Mechanisms of Organ Injury and Repair by Macrophages

Exploring the full spectrum of macrophage activation

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Protective and pathogenic functions of macrophage subsets

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Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages

Ginhoux, F., Greter, M., Leboeuf, M., Nandi, S., See, P., Gokhan, S., Mehler, M. F., Conway, S. J., Ng, L. G., Stanley, E. R., et al. (2010) · Science · doi:10.1126/science.1194637 · Cited by 5,175

Macrophage biology in development, homeostasis and disease

Wynn, T. A., Chawla, A., & Pollard, J. W. (2013) · Nature · doi:10.1038/nature12034 · Cited by 4,684

Macrophages in Tissue Repair, Regeneration, and Fibrosis

Wynn, T. A., & Vannella, K. M. (2016) · Immunity · doi:10.1016/j.immuni.2016.02.015 · Cited by 4,481

NLRP3 inflammasomes are required for atherogenesis and activated by cholesterol crystals

Duewell, P., Kono, H., Rayner, K. J., Sirois, C. M., Vladimer, G., Bauernfeind, F. G., Abela, G. S., Franchi, L., Nuñez, G., Schnurr, M., et al. (2010) · Nature · doi:10.1038/nature08938 · Cited by 4,026

Mechanisms of fibrosis: therapeutic translation for fibrotic disease

Wynn, T. A., & Ramalingam, T. R. (2012) · Nature Medicine · doi:10.1038/nm.2807 · Cited by 3,541

NLRP3 is activated in Alzheimer’s disease and contributes to pathology in APP/PS1 mice

Heneka, M. T., Kummer, M. P., Stutz, A., Delekate, A., Schwartz, S., Vieira-Saecker, A., Griep, A., Axt, D., Remus, A., Tzeng, T.-C., et al. (2013) · Nature · doi:10.1038/nature11729 · Cited by 2,898

A Lineage of Myeloid Cells Independent of Myb and Hematopoietic Stem Cells

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Fibrosis: from mechanisms to medicines

Henderson, N. C., Rieder, F., & Wynn, T. A. (2020) · Nature · doi:10.1038/s41586-020-2938-9 · Cited by 1,868

The Role of Macrophages in Acute and Chronic Wound Healing and Interventions to Promote Pro-wound Healing Phenotypes

Krzyszczyk, P., Schloss, R. S., Palmer, A. F., & Francois Berthiaume, B. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00419 · Cited by 1,598

IFNγ: signalling, epigenetics and roles in immunity, metabolism, disease and cancer immunotherapy

Ivashkiv, L. B. (2018) · Nature reviews. Immunology · doi:10.1038/s41577-018-0029-z · Cited by 1,418

Inflammation and metabolism in tissue repair and regeneration

Eming, S. A., Wynn, T. A., & Martin, P. (2017) · Science · doi:10.1126/science.aam7928 · Cited by 1,369

The role of macrophages in the resolution of inflammation

Watanabe, S., Alexander, M., Misharin, A. V., & Budinger, G. R. S. (2019) · Journal of Clinical Investigation · doi:10.1172/jci124615 · Cited by 925

TGF-β1 Signaling and Tissue Fibrosis

Kim, K. K., Sheppard, D., & Chapman, H. A. (2018) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a022293 · Cited by 800

Mesenchymal stem cell-derived exosomes and other extracellular vesicles as new remedies in the therapy of inflammatory diseases

Harrell, C. R., Jovicic, N., Djonov, V., Arsenijevic, N., & Volarevic, V. (2019) · Cells · doi:10.3390/cells8121605 · Cited by 795

Cytokine Networks in the Pathophysiology of Inflammatory Bowel Disease

Friedrich, M., Pohin, M., & Powrie, F. M. (2019) · Immunity · doi:10.1016/j.immuni.2019.03.017 · Cited by 776

Moving beyond the glial scar for spinal cord repair

Bradbury, E. J., & Burnside, E. R. (2019) · Nature Communications · doi:10.1038/s41467-019-11707-7 · Cited by 774

Macrophages in inflammation, repair and regeneration

Oishi, Y., & Manabe, I. (2018) · International Immunology · doi:10.1093/intimm/dxy054 · Cited by 770

Macrophages as a therapeutic target to promote diabetic wound healing

Sharifiaghdam, M., Shaabani, E., Majidi, R. F., Smedt, S. C. D., Braeckmans, K., & Fraire, J. C. (2022) · Molecular Therapy · doi:10.1016/j.ymthe.2022.07.016 · Cited by 606

Macrophage Polarization in Chronic Inflammatory Diseases: Killers or Builders?

