Key players in the immune response to biomaterial scaffolds for regenerative medicine

被引:259
作者
Chung, Liam [1 ,2 ]
Maestas, David R., Jr. [1 ]
Housseau, Franck [2 ,3 ]
Elisseeff, Jennifer H. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Translat Tissue Engn Ctr, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
关键词
Immunoengineering; ECM; Innate immune response; Adaptive immune response; Regenerative medicine; Fibrosis; T cells; Wound healing; Wound repair; Interleukin expression; INNATE LYMPHOID-CELLS; FOREIGN-BODY RESPONSE; REGULATORY T-CELLS; MACROPHAGE POLARIZATION; BREAST IMPLANTS; CYSTIC-FIBROSIS; IN-VIVO; TISSUE; NEUTROPHILS; INFLAMMATION;
D O I
10.1016/j.addr.2017.07.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The compatibility of biomaterials is critical to their structural and biological function in medical applications. The immune system is the first responder to tissue trauma and to a biomaterial implant. The innate immune effector cells, most notably macrophages, play a significant role in the defense against foreign bodies and the formation of a fibrous capsule around synthetic implants. Alternatively, macrophages participate in the pro-regenerative capacity of tissue-derived biological scaffolds. Research is now elucidating the role of the adaptive immune system, and T cells in particular, in directing macrophage response to synthetic and biological materials. Here, we review basic immune cell types and discuss recent research on the role of the immune system in tissue repair and its potential relevance to scaffold design. We will also discuss new emerging immune cell types relevant to biomaterial responses and tissue repair. Finally, prospects for specifically targeting and modulating the immune response to biomaterial scaffolds for enhancing tissue repair and regeneration will be presented. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:184 / 192
页数:9
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