Immunomodulation of Skin Repair: Cell-Based Therapeutic Strategies for Skin Replacement (A Comprehensive Review)
Tóm tắt
Từ khóa
Tài liệu tham khảo
Vig, K., Chaudhari, A., Tripathi, S., Dixit, S., Sahu, R., Pillai, S., Dennis, V.A., and Singh, S.R. (2017). Advances in Skin Regeneration Using Tissue Engineering. Int. J. Mol. Sci., 18.
Gaur, M., Dobke, M., Lunyak, V.V., Piatelli, A., and Zavan, B. (2017). Molecular Sciences Mesenchymal Stem Cells from Adipose Tissue in Clinical Applications for Dermatological Indications and Skin Aging. Int. J. Mol. Sci., 18.
Nybo, 2010, Injury is a major inducer of epidermal innate immune responses during wound healing, J. Investig. Dermatol., 130, 910, 10.1038/jid.2009.414
Klar, 2014, Tissue-engineered dermo-epidermal skin grafts prevascularized with adipose-derived cells, Biomaterials, 35, 5065, 10.1016/j.biomaterials.2014.02.049
Klar, 2013, “Trooping the color”: Restoring the original donor skin color by addition of melanocytes to bioengineered skin analogs, Pediatr. Surg. Int., 29, 239, 10.1007/s00383-012-3217-0
Klar, 2014, Analysis of blood and lymph vascularization patterns in tissue-engineered human dermo-epidermal skin analogs of different pigmentation, Pediatr. Surg. Int., 30, 223, 10.1007/s00383-013-3451-0
Tavakoli, S., and Klar, A.S. (2021). Bioengineered Skin Substitutes: Advances and Future Trends. Appl. Sci., 11.
Klar, 2016, Characterization of vasculogenic potential of human adipose-derived endothelial cells in a three-dimensional vascularized skin substitute, Pediatr. Surg. Int., 32, 17, 10.1007/s00383-015-3808-7
Klar, 2014, Differential expression of granulocyte, macrophage, and hypoxia markers during early and late wound healing stages following transplantation of tissue-engineered skin substitutes of human origin, Pediatr. Surg. Int., 30, 1257, 10.1007/s00383-014-3616-5
Zimoch, 2018, Polyisocyanopeptide hydrogels: A novel thermo-responsive hydrogel supporting pre-vascularization and the development of organotypic structures, Acta Biomater., 70, 129, 10.1016/j.actbio.2018.01.042
Halim, 2010, Biologic and synthetic skin substitutes: An overview, Indian J. Plast Surg., 43, S23, 10.4103/0970-0358.70712
Klar, 2017, The Use of Adipose Derived Cells for Skin Nerve Regeneration-Short Review of Experimental Research, J. Tissue Sci. Eng., 8, 2, 10.4172/2157-7552.1000191
Shevchenko, 2010, A review of tissue-engineered skin bioconstructs available for skin reconstruction, J. R. Soc. Interface, 7, 229, 10.1098/rsif.2009.0403
Vacanti, 1999, Tissue engineering: The design and fabrication of living replacement devices for surgical reconstruction and transplantation, Lancet, 354, 32, 10.1016/S0140-6736(99)90247-7
Chen, 2009, Stem cells for skin tissue engineering and wound healing, Crit. Rev. Biomed. Eng., 37, 399, 10.1615/CritRevBiomedEng.v37.i4-5.50
Klar, 2017, Skin tissue engineering: Application of adipose-derived stem cells, Biomed Res. Int., 2017, 9747010, 10.1155/2017/9747010
Metcalfe, 2007, Bioengineering skin using mechanisms of regeneration and repair, Biomaterials, 28, 5100, 10.1016/j.biomaterials.2007.07.031
Metcalfe, 2007, Tissue engineering of replacement skin: The crossroads of biomaterials, wound healing, embryonic development, stem cells and regeneration, J. R. Soc. Interface, 4, 413, 10.1098/rsif.2006.0179
Clayton, 2017, Langerhans cells-programmed by the epidermis, Front. Immunol., 8, 1676, 10.3389/fimmu.2017.01676
(2017). MA Nilforoushzadeh Dermal Fibroblast Cells: Biology and Function in Skin Regeneration. J. Ski., Available online: https://sites.kowsarpub.com/jssc/articles/69080.html.
Moore, 2006, Prediction and monitoring the therapeutic response of chronic dermal wounds, Int. Wound J., 3, 89, 10.1111/j.1742-4801.2006.00212.x
Lazarus, 1994, Definitions and guidelines for assessment of wounds and evaluation of healing, Wound Repair Regen., 2, 165, 10.1046/j.1524-475X.1994.20305.x
Boateng, 2008, Wound healing dressings and drug delivery systems: A review, J. Pharm. Sci., 97, 2892, 10.1002/jps.21210
Percival, 2002, Classification of Wounds and their Management, Surgery, 20, 114
Larson, 2010, Scarless fetal wound healing: A basic science review, Plast. Reconstr. Surg., 126, 1172, 10.1097/PRS.0b013e3181eae781
Zengaffinen, 2014, Primary wound closure with a Limberg flap vs. secondary wound healing after excision of a pilonidal sinus: A multicentre randomised controlled study, Int. J. Colorectal Dis., 30, 97
Martin, 1997, Wound Healing-Aiming for Perfect Skin Regeneration, Science, 276, 75, 10.1126/science.276.5309.75
Wallace, H., Basehore, B., and Zito, P. (2020, December 08). Wound Healing Phases; StatPearls Publishing, Treasure Island (FL) 2020. Available online: https://europepmc.org/books/n/statpearls/article-34001/.
Kloc, 2019, Macrophage functions in wound healing, J. Tissue Eng. Regen. Med., 13, 99
Gilmore, 1991, Phases of wound healing, Dimens Oncol. Nurs., 5, 32
Wilgus, 2013, Neutrophils and Wound Repair: Positive Actions and Negative Reactions, Adv. Wound Care, 2, 379, 10.1089/wound.2012.0383
Iacob, A.T., Drăgan, M., Ionescu, O.M., Profire, L., Ficai, A., Andronescu, E., Confederat, L.G., and Lupașcu, D. (2020). An Overview of Biopolymeric Electrospun Nanofibers Based on Polysaccharides for Wound Healing Management. Pharmaceutics, 12.
McCartney-Francis, N.L., and Wahl, S.M. (2001). TGF-β and macrophages in the rise and fall of inflammation. TGF-β and Related Cytokines in Inflammation, Birkhäuser.
