生物材料
免疫系统
伤口愈合
机械生物学
化学
组织工程
天然组织
巨噬细胞
重编程
细胞生物学
细胞
生物医学工程
免疫学
体外
医学
生物
生物化学
作者
Ricardo Whitaker,Beatriz Hernaez-Estrada,Rosa Marı́a Hernández,Edorta Santos‐Vizcaíno,Kara L. Spiller
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2021-08-20
卷期号:121 (18): 11305-11335
被引量:163
标识
DOI:10.1021/acs.chemrev.0c00895
摘要
All implanted biomaterials are targets of the host's immune system. While the host inflammatory response was once considered a detrimental force to be blunted or avoided, in recent years, it has become a powerful force to be leveraged to augment biomaterial-tissue integration and tissue repair. In this review, we will discuss the major immune cells that mediate the inflammatory response to biomaterials, with a focus on how biomaterials can be designed to modulate immune cell behavior to promote biomaterial-tissue integration. In particular, the intentional activation of monocytes and macrophages with controlled timing, and modulation of their interactions with other cell types involved in wound healing, have emerged as key strategies to improve biomaterial efficacy. To this end, careful design of biomaterial structure and controlled release of immunomodulators can be employed to manipulate macrophage phenotype for the maximization of the wound healing response with enhanced tissue integration and repair, as opposed to a typical foreign body response characterized by fibrous encapsulation and implant isolation. We discuss current challenges in the clinical translation of immunomodulatory biomaterials, such as limitations in the use of in vitro studies and animal models to model the human immune response. Finally, we describe future directions and opportunities for understanding and controlling the biomaterial-immune system interface, including the application of new imaging tools, new animal models, the discovery of new cellular targets, and novel techniques for in situ immune cell reprogramming.
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