The DOI matches its Crossref record; 178 of the 178 references it cites were found in a registry or an index.
Protective and pathogenic functions of macrophage subsets
Open accessAbstract
Macrophages are strategically located throughout the body tissues, where they ingest and process foreign materials, dead cells and debris and recruit additional macrophages in response to inflammatory signals. They are highly heterogeneous cells that can rapidly change their function in response to local microenvironmental signals. In this Review, we discuss the four stages of orderly inflammation mediated by macrophages: recruitment to tissues; differentiation and activation in situ; conversion to suppressive cells; and restoration of tissue homeostasis. We also discuss the protective and pathogenic functions of the various macrophage subsets in antimicrobial defence, antitumour immune responses, metabolism and obesity, allergy and asthma, tumorigenesis, autoimmunity, atherosclerosis, fibrosis and wound healing. Finally, we briefly discuss the characterization of macrophage heterogeneity in humans.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“CD68 and reelin, markers for MΦs and HSCs, respectively (12,13), were expressed in our system at the end of the experiment, reflecting the maintenance of the cell types in a differentiated state.”
From Development of an in vitro human liver system for interrogating nonalcoholic steatohepatitis (2016) · cites this paper as [13]
In the citing paper
“Macrophage polarization and plasticity have been shown to play important roles in a diverse spectrum of disease processes [32,33].”
From Macrophage polarization: an opportunity for improved outcomes in biomaterials and regenerative medicine (2012) · cites this paper as [32]
In the citing paper
“In some cases, as will be discussed in further detail, prolonged inflammation and remodeling leading to fibrosis or hypertrophic scar formation may occur due to dysregulation of the default healing process [32,86,101,102].”
From Macrophage polarization: an opportunity for improved outcomes in biomaterials and regenerative medicine (2012) · cites this paper as [32]
In the citing paper
“One of the major events at this time is a change in the phenotype of macrophages from an inflammatory and microbicidal phenotype, grouped as M1 macrophages, secreting IL-1, TNFα, IL-6, IL-12, MMPs, and other cytokines, to an anti-inflammatory, regulatory, and reparative phenotype, classed and grouped as M2, producing arginase, TGFβ, CCL18, PGE2, and IL-10 (Fig. 4).”
From The Innate Immune System in Acute and Chronic Wounds (2016) · cites this paper as [93]
In the citing paper
“However, chronic inflammation and persistent Mp accumulation are often associated with tissue destruction and fibrosis [6 -8].”
From Macrophage phenotypes during tissue repair (2013) · cites this paper as [8]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
RETRACTED: Foxp3-positive macrophages display immunosuppressive properties and promote tumor growth
Manrique, S. Z., Correa, M. A. D., Hoelzinger, D. B., Dominguez, A. L., Mirza, N. N., Lin, H., Stein‐Streilein, J., Gordon, S., & Lustgarten, J. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20100730 · Cited by 72
RetractedHallmarks of Cancer: The Next Generation
Hanahan, D., & Weinberg, R. A. (2011) · Cell · doi:10.1016/j.cell.2011.02.013 · Cited by 66,590
Exploring the full spectrum of macrophage activation
Mosser, D. M., & Edwards, J. P. (2008) · Nature Reviews Immunology · doi:10.1038/nri2448 · Cited by 9,144
Alternative activation of macrophages
Gordon, S. (2003) · Nature Reviews Immunology · doi:10.1038/nri978 · Cited by 6,189
Monocyte and macrophage heterogeneity
Gordon, S., & Taylor, P. R. (2005) · Nature Reviews Immunology · doi:10.1038/nri1733 · Cited by 5,190
Curiel, T. J., Coukos, G., Zou, L., Alvarez, X., Cheng, P., Mottram, P., Evdemon-Hogan, M., Conejo-Garcia, J. R., Zhang, L., Burow, M., et al. (2004) · Nature Medicine · doi:10.1038/nm1093 · Cited by 5,151
