Department of Health Sciences, Università del Piemonte Orientale, 28100 Novara, Italy.
Interdisciplinary Research Center of Autoimmune Diseases, Università del Piemonte Orientale, 28100 Novara, Italy.
Int J Mol Sci. 2019 Jan 8;20(1):204. doi: 10.3390/ijms20010204.
Tolerogenic vaccines are aimed at inhibiting antigen-specific immune responses. Antigen-loaded nanoparticles (NPs) have been recently emerged as ideal tools for tolerogenic vaccination because their composition, size, and capability of loading immunomodulatory molecules can be readily exploited to induce peripheral tolerance. Among polymeric NPs, poly(lactic-co-glycolic acid) (PLGA) NPs have the advantage of currently holding approval for several applications in drug delivery, diagnostics, and other clinical uses by the Food and Drug Administration (FDA). PLGA-NPs are non-toxic and display excellent biocompatibility and biodegradability properties. Moreover, surface functionalization may improve their interaction with biological materials, thereby optimizing targeting and performance. PLGA-NPs are the most extensively studied in pre-clinical model in the field of tolerogenic vaccination. Thus, this review describes their potential applications in the treatment of autoimmune diseases.
耐受原疫苗旨在抑制抗原特异性免疫反应。负载抗原的纳米颗粒(NPs)最近已成为耐受原疫苗接种的理想工具,因为其组成、大小和负载免疫调节分子的能力可以被充分利用来诱导外周耐受。在聚合物 NPs 中,聚(乳酸-共-乙醇酸)(PLGA) NPs 的优势在于目前已获得美国食品和药物管理局(FDA)批准,可用于药物输送、诊断和其他临床用途。PLGA-NPs 无毒,具有优异的生物相容性和生物降解性。此外,表面功能化可以改善它们与生物材料的相互作用,从而优化靶向性和性能。PLGA-NPs 是耐受原疫苗接种领域中在临床前模型中研究最多的。因此,本综述描述了它们在治疗自身免疫性疾病中的潜在应用。