Department of Orthopaedic Surgery, Washington University, St. Louis, MO 63110, USA; Shriners Hospitals for Children - St. Louis, St. Louis, MO 63110, USA; Department of Biomedical Engineering, Washington University, St. Louis, MO 63110, USA; Center of Regenerative Medicine, Washington University, St. Louis, MO 63110, USA.
Department of Orthopaedic Surgery, Washington University, St. Louis, MO 63110, USA; Shriners Hospitals for Children - St. Louis, St. Louis, MO 63110, USA; Center of Regenerative Medicine, Washington University, St. Louis, MO 63110, USA.
Acta Biomater. 2021 Oct 1;133:74-86. doi: 10.1016/j.actbio.2021.03.062. Epub 2021 Apr 3.
Immunoengineering continues to revolutionize healthcare, generating new approaches for treating previously intractable diseases, particularly in regard to cancer immunotherapy. In joint diseases, such as osteoarthritis (OA) and rheumatoid arthritis (RA), biomaterials and anti-cytokine treatments have previously been at that forefront of therapeutic innovation. However, while many of the existing anti-cytokine treatments are successful for a subset of patients, these treatments can also pose severe risks, adverse events and off-target effects due to continuous delivery at high dosages or a lack of disease-specific targets. The inadequacy of these current treatments has motivated the development of new immunoengineering strategies that offer safer and more efficacious alternative therapies through the precise and controlled targeting of specific upstream immune responses, including direct and mechanistically-driven immunoengineering approaches. Advances in the understanding of the immunomodulatory pathways involved in musculoskeletal disease, in combination with the growing emphasis on personalized medicine, stress the need for carefully considering the delivery strategies and therapeutic targets when designing therapeutics to better treat RA and OA. Here, we focus on recent advances in biomaterial and cell-based immunomodulation, in combination with genetic engineering, for therapeutic applications in joint diseases. The application of immunoengineering principles to the study of joint disease will not only help to elucidate the mechanisms of disease pathogenesis but will also generate novel disease-specific therapeutics by harnessing cellular and biomaterial responses. STATEMENT OF SIGNIFICANCE: It is now apparent that joint diseases such as osteoarthritis and rheumatoid arthritis involve the immune system at both local (i.e., within the joint) and systemic levels. In this regard, targeting the immune system using both biomaterial-based or cellular approaches may generate new joint-specific treatment strategies that are well-controlled, safe, and efficacious. In this review, we focus on recent advances in immunoengineering that leverage biomaterials and/or genetically engineered cells for therapeutic applications in joint diseases. The application of such approaches, especially synergistic strategies that target multiple immunoregulatory pathways, has the potential to revolutionize our understanding, treatment, and prevention of joint diseases.
免疫工程继续彻底改变医疗保健,为治疗以前难以治疗的疾病,特别是癌症免疫疗法,提供新的方法。在联合疾病中,如骨关节炎(OA)和类风湿性关节炎(RA),生物材料和抗细胞因子治疗一直处于治疗创新的前沿。然而,尽管许多现有的抗细胞因子治疗对一部分患者有效,但这些治疗方法也可能由于高剂量的持续输送或缺乏疾病特异性靶标而带来严重的风险、不良反应和脱靶效应。这些现有治疗方法的不足促使人们开发新的免疫工程策略,通过精确和控制针对特定上游免疫反应,包括直接和机械驱动的免疫工程方法,提供更安全、更有效的替代疗法。对肌肉骨骼疾病中涉及的免疫调节途径的理解的进步,结合对个性化医学的日益重视,强调在设计治疗方法以更好地治疗 RA 和 OA 时,需要仔细考虑输送策略和治疗靶标。在这里,我们重点介绍生物材料和基于细胞的免疫调节与基因工程相结合的联合疾病治疗的最新进展。将免疫工程原理应用于关节疾病的研究不仅有助于阐明疾病发病机制的机制,还可以通过利用细胞和生物材料反应产生新的疾病特异性治疗方法。意义声明:现在很明显,骨关节炎和类风湿性关节炎等关节疾病涉及局部(即在关节内)和全身水平的免疫系统。在这方面,使用基于生物材料或细胞的方法靶向免疫系统可能会产生新的关节特异性治疗策略,这些策略是可控的、安全的和有效的。在这篇综述中,我们重点介绍了利用生物材料和/或基因工程细胞治疗关节疾病的最新免疫工程进展。这些方法的应用,特别是靶向多个免疫调节途径的协同策略,有可能彻底改变我们对关节疾病的理解、治疗和预防。