Turner, 2014, Cytokines and chemokines: At the crossroads of cell signalling and inflammatory disease, Biochim. Biophys. Acta, 1843, 2563, 10.1016/j.bbamcr.2014.05.014
Werner, 2007, Keratinocyte–fibroblast interactions in wound healing, Keratinocyte–Fibroblast Interact. Wound Health, 127, 998
Nelson, 2003, Nutrition for optimum wound healing, Nurs. Stand., 18, 55
Gordillo, 2003, Revisiting the essential role of oxygen in wound healing, Am. J. Surg., 186, 259, 10.1016/S0002-9610(03)00211-3
Phan, 2008, Biology of Fibroblasts and Myofibroblasts, Proc. Am. Thorac. Soc., 5, 334, 10.1513/pats.200708-146DR
Varney, 2013, Mechanoregulation of the Myofibroblast in Wound Contraction, Scarring, and Fibrosis: Opportunities for New Therapeutic Intervention, Adv. Wound Care, 2, 122, 10.1089/wound.2012.0393
Darby, 2014, Fibroblasts and myofibroblasts in wound healing, Clin. Cosmet. Investig. Dermatol., 7, 301
Basu, A., Kligman, L.H., Samulewicz, S.J., and Howe, C.C. (2001). Impaired wound healing in mice deficient in a matricellular protein SPARC (osteonectin, BM-40). BMC Cell Biol., 2.
Chen, 2016, Insight into reepithelialization: How do mesenchymal stem cells perform?, Stem Cells Int., 3, 1
Santoro, 2005, Cellular and molecular facets of keratinocyte reepithelization during wound healing, Exp. Cell Res., 304, 274, 10.1016/j.yexcr.2004.10.033
Martins, 2013, Matrix metalloproteinases and epidermal wound repair, Cell Tissue Res., 351, 255, 10.1007/s00441-012-1410-z
Nguyen, T.T., Mobashery, S., and Chang, M. (2016). Roles of Matrix Metalloproteinases in Cutaneous Wound Healing. Wound Health New Insights Into Anc. Chall., 37–71.
Michopoulou, 2015, How do epidermal matrix metalloproteinases support re-epithelialization during skin healing?, Artic. Eur. J. Dermatol., 25, 33, 10.1684/ejd.2015.2553
Pastar, 2014, Epithelialization in Wound Healing: A Comprehensive Review, Adv. Wound Care, 3, 445, 10.1089/wound.2013.0473
Krzyszczyk, 2018, The Role of Macrophages in Acute and Chronic Wound Healing and Interventions to Promote Pro-wound Healing Phenotypes, Front. Physiol., 9, 419, 10.3389/fphys.2018.00419
Wynn, 2016, Macrophages in Tissue Repair, Regeneration, and Fibrosis, Immunity, 44, 450, 10.1016/j.immuni.2016.02.015
Martinez, F.O., and Gordon, S. (2014). The M1 and M2 paradigm of macrophage activation: Time for reassessment. F1000Prime Rep., 6.
Schnoor, 2008, Production of type VI collagen by human macrophages: A new dimension in macrophage functional heterogeneity, J. Immunol., 180, 5707, 10.4049/jimmunol.180.8.5707
Weitkamp, 1999, Human macrophages synthesize type VIII collagen in vitro and in the atherosclerotic plaque, FASEB J., 13, 1445, 10.1096/fasebj.13.11.1445
Ogle, 2016, Monocytes and macrophages in tissue repair: Implications for immunoregenerative biomaterial design, Exp. Biol. Med., 241, 1084, 10.1177/1535370216650293
Recalcati, 2010, Differential regulation of iron homeostasis during human macrophage polarized activation, Eur. J. Immunol., 40, 824, 10.1002/eji.200939889
Mantovani, 2004, The chemokine system in diverse forms of macrophage activation and polarization, Trends Immonology, 25, 677, 10.1016/j.it.2004.09.015
Murray, 2011, Protective and pathogenic functions of macrophage subsets, Nat. Rev. Immunol., 11, 723, 10.1038/nri3073
Zhu, 2016, The pentacyclic triterpene Lupeol switches M1 macrophages to M2 and ameliorates experimental inflammatory bowel disease, Int. Immunopharmacol., 30, 74, 10.1016/j.intimp.2015.11.031
Ferrante, 2012, Regulation of Macrophage Polarization and Wound Healing, Adv. Wound Care, 1, 10, 10.1089/wound.2011.0307
Martinez, 2008, Alternative Activation of Macrophages: An Immunologic Functional Perspective, Annu. Rev. Immunol., 27, 451, 10.1146/annurev.immunol.021908.132532
Wang, 2019, M2b macrophage polarization and its roles in diseases, J. Leukoc. Biol., 106, 345, 10.1002/JLB.3RU1018-378RR
Das, 2015, Monocyte and Macrophage Plasticity in Tissue Repair and Regeneration, Am. J. Pathol., 185, 2596, 10.1016/j.ajpath.2015.06.001
Larouche, 2018, Immune regulation of skin wound healing: Mechanisms and novel therapeutic targets, Adv. Wound Care, 7, 209, 10.1089/wound.2017.0761
Zhao, R., Liang, H., Clarke, E., Jackson, C., and Xue, M. (2016). Inflammation in Chronic Wounds. Int. J. Mol. Sci., 17.
Dinarello, 2018, Introduction to the interleukin-1 family of cytokines and receptors: Drivers of innate inflammation and acquired immunity, Immunol. Rev., 281, 5, 10.1111/imr.12624
Frykberg, 2015, Challenges in the Treatment of Chronic Wounds, Adv. Wound Care, 4, 560, 10.1089/wound.2015.0635
Wysocki, 1993, Wound fluid from chronic leg ulcers contains elevated levels of metalloproteinases MMP-2 and MMP-9, J. Investig. Dermatol., 10, 64, 10.1111/1523-1747.ep12359590
Wallace, 1998, Levels of tumor necrosis factor-α (TNF-α) and soluble TNF receptors in chronic venous leg ulcers–correlations to healing status, J. Investig. Dermatol., 110, 292, 10.1046/j.1523-1747.1998.00113.x
Takeo, 2015, Wound Healing and Skin Regeneration, Cold Spring Harb. Perspect Med., 5, a023267, 10.1101/cshperspect.a023267
Jin, 2018, Macrophages in keloid are potent at promoting the differentiation and function of regulatory T cells, Exp. Cell Res., 362, 472, 10.1016/j.yexcr.2017.12.011
Li, 2017, Status of M1 and M2 type macrophages in keloid, Int. J. Clin. Exp. Pathol., 10, 11098
Ostuni, 2015, Macrophages and cancer: From mechanisms to therapeutic implications, Trends Immunol., 36, 229, 10.1016/j.it.2015.02.004
Cromack, 1987, Transforming growth factor beta levels in rat wound chambers, J. Surg. Res., 42, 622, 10.1016/0022-4804(87)90005-9
Yamakawa, 2019, Advances in surgical applications of growth factors for wound healing, Burn. Trauma, 7, 10, 10.1186/s41038-019-0148-1
Yoshida, 2003, Neutralization of hepatocyte growth factor leads to retarded cutaneous wound healing associated with decreased neovascularization and granulation tissue formation, J. Investig. Dermatol., 120, 335, 10.1046/j.1523-1747.2003.12039.x
Wang, 2009, MEK, p38, and PI-3K mediate cross talk between EGFR and TNFR in enhancing hepatocyte growth factor production from human mesenchymal stem cells, Am. J. Physiol. Cell Physiol., 297, C1284, 10.1152/ajpcell.00183.2009
Joseph, P., and Christopher, C. (2020, December 08). Skin Grafting -StatPearls -NCBI Bookshelf, Available online: https://www.ncbi.nlm.nih.gov/books/NBK532874/.
