Design, clinical translation and immunological response of biomaterials in regenerative medicine

被引:213
作者
Sadtler, Kaitlyn [1 ,2 ]
Singh, Anirudha [1 ,2 ,3 ]
Wolf, Matthew T. [1 ,2 ]
Wang, Xiaokun [1 ,2 ]
Pardoll, Drew M. [4 ]
Elisseeff, Jennifer H. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Translat Tissue Engn Ctr, Dept Biomed Engn, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Wilmer Eye Inst, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Sch Med, Dept Urol, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
来源
NATURE REVIEWS MATERIALS | 2016年 / 1卷 / 07期
关键词
MESENCHYMAL STEM-CELLS; TISSUE-ENGINEERED CORNEA; IN-VIVO; INVIVO BIOCOMPATIBILITY; EXTRACELLULAR-MATRIX; CHONDROITIN SULFATE; CARTILAGE DEFECTS; EPITHELIAL-CELLS; HIGH-THROUGHPUT; IMMUNE-SYSTEM;
D O I
10.1038/natrevmats.2016.40
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The field of regenerative medicine aims to replace tissues lost as a consequence of disease, trauma or congenital abnormalities. Biomaterials serve as scaffolds for regenerative medicine to deliver cells, provide biological signals and physical support, and mobilize endogenous cells to repair tissues. Sophisticated chemistries are used to synthesize materials that mimic and modulate native tissue microenvironments, to replace form and to elucidate structure-function relationships of cell-material interactions. The therapeutic relevance of these biomaterial properties can only be studied after clinical translation, whereby key parameters for efficacy can be defined and then used for future design. In this Review, we present the development and translation of biomaterials for two tissue engineering targets, cartilage and cornea, both of which lack the ability to self-repair. Finally, looking to the future, we discuss the role of the immune system in regeneration and the potential for biomaterial scaffolds to modulate immune signalling to create a pro-regenerative environment.
引用
收藏
页数:17
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共 195 条
  • [1] Human mesenchymal stem cells modulate allogeneic immune cell responses
    Aggarwal, S
    Pittenger, MF
    [J]. BLOOD, 2005, 105 (04) : 1815 - 1822
  • [2] Proteogenomic Analysis of Human Chromosome 9-Encoded Genes from Human Samples and Lung Cancer Tissues
    Ahn, Jung-Mo
    Kim, Min-Sik
    Kim, Yong-In
    Jeong, Seul-Ki
    Lee, Hyoung-Joo
    Lee, Sun Hee
    Paik, Young-Ki
    Pandey, Akhilesh
    Cho, Je-Yoel
    [J]. JOURNAL OF PROTEOME RESEARCH, 2014, 13 (01) : 137 - 146
  • [3] SUPPRESSION OF RETINAL NEOVASCULARIZATION IN-VIVO BY INHIBITION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR (VEGF) USING SOLUBLE VEGF-RECEPTOR CHIMERIC PROTEINS
    AIELLO, LP
    PIERCE, EA
    FOLEY, ED
    TAKAGI, H
    CHEN, H
    RIDDLE, L
    FERRARA, N
    KING, GL
    SMITH, LEH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (23) : 10457 - 10461
  • [4] Immunologically Active Biomaterials for Cancer Therapy
    Ali, Omar A.
    Mooney, David J.
    [J]. CANCER IMMUNOLOGY AND IMMUNOTHERAPY, 2011, 344 : 279 - 297
  • [5] Ali OA, 2009, SCI TRANSL MED, V1, DOI 10.1126/scitranslmed.3000359
  • [6] Biosynthetic hydrogel scaffolds made from fibrinogen and polyethylene glycol for 3D cell cultures
    Almany, L
    Seliktar, D
    [J]. BIOMATERIALS, 2005, 26 (15) : 2467 - 2477
  • [7] Silk matrix for tissue engineered anterior cruciate ligaments
    Altman, GH
    Horan, RL
    Lu, HH
    Moreau, J
    Martin, I
    Richmond, JC
    Kaplan, DL
    [J]. BIOMATERIALS, 2002, 23 (20) : 4131 - 4141
  • [8] Inflammatory response to implants
    Anderson, J.M.
    [J]. ASAIO Transactions, 1988, 34 (02): : 101 - 107
  • [9] Foreign body reaction to biomaterials
    Anderson, James M.
    Rodriguez, Analiz
    Chang, David T.
    [J]. SEMINARS IN IMMUNOLOGY, 2008, 20 (02) : 86 - 100
  • [10] Biological responses to materials
    Anderson, JM
    [J]. ANNUAL REVIEW OF MATERIALS RESEARCH, 2001, 31 : 81 - 110