Parisi, L., Gini, E., Baci, D., Tremolati, M., Fanuli, M., Bassani, B., Farronato, G., Bruno, A., & Mortara, L. (2018) · Journal of Immunology Research · doi:10.1155/2018/8917804 · Cited by 508

Myofibroblast proliferation and heterogeneity are supported by macrophages during skin repair

Shook, B. A., Wasko, R. R., Rivera-Gonzalez, G. C., Salazar-Gatzimas, E., López-Giráldez, F., Dash, B. C., Muñoz-Rojas, A. R., Aultman, K. D., Zwick, R. K., Lei, V., et al. (2018) · Science · doi:10.1126/science.aar2971 · Cited by 519

TGF-β1 – A truly transforming growth factor in fibrosis and immunity

Lodyga, M., & Hinz, B. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.12.010 · Cited by 466

The big five in fibrosis: Macrophages, myofibroblasts, matrix, mechanics, and miscommunication

Pakshir, P., & Hinz, B. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.01.019 · Cited by 396

Macrophage Polarization and Osteoporosis: A Review

Muñoz, J., Akhavan, N. S., Mullins, A. P., & Arjmandi, B. H. (2020) · Nutrients · doi:10.3390/nu12102999 · Cited by 391

Inflammation and Skeletal Muscle Regeneration: Leave It to the Macrophages!

Chazaud, B. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.04.006 · Cited by 397

Lung Myofibroblasts Promote Macrophage Profibrotic Activity through Lactate-induced Histone Lactylation

Cui, H., Xie, N., Banerjee, S., Ge, J., Jiang, D., Dey, T., Matthews, Q. L., Liu, R.-M., & Liu, G. (2020) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2020-0360oc · Cited by 373

Macrophage plasticity: signaling pathways, tissue repair, and regeneration

Yan, L., Wang, J., Cai, X., Liou, Y., Shen, H., Hao, J., Huang, C., Luo, G., & He, W. (2024) · MedComm · doi:10.1002/mco2.658 · Cited by 406

Extracellular vesicle activities regulating macrophage- and tissue-mediated injury and repair responses

Hu, Q., Lyon, C. J., Fletcher, J. K., Tang, W., Wan, M., & Hu, Y. (2020) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2020.12.014 · Cited by 318

Macrophage phenotypes and functions: resolving inflammation and restoring homeostasis

Rodríguez-Morales, P., & Franklin, R. A. (2023) · Trends in Immunology · doi:10.1016/j.it.2023.10.004 · Cited by 341

Gut microbiota-derived butyrate regulates gut mucus barrier repair by activating the macrophage/WNT/ERK signaling pathway

Liang, L., Liu, L., Zhou, W., Yang, C., Mai, G., Li, H., & Chen, Y. (2022) · Clinical Science · doi:10.1042/cs20210778 · Cited by 291

Insulin-Like Growth Factor (IGF) System in Liver Diseases

Adamek, A., & Kasprzak, A. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19051308 · Cited by 284

Role of Macrophages in Acute Lung Injury and Chronic Fibrosis Induced by Pulmonary Toxicants

Laskin, D. L., Malaviya, R., & Laskin, J. D. (2018) · Toxicological Sciences · doi:10.1093/toxsci/kfy309 · Cited by 272

Comparative regenerative mechanisms across different mammalian tissues

Iismaa, S. E., Kaidonis, X., Nicks, A. M., Bogush, N., Kikuchi, K., Naqvi, N., Harvey, R. P., Husain, A., & Graham, R. M. (2018) · npj Regenerative Medicine · doi:10.1038/s41536-018-0044-5 · Cited by 270

The Impact of Estrogens and Their Receptors on Immunity and Inflammation during Infection

Harding, A. T., & Heaton, N. S. (2022) · Cancers · doi:10.3390/cancers14040909 · Cited by 278

Mechanobiology of Macrophages: How Physical Factors Coregulate Macrophage Plasticity and Phagocytosis

Jain, N., Moeller, J., & Vogel, V. (2019) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-062117-121224 · Cited by 237