(2020, December 08). Immunobiology-NCBI Bookshelf, (n.d.), Available online: https://www.ncbi.nlm.nih.gov/books/NBK10757/.
Middelkoop, E. (2018). Skin substitutes and “the next level”. Total Burn Care, Elsevier. Available online: https://www.sciencedirect.com/science/article/pii/B9780323476614000150.
Hardin-Young, J., Teumer, J., and Ross, R.N. (2020). Approaches to transplanting engineered cells and tissues. Princ. Tissue Eng., 281–291. Available online: http://www.academia.edu/download/61780013/Principles_of_Tissue_Engineering20200114-84151-1u473co.pdf#page=324.
Buchbinder, 2007, Wound healing: Adjuvant therapy and treatment adherence, Venous Ulcers, 8, 91, 10.1016/B978-012373565-2.50012-9
Carter, J.E., and Holmes, J.H. (2016). The Surgical Management of Burn Wounds. Skin Tissue Engineering and Regenerative Medicine, Elsevier Inc.
Cascalho, M. (2008). Challenges and potentials of xenotransplantation. Clin. Immunol., 1215–1222. Available online: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152187/.
Kuo, 2018, Comparison of two decellularized dermal equivalents, J. Tissue Eng. Regen. Med., 12, 983, 10.1002/term.2530
Bello, 2001, Tissue-engineered skin: Current status in wound healing, Am. J. Clin. Dermatol., 2, 305, 10.2165/00128071-200102050-00005
Pourmoussa, 2016, An update and review of cell-based wound dressings and their integration into clinical practice, Ann. Transl. Med., 4, 457, 10.21037/atm.2016.12.44
Becker, 1963, Cytological Demonstration of the Clonal Nature of Spleen Colonies Derived from Transplanted Mouse Marrow Cells, Nature, 197, 452, 10.1038/197452a0
Siminovitch, 1963, The Distribution of Colony-Forming Cells among Spleen Colonies, J. Cell. Comp. Physiol., 62, 327, 10.1002/jcp.1030620313
Duscher, 2016, Stem cells in wound healing: The future of regenerative medicine? A mini-review, Gerontology, 62, 216, 10.1159/000381877
Gorecka, 2019, The potential and limitations of induced pluripotent stem cells to achieve wound healing, Stem Cell Res. Ther., 10, 1, 10.1186/s13287-019-1185-1
Dash, B., Xu, Z., Lin, L., Koo, A., Ndon, S., Berthiaume, F., Dardik, A., and Hsia, H. (2018). Stem Cells and Engineered Scaffolds for Regenerative Wound Healing. Bioengineering, 5.
Smith, 2001, Embryo-derived stem cells: Of mice and men, Annu. Rev. Cell Dev. Biol., 17, 435, 10.1146/annurev.cellbio.17.1.435
Martin, 1981, Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells, Proc. Natl. Acad Sci. USA, 78, 7634, 10.1073/pnas.78.12.7634
Medvedev, 2010, Induced pluripotent stem cells: Problems and advantages when applying them in regenerative medicine, Acta Nat., 2, 18, 10.32607/20758251-2010-2-2-18-27
Aoi, 2008, Generation of pluripotent stem cells from adult mouse liver and stomach cells, Science, 321, 699, 10.1126/science.1154884
Hanna, 2008, Direct reprogramming of terminally differentiated mature B lymphocytes to pluripotency, Cell, 133, 250, 10.1016/j.cell.2008.03.028
Kim, 2014, Pluripotent stem cells induced from adult neural stem cells by reprogramming with two factors, nature.com, Nature, 454, 646, 10.1038/nature07061
Eminli, 2008, Reprogramming of Neural Progenitor Cells into Induced Pluripotent Stem Cells in the Absence of Exogenous Sox2 Expression, Stem Cells, 26, 2467, 10.1634/stemcells.2008-0317
Takahashi, 2007, Induction of pluripotent stem cells from adult human fibroblasts by defined factors, Cell, 131, 861, 10.1016/j.cell.2007.11.019
Yu, 2007, Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells, Science, 21, 1917, 10.1126/science.1151526
Lian, 2014, Paracrine Mechanisms of Mesenchymal Stem Cell-Based Therapy: Current Status and Perspectives, Cell Transplant., 23, 1045, 10.3727/096368913X667709
Baraniak, 2010, Stem cell paracrine actions and tissue regeneration, Regen. Med., 5, 121, 10.2217/rme.09.74
Devrim, 2004, Comparison of Keratinocyte Proliferation in Diabetic and Non-Diabetic Inflamed Gingiva, J. Periodontol., 75, 989, 10.1902/jop.2004.75.7.989
Kim, 2013, Cooperation of endothelial and smooth muscle cells derived from human induced pluripotent stem cells enhances neovascularization in dermal wounds, Proceedings of the Tissue Engineering—Part A, Volume 19, 2478, 10.1089/ten.tea.2012.0768
Clayton, 2018, Induced pluripotent stem cell-derived endothelial cells promote angiogenesis and accelerate wound closure in a murine excisional wound healing model, Biosci. Rep., 38, BSR20180563, 10.1042/BSR20180563
Casqueiro, 2012, Infections in patients with diabetes mellitus: A review of pathogenesis, Indian J. Endocrinol. Metab., 16, S27, 10.4103/2230-8210.94253
Zhang, 2015, Exosomes released from human induced pluripotent stem cells-derived MSCs facilitate cutaneous wound healing by promoting collagen synthesis and angiogenesis, J. Transl. Med., 13, 1, 10.1186/s12967-015-0417-0
Itoh, M., Umegaki-Arao, N., Guo, Z., Liu, L., Higgins, C.A., and Christiano, A.M. (2013). Generation of 3D Skin Equivalents Fully Reconstituted from Human Induced Pluripotent Stem Cells (iPSCs). PLoS ONE, 8.
Kuzuya, 1995, Induction of angiogenesis by smooth muscle cell-derived factor: Possible role in neovascularization in atherosclerotic plaque, J. Cell. Physiol., 164, 658, 10.1002/jcp.1041640324
Shen, 2016, Engineered human vascularized constructs accelerate diabetic wound healing, Biomaterials, 102, 107, 10.1016/j.biomaterials.2016.06.009
Tan, 2018, Integration of induced pluripotent stem cell-derived endothelial cells with polycaprolactone/gelatin-based electrospun scaffolds for enhanced therapeutic angiogenesis, Stem Cell Res. Ther., 9, 1, 10.1186/s13287-018-0824-2
Kashpur, 2019, Differentiation of diabetic foot ulcer-derived induced pluripotent stem cells reveals distinct cellular and tissue phenotypes, FASEB J., 33, 1262, 10.1096/fj.201801059
Nakayama, 2018, The development of induced pluripotent stem cell-derived mesenchymal stem/stromal cells from normal human and RDEB epidermal keratinocytes, J. Dermatol. Sci., 91, 301, 10.1016/j.jdermsci.2018.06.004
Kobayashi, H. (2018). Effects of Exosomes Derived from the Induced Pluripotent Stem Cells on Skin Wound Healing, Nagoya University. Available online: https://ci.nii.ac.jp/naid/500001336521/.