Cytokine-mediated regulation of CXCR4 expression in human neutrophils
Nagase, H., Miyamasu, M., Yamaguchi, M., Imanishi, M., Tsuno, N. H., Matsushima, K., Yamamoto, K., Morita, Y., & Hirai, K. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.71.4.711 · Cited by 4,713
Obesity induces a phenotypic switch in adipose tissue macrophage polarization
Lumeng, C. N., Bodzin, J. L., & Saltiel, A. R. (2007) · Journal of Clinical Investigation · doi:10.1172/jci29881 · Cited by 4,664
Cellular and molecular mechanisms of fibrosis
Wynn, T. (2008) · The Journal of Pathology · doi:10.1002/path.2277 · Cited by 4,495
Self-citationMacrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm
Biswas, S. K., & Mantovani, A. (2010) · Nature Immunology · doi:10.1038/ni.1937 · Cited by 3,840
Flagged first, then by citations
Cited by
Sorted by citations
Items 401–500 of 1,030
Microcystin-LR ameliorates pulmonary fibrosis via modulating CD206+ M2-like macrophage polarization
Wang, J., Xu, L., Xiang, Z., Ren, Y., Zheng, X., Zhao, Q., Zhou, Q., Zhou, Y., Xu, L., & Wang, Y. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2329-z · Cited by 172
Ding, J., Zhang, Y., Cai, X., Zhang, Y., Yan, S., Wang, J., Zhang, S., Yin, T., Yang, C., & Yang, J. (2021) · Theranostics · doi:10.7150/thno.58731 · Cited by 172
Wang, Z., Brandt, S., Medeiros, A., Wang, S., Wu, H., Dent, A., & Serezani, C. H. (2015) · PLOS ONE · doi:10.1371/journal.pone.0115855 · Cited by 169
Wager, C. M. L., & Wormley, F. L. (2014) · Mucosal Immunology · doi:10.1038/mi.2014.65 · Cited by 171
C-Type Lectin Receptors in Antiviral Immunity and Viral Escape
Bermejo‐Jambrina, M., Eder, J., Helgers, L. C., Hertoghs, N., Nijmeijer, B. M., Stunnenberg, M., & Geijtenbeek, T. B. H. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00590 · Cited by 184
Hypothalamic innate immune reaction in obesity
Kälin, S., Heppner, F. L., Bechmann, I., Prinz, M., Tschöp, M. H., & Yi, C.-X. (2015) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2015.48 · Cited by 167
da Silva, M. D., Bobinski, F., Sato, K., Kolker, S. J., Sluka, K. A., & Santos, A. R. S. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8790-x · Cited by 173
Pathogenic Role of IL-17-Producing Immune Cells in Obesity, and Related Inflammatory Diseases
Chehimi, M., Vidal, H., & Eljaafari, A. (2017) · Journal of Clinical Medicine · doi:10.3390/jcm6070068 · Cited by 172
Rong, L., Zhang, Y., Li, W., Su, Z., Fadhil, J. I., & Zhang, C. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.119515 · Cited by 167
A unique role for p53 in the regulation of M2 macrophage polarization
Li, L., Ng, D. S. W., Mah, W.-C., Almeida, F. F., Rahmat, S. A. B., Rao, V. K., Leow, S. C., Laudisi, F., Peh, M. T., Goh, A. M., et al. (2014) · Cell Death and Differentiation · doi:10.1038/cdd.2014.212 · Cited by 169
Dou, C., Ding, N., Zhao, C., Hou, T., Kang, F., Cao, Z., Liu, C., Bai, Y., Dai, Q., Ma, Q., et al. (2017) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3364 · Cited by 169
Kauder, S. E., Kuo, T. C., Harrabi, O., Chen, A. Y.-C., Sangalang, E., Doyle, L. V., Rocha, S. S., Bollini, S. S., Han, B., Sim, J., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0201832 · Cited by 170
Macrophage Plasticity and Atherosclerosis Therapy
Lin, P. C., Ji, H., Li, Y., & Guo, S. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.679797 · Cited by 172
Marrocco, A., & Ortiz, L. A. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.936167 · Cited by 173
Niche signals and transcription factors involved in tissue-resident macrophage development
T’Jonck, W., Guilliams, M., & Bonnardel, J. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.02.005 · Cited by 173
Li, T., Peng, M., Yang, Z., Zhou, X., Deng, Y., Jiang, C., Xiao, M., & Wang, J. (2018) · Acta Biomaterialia · doi:10.1016/j.actbio.2018.03.012 · Cited by 169
