Macrophage Phenotype as a Determinant of Biologic Scaffold Remodeling

The chemokine system in diverse forms of macrophage activation and polarization

MANTOVANI, A., SICA, A., SOZZANI, S., ALLAVENA, P., VECCHI, A., & LOCATI, M. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.09.015 · Cited by 6,534

Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes

MANTOVANI, A., SOZZANI, S., LOCATI, M., ALLAVENA, P., & SICA, A. (2002) · Trends in Immunology · doi:10.1016/s1471-4906(02)02302-5 · Cited by 5,528

Monocyte and macrophage heterogeneity

Gordon, S., & Taylor, P. R. (2005) · Nature Reviews Immunology · doi:10.1038/nri1733 · Cited by 5,190

Foreign body reaction to biomaterials

Anderson, J. M., Rodriguez, A., & Chang, D. T. (2008) · Seminars in Immunology · doi:10.1016/j.smim.2007.11.004 · Cited by 5,138 · cited 1×

Biomaterials Science: An Introduction to Materials in Medicine

Ratner, B. D., Hoffman, A. S., Schöen, F. J., & Lemons, J. E. (1996) · doi:10.1016/c2009-0-02433-7 · Cited by 5,125

M-1/M-2 Macrophages and the Th1/Th2 Paradigm

Mills, C. D., Kincaid, K., Alt, J. M., Heilman, M. J., & Hill, A. M. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.12.6166 · Cited by 3,287

The many faces of macrophage activation

Mosser, D. M. (2003) · Journal of Leukocyte Biology · doi:10.1189/jlb.0602325 · Cited by 1,902

Biological Responses to Materials

Anderson, J. M. (2001) · Annual Review of Materials Research · doi:10.1146/annurev.matsci.31.1.81 · Cited by 1,465

Macrophage Polarization Comes of Age

Mantovani, Sica, & Locati, M. (2005) · Immunity · doi:10.1016/j.immuni.2005.10.001 · Cited by 1,259

Arginase inhibition ameliorates adipose tissue inflammation in mice with diet-induced obesity

Hu, H., Moon, J., Chung, J. H., Kim, O. Y., Yu, R., & Shin, M. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.07.048 · Cited by 25

Effect of bone marrow-derived extracellular matrix on cardiac function after ischemic injury

Ravi, S., Caves, J. M., Martinez, A. W., Xiao, J., Wen, J., Haller, C. A., Davis, M. E., & Chaikof, E. L. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.07.010 · Cited by 25

Leukocyte Inflammatory Response in a Rat Urinary Bladder Regeneration Model Using Porcine Small Intestinal Submucosa Scaffold

Ashley, R., Palmer, B. W., Schultz, A. D., Woodson, B. W., Roth, C. C., Routh, J. C., Fung, K.-M. A., Frimberger, D. C., Lin, H., & Kropp, B. P. (2009) · Tissue Engineering Part A · doi:10.1089/ten.tea.2008.0699 · Cited by 25

Urinary Bladder Tissue Engineering Using Natural Scaffolds in a Porcine Model: Role of Toll-Like Receptors and Impact of Biomimetic Molecules

Evren, S., Loai, Y., Antoon, R., Islam, S. S., Yeger, H., Moore, K., Wong, K. K. W., Gorczynski, R. M., & Farhat, W. A. (2010) · Cells Tissues Organs · doi:10.1159/000317332 · Cited by 26

Localized delivery of dexamethasone-21-phosphate via microdialysis implants in rat induces M(GC) macrophage polarization and alters CCL2 concentrations

Keeler, G. D., Durdik, J. M., & Stenken, J. A. (2014) · Acta Biomaterialia · doi:10.1016/j.actbio.2014.10.022 · Cited by 25

The Effect of Platelet Proteins Released in Response to Titanium Implant Surfaces on Macrophage Pro‐Inflammatory Cytokine Gene Expression

Alfarsi, M. A., Hamlet, S. M., & Ivanovski, S. (2014) · Clinical Implant Dentistry and Related Research · doi:10.1111/cid.12231 · Cited by 25

Biocompatibility and Immunophenotypic Characterization of a Porcine Cholecyst–derived Scaffold Implanted in Rats

Muhamed, J., Revi, D., Rajan, A., Geetha, S., & Anilkumar, T. V. (2014) · Toxicologic Pathology · doi:10.1177/0192623314550722 · Cited by 25

