Immunomodulatory Biomaterials for Tissue Repair

被引:201
作者
Whitaker, Ricardo [1 ]
Hernaez-Estrada, Beatriz [1 ,2 ]
Maria Hernandez, Rosa [2 ,3 ]
Santos-Vizcaino, Edorta [2 ,3 ]
Spiller, Kara L. [1 ]
机构
[1] Drexel Univ, Sch Biomed Engn Sci & Hlth Syst, Philadelphia, PA 19104 USA
[2] Univ Basque Country UPV EHU, Sch Pharm, Lab Pharmaceut, NanoBioCel Grp, Vitoria 01006, Spain
[3] Biomed Res Networking Ctr Bioengn Biomat & Nanome, Vitoria 01006, Spain
基金
美国国家科学基金会;
关键词
FOREIGN-BODY RESPONSE; MESENCHYMAL STEM-CELLS; UTERINE ARTERY EMBOLIZATION; CONDITIONAL MACROPHAGE DEPLETION; MESOPOROUS SILICA NANOPARTICLES; VIVO HOST RESPONSE; IN-VIVO; PORE-SIZE; IMMUNE-RESPONSE; ANTIINFLAMMATORY MONOCYTES;
D O I
10.1021/acs.chemrev.0c00895
中图分类号
O6 [化学];
学科分类号
0703 ;
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.
引用
收藏
页码:11305 / 11335
页数:31
相关论文
共 275 条
[1]   Organ-On-A-Chip Platforms: A Convergence of Advanced Materials, Cells, and Microscale Technologies [J].
Ahadian, Samad ;
Civitarese, Robert ;
Bannerman, Dawn ;
Mohammadi, Mohammad Hossein ;
Lu, Rick ;
Wang, Erika ;
Davenport-Huyer, Locke ;
Lai, Ben ;
Zhang, Boyang ;
Zhao, Yimu ;
Mandla, Serena ;
Korolj, Anastasia ;
Radisic, Milica .
ADVANCED HEALTHCARE MATERIALS, 2018, 7 (02)
[2]   Controlled M1-to-M2 transition of aged macrophages by calcium phosphate coatings [J].
Alhamdi, Jumana R. ;
Peng, Tao ;
Al-Naggar, Iman M. ;
Hawley, Kelly L. ;
Spiller, Kara L. ;
Kuhn, Liisa T. .
BIOMATERIALS, 2019, 196 :90-99
[3]   Impact of 3-D printed PLA- and chitosan-based scaffolds on human monocyte/macrophage responses: Unraveling the effect of 3-D structures on inflammation [J].
Almeida, Catarina R. ;
Serra, Tiziano ;
Oliveira, Marta I. ;
Planell, Josep A. ;
Barbosa, Mario A. ;
Navarro, Melba .
ACTA BIOMATERIALIA, 2014, 10 (02) :613-622
[4]   Inflammation via myeloid differentiation primary response gene 88 signaling mediates the fibrotic response to implantable synthetic poly(ethylene glycol) hydrogels [J].
Amer, Luke D. ;
Saleh, Leila S. ;
Walker, Cierra ;
Thomas, Stacey ;
Janssen, William J. ;
Alper, Scott ;
Bryant, Stephanie J. .
ACTA BIOMATERIALIA, 2019, 100 :105-117
[5]   Foreign body reaction to biomaterials [J].
Anderson, James M. ;
Rodriguez, Analiz ;
Chang, David T. .
SEMINARS IN IMMUNOLOGY, 2008, 20 (02) :86-100
[6]  
ANDERSON JM, 1984, BIOMATERIALS, V5, P5, DOI 10.1016/0142-9612(84)90060-7
[7]  
[Anonymous], 2018, NATL PLAST SURG STAT
[8]  
[Anonymous], 2020, NATL DIAB STAT REP 2
[9]  
[Anonymous], 2019, NATL BREAST IMPL REG
[10]   The enhancement of bone allograft incorporation by the local delivery of the sphingosine 1-phosphate receptor targeted drug FTY720 [J].
Aronin, Caren E. Petrie ;
Shin, Soo J. ;
Naden, Kimberly B. ;
Rios, Peter D., Jr. ;
Sefcik, Lauren S. ;
Zawodny, Sarah R. ;
Bagayoko, Namory D. ;
Cui, Quanjun ;
Khan, Yusuf ;
Botchwey, Edward A. .
BIOMATERIALS, 2010, 31 (25) :6417-6424