Montaño Javier, Garnica Josep, Santamaria Pere
Institut D'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, 08036, Spain.
Institut D'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, 08036, Spain; Julia McFarlane Diabetes Research Centre (JMDRC) and Department of Microbiology, Immunology and Infectious Diseases, Snyder Institute for Chronic Diseases and Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Alberta, T2N 4N1, Canada.
Semin Immunol. 2021 Aug;56:101535. doi: 10.1016/j.smim.2021.101535. Epub 2021 Dec 27.
Autoimmune diseases, caused by cellularly and molecularly complex immune responses against self-antigens, are largely treated with broad-acting, non-disease-specific anti-inflammatory drugs. These compounds can attenuate autoimmune inflammation, but tend to impair normal immunity against infection and cancer, cannot restore normal immune homeostasis and are not curative. Nanoparticle (NP)- and microparticle (MP)-based delivery of immunotherapeutic agents affords a unique opportunity to not only increase the specificity and potency of broad-acting immunomodulators, but also to elicit the formation of organ-specific immunoregulatory cell networks capable of inducing bystander immunoregulation. Here, we review the various NP/MP-based strategies that have so far been tested in models of experimental and/or spontaneous autoimmunity, with a focus on mechanisms of action.
自身免疫性疾病是由针对自身抗原的细胞和分子复杂免疫反应引起的,目前主要使用作用广泛、非疾病特异性的抗炎药物进行治疗。这些化合物可以减轻自身免疫性炎症,但往往会损害针对感染和癌症的正常免疫力,无法恢复正常的免疫稳态,也无法治愈疾病。基于纳米颗粒(NP)和微粒(MP)的免疫治疗药物递送提供了一个独特的机会,不仅可以提高作用广泛的免疫调节剂的特异性和效力,还可以引发能够诱导旁观者免疫调节的器官特异性免疫调节细胞网络的形成。在这里,我们综述了迄今为止在实验性和/或自发性自身免疫模型中测试的各种基于NP/MP的策略,重点关注其作用机制。