Liubaviciute, 2020, Modulated mesenchymal stromal cells improve skin wound healing, Biologicals, 67, 1, 10.1016/j.biologicals.2020.08.003
Tencerova, 2016, The bone marrow-derived stromal cells: Commitment and regulation of adipogenesis, Front. Endocrinol., 7, 127, 10.3389/fendo.2016.00127
Rosen, 2015, Energy Excess, Glucose Utilization, and Skeletal Remodeling: New Insights, J. Bone Miner. Res., 30, 1356, 10.1002/jbmr.2574
Lindner, 2010, Mesenchymal Stem or Stromal Cells: Toward a Better Understanding of Their Biology?, Transfus Med. Hemother., 37, 75, 10.1159/000290897
Abboud, 1993, A bone marrow stromal cell line is a source and target for platelet-derived growth factor, Blood, 81, 2547, 10.1182/blood.V81.10.2547.2547
Rocha, 2012, Metabolic labeling of human bone marrow mesenchymal stem cells for the quantitative analysis of their chondrogenic differentiation, J. Proteome Res., 11, 5350, 10.1021/pr300572r
Wu, 2007, Bone marrow-derived stem cells in wound healing: A review, Wound Repair Regen., 15, S18, 10.1111/j.1524-475X.2007.00221.x
Hao, 2009, Transplantation of BMSCs expressing hPDGF-A/hBD2 promotes wound healing in rats with combined radiation-wound injury, Gene Ther., 16, 34, 10.1038/gt.2008.133
Basiouny, 2013, Effect of bone marrow derived mesenchymal stem cells on healing of induced full-thickness skin wounds in albino rat, Int. J. Stem Cells, 6, 12, 10.15283/ijsc.2013.6.1.12
Wu, 2007, Mesenchymal Stem Cells Enhance Wound Healing Through Differentiation and Angiogenesis, Stem Cells, 25, 2648, 10.1634/stemcells.2007-0226
Dash, 2009, Targeting nonhealing ulcers of lower extremity in human through autologous bone marrow-derived mesenchymal stem cells, Rejuvenation Res., 12, 359, 10.1089/rej.2009.0872
Sorrell, 2010, Topical delivery of mesenchymal stem cells and their function in wounds, Stem Cell Res. Ther., 1, 1, 10.1186/scrt30
Horwitz, 1999, Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfecta, Nat. Med., 5, 309, 10.1038/6529
Salinas, 2009, Mesenchymal stem cells for craniofacial tissue regeneration: Designing hydrogel delivery vehicles, J. Dent. Res., 88, 681, 10.1177/0022034509341553
Lei, 2018, Bone marrow-derived mesenchymal stem cells laden novel thermo-sensitive hydrogel for the management of severe skin wound healing, Mater. Sci. Eng. C Mater. Biol. Appl., 1, 159, 10.1016/j.msec.2018.04.045
Viezzer, 2020, A new waterborne chitosan-based polyurethane hydrogel as a vehicle to transplant bone marrow mesenchymal cells improved wound healing of ulcers in a diabetic, Carbohydr. P, 231, 115734, 10.1016/j.carbpol.2019.115734
Bharti, 2020, Effect of cryopreservation on therapeutic potential of canine bone marrow derived mesenchymal stem cells augmented mesh scaffold for wound healing in guinea pig, Biomed. Pharmacother., 121, 109573, 10.1016/j.biopha.2019.109573
Erben, 1997, Short-Term Treatment of Rats with High Dose 1,25-Dihydroxyvitamin D3 Stimulates Bone Formation and Increases the Number of Osteoblast Precursor Cells in Bone, Endocrinology, 138, 4629, 10.1210/endo.138.11.5511
Yoshimura, 2006, Characterization of freshly isolated and cultured cells derived from the fatty and fluid portions of liposuction aspirates, J. Cell. Physiol., 208, 64, 10.1002/jcp.20636
Conese, 2020, The Role of Adipose-Derived Stem Cells, Dermal Regenerative Templates, and Platelet-Rich Plasma in Tissue Engineering-Based Treatments of Chronic Skin Wounds, Stem Cells Int., 2020, 7056261, 10.1155/2020/7056261
Patrikoski, 2019, Perspectives for clinical translation of adipose stromal/stem cells, Stem Cells Int., 2019, 1, 10.1155/2019/5858247
Ntege, 2020, Advances in regenerative therapy: A review of the literature and future directions, Regen. Ther., 14, 136, 10.1016/j.reth.2020.01.004
Peng, Q., Alipour, H., Porsborg, S., Fink, T., and Zachar, V. (2020). Evolution of ASC Immunophenotypical Subsets During Expansion In Vitro. Int. J. Mol. Sci. Artic., 21.
Fristad, 2018, Adipose-derived and bone marrow mesenchymal stem cells: A donor-matched comparison, Stem Cell Res. Ther., 9, 1
Yu, 2010, Yield and characterization of subcutaneous human adipose-derived stem cells by flow cytometric and adipogenic mRNA analyzes, Cytotherapy, 12, 538, 10.3109/14653241003649528
Gimble, 2007, Adipose-derived stem cells for regenerative medicine, Circ. Res., 100, 1249, 10.1161/01.RES.0000265074.83288.09
Gimble, 2011, Adipose-derived stromal/stem cells (ASC) in regenerative medicine: Pharmaceutical applications, Curr. Pharm. Des., 17, 332, 10.2174/138161211795164220
Rodriguez, J., Pratta, A., Abbassi, N., and Fabre, H. (2017). Evaluation of three devices for the isolation of the stromal vascular fraction from adipose tissue and for ASC culture: A comparative study. Stem Cells Int., 2017.
Hur, W., Lee, H.Y., Min, H.S., Wufuer, M., Lee, C.W., Hur, J.A., Kim, S.H., Kim, B.K., and Choi, T.H. (2017). Regeneration of full-thickness skin defects by differentiated adipose-derived stem cells into fibroblast-like cells by fibroblast-conditioned medium. Stem Cell Res. Ther., 8.
Kim, 2007, Wound healing effect of adipose-derived stem cells: A critical role of secretory factors on human dermal fibroblasts, J. Dermatol. Sci., 48, 15, 10.1016/j.jdermsci.2007.05.018
Lee, 2012, Safety and Effect of Adipose Tissue-Derived Stem Cell Implantation in Patients With Critical Limb Ischemia, Circ. J., 76, 1750, 10.1253/circj.CJ-11-1135
Bura, 2014, Phase I trial: The use of autologous cultured adipose-derived stroma/stem cells to treat patients with non-revascularizable critical limb ischemia, Cytotherapy, 16, 245, 10.1016/j.jcyt.2013.11.011
Parvizi, 2015, Therapeutic Prospect of Adipose-Derived Stromal Cells for the Treatment of Abdominal Aortic Aneurysm, Stem Cells Dev., 24, 1493, 10.1089/scd.2014.0517
Rennert, 2014, Diabetes impairs the angiogenic potential of adipose-derived stem cells by selectively depleting cellular subpopulations, Stem Cell Res. Ther., 5, 1, 10.1186/scrt468
Siennicka, K., Zolocinska, A., Stepien, K., Lubina-Dabrowska, N., Maciagowska, M., Zolocinska, E., Slysz, A., Piusinska-Macoch, R., Mazur, S., and Zdanowicz, U. (2016). Adipose-Derived Cells (Stromal Vascular Fraction) Transplanted for Orthopedical or Neurological Purposes: Are They Safe Enough?. Stem Cells Int., 2016.