The Role of Myofibroblasts in Physiological and Pathological Tissue Repair

Schuster, R., Younesi, F., Ezzo, M., & Hinz, B. (2023) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041231 · Cited by 232

Microenvironment-responsive immunoregulatory electrospun fibers for promoting nerve function recovery

Xi, K., Gu, Y., Tang, J., Chen, H., Xu, Y., Wu, L., Cai, F., Deng, L., Yang, H., Shi, Q., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18265-3 · Cited by 231

Macrophages and fibroblasts during inflammation and tissue repair in models of organ regeneration

Mescher, A. L. (2017) · Regeneration · doi:10.1002/reg2.77 · Cited by 238

Canonical and Non-Canonical Wnt Signaling in Immune Cells

Chae, W.-J., & Bothwell, A. L. M. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.08.006 · Cited by 221

Prostaglandin E2 hydrogel improves cutaneous wound healing via M2 macrophages polarization

Zhang, S., Liu, Y., Zhang, X., Zhu, D., Qi, X., Cao, X., Fang, Y., Che, Y., Han, Z., He, Z., et al. (2018) · Theranostics · doi:10.7150/thno.27385 · Cited by 214

Osteoimmunology in Bone Fracture Healing

Ono, T., & Takayanagi, H. (2017) · Current Osteoporosis Reports · doi:10.1007/s11914-017-0381-0 · Cited by 222

The role of macrophage subtypes and exosomes in immunomodulation

Gharavi, A. T., Hanjani, N. A., Movahed, E., & Doroudian, M. (2022) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-022-00384-y · Cited by 214

Building and Regenerating the Lung Cell by Cell

Whitsett, J. A., Kalin, T. V., Xu, Y. J., & Kalinichenko, V. V. (2018) · Physiological Reviews · doi:10.1152/physrev.00001.2018 · Cited by 210

Inflammation and Its Role in Regeneration and Repair

Cooke, J. P. (2019) · Circulation Research · doi:10.1161/circresaha.118.314669 · Cited by 210

Immune responses to injury and their links to eye disease

Stepp, M. A., & Menko, A. S. (2021) · Translational research · doi:10.1016/j.trsl.2021.05.005 · Cited by 204

Pro-Angiogenic Macrophage Phenotype to Promote Myocardial Repair

Ferraro, B., Leoni, G., Hinkel, R., Ormanns, S., Paulin, N., Ortega‐Gómez, A., Viola, J. R., de Jong, R., Bongiovanni, D., Bozoglu, T. M., et al. (2019) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2019.03.503 · Cited by 201

Macrophage phenotypic switch orchestrates the inflammation and repair/regeneration following acute pancreatitis injury

Wu, J., Zhang, L., Shi, J., He, R., Yang, W., Habtezion, A., Niu, N., Lu, P., & Xue, J. (2020) · EBioMedicine · doi:10.1016/j.ebiom.2020.102920 · Cited by 189

Roles of Macrophages in the Development and Treatment of Gut Inflammation

Han, X., Ding, S., Jiang, H., & Liu, G. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.625423 · Cited by 196

Regulation of tissue iron homeostasis: the macrophage “ferrostat”

Winn, N. C., Volk, K. M., & Hasty, A. H. (2020) · JCI Insight · doi:10.1172/jci.insight.132964 · Cited by 184

Monocytes deposit migrasomes to promote embryonic angiogenesis

Zhang, C., Li, T., Yin, S., Gao, M., He, H., Li, Y., Jiang, D., Shi, M., Wang, J., & Yu, L. (2022) · Nature Cell Biology · doi:10.1038/s41556-022-01026-3 · Cited by 173

Role of gut microbiota in intestinal wound healing and barrier function

Alam, A., & Neish, A. (2018) · Tissue Barriers · doi:10.1080/21688370.2018.1539595 · Cited by 166

Losartan attenuates sepsis-induced cardiomyopathy by regulating macrophage polarization via TLR4-mediated NF-κB and MAPK signaling

Chen, X.-S., Wang, S., Liu, C.-Y., Gao, Y., Meng, X.-L., Wei, W., Shou, S., Liu, Y., & Chai, Y. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106473 · Cited by 173

Analysis of the immune response to sciatic nerve injury identifies efferocytosis as a key mechanism of nerve debridement