Biomimetic Concealing of PLGA Microspheres in a 3D Scaffold to Prevent Macrophage Uptake

Minardi, S., Corradetti, B., Taraballi, F., Sandri, M., Martinez, J. O., Powell, S. T., Tampieri, A., Weiner, B. K., & Tasciotti, E. (2016) · Small · doi:10.1002/smll.201503484 · Cited by 25

Enhancement of wound closure by modifying dual release patterns of stromal-derived cell factor-1 and a macrophage recruitment agent from gelatin hydrogels

Kim, Y., & Tabata, Y. (2016) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.2202 · Cited by 25

Specialized Histological and Histomorphometrical Analytical Methods for Biocompatibility Testing of Biomaterials for Maxillofacial Surgery in (Pre-) Clinical Studies

Lindner, C., Pröhl, A., Abels, M., LÖFFLER, T., Batinic, M., Jung, O., & Barbeck, M. (2020) · In Vivo · doi:10.21873/invivo.12148 · Cited by 25

Bioinspired Hybrid Nanostructured PEEK Implant with Enhanced Antibacterial and Anti-inflammatory Synergy

Ao, J., Zhang, X., You, Y., Chen, Y., Liu, Z., Gao, J., Qin, C., Hao, L., Zhao, J., & Jiang, R. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c06322 · Cited by 25

A Magnetically Responsive Biomaterial System for Flexibly Regulating the Duration between Pro‐ and Anti‐Inflammatory Cytokine Deliveries

Tolouei, A. E., Dülger, N., Ghatee, R., & Kennedy, S. M. (2018) · Advanced Healthcare Materials · doi:10.1002/adhm.201800227 · Cited by 26

Polymeric Electrospun Scaffolds: Neuregulin Encapsulation and Biocompatibility Studies in a Model of Myocardial Ischemia

Simón‐Yarza, T., Rossi, A., Heffels, K., Prósper, F., Gröll, J., & Blanco‐Prieto, M. J. (2015) · Tissue Engineering Part A · doi:10.1089/ten.tea.2014.0523 · Cited by 24

How Biomaterials Can Influence Various Cell Types in the Repair and Regeneration of the Heart after Myocardial Infarction

Lister, Z., Rayner, K. J., & Suuronen, E. J. (2016) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2016.00062 · Cited by 25

A novel chemotactic factor derived from the extracellular matrix protein decorin recruits mesenchymal stromal cells in vitro and in vivo

Dempsey, S. G., Miller, C. H., Schüler, J. B., Veale, R. W. F., Day, D. J., & May, B. C. H. (2020) · PLoS ONE · doi:10.1371/journal.pone.0235784 · Cited by 24

Extracellular matrix-based biomaterials in burn wound repair: A promising therapeutic strategy

Song, Y., Liu, P., Zhou, X., Chen, Y., Wu, W., Zhang, J.-Y., Li‐Ling, J., & Xie, H. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.137633 · Cited by 25

A Comparative Study of Porcine Small Intestine Submucosa and Cross-Linked Bovine Type I Collagen as a Nerve Conduit

Zhukauskas, R. M., Fischer, D. N., Deister, C. A., Alsmadi, N. Z., & Mercer, D. M. (2021) · Journal of Hand Surgery Global Online · doi:10.1016/j.jhsg.2021.06.006 · Cited by 24

The interaction of transient receptor potential melastatin 7 with macrophages promotes vascular adventitial remodeling in transverse aortic constriction rats

Li, Y., Jiang, H., Ruan, C., Zhong, J., Gao, P., Zhu, D., Niu, W., & Guo, S. (2013) · Hypertension Research · doi:10.1038/hr.2013.110 · Cited by 23

Potential Synergistic Effects of Stem Cells and Extracellular Matrix Scaffolds

Gaffney, L. S., Wrona, E. A., & Freytes, D. O. (2017) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.7b00083 · Cited by 23

An injectable dental pulp-derived decellularized matrix hydrogel promotes dentin repair through modulation of macrophage response.