Kim, 2018, Effects of donor age on human adipose-derived adherent stromal cells under oxidative stress conditions, J. Int. Med. Res., 46, 951, 10.1177/0300060517731684
Klar, 2018, Characterization of M1 and M2 polarization of macrophages in vascularized human dermo-epidermal skin substitutes in vivo, Pediatr. Surg. Int., 34, 129, 10.1007/s00383-017-4179-z
Barsotti, 2011, Fibrin acts as biomimetic niche inducing both differentiation and stem cell marker expression of early human endothelial progenitor cells, Cell Prolif., 44, 33, 10.1111/j.1365-2184.2010.00715.x
Davis, 2011, Supplementation of fibrin gels with sodium chloride enhances physical properties and ensuing osteogenic response, Acta Biomater., 7, 691, 10.1016/j.actbio.2010.09.007
Murphy, 2017, Engineering fibrin hydrogels to promote the wound healing potential of mesenchymal stem cell spheroids, Acta Biomater., 64, 176, 10.1016/j.actbio.2017.10.007
Chae, 2017, Stromal vascular fraction shows robust wound healing through high chemotactic and epithelialization property, Cytotherapy, 19, 543, 10.1016/j.jcyt.2017.01.006
Gobin, 2003, Effects of Epidermal Growth Factor on Fibroblast Migration through Biomimetic Hydrogels, Biotechnol. Prog., 19, 1781, 10.1021/bp0341390
Blay, 1985, Epidermal growth factor promotes the chemotactic migration of cultured rat intestinal epithelial cells, J. Cell. Physiol., 124, 107, 10.1002/jcp.1041240117
Matthay, 1993, Transient effect of epidermal growth factor on the motility of an immortalized mammary epithelial cell line, J. Cell. Sci., 106, 869, 10.1242/jcs.106.3.869
Nilforoushzadeh, 2020, Engineered skin graft with stromal vascular fraction cells encapsulated in fibrin–collagen hydrogel: A clinical study for diabetic wound healing, J. Tissue Eng. Regen. Med., 14, 424, 10.1002/term.3003
Guo, 2018, Adipose-derived mesenchymal stem cells accelerate diabetic wound healing in a similar fashion as bone marrow-derived cells, Am. J. Physiol.Cell Physiol., 315, C885, 10.1152/ajpcell.00120.2018
Morizono, 2003, Comparison of multi-lineage cells from human adipose tissue and bone marrow, Cells Tissues Organs, 174, 101, 10.1159/000071150
Koenen, 2013, Adipose-Derived Stem Cells in Wound Healing: Recent Results In Vitro and In Vivo, OA Mol. Cell Biol., 1, 8
Aggarwal, 2004, Human mesenchymal stem cells modulate allogeneic immune cell responses, Blood, 105, 1815, 10.1182/blood-2004-04-1559
Magni, 2002, Human bone marrow stromal cells suppress T-lymphocyte proliferation induced by cellular or nonspecific mitogenic stimuli, Blood, 99, 3838, 10.1182/blood.V99.10.3838
Montesinos, 2015, Immunoregulation by Mesenchymal Stem Cells: Biological Aspects and Clinical Applications, J. Immunol. Res., 2015, 394917
Krampera, 2003, Bone marrow mesenchymal stem cells inhibit the response of naive and memory antigen-specific T cells to their cognate peptide, Blood, 101, 3722, 10.1182/blood-2002-07-2104
Meisel, 2004, Human bone marrow stromal cells inhibit allogeneic T-cell responses by indoleamine 2,3-dioxygenase-mediated tryptophan degradation, Blood, 103, 4619, 10.1182/blood-2003-11-3909
Rhijn, 2012, Mesenchymal stem cells derived from adipose tissue are not affected by renal disease, Kidney Int., 82, 748, 10.1038/ki.2012.187
2010, Mesenchymal stem cells: A new therapeutic tool for AKI, Nat. Rev. Nephrol., 6, 179, 10.1038/nrneph.2009.229
Rahimnejad, 2017, Biomaterials and tissue engineering for scar management in wound care, Burn. Trauma, 5, 4, 10.1186/s41038-017-0069-9
Li, 2015, Three-dimensional graphene foams loaded with bone marrow derived mesenchymal stem cells promote skin wound healing with reduced scarring, Mater. Sci. Eng. C Mater. Biol. Appl., 1, 181, 10.1016/j.msec.2015.07.062
Maggini, J., Mirkin, G., Bognanni, I., Holmberg, J., Piazzón, I.M., Nepomnaschy, I., Costa, H., Cañones, C., Raiden, S., and Vermeulen, M. (2010). Mouse bone marrow-derived mesenchymal stromal cells turn activated macrophages into a regulatory-like profile. PLoS ONE, 5.
