Tu Zhaoxu, Zhong Yiling, Hu Hanze, Shao Dan, Haag Rainer, Schirner Michael, Lee Jaewoo, Sullenger Bruce, Leong Kam W
School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, China.
Department of Biomedical Engineering, Columbia University, New York, NY USA.
Nat Rev Mater. 2022;7(7):557-574. doi: 10.1038/s41578-022-00426-z. Epub 2022 Feb 28.
Inflammation plays an important role in the response to danger signals arising from damage to our body and in restoring homeostasis. Dysregulated inflammatory responses occur in many diseases, including cancer, sepsis and autoimmunity. The efficacy of anti-inflammatory drugs, developed for the treatment of dysregulated inflammation, can be potentiated using biomaterials, by improving the bioavailability of drugs and by reducing side effects. In this Review, we first outline key elements and stages of the inflammatory environment and then discuss the design of biomaterials for different anti-inflammatory therapeutic strategies. Biomaterials can be engineered to scavenge danger signals, such as reactive oxygen and nitrogen species and cell-free DNA, in the early stages of inflammation. Materials can also be designed to prevent adhesive interactions of leukocytes and endothelial cells that initiate inflammatory responses. Furthermore, nanoscale platforms can deliver anti-inflammatory agents to inflammation sites. We conclude by discussing the challenges and opportunities for biomaterial innovations in addressing inflammation.
炎症在机体对因身体损伤产生的危险信号的反应以及恢复内环境稳态过程中发挥着重要作用。许多疾病,包括癌症、脓毒症和自身免疫性疾病,都会出现炎症反应失调的情况。通过生物材料提高药物的生物利用度并减少副作用,可以增强为治疗炎症反应失调而研发的抗炎药物的疗效。在本综述中,我们首先概述炎症环境的关键要素和阶段,然后讨论针对不同抗炎治疗策略的生物材料设计。生物材料可以设计成在炎症早期清除危险信号,如活性氧和氮物种以及游离DNA。材料还可以设计成防止引发炎症反应的白细胞与内皮细胞之间的黏附相互作用。此外,纳米级平台可以将抗炎剂递送至炎症部位。我们通过讨论生物材料创新在应对炎症方面所面临的挑战和机遇来结束本文。