Yi, P., Chen, S.-X., Zhao, Y., Ku, W., Lu, H., Yu, D.-S., & Zhao, W. (2024) · Biomaterials Advances · doi:10.1016/j.bioadv.2024.213883 · Cited by 24

Extracellular matrix scaffolds derived from different musculoskeletal tissues drive distinct macrophage phenotypes and direct tissue-specific cellular differentiation

Mahon, O. R., Browe, D. C., Díaz‐Payno, P. J., Pitacco, P., Cunningham, K. T., Mills, K. H. G., Dunne, A., & Kelly, D. J. (2021) · Journal of Immunology and Regenerative Medicine · doi:10.1016/j.regen.2021.100041 · Cited by 21

Morphologic Analysis of M2 Macrophage in Glioblastoma: Involvement of Macrophage Extracellular Traps (METs)

Michiba, A., Shiogama, K., Tsukamoto, T., Hirayama, M., Yamada, S., & Abe, M. (2022) · ACTA HISTOCHEMICA ET CYTOCHEMICA · doi:10.1267/ahc.22-00018 · Cited by 22

Extracellular Matrices as Bioactive Materials for In Situ Tissue Regeneration

Zhao, P., Yang, F., Jia, X., Xiao, Y., Hua, C., Xing, M. M. Q., & Lyu, G. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15122771 · Cited by 22

Ixmyelocel-T, an expanded multicellular therapy, contains a unique population of M2-like macrophages

Ledford, K. J., Zeigler, F., & Bartel, R. L. (2013) · Stem Cell Research & Therapy · doi:10.1186/scrt345 · Cited by 21

Developing Repair Materials for Stress Urinary Incontinence to Withstand Dynamic Distension

Hillary, C. J., Román, S., Bullock, A. J., Green, N. H., Chapple, C. R., & MacNeil, S. (2016) · PLoS ONE · doi:10.1371/journal.pone.0149971 · Cited by 22

Localized SDF-1α Delivery Increases Pro-Healing Bone Marrow-Derived Cells in the Supraspinatus Muscle Following Severe Rotator Cuff Injury

Tellier, L. E., Krieger, J. R., Brimeyer, A. L., Coogan, A. C., Falis, A. A., Rinker, T. E., Schudel, A., Thomas, S. N., Jarrett, C. D., Willett, N. J., et al. (2018) · Regenerative Engineering and Translational Medicine · doi:10.1007/s40883-018-0052-4 · Cited by 22

Subarachnoid Hemorrhage Induces Dynamic Immune Cell Reactions in the Choroid Plexus

Solar, P., Klusáková, I., Jančálek, R., Dubový, P., & Joukal, M. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00018 · Cited by 22

Immunomodulation for maxillofacial reconstructive surgery

Kim, S. (2020) · Maxillofacial Plastic and Reconstructive Surgery · doi:10.1186/s40902-020-00249-4 · Cited by 22

Extracellular Matrix as an Inductive Scaffold for Functional Tissue Reconstruction

Brown, B. N., & Badylak, S. F. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800548-4.00002-4 · Cited by 21

Adipose Stromal Cells Enhance Decellularized Adipose Tissue Remodeling Through Multimodal Mechanisms

Robb, K. P., Juignet, L., Martin, P. M., Walker, J. T., Brooks, C. R., Barreira, C., Dekaban, G. A., & Flynn, L. E. (2020) · Tissue Engineering Part A · doi:10.1089/ten.tea.2020.0180 · Cited by 21

The performance of photooxidatively crosslinked acellular bovine jugular vein conduits in the reconstruction of connections between pulmonary arteries and right ventricles

Lü, W., Zhang, M., Wu, Z., Hu, T., Xu, Z., Liu, W., & Hu, Y. (2010) · Biomaterials · doi:10.1016/j.biomaterials.2009.12.046 · Cited by 22

Strategies for skeletal muscle tissue engineering: seed vs. soil

Sicari, B. M., Londoño, R., & Badylak, S. F. (2015) · Journal of Materials Chemistry B · doi:10.1039/c5tb01714a · Cited by 22

Host Response to Naturally Derived Biomaterials

Lopresti, S. T., & Brown, B. N. (2015) · Host Response to Biomaterials · doi:10.1016/b978-0-12-800196-7.00004-9 · Cited by 24

Tumor and Peritoneum-Associated Macrophage Gene Signature as a Novel Molecular Biomarker in Gastric Cancer

Sullivan, K. M., Li, H., Yang, A., Zhang, Z., Muñoz, R. M., Mahuron, K. M., Yuan, Y., Paz, I. B., Hoff, D. D. V., Han, H., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25074117 · Cited by 22