Kalinski, A. L., Yoon, C., Huffman, L. D., Duncker, P. C., Kohen, R., Passino, R., Hafner, H., Johnson, C. N., Kawaguchi, R., Carbajal, K. S., et al. (2020) · eLife · doi:10.7554/elife.60223 · Cited by 168

Barrier-tissue macrophages: functional adaptation to environmental challenges

Mowat, A. M., Scott, C. L., & Bain, C. C. (2017) · Nature Medicine · doi:10.1038/nm.4430 · Cited by 162

The twin cytokines interleukin-34 and CSF-1: masterful conductors of macrophage homeostasis

Muñoz-García, J., Cochonneau, D., Télétchéa, S., Moranton, E., Lanoé, D., Brion, R., Lézot, F., Heymann, M., & Heymann, D. (2020) · Theranostics · doi:10.7150/thno.50683 · Cited by 159

Macrophages and hepatocellular carcinoma

Tian, Z., Hou, X., Liu, W., Han, Z., & Wei, L. (2019) · Cell & Bioscience · doi:10.1186/s13578-019-0342-7 · Cited by 158

IL-4 and IL-13: Regulators and Effectors of Wound Repair

Allen, J. E. (2023) · Annual Review of Immunology · doi:10.1146/annurev-immunol-101921-041206 · Cited by 158

Distinct myeloid cell subsets promote meningeal remodeling and vascular repair after mild traumatic brain injury

Russo, M. V., Latour, L. L., & McGavern, D. B. (2018) · Nature Immunology · doi:10.1038/s41590-018-0086-2 · Cited by 149

Intra- and Extracellular Degradation of Neutrophil Extracellular Traps by Macrophages and Dendritic Cells

Lazzaretto, B., & Fadeel, B. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1800159 · Cited by 150

Reduction of the relative centrifugal force influences cell number and growth factor release within injectable PRF-based matrices

Wend, S., Kubesch, A., Orłowska, A., Al‐Maawi, S., Zender, N., Dias, A., Miron, R. J., Sader, R., Booms, P., Kirkpatrick, C. J., et al. (2017) · Journal of Materials Science Materials in Medicine · doi:10.1007/s10856-017-5992-6 · Cited by 155

Cutaneous innervation in impaired diabetic wound healing

Nowak, N. C., Menichella, D. M., Miller, R., & Paller, A. S. (2021) · Translational research · doi:10.1016/j.trsl.2021.05.003 · Cited by 146

Conventional and pathogenic Th2 cells in inflammation, tissue repair, and fibrosis

Kokubo, K., Onodera, A., Kiuchi, M., Tsuji, K., Hirahara, K., & Nakayama, T. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.945063 · Cited by 155

Evolving Roles of Muscle-Resident Fibro-Adipogenic Progenitors in Health, Regeneration, Neuromuscular Disorders, and Aging

Théret, M., Rossi, F. M. V., & Contreras, O. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.673404 · Cited by 154

Modulation of macrophages by a paeoniflorin-loaded hyaluronic acid-based hydrogel promotes diabetic wound healing

Yang, H., Song, L., Sun, B., Chu, D., Yang, L., Li, M., Li, H., Dai, Y., Yu, Z., & Guo, J. (2021) · Materials Today Bio · doi:10.1016/j.mtbio.2021.100139 · Cited by 137

Lymphatic Dysfunction, Leukotrienes, and Lymphedema

Jiang, X., Nicolls, M. R., Tian, W., & Rockson, S. G. (2017) · Annual Review of Physiology · doi:10.1146/annurev-physiol-022516-034008 · Cited by 133

Long noncoding RNA Malat1 regulates differential activation of macrophages and response to lung injury

Cui, H., Banerjee, S., Guo, S., Xie, N., Ge, J., Jiang, D., Zörnig, M., Thannickal, V. J., & Liu, G. (2019) · JCI Insight · doi:10.1172/jci.insight.124522 · Cited by 133

Inflammation associated with noise-induced hearing loss

Frye, M. D., Ryan, A. F., & Kurabi, A. (2019) · The Journal of the Acoustical Society of America · doi:10.1121/1.5132545 · Cited by 138

Wnt Signaling in the Regulation of Immune Cell and Cancer Therapeutics

Haseeb, M., Pirzada, R. H., Ain, Q. U., & Choi, S. (2019) · Cells · doi:10.3390/cells8111380 · Cited by 133