Jackson, 2012, Mesenchymal stem cell therapy for attenuation of scar formation during wound healing, Stem Cell Res. Ther., 3, 20, 10.1186/scrt111
Moore, 2001, Interleukin-10 and the interleukin-10 receptor, Annu. Rev. Immunol., 19, 683, 10.1146/annurev.immunol.19.1.683
Liechty, 2000, Fetal wound repair results in scar formation in interleukin-10–deficient mice in a syngeneic murine model of scarless fetal wound repair, J. Pediatr. Surg., 35, 866, 10.1053/jpsu.2000.6868
Peranteau, 2008, IL-10 overexpression decreases inflammatory mediators and promotes regenerative healing in an adult model of scar formation, J. Investig. Dermatol, 128, 1852, 10.1038/sj.jid.5701232
Gordon, 2008, Permissive environment in postnatal wounds induced by adenoviral-mediated overexpression of the anti-inflammatory cytokine interleukin-10 prevents scar formation, Wound Repair Regen., 16, 70, 10.1111/j.1524-475X.2007.00326.x
Mattar, 2015, Comparing the immunomodulatory properties of bone marrow, adipose tissue, and birth-associated tissue mesenchymal stromal cells, Front. Immunol., 6, 560, 10.3389/fimmu.2015.00560
Ceccarelli, 2020, Immunomodulatory Effect of Adipose-Derived Stem Cells: The Cutting Edge of Clinical Application, Front. Cell Dev. Biol., 8, 236, 10.3389/fcell.2020.00236
Cao, 2020, Characterization of the immunomodulatory properties of alveolar bone-derived mesenchymal stem cells, Stem Cell Res. Ther., 11, 120, 10.1186/s13287-020-01605-x
Rostami, 2020, Immunoregulatory properties of mesenchymal stem cells: Micro-RNAs, Immunol. Lett., 219, 34, 10.1016/j.imlet.2019.12.011
Wang, 2020, Immunomodulatory Properties of Stem Cells in Periodontitis: Current Status and Future Prospective, Stem Cell Int., 2020, 9836518
Anderson, 2009, Human adult stem cells derived from adipose tissue protect against experimental colitis and sepsis, Gut, 57, 929
Hong, 2010, Therapeutic potential of adipose-derived stem cells in vascular growth and tissue repair, Curr. Opin. Organ. Transplant., 15, 86, 10.1097/MOT.0b013e328334f074
Mitchell, 2006, Immunophenotype of Human Adipose-Derived Cells: Temporal Changes in Stromal-Associated and Stem Cell-Associated Markers, Stem Cells, 24, 376, 10.1634/stemcells.2005-0234
Puissant, 2005, Immunomodulatory effect of human adipose tissue-derived adult stem cells: Comparison with bone marrow mesenchymal stem cells, Br. J. Haematol., 129, 118, 10.1111/j.1365-2141.2005.05409.x
Wolbank, 2007, Dose-dependent immunomodulatory effect of human stem cells from amniotic membrane: A comparison with human mesenchymal stem cells from adipose tissue, Tissue Eng., 13, 1173, 10.1089/ten.2006.0313
Yoo, 2009, Comparison of immunomodulatory properties of mesenchymal stem cells derived from adult human tissues, Cell Immunol., 259, 150, 10.1016/j.cellimm.2009.06.010
Lindroos, 2011, The Potential of Adipose Stem Cells in Regenerative Medicine, Stem Cell Rev. Reports, 7, 269, 10.1007/s12015-010-9193-7
Kucerova, 2007, Adipose Tissue-Derived Human Mesenchymal Stem Cells Mediated Prodrug Cancer Gene Therapy, Cancer Res., 67, 6304, 10.1158/0008-5472.CAN-06-4024
Yu, 2008, Mesenchymal stem cells derived from human adipose tissues favor tumor cell growth in vivo, Stem Cells Dev., 17, 463, 10.1089/scd.2007.0181
Barone, 2013, Immunomodulatory effects of adipose-derived stem cells: Fact or fiction?, Biomed. Res. Int., 2013, 383685
Cui, 2007, Expanded adipose-derived stem cells suppress mixed lymphocyte reaction by secretion of prostaglandin E2, Tissue Eng., 13, 1185, 10.1089/ten.2006.0315
Lin, 2012, Allogeneic and xenogeneic transplantation of adipose-derived stem cells in immunocompetent recipients without immunosuppressants, Stem Cells Dev., 21, 2770, 10.1089/scd.2012.0176
Gonzalez, 2010, Human adipose-derived mesenchymal stem cells reduce inflammatory and T cell responses and induce regulatory T cells in vitro in rheumatoid arthritis, Ann. Rheum. Dis., 69, 241, 10.1136/ard.2008.101881
Fang, 2007, Favorable response to human adipose tissue-derived mesenchymal stem cells in steroid-refractory acute graft-versus-host disease, Transpl. Proc., 39, 3358, 10.1016/j.transproceed.2007.08.103
Fang, 2007, Human adipose tissue-derived mesenchymal stromal cells as salvage therapy for treatment of severe refractory acute graft-vs.-host disease in two children, Pediatr. Transplant., 11, 814, 10.1111/j.1399-3046.2007.00780.x
Fang, 2007, Using human adipose tissue-derived mesenchymal stem cells as salvage therapy for hepatic graft-versus-host disease resembling acute hepatitis, Transpl. Proc., 39, 1710, 10.1016/j.transproceed.2007.02.091
Park, 2011, Cell cycle regulators are critical for maintaining the differentiation potential and immaturity in adipogenesis of adipose-derived stem cells, Differentiation, 82, 136, 10.1016/j.diff.2011.06.002
Jiang, 2020, Immune modulation by mesenchymal stem cells, Cell Prolif., 53, e12712, 10.1111/cpr.12712
Bartholomew, 2002, Mesenchymal stem cells suppress lymphocyte proliferation in vitro and prolong skin graft survival in vivo, Exp. Hematol., 30, 42, 10.1016/S0301-472X(01)00769-X
Koppula, 2009, Histocompatibility testing of cultivated human bone marrow stromal cells—A promising step towards pre-clinical screening for allogeneic stem cell therapy, Cell. Immunol., 259, 61, 10.1016/j.cellimm.2009.05.014
Mohanty, 2020, Immunomodulatory properties of bone marrow mesenchymal stem cells, J. Biosci., 45, 1, 10.1007/s12038-020-00068-9
Bertozzi, 2017, The biological and clinical basis for the use of adipose-derived stem cells in the field of wound healing, Ann. Med. Surg, 20, 41, 10.1016/j.amsu.2017.06.058
Franz, 2011, Immune responses to implants—A review of the implications for the design of immunomodulatory biomaterials, Biomaterials, 32, 6692, 10.1016/j.biomaterials.2011.05.078
Sun, 2018, Engineering Pro-Regenerative Hydrogels for Scarless Wound Healing, Adv. Healthc. Mater., 7, 1800016, 10.1002/adhm.201800016
Vishwakarma, 2016, Engineering Immunomodulatory Biomaterials To Tune the Inflammatory Response, Trends Biotechnol., 34, 470, 10.1016/j.tibtech.2016.03.009
Mantovani, 2013, Macrophage plasticity and polarization in tissue repair and remodelling, J. Pathol., 229, 176, 10.1002/path.4133
Brown, 2012, Macrophage polarization: An opportunity for improved outcomes in biomaterials and regenerative medicine, Biomaterials, 33, 3792, 10.1016/j.biomaterials.2012.02.034
Williams, 2008, On the mechanisms of biocompatibility, Biomaterials, 29, 2941, 10.1016/j.biomaterials.2008.04.023
Li, J., and Hastings, G.W. (2016). Oxide bioceramics: Inert ceramic materials in medicine and dentistry. Handbook of Biomaterial Properties, Springer. [2nd ed.].
Hayashi, 1993, Bone-implant interface mechanics of in vivo bio-inert ceramics, Biomaterials, 14, 1173, 10.1016/0142-9612(93)90163-V
Ehashi, T., Takemura, T., Hanagata, N., Minowa, T., Kobayashi, H., Ishihara, K., and Yamaoka, T. (2014). Comprehensive genetic analysis of early host body reactions to the bioactive and bio-inert porous scaffolds. PLoS ONE, 9.
Desai, 2017, Advances in islet encapsulation technologies, Nat. Rev. Drug Discov., 16, 338, 10.1038/nrd.2016.232
Onuki, 2008, A review of the biocompatibility of implantable devices: Current challenges to overcome foreign body response, J. Diabetes Sci. Technol., 2, 1003, 10.1177/193229680800200610
Mohammadi, 2020, Silk based scaffolds with immunomodulatory capacity: Anti-inflammatory effects of nicotinic acid, Biomater. Sci., 8, 148, 10.1039/C9BM00814D
Hench, 2010, Twenty-first century challenges for biomaterials, Royalsocietypublishing.Org, J. R. Soc. Interface, 7, S379, 10.1098/rsif.2010.0151.focus
Dziki, 2017, Extracellular Matrix Bioscaffolds as Immunomodulatory Biomaterials, Tissue Eng. Part. A, 23, 1152, 10.1089/ten.tea.2016.0538
Anderson, 2008, Foreign body reaction to biomaterials, Semin. Immunol., 20, 86, 10.1016/j.smim.2007.11.004
Bensiamar, 2015, Topographical cues regulate the crosstalk between MSCs and macrophages, Biomaterials, 37, 124, 10.1016/j.biomaterials.2014.10.028
Broughton, 2006, The Basic Science of Wound Healing, Plast Reconstr. Surg., 117, 12S, 10.1097/01.prs.0000225430.42531.c2
Badylak, 2008, Macrophage phenotype as a determinant of biologic scaffold remodeling, Tissue Eng. Part. A., 14, 1835, 10.1089/ten.tea.2007.0264
Brown, 2009, Macrophage phenotype and remodeling outcomes in response to biologic scaffolds with and without a cellular component, Biomaterials, 30, 1482, 10.1016/j.biomaterials.2008.11.040
Koh, 2011, Inflammation and wound healing: The role of the macrophage, Expert Rev. Mol., 13, e23, 10.1017/S1462399411001943
Sridharan, 2015, Biomaterial based modulation of macrophage polarization: A review and suggested design principles, Materialstoday, 18, 313
Singh, 2017, Unbiased Analysis of the Impact of Micropatterned Biomaterials on Macrophage Behavior Provides Insights beyond Predefined Polarization States, ACS Biomater. Sci. Eng., 3, 969, 10.1021/acsbiomaterials.7b00104
Corliss, 2016, Macrophages: An Inflammatory Link Between Angiogenesis and Lymphangiogenesis, Microcirculation, 23, 95, 10.1111/micc.12259
Ashouri, 2019, Macrophage polarization in wound healing: Role of aloe vera/chitosan nanohydrogel, Drug Deliv. Transl. Res., 9, 1027, 10.1007/s13346-019-00643-0
Kumar, 2018, Immunomodulatory injectable silk hydrogels maintaining functional islets and promoting anti-inflammatory M2 macrophage polarization, Biomaterials, 187, 1, 10.1016/j.biomaterials.2018.09.037
Li, 2016, Transition from inflammation to proliferation: A critical step during wound healing, Cell. Mol. Life Sci., 73, 3861, 10.1007/s00018-016-2268-0
Lucas, 2010, Differential roles of macrophages in diverse phases of skin repair, J. Immunol., 184, 3964, 10.4049/jimmunol.0903356
Klar, 2017, Comparison of in vivo immune responses following transplantation of vascularized and non-vascularized human dermo-epidermal skin substitutes, Pediatr. Surg., 33, 377, 10.1007/s00383-016-4031-x
Brown, 2012, Macrophage phenotype as a predictor of constructive remodeling following the implantation of biologically derived surgical mesh materials, Acta Biomater., 8, 978, 10.1016/j.actbio.2011.11.031
Meng, 2015, Solubilized extracellular matrix from brain and urinary bladder elicits distinct functional and phenotypic responses in macrophages, Biomaterials, 46, 131, 10.1016/j.biomaterials.2014.12.044
Chakraborty, 2020, Regulation of decellularized matrix mediated immune response, Biomater. Sci., 8, 1194, 10.1039/C9BM01780A
Kharaziha, 2021, Rational Design of Immunomodulatory Hydrogels for Chronic Wound Healing, Adv. Mater, 33, 2100176, 10.1002/adma.202100176
Raynal, 2009, Identification of multiple potent binding sites for human leukocyte associated Ig-like receptor LAIR on collagens II and III, Matrix Biol., 28, 202, 10.1016/j.matbio.2009.03.005
Chaffee, 2019, Stabilized collagen matrix dressing improves wound macrophage function and epithelialization, FASEB J., 33, 2144, 10.1096/fj.201800352R
Inv, 1993, Fibroblast Migration in Fibrin Gel Matrices, Am. J. Pathol., 142, 273
Clark, 2001, Fibrin and wound healing, Ann. N. Y. Acad. Sci., 936, 355, 10.1111/j.1749-6632.2001.tb03522.x
Stone, 2018, Advancements in regenerative strategies through the continuum of burn care, Front. Pharmacol., 9, 672, 10.3389/fphar.2018.00672
Hsieh, 2017, Differential regulation of macrophage inflammatory activation by fibrin and fibrinogen, Acta Biomater., 1, 14, 10.1016/j.actbio.2016.09.024
Qu, 2010, Interface between hemostasis and adaptive immunity, Curr. Opin. Immunol., 22, 634, 10.1016/j.coi.2010.08.017
Pravda, 2016, Hyaluronic Acid and Its Derivatives in Coating and Delivery Systems: Applications in Tissue Engineering, Regenerative Medicine and Immunomodulation, Adv. Healthc. Mater., 5, 2841, 10.1002/adhm.201600316
Rayahin, 2015, High and Low Molecular Weight Hyaluronic Acid Differentially Influence Macrophage Activation, ACS Biomater. Sci. Eng., 1, 481, 10.1021/acsbiomaterials.5b00181
Fong, 2018, Chitosan immunomodulatory properties: Perspectives on the impact of structural properties and dosage, Futur. Sci. OA, 4, FSO225, 10.4155/fsoa-2017-0064
Takei, 2012, Synthesis of a chitosan derivative soluble at neutral pH and gellable by freeze–thawing, and its application in wound care, Acta Biomater., 8, 686, 10.1016/j.actbio.2011.10.005
Porporatto, 2003, Chitosan induces different L L-arginine metabolic pathways in resting and inflammatory macrophages, Biochem. Biophys. Res. Commun., 304, 266, 10.1016/S0006-291X(03)00579-5
Moura, 2013, Chitosan-based dressings loaded with neurotensin-an efficient strategy to im-prove early diabetic wound healing, Acta Biomater., 10, 843, 10.1016/j.actbio.2013.09.040
Wijesekara, 2011, Biological activities and potential health benefits of sulfated polysaccharides derived from marine algae, Carbohydr. Polym., 84, 14, 10.1016/j.carbpol.2010.10.062
Kalitnik, 2015, Oligosaccharides of κ/β-carrageenan from the red alga Tichocarpus crinitus and their ability to induce interleukin 10, J. Appl. Phycol., 1, 545
He, 2014, Arginine-based polyester amide/polysaccharide hydrogels and their biological response, Acta Biomater., 10, 2482, 10.1016/j.actbio.2014.02.011
Salabas, 2013, The pathophysiology of Peyronie’s disease, Arab J. Urol., 11, 272, 10.1016/j.aju.2013.06.006