Biomaterial-Based Regenerative Strategies for Volumetric Muscle Loss: Challenges and Solutions

Cai, C. W., Grey, J. A., Hubmacher, D., & Han, W. M. (2024) · Advances in Wound Care · doi:10.1089/wound.2024.0079 · Cited by 23

The Synthetic Melanocortin (CKPV)2 Exerts Anti-Fungal and Anti-Inflammatory Effects against Candida albicans Vaginitis via Inducing Macrophage M2 Polarization

Ji, H., Zou, Y., Duan, J., Jia, Z., Li, X.-J., Wang, Z., Li, L., Li, Y., Liu, G., Ming-qing, T., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056004 · Cited by 21

An In Vivo Model System for Evaluation of the Host Response to Biomaterials

Sicari, B. M., Turner, N. J., & Badylak, S. F. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-505-7_1 · Cited by 21

Implantation of atelocollagen sheet for vocal fold scar

Kishimoto, Y., Welham, N. V., & Hirano, S. (2010) · Current Opinion in Otolaryngology & Head & Neck Surgery · doi:10.1097/moo.0b013e32833febdc · Cited by 21

In vitro characterization of a novel tissue engineered based hybridized nano and micro structured collagen implant and its in vivo role on tenoinduction, tenoconduction, tenogenesis and tenointegration

Oryan, A., Moshiri, A., & Meimandi-Parizi, A. (2013) · Journal of Materials Science Materials in Medicine · doi:10.1007/s10856-013-5110-3 · Cited by 21

Comprehensive Genetic Analysis of Early Host Body Reactions to the Bioactive and Bio-Inert Porous Scaffolds

Ehashi, T., Takemura, T., Hanagata, N., Minowa, T., Kobayashi, H., Ishihara, K., & Yamaoka, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085132 · Cited by 20

Characterization of and host response to tyramine substituted-hyaluronan enriched fascia extracellular matrix

Chin, L., Calabro, A. R., Rodríguez, E. R., Tan, C. D., Walker, E., & Derwin, K. A. (2011) · Journal of Materials Science Materials in Medicine · doi:10.1007/s10856-011-4325-4 · Cited by 21

Proinflammatory polarization of stifle synovial macrophages in dogs with cruciate ligament rupture

Yarnall, B. W., Chamberlain, C. S., Hao, Z., & Muir, P. (2019) · Veterinary Surgery · doi:10.1111/vsu.13261 · Cited by 23

Inflammatory response and macrophage polarization using different physicochemical biomaterials for oral and maxillofacial reconstruction

Munerato, M. S., Biguetti, C. C., da Silva, R. B. P., da Silva, A. C. R., Bacelar, A. C. Z., da Silva, J. L., Couto, M. C. R., Duarte, M. A. H., Santiago, J. F., Bossini, P. S., et al. (2019) · Materials Science and Engineering C · doi:10.1016/j.msec.2019.110229 · Cited by 21

The Condensation of Collagen Leads to an Extended Standing Time and a Decreased Pro-inflammatory Tissue Response to a Newly Developed Pericardium-based Barrier Membrane for Guided Bone Regeneration

GUELDENPFENNIG, T., Houshmand, A., Najman, S. J., Stojanović, S., Koržinskas, T., Smeets, R., Gosau, M., Pissarek, J., Emmert, S., Jung, O., et al. (2020) · In Vivo · doi:10.21873/invivo.11867 · Cited by 21

Whole liver engineering: A promising approach to develop functional liver surrogates

Meng, F., Assiri, A. M., Dhar, D. K., & Broering, D. (2017) · Liver International · doi:10.1111/liv.13444 · Cited by 23

Enhancing Viability in Static and Perfused 3D Tissue Constructs Using Sacrificial Gelatin Microparticles

Hudson, A. R., Shiwarski, D. J., Kramer, A. J., & Feinberg, A. W. (2025) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.4c02169 · Cited by 20

Modulation of the inflammatory response to decellularized collagen matrix for cartilage regeneration

Gvaramia, D., Kern, J., Jakob, Y., Tritschler, H., Brenner, R. E., Breiter, R., Kzhyshkowska, J. G., & Rotter, N. (2021) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.37349 · Cited by 20