Overexpression of S100A9 in obesity impairs macrophage differentiation via TLR4-NFkB-signaling worsening inflammation and wound healing

Franz, S., Ertel, A., Engel, K. M., Simon, J. C., & Saalbach, A. (2022) · Theranostics · doi:10.7150/thno.67174 · Cited by 129

Therapeutic Use of Mesenchymal Stem Cell-Derived Exosomes: From Basic Science to Clinics

Harrell, C. R., Jovicic, N. U., Djonov, V., & Volarević, V. (2020) · Pharmaceutics · doi:10.3390/pharmaceutics12050474 · Cited by 131

Thou shall not heal: Overcoming the non-healing behaviour of diabetic foot ulcers by engineering the inflammatory microenvironment

Monaghan, M. G., Borah, R., Thomsen, C., & Browne, S. (2023) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2023.115120 · Cited by 131

Microglia maintain structural integrity during fetal brain morphogenesis

Lawrence, A. R., Canzi, A., Bridlance, C., Olivié, N., Lansonneur, C., Catale, C., Pizzamiglio, L., Kloeckner, B., Silvin, A., Munro, D. A. D., et al. (2024) · Cell · doi:10.1016/j.cell.2024.01.012 · Cited by 126

Role of Hyaluronic Acids and Potential as Regenerative Biomaterials in Wound Healing

Yang, H., Song, L., Zou, Y., Sun, D., Wang, L., Yu, Z., & Guo, J. (2020) · ACS Applied Bio Materials · doi:10.1021/acsabm.0c01364 · Cited by 124

Fra-2–expressing macrophages promote lung fibrosis

Ucero, A. C., Bakiri, L., Roediger, B., Suzuki, M., Jiménez, M., Mandal, P., Braghetta, P., Bonaldo, P., Paz-Ares, L. G., Torre, C. F., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci125366 · Cited by 120

The Cross-Talk between Mesenchymal Stem Cells and Immune Cells in Tissue Repair and Regeneration

Harrell, C. R., Djonov, V., & Volarević, V. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052472 · Cited by 119

Temporally distinct myeloid cell responses mediate damage and repair after cerebrovascular injury

Mastorakos, P., Mihelson, N., Luby, M., Burks, S. R., Johnson, K., Hsia, A. W., Witko, J., Frank, J. A., Latour, L., & McGavern, D. B. (2021) · Nature Neuroscience · doi:10.1038/s41593-020-00773-6 · Cited by 113

CCR2 deficiency in monocytes impairs angiogenesis and functional recovery after ischemic stroke in mice

Pedragosa, J., Miró‐Mur, F., Otxoa-de-Amezaga, A., Justicia, C., Ruíz-Jaén, F., Ponsaerts, P., Pasparakis, M., & Planas, A. M. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20909055 · Cited by 115

The Immune-Centric Revolution in the Diabetic Foot: Monocytes and Lymphocytes Role in Wound Healing and Tissue Regeneration—A Narrative Review

Rehak, L., Giurato, L., Meloni, M., Panunzi, A., Manti, G. M., & Uccioli, L. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11030889 · Cited by 112

Fibrosis: cross-organ biology and pathways to development of innovative drugs

Rieder, F., Nagy, L. E., Maher, T. M., Distler, J. H. W., Kramann, R., Hinz, B., & Prunotto, M. (2025) · Nature Reviews Drug Discovery · doi:10.1038/s41573-025-01158-9 · Cited by 134

Resident tissue macrophages: Key coordinators of tissue homeostasis beyond immunity

Zhao, J., Andreev, I., & Silva, H. M. (2024) · Science Immunology · doi:10.1126/sciimmunol.add1967 · Cited by 109

Generation, localization and functions of macrophages during the development of testis

Lokka, E., Lintukorpi, L., Cisneros-Montalvo, S., Mäkelä, J., Tyystjärvi, S., Ojasalo, V., Gerke, H., Toppari, J., Rantakari, P., & Salmi, M. (2020) · Nature Communications · doi:10.1038/s41467-020-18206-0 · Cited by 102

The Role of Tumor Associated Macrophages in Hepatocellular Carcinoma

Huang, Y., Ge, W., Zhou, J., Gao, B., Qian, X., & Wang, W. (2021) · Journal of Cancer · doi:10.7150/jca.51346 · Cited by 101

Is the Macrophage Phenotype Determinant for Fibrosis Development?