He, 2019, Biodegradable amino acid-based poly(ester amine) with tunable immunomodulating properties and their in vitro and in vivo wound healing studies in diabetic rats’ wounds, Acta Biomater., 84, 114, 10.1016/j.actbio.2018.11.053
Singh, 2014, Hydrogels and scaffolds for immunomodulation, Adv. Mater., 26, 6530, 10.1002/adma.201402105
Vaday, 2000, Extracellular matrix moieties, cytokines, and enzymes: Dynamic effects on immune cell behavior and inflammation, J. Leukoc. Biol., 67, 149, 10.1002/jlb.67.2.149
Rowley, 2019, Extracellular Matrix-Based Strategies for Immunomodulatory Biomaterials Engineering, Adv. Healthc. Mater., 8, e1801578, 10.1002/adhm.201801578
Badylak, 2008, Immune response to biologic scaffold materials, Semin. Immunol., 20, 109, 10.1016/j.smim.2007.11.003
Taraballi, 2018, Biomimetic Tissue Engineering: Tuning the Immune and Inflammatory Response to Implantable Biomaterials, Adv. Healthc. Mater., 7, 1800490, 10.1002/adhm.201800490
Cramer, 2019, Extracellular matrix-based biomaterials and their influence upon cell behavior, Biomater. Eng. Cell Behav., 48, 2132
Huleihel, 2017, Macrophage phenotype in response to ECM bioscaffolds, Semin. Immunol, 29, 2, 10.1016/j.smim.2017.04.004
Abraham, 2000, Evaluation of the porcine intestinal collagen layer as a biomaterial, J. Biomed. Mater. Res., 51, 442, 10.1002/1097-4636(20000905)51:3<442::AID-JBM19>3.0.CO;2-4
Parmaksiz, 2016, Clinical applications of decellularized extracellular matrices for tissue engineering and regenerative medicine, Biomed. Mater., 11, 022003, 10.1088/1748-6041/11/2/022003
Mokhtari, 2019, An injectable mechanically robust hydrogel of Kappa-carrageenan-dopamine functionalized graphene oxide for promoting cell growth, Carbohydr. Polym., 214, 234, 10.1016/j.carbpol.2019.03.030
Tavakoli, 2021, Nanocomposite hydrogel based on carrageenan-coated starch/cellulose nanofibers as a hemorrhage control material, Carbohydr. Polym., 251, 117013, 10.1016/j.carbpol.2020.117013
Tavakoli, 2019, Sprayable and injectable visible-light Kappa-carrageenan hydrogel for in-situ soft tissue engineering, Int. J. Biol. Macromol., 138, 590, 10.1016/j.ijbiomac.2019.07.126
Tavakoli, 2020, A multifunctional nanocomposite spray dressing of Kappa-carrageenan-polydopamine modified ZnO/L-glutamic acid for diabetic wounds, Mater. Sci. Eng. C, 111, 110837, 10.1016/j.msec.2020.110837
Yu, 2018, Injectable Bioresponsive Gel Depot for Enhanced Immune Checkpoint Blockade, Adv. Mater., 30, e1801527, 10.1002/adma.201801527
Yang, 2018, Engineering Dendritic-Cell-Based Vaccines and PD-1 Blockade in Self-Assembled Peptide Nanofibrous Hydrogel to Amplify Antitumor T-Cell Immunity, ACS Publ., 18, 4377
Sun, 2018, Injectable Hydrogels Coencapsulating Granulocyte-Macrophage Colony-Stimulating Factor and Ovalbumin Nanoparticles to Enhance Antigen Uptake Efficiency, ACS Appl. Mater. Interfaces, 10, 20315, 10.1021/acsami.8b04312
Zaveri, 2014, Integrin-directed modulation of macrophage responses to biomaterials, Biomaterials, 35, 3504, 10.1016/j.biomaterials.2014.01.007
Wilgus, 2008, Immune cells in the healing skin wound: Influential players at each stage of repair, Pharmacol. Res., 58, 112, 10.1016/j.phrs.2008.07.009
Jones, 2007, Proteomic analysis and quantification of cytokines and chemokines from biomaterial surface-adherent macrophages and foreign body giant cells, J. Biomed. Mater. Res. Part. A, 83, 585, 10.1002/jbm.a.31221
Zakrzewski, 2014, Overcoming immunological barriers in regenerative medicine, Nat. Biotechnol., 32, 786, 10.1038/nbt.2960
Babensee, 2005, Differential levels of dendritic cell maturation on different biomaterials used in combination products, J. Biomed. Mater. Res. Part A, 74, 503, 10.1002/jbm.a.30429
Zhou, 1996, CD14+ blood monocytes can differentiate into functionally mature CD83+ dendritic cells, Proc. Natl. Acad. Sci. USA, 93, 2588, 10.1073/pnas.93.6.2588
Adelmeijer, 2006, Collagens are functional, high affinity ligands for the inhibitory immune receptor LAIR-1, J. Exp. Med., 203, 1419, 10.1084/jem.20052554
Chattopadhyay, 2014, Review collagen-based biomaterials for wound healing, Biopolymers, 101, 821, 10.1002/bip.22486
Witherel, 2016, Response of human macrophages to wound matrices in vitro, Wound Repair Regen., 24, 514, 10.1111/wrr.12423
Orlandi, 2018, Long-term follow-up comparison of two different bi-layer dermal substitutes in tissue regeneration: Clinical outcomes and histological findings, Int. Wound J., 15, 695, 10.1111/iwj.12912
Agrawal, 2012, Macrophage phenotypes correspond with remodeling outcomes of various acellular dermal matrices, Open J. Regen. Med., 1, 25919
Podolnikova, 2003, Identification of a Novel Binding Site for Platelet Integrins IIb 3 (GPIIbIIIa) and 5 1 in the C-domain of Fibrinogen, J. Biol. Chem., 278, 32251, 10.1074/jbc.M300410200
(2017). Local induction of lymphangiogenesis with engineered fibrin-binding VEGF-C promotes wound healing by increasing immune cell trafficking and matrix. Biomaterials, 131, 160–175. Available online: https://www.sciencedirect.com/science/article/pii/S0142961217301825.
Mokarram, 2014, A perspective on immunomodulation and tissue repair, Ann. Biomed. Eng., 42, 338, 10.1007/s10439-013-0941-0
Hashimoto, 2020, Gene expression advances skin reconstruction and wound repair better on silk fibroin-based materials than on collagen-based materials, Materialia, 9, 100519, 10.1016/j.mtla.2019.100519
Burdick, 2011, Hyaluronic acid hydrogels for biomedical applications, Adv. Mater., 23, 41, 10.1002/adma.201003963
Wang, H., Morales, R.T.T., Cui, X., Huang, J., Qian, W., Tong, J., and Chen, W. (2019). A Photoresponsive Hyaluronan Hydrogel Nanocomposite for Dynamic Macrophage Immunomodulation. Adv. Healthc. Mater., 8.
Zamboni, 2018, The potential of hyaluronic acid in immunoprotection and immunomodulation: Chemistry, processing and function, Prog. Mater., 97, 97, 10.1016/j.pmatsci.2018.04.003
Ruppert, 2014, Tissue integrity signals communicated by high-molecular weight hyaluronan and the resolution of inflammation, Immunol Res., 58, 186, 10.1007/s12026-014-8495-2
Saini, 2020, Immunomodulatory Properties of Chitosan: Impact on Wound Healing and Tissue Repair, Endocr Metab. Immune. Disord Drug. Targets, 20, 1611, 10.2174/1871530320666200503054605