Chen, X., Yang, M., Yin, J., Li, P., Zeng, S., Zheng, G., He, Z., Liu, H., Wang, Q., Zhang, F., et al. (2022) · Cell Communication and Signaling · doi:10.1186/s12964-022-00888-2 · Cited by 165
The Role of Reactive Oxygen Species in the Rheumatoid Arthritis-Associated Synovial Microenvironment
Wang, X., Fan, D., Cao, X., Ye, Q., Wang, Q., Zhang, M., & Xiao, C. (2022) · Antioxidants · doi:10.3390/antiox11061153 · Cited by 176
Pharmacokinetics of magnetic iron oxide nanoparticles for medical applications
Nowak‐Jary, J., & Machnicka, B. (2022) · Journal of Nanobiotechnology · doi:10.1186/s12951-022-01510-w · Cited by 170
Boer, M. C., Joosten, S. A., & Ottenhoff, T. H. M. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00217 · Cited by 170
Sima, C., & Glogauer, M. (2013) · Periodontology 2000 · doi:10.1111/prd.12032 · Cited by 165
Interferon-Regulatory Factors Determine Macrophage Phenotype Polarization
Günthner, R., & Anders, H. (2013) · Mediators of Inflammation · doi:10.1155/2013/731023 · Cited by 172
Electric fields are novel determinants of human macrophage functions
Hoare, J. I., Rajnicek, A. M., McCaig, C., Barker, R. N., & Wilson, H. M. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.3a0815-390r · Cited by 169
NF-κB dynamics determine the stimulus specificity of epigenomic reprogramming in macrophages
Cheng, Q. J., Ohta, S., Sheu, K. M., Spreafico, R., Adelaja, A., Taylor, B. E., & Hoffmann, A. (2021) · Science · doi:10.1126/science.abc0269 · Cited by 168
Pathophysiology of NASH: perspectives for a targeted treatment
Marra, F., & Lotersztajn, S. (2013) · Current Pharmaceutical Design · doi:10.2174/13816128113199990344 · Cited by 163
Yao, A., Liu, F., Chen, K., Tang, L. V., Liu, L., Zhang, K., Yu, C., Bian, G., Guo, H., Zheng, J., et al. (2014) · Neurotherapeutics · doi:10.1007/s13311-013-0254-x · Cited by 163
Kiss, M., Czimmerer, Z., & Nagy, L. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2013.05.044 · Cited by 166
Acute injury in the peripheral nervous system triggers an alternative macrophage response
Ydens, E., Cauwels, A., Asselbergh, B., Goethals, S., Peeraer, L., Lornet, G., Almeida-Souza, L., Ginderachter, J. A. V., Timmerman, V., & Janssens, S. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-176 · Cited by 171
Fan, Y., Zhang, Y., Zhao, Q., Xie, Y., Luo, R., Yang, P., & Weng, Y. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.03.007 · Cited by 164
Recent advancements in the development of heterocyclic anti-inflammatory agents
Sharma, S., Kumar, D., Singh, G., Monga, V., & Kumar, B. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2020.112438 · Cited by 163
Clearance of Amyloid-β Peptides By Microglia and Macrophages: the Issue of What, When and Where
Lai, A. Y., & McLaurin, J. (2012) · Future Neurology · doi:10.2217/fnl.12.6 · Cited by 166
Lactic acid promotes macrophage polarization through MCT-HIF1α signaling in gastric cancer
Zhang, L., & Li, S. (2020) · Experimental Cell Research · doi:10.1016/j.yexcr.2020.111846 · Cited by 168
MiR-146a modulates macrophage polarization by inhibiting Notch1 pathway in RAW264.7 macrophages
Huang, C., Liu, X.-J., QunZhou, Xie, J., Ma, T.-T., Meng, X.-M., & Li, J. (2016) · International Immunopharmacology · doi:10.1016/j.intimp.2016.01.009 · Cited by 160
Macrophage-based nanotherapeutic strategies in ulcerative colitis
Zhang, J., Zhao, Y., Hou, T., Zeng, H., Kalambhe, D., Wang, B., Shen, X., & Huang, Y. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.01.047 · Cited by 160
Lactate-Dependent Regulation of Immune Responses by Dendritic Cells and Macrophages
Manoharan, I., Prasad, P. D., Thangaraju, M., & Manicassamy, S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.691134 · Cited by 171
Functional muscle recovery with nanoparticle-directed M2 macrophage polarization in mice
Raimondo, T. M., & Mooney, D. J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1806908115 · Cited by 159