Lis-López, L., Bauset, C., Seco-Cervera, M., & Cosín‐Roger, J. (2021) · Biomedicines · doi:10.3390/biomedicines9121747 · Cited by 104

Innate Immunity and Pathogenesis of Biliary Atresia

Ortiz‐Perez, A., Donnelly, B., Temple, H., Tiao, G. M., Bansal, R., & Mohanty, S. K. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00329 · Cited by 102

The Role of Macrophages in Vascular Repair and Regeneration after Ischemic Injury

Hong, H., & Tian, X. Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21176328 · Cited by 106

Accelerated Wound Closure of Deep Partial Thickness Burns with Acellular Fish Skin Graft

Stone, R., Saathoff, E. C., Larson, D. A., Wall, J. T., Wienandt, N., Magnússon, S., Kjartansson, H., Natesan, S., & Christy, R. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041590 · Cited by 98

Quadruple abnormal protein aggregates in brainstem pathology and exogenous metal-rich magnetic nanoparticles (and engineered Ti-rich nanorods). The substantia nigrae is a very early target in young urbanites and the gastrointestinal tract a key brainstem portal

Calderón‐Garcidueñas, L., González-Maciel, A., Reynoso-Robles, R., Hammond, J., Kulesza, R. J., Lachmann, I., Torres‐Jardón, R., Mukherjee, P. S., & Maher, B. A. (2020) · Environmental Research · doi:10.1016/j.envres.2020.110139 · Cited by 98

Essential involvement of the CX3CL1-CX3CR1 axis in bleomycin-induced pulmonary fibrosis via regulation of fibrocyte and M2 macrophage migration

Ishida, Y., Kimura, A., Nosaka, M., Kuninaka, Y., Hemmi, H., Sasaki, I., Kaisho, T., Mukaida, N., & Kondo, T. (2017) · Scientific Reports · doi:10.1038/s41598-017-17007-8 · Cited by 97

Targeting vascular normalization: a promising strategy to improve immune–vascular crosstalk in cancer immunotherapy

Qian, C., Liu, C., Liu, W., Zhou, R., & Zhao, L. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1291530 · Cited by 99

Macrophage Transitions in Heart Valve Development and Myxomatous Valve Disease

Hulin, A., Anstine, L. J., Kim, A. J., Potter, S. J., DeFalco, T., Lincoln, J., & Yutzey, K. E. (2018) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.117.310667 · Cited by 88

Pulmonary inflammation and fibroblast immunoregulation: from bench to bedside

Ghonim, M. A., Boyd, D. F., Flerlage, T., & Thomas, P. G. (2023) · Journal of Clinical Investigation · doi:10.1172/jci170499 · Cited by 90

The Many Roles of Macrophages in Skeletal Muscle Injury and Repair

Wang, X., & Zhou, L. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.952249 · Cited by 101

Low-intensity pulsed ultrasound promotes skeletal muscle regeneration via modulating the inflammatory immune microenvironment

Qin, H., Luo, Z., Sun, Y., He, Z., Qi, B., Chen, Y., Wang, J., Li, C., Lin, W., Han, Z., et al. (2023) · International Journal of Biological Sciences · doi:10.7150/ijbs.79685 · Cited by 86

Immune System and Hepatocellular Carcinoma (HCC): New Insights into HCC Progression

Kotsari, M., Dimopoulou, V., Koskinas, J. S., & Armakolas, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241411471 · Cited by 93

Cellular Mechanisms of Psoriasis Pathogenesis: A Systemic Review

Wu, M., Dai, C., & Zeng, F. (2023) · Clinical Cosmetic and Investigational Dermatology · doi:10.2147/ccid.s420850 · Cited by 88

Inhibitory actions of the NRG-1/ErbB4 pathway in macrophages during tissue fibrosis in the heart, skin, and lung

Vermeulen, Z., Hervent, A.-S., Dugaucquier, L., Vandekerckhove, L., Rombouts, M., Beyens, M., Schrijvers, D. M., Meyer, G. R. Y. D., Maudsley, S. R., Keulenaer, G. W. D., et al. (2017) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00206.2017 · Cited by 83

Flavonoid-mediated immunomodulation of human macrophages involves key metabolites and metabolic pathways

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Resolution of Inflammation and Gut Repair in IBD: Translational Steps Towards Complete Mucosal Healing

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