Macrophage response mediated by extracellular matrix: recent progress

Xiao, W., Yang, Y., Chu, C., Rung, S., Wang, Z., Man, Y., Lin, J., & Qu, Y. (2022) · Biomedical Materials · doi:10.1088/1748-605x/aca946 · Cited by 21

Process Development and Manufacturing of Human and Animal Acellular Dermal Matrices

Bush, K., & Gertzman, A. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801654-1.00005-x · Cited by 21

Parallel evolution of polymer chemistry and immunology: Integrating mechanistic biology with materials design

Sadtler, K., Collins, J., Byrne, J. D., & Langer, R. (2020) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2020.06.021 · Cited by 20

Esophagus and regenerative medicine

Londoño, R. (2012) · World Journal of Gastroenterology · doi:10.3748/wjg.v18.i47.6894 · Cited by 19

Effect of iRoot SP and mineral trioxide aggregate (MTA) on the viability and polarization of macrophages

Zhu, X., Yuan, Z., Yan, P., Li, Y., Jiang, H., & Huang, S. (2017) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2017.03.010 · Cited by 19

Fibroadhesive scarring of grafted collagen scaffolds interferes with implant–host neural tissue integration and bridging in experimental spinal cord injury

Altinova, H., Hammes, S., Palm, M., Gerardo‐Nava, J., Achenbach, P., Deumens, R., Hermans, E., Führmann, T., Boecker, A. H., van Neerven, S. G. A., et al. (2019) · Regenerative Biomaterials · doi:10.1093/rb/rbz006 · Cited by 19

Impact of Electrospun Conduit Fiber Diameter and Enclosing Pouch Pore Size on Vascular Constructs Grown Within Rat Peritoneal Cavities

Bashur, C. A., Eagleton, M. J., & Ramamurthi, A. (2012) · Tissue Engineering Part A · doi:10.1089/ten.tea.2012.0309 · Cited by 19

Biodegradable lysine-derived polyurethane scaffolds promote healing in a porcine full-thickness excisional wound model

Adolph, E. J., Pollins, A. C., Cardwell, N. L., Davidson, J. M., Guelcher, S. A., & Nanney, L. B. (2014) · Journal of Biomaterials Science Polymer Edition · doi:10.1080/09205063.2014.965997 · Cited by 18

FTY720 attenuates tubulointerstitial inflammation and fibrosis in subtotally nephrectomized rats

Ni, H.-F., Chen, J., Zhang, M., Pan, M.-M., Zhang, J., Liu, H., Tang, R., Ma, K., & Liu, B. (2013) · Renal Failure · doi:10.3109/0886022x.2013.809006 · Cited by 18

An Immunopathological Evaluation of the Porcine Cholecyst Matrix as a Muscle Repair Graft in a Male Rat Abdominal Wall Defect Model

Dhanush Krishna, B., Nair, N. D., Venugopal, S. K., Das, V. N., George, S., Abraham, M. J., Eassow, S., Alison, M. R., Sainulabdeen, A., & Anilkumar, T. V. (2018) · Toxicologic Pathology · doi:10.1177/0192623317752894 · Cited by 18

First Insights Into the M2 Inflammatory Response After Adipose-Tissue-Derived Stem Cell Injections in Radiation-Injured Muscles

Riccobono, D., Nikovics, K., Francois, S., Favier, A., Jullien, N., Schrock, G., Scherthan, H., & Drouet, M. (2018) · Health Physics · doi:10.1097/hp.0000000000000822 · Cited by 14

Extent of Inflammation and Foreign Body Reaction to Porous Polyethylene In Vitro and In Vivo

Vollkommer, T., Henningsen, A., Friedrich, R. E., Felthaus, O. H., Eder, F., Morsczeck, C. O., Smeets, R., Gehmert, S., & Gosau, M. (2019) · In Vivo · doi:10.21873/invivo.11479 · Cited by 18

Macrophage Polarization with Angiopoietin-1 Peptide QHREDGS

Mandla, S., Huyer, L. D., Wang, Y., & Radisic, M. (2019) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.9b00483 · Cited by 19

Peritoneal pre-conditioning reduces macrophage marker expression in collagen-containing engineered vascular grafts

Shojaee, M., Wood, K. B., Moore, L. K., & Bashur, C. A. (2017) · Acta Biomaterialia · doi:10.1016/j.actbio.2017.10.006 · Cited by 18