Osteoimmunology: Inflammatory osteolysis and regeneration of the alveolar bone
Gruber, R. (2019) · Journal Of Clinical Periodontology · doi:10.1111/jcpe.13056 · Cited by 161
Hu, G., Su, Y., Kang, B. H., Fan, Z., Dong, T., Brown, D. R., Cheah, J. H., Wittrup, K. D., & Chen, J. (2021) · Nature Communications · doi:10.1038/s41467-021-21066-x · Cited by 162
Metabolic reprogramming consequences of sepsis: adaptations and contradictions
Liu, J., Zhou, G., Wang, X., & Liu, D. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04490-0 · Cited by 161
Hucke, S., Eschborn, M., Liebmann, M., Herold, M. V. B., Freise, N., Engbers, A., Ehling, P., Meuth, S. G., Roth, J., Kuhlmann, T., et al. (2015) · Journal of Autoimmunity · doi:10.1016/j.jaut.2015.11.001 · Cited by 161
Ko, J. H., Lee, H. J., Jeong, H. J., Kim, M. K., Wee, W. R., Yoon, S.-O., Choi, H., Prockop, D. J., & Oh, J. Y. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1522905113 · Cited by 164
Herová, M., Schmid, M., Gemperle, C., & Hersberger, M. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402166 · Cited by 157
Grailer, J. J., Haggadone, M. D., Sarma, J. V., Zetoune, F. S., & Ward, P. A. (2014) · Journal of Innate Immunity · doi:10.1159/000358524 · Cited by 157
Arnold, C. E., Whyte, C. S., Gordon, P., Barker, R. N., Rees, A. J., & Wilson, H. M. (2013) · Immunology · doi:10.1111/imm.12173 · Cited by 163
Interleukin-36γ–producing macrophages drive IL-17–mediated fibrosis
Sommerfeld, S. D., Cherry, C., Schwab, R. M., Chung, L., Maestas, D. R., Laffont, P., Stein, J. E., Tam, A. J., Ganguly, S., Housseau, F., et al. (2019) · Science Immunology · doi:10.1126/sciimmunol.aax4783 · Cited by 160
Synergistic immunotherapy of glioblastoma by dual targeting of IL-6 and CD40
Yang, F., He, Z., Duan, H., Zhang, D., Li, J., Yang, H., Dorsey, J. F., Zou, W., Nabavizadeh, S. A., Bagley, S. J., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23832-3 · Cited by 161
Monocyte-endothelial cell interactions in vascular and tissue remodeling
Medrano-Bosch, M., Simón-Codina, B., Jiménez, W., Edelman, E. R., & Melgar‐Lesmes, P. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1196033 · Cited by 168
Inflammatory pathways in the early steps of colorectal cancer development
Mariani, F. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i29.9716 · Cited by 161
Ambarus, C. A., Noordenbos, T., de Hair, M. J. H., Tak, P. P., & Baeten, D. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3796 · Cited by 161
The key role of the scaffold on the efficiency of dendrimer nanodrugs
Caminade, A., Fruchon, S., Turrin, C., Poupot, M., Ouali, A., Maraval, A., Garzoni, M., Maly, M., Furer, V. L., Коваленко, В. И., et al. (2015) · Nature Communications · doi:10.1038/ncomms8722 · Cited by 162
Host Responses to Biomaterials and Anti‐Inflammatory Design—a Brief Review
Zhou, G., & Groth, T. (2018) · Macromolecular Bioscience · doi:10.1002/mabi.201800112 · Cited by 160
Yu, Y., Dai, K., Gao, Z., Tang, W., Shen, T., Yuan, Y., Wang, J., & Liu, C. (2021) · Science Advances · doi:10.1126/sciadv.abd8217 · Cited by 156
Tan, H.-Y., Wang, N., Man, K., Tsao, S., Che, C., & Feng, Y. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.271 · Cited by 155
Therapeutic strategies for preventing skeletal muscle fibrosis after injury
Garg, K., Corona, B. T., & Walters, T. (2015) · Frontiers in Pharmacology · doi:10.3389/fphar.2015.00087 · Cited by 151
Regulation of Embryonic and Postnatal Development by the CSF-1 Receptor
Chiţu, V., & Stanley, E. R. (2016) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2016.10.004 · Cited by 163
Foo, S., Chen, W., Chan, Y., Bowman, J. W., Chang, L.-C., Choi, Y., Yoo, J., Ge, J., Cheng, G., Bonnin, A., et al. (2017) · Nature Microbiology · doi:10.1038/s41564-017-0016-3 · Cited by 155
Tenbrock, L., Wolf, J., Boneva, S., Schlecht, A., Agostini, H. T., Wieghofer, P., Schlunck, G., & Lange, C. (2021) · Cell and Tissue Research · doