Ackun-Farmmer Marian A, Jewell Christopher M
Fischell Department of Bioengineering, University of Maryland, College Park, MD, 20742, USA.
US Department of Veterans Affairs, VA Maryland Health Care System, Baltimore, MD, 21201, USA.
Adv Nanobiomed Res. 2023 Mar;3(3). doi: 10.1002/anbr.202200135. Epub 2023 Jan 29.
Disease modifying drugs and biologics used to treat autoimmune diseases, although promising, are non-curative. As the field moves towards development of new approaches to treat autoimmune disease, antigen-specific therapies immunotherapies (ASITs) have emerged. Despite clinical approval of ASITs for allergies, clinical trials using soluble ASITs for autoimmunity have been largely unsuccessful. A major effort to address this shortcoming is the use of biomaterials to harness the features unique to specific delivery routes. This review focuses on biomaterials being developed for delivery route-specific strategies to induce antigen-specific responses in autoimmune diseases such as multiple sclerosis, type 1 diabetes, rheumatoid arthritis, and celiac disease. We first discuss the delivery strategies used in ongoing and completed clinical trials in autoimmune ASITs. Next, we highlight pre-clinical biomaterial approaches from the most recent 3 years in the context of these same delivery route considerations. Lastly, we provide discussion on the gaps remaining in biomaterials development and comment on the need to consider delivery routes in the process of designing biomaterials for ASITs.
用于治疗自身免疫性疾病的疾病修正药物和生物制剂虽然前景广阔,但无法治愈疾病。随着该领域朝着开发治疗自身免疫性疾病的新方法发展,抗原特异性疗法即免疫疗法(ASITs)应运而生。尽管ASITs已获临床批准用于治疗过敏,但使用可溶性ASITs治疗自身免疫性疾病的临床试验大多未取得成功。解决这一缺陷的一项主要努力是利用生物材料来发挥特定给药途径所独有的特性。本综述重点关注正在开发的用于特定给药途径策略的生物材料,以在诸如多发性硬化症、1型糖尿病、类风湿性关节炎和乳糜泻等自身免疫性疾病中诱导抗原特异性反应。我们首先讨论在自身免疫性ASITs的正在进行和已完成的临床试验中所使用的给药策略。接下来,我们在这些相同的给药途径考量背景下,突出最近3年的临床前生物材料方法。最后,我们讨论生物材料开发中仍然存在的差距,并评论在为ASITs设计生物材料的过程中考虑给药途径的必要性。