Cartilage Tissue Engineering

Faust, H. J., Guo, Q., & Elisseeff, J. H. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809880-6.00053-9 · Cited by 18

Integration and functional performance of a decellularised porcine superflexor tendon graft in an ovine model of anterior cruciate ligament reconstruction

Edwards, J. H., Jones, G. L., Herbert, A., Fisher, J., & Ingham, E. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121204 · Cited by 17

STS loaded PCL-MECM based hydrogel hybrid scaffolds promote meniscal regeneration via modulating macrophage phenotype polarization

Li, M., Yin, H., Chen, M., Deng, H., Tian, G., Guo, W., Yi, G., Guo, Q., Chen, Z., & Liu, S. (2023) · Biomaterials Science · doi:10.1039/d2bm00526c · Cited by 17

Effects of Scaffold Material Used in Cardiovascular Surgery on Mesenchymal Stem Cells and Cardiac Progenitor Cells

Hodonsky, C. J., Mundada, L. V., Wang, S., Witt, R. G., Raff, G. W., Kaushal, S., & Si, M. (2014) · The Annals of Thoracic Surgery · doi:10.1016/j.athoracsur.2014.08.071 · Cited by 17

Winner of the student award in the undergraduate category, 10th World Biomaterials Congress, May 17–22, 2016, Montreal QC, Canada: Evaluation of the tissue response to alginate encapsulated islets in an omentum pouch model

Ibarra, V., Appel, A. A., Anastasio, M. A., Opara, E. C., & Brey, E. M. (2016) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.35769 · Cited by 17

The Role of the Host Immune Response in Tissue Engineering and Regenerative Medicine

Brown, B. N., & Badylak, S. F. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-398358-9.00025-2 · Cited by 17

Biologic Scaffolds Composed of Extracellular Matrix for Regenerative Medicine

Scarritt, M. E., Murdock, M. H., & Badylak, S. F. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809880-6.00035-7 · Cited by 19

Effect of cyclic deformation on xenogeneic heart valve biomaterials

Dalgliesh, A. J., Parvizi, M., Noble, C., & Griffiths, L. G. (2019) · PLoS ONE · doi:10.1371/journal.pone.0214656 · Cited by 17

Modification of decellularized vascular xenografts with 8‐arm polyethylene glycol suppresses macrophage infiltration but maintains graft degradability

Mahara, A., Kitai, M., Masunaga, H., Hikima, T., Ohya, Y., Sasaki, S., Sakurai, S., & Yamaoka, T. (2020) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.36960 · Cited by 17

Addition of platelet‐rich plasma supports immune modulation and improved mechanical integrity in Alloderm mesh for ventral hernia repair in a rat model

Fernandez-Moure, J. S., Eps, J. L. V., Scherba, J. C., Yazdi, I. K., Robbins, A. B., Cabrera, F. J., Vatsaas, C., Moreno, M. R., Weiner, B. K., & Tasciotti, E. (2020) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.3156 · Cited by 17

Promoting endogenous repair of skeletal muscle using regenerative biomaterials

Carleton, M. M., & Sefton, M. V. (2021) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.37239 · Cited by 19

Assessing the Effects of VEGF Releasing Microspheres on the Angiogenic and Foreign Body Response to a 3D Printed Silicone-Based Macroencapsulation Device

Levey, R. E., Coulter, F. B., Scheiner, K. C., Deotti, S., Robinson, S. T., McDonough, L., Nguyễn, T. T., Steendam, R., Canney, M., Wylie, R., et al. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13122077 · Cited by 18

Beyond Encapsulation: Exploring Macrophage-Fibroblast Cross Talk in Implant-Induced Fibrosis

Sudarsanam, P. K., Alsema, E. C., Beijer, N. R. M., van Kooten, T. G., & de Boer, J. (2024) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2023.0300 · Cited by 18

High salt aggravates renal inflammation via promoting pro-inflammatory macrophage in 5/6-nephrectomized rat

Liu, Y., Dai, X., Yang, S., Peng, Y., Hou, F. F., & Zhou, Q. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119109 · Cited by 17

Modulating immune responses for enhanced cell therapies: The dual role of multi-scale biomaterials

Zeng, J., Jin, Y., Ao, Y., Li, W., Liang, K., Chen, H., Long, Y., & Du, Y. (2024) · EngMedicine · doi:10.1016/j.engmed.2024.100038 · Cited by 16

