrigendum to “Editorial: Advanced strategies to bridge the gap between inflammation and tissue regeneration” [Adv. Drug Deliv. Rev. 209 (2024) 115328]
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