Rafiei Mehrnoosh, Chung Jin Teng, Chau Ying
Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Hong Kong, China.
Institute for Nanoscience and Nanotechnology, Sharif University of Technology, Tehran, Iran.
Front Drug Deliv. 2023 Feb 15;3:1077253. doi: 10.3389/fddev.2023.1077253. eCollection 2023.
The eye is a hard-to-treat organ due to its poor regenerative capacity and susceptibility to inflammation; as a result, it has an immune privilege mechanism. In the case of ocular degenerative disorders, chronic and uncontrolled ocular inflammations can overcome this immune response to initiate and exacerbate tissue degeneration, ultimately leading to blindness. Recent landmark discoveries on the key roles of the ocular innate immune system in regulating acute and chronic inflammations as well as tissue fibrosis and homeostasis have shed light on the value of novel treatment interventions in modulating ocular immune responses at the molecular, cellular, and tissue levels. This strategy can be attained by using therapeutics to target resident phagocytes and antigen-presenting cells, namely, microglia and dendritic cells, as well as infiltrating neutrophils and macrophages. Biomaterials are foreign materials to the host and interact with innate immune cells. To leverage such intrinsic immunomodulatory properties, biomaterials such as implants, injectable depots, and nano/micro particles can be used alone as a treatment or with different payloads as carriers in immune-related ocular disorders. This article discusses how physicochemical properties such as biodegradability, size, shape, and charge affect biomaterials' interaction with the eye's innate immune system, therefore influencing outcomes towards pro- or anti-inflammatory responses. Knowledge about the eye's immunological response is required for designing tolerogenic biomaterials including intraocular lenses, cellular scaffolds, therapeutic molecule depots, or carriers of gene therapies. The discussion presented in this review will shed light on the potential use of biomaterials to direct immune responses toward favorable treatment outcomes.
眼睛是一个难以治疗的器官,因为其再生能力差且易受炎症影响;因此,它具有免疫赦免机制。在眼部退行性疾病的情况下,慢性且不受控制的眼部炎症会克服这种免疫反应,引发并加剧组织退化,最终导致失明。最近关于眼部固有免疫系统在调节急性和慢性炎症以及组织纤维化和内环境稳态中的关键作用的重大发现,揭示了新型治疗干预措施在分子、细胞和组织水平上调节眼部免疫反应的价值。这一策略可以通过使用治疗药物来靶向驻留吞噬细胞和抗原呈递细胞,即小胶质细胞和树突状细胞,以及浸润的中性粒细胞和巨噬细胞来实现。生物材料对于宿主来说是外来物质,并与固有免疫细胞相互作用。为了利用这种内在的免疫调节特性,诸如植入物、可注射贮库以及纳米/微粒等生物材料可以单独用作治疗手段,或者与不同的负载物一起用作免疫相关眼部疾病的载体。本文讨论了诸如生物可降解性、尺寸、形状和电荷等物理化学性质如何影响生物材料与眼睛固有免疫系统的相互作用,从而影响促炎或抗炎反应的结果。设计包括人工晶状体、细胞支架、治疗分子贮库或基因治疗载体在内的耐受性生物材料需要了解眼睛的免疫反应。本综述中的讨论将阐明生物材料在引导免疫反应以实现有利治疗结果方面的潜在用途。