Effect of implantation site and injury condition on host response to human‐derived fascia lata ECM in a rat model

Leigh, D. R., Baker, A. R., Mesiha, M., Rodríguez, E. R., Tan, C. D., Walker, E., & Derwin, K. A. (2011) · Journal of Orthopaedic Research® · doi:10.1002/jor.21529 · Cited by 16

Biocompatibility and Bioresponse to Biomaterials

Anderson, J. M. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-381422-7.10038-0 · Cited by 19

In vivo response to decellularized mesothelium scaffolds

Cronce, M. J., Faulknor, R., Pomerantseva, I., Liu, X., Goldman, S., Ekwueme, E. C., Mwizerwa, O., Neville, C. M., & Sundback, C. A. (2017) · Journal of Biomedical Materials Research Part B Applied Biomaterials · doi:10.1002/jbm.b.33879 · Cited by 16

Electrosprayed extracellular matrix nanoparticles induce a pro‐regenerative cell response

Link, P. A., Ritchie, A. M., Cotman, G. M., Valentine, M. S., Dereski, B. S., & Heise, R. L. (2018) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.2768 · Cited by 16

Development and characterisation of cytocompatible polyester substrates with tunable mechanical properties and degradation rate

Ribeiro, S., Carvalho, A. M., Fernandes, E. M., Gomes, M. E., Reis, R. L., Bayon, Y., & Zeugolis, D. I. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.11.026 · Cited by 16

Inductive Remodeling of Extracellular Matrix Scaffolds in the Temporomandibular Joint of Pigs

Brown, B. N., Chung, W. L., Lowe, J., LoPresti, S. T., Cheetham, J., Almarza, A. J., & Badylak, S. F. (2021) · Tissue Engineering Part A · doi:10.1089/ten.tea.2021.0123 · Cited by 17

Effect of poly(ethylene glycol) diacrylate concentration on network properties and in vivo response of poly(β‐amino ester) networks

Safranski, D. L., Weiss, D., Clark, J., Caspersen, B. S., Taylor, W. R., & Gall, K. (2010) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.32983 · Cited by 16

Endo180 and MT1-MMP are involved in the phagocytosis of collagen scaffolds by macrophages and is regulated by interferon-gamma

Ye, Q., Xing, Q., Ren, Y., Harmsen, M. C., & Bank, R. (2010) · European Cells and Materials · doi:10.22203/ecm.v020a16 · Cited by 16

Site-specific prolapse surgery. II. Vaginal paravaginal repair augmented with either synthetic mesh or remodelling xenograft

Reid, R. I., & Luo, K. (2011) · International Urogynecology Journal · doi:10.1007/s00192-010-1346-3 · Cited by 15

Transcriptomic Regulation of Macrophages by Matrix-Bound Nanovesicle-Associated Interleukin-33

Cramer, M. C., Molina, C. P., Hussey, G. S., Turnquist, H. R., & Badylak, S. F. (2022) · Tissue Engineering Part A · doi:10.1089/ten.tea.2022.0006 · Cited by 15

Biomaterials-based immunomodulation enhances survival of murine vascularized composite allografts

Sommerfeld, S. D., Zhou, X., Mejías, J. C., Oh, B. C., Maestas, D. R., Furtmüller, G. J., Laffont, P., Elisseeff, J. H., & Brandacher, G. (2023) · Biomaterials Science · doi:10.1039/d2bm01845d · Cited by 17

Suspension electrospinning of decellularized extracellular matrix: A new method to preserve bioactivity

Jones, S., VandenHeuvel, S. N., Martinez, A. L., Birur, R., Burgeson, E. M., Gilbert, I., Baker, A. B., Wolf, M. T., Raghavan, S. A., Rogers, S. A., et al. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.08.012 · Cited by 17

Engineering Myocardium for Heart Regeneration—Advancements, Considerations, and Future Directions

Jarrell, D. K., Vanderslice, E. J., VeDepo, M. C., & Jacot, J. G. (2020) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2020.586261 · Cited by 15

Macrophages of Different Phenotypes Influence the Migration of BMSCs in PLGA Scaffolds with Different Pore Size

Dai, Y., Li, X., Wu, R., Jin, Y., & Gao, C. (2017) · Biotechnology Journal · doi:10.1002/biot.201700297 · Cited by 15

Bovine hydroxyapatite-based scaffold accelerated the inflammatory phase and bone growth in rats with bone defect

Gani, M. A., Budiatin, A. S., Shinta, D. W., Ardianto, C., & Khotib, J. (2023) · Journal of Applied Biomaterials & Functional Materials · doi:10.1177/22808000221149193 · Cited by 18

Macrophage Plasticity and Polarization

Galdiero, M. R., & Mantovani, A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800196-7.00006-2 · Cited by 14

Biocompatibility and Immune Response to Biomaterials

Brown, B. N., & Badylak, S. F. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-398523-1.00011-2 · Cited by 15

Guidelines for Models of Skeletal Muscle Injury and Therapeutic Assessment

Willett, N. J., Krishnan, L., Li, M. T. A., Guldberg, R. E., & Warren, G. L. (2016) · Cells Tissues Organs · doi:10.1159/000445345 · Cited by 15

Analyzing the scaffold immune microenvironment using flow cytometry: practices, methods and considerations for immune analysis of biomaterials

Sadtler, K., & Elisseeff, J. H. (2019) · Biomaterials Science · doi:10.1039/c9bm00349e · Cited by 16

Tissue Engineering with Decellularized Tissues

Badylak, S. F., Brown, B. N., & Gilbert, T. W. (2012) · Elsevier eBooks · doi:10.1016/b978-0-08-087780-8.00140-6 · Cited by 14

Biodegradable materials for surgical management of stress urinary incontinence: A narrative review

MacCraith, E., O’Brien, F. J., & Davis, N. F. (2021) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/j.ejogrb.2021.02.024 · Cited by 13

Immunomodulatory contribution of mast cells to the regenerative biomaterial microenvironment

Wang, R. M., Mesfin, J. M., Karkanitsa, M. L., Ungerleider, J. L., Zelus, E. I., Zhang, Y., Kawakami, Y., Kawakami, Y., Kawakami, T., & Christman, K. L. (2023) · npj Regenerative Medicine · doi:10.1038/s41536-023-00324-0 · Cited by 13

Guidance on the assessment of the functionality of biomaterials for periodontal tissue regeneration: Methodologies and testing procedures

Daghrery, A., Dal‐Fabbro, R., dos Reis‐Prado, A. H., Araújo, I. J. D. S., Fischer, N. G., Rosa, V., Silikas, N., Aparicio, C., Watts, D. C., & Bottino, M. C. (2025) · Dental Materials · doi:10.1016/j.dental.2024.12.018 · Cited by 14

Strategies for functional bioscaffold-based skeletal muscle reconstruction.

Sicari, B. M., Dziki, J. L., & Badylak, S. F. (2015) · Europe PMC (PubMed Central) · doi:10.3978/j.issn.2305-5839.2015.09.45 · Cited by 14

Macrophage Involvement in the Remodeling of an Extracellular Matrix Scaffold

Valentin, J. E. (2010) · D-Scholarship@Pitt (University of Pittsburgh)

Macrophage phenotype and remodeling outcomes in response to biologic scaffolds with and without a cellular component

Brown, B. N., Valentin, J. E., Stewart-Akers, A. M., McCabe, G. P., & Badylak, S. F. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2008.11.040 · Cited by 896

Macrophage phenotype as a predictor of constructive remodeling following the implantation of biologically derived surgical mesh materials

Brown, B. N., Londono, R., Tottey, S., Zhang, L., Kukla, K. A., Wolf, M. T., Daly, K. A., Reing, J. E., & Badylak, S. F. (2012) · Acta Biomaterialia · doi:10.1016/j.actbio.2011.11.031 · Cited by 745

Macrophage Phenotype in Response to Implanted Synthetic Scaffolds: An Immunohistochemical Study in the Rat

Palmer, J. A., Abberton, K. M., Mitchell, G. M., & Morrison, W. A. (2014) · Cells Tissues Organs · doi:10.1159/000363693 · Cited by 42

Mechanisms underlying heterologous skin scaffold-mediated tissue remodeling

Mimura, K. K., Moraes, A. R., Miranda, A. C., Greco, R., Ansari, T., Sibbons, P., Greco, K. V., & Oliani, S. M. (2016) · Scientific Reports · doi:10.1038/srep35074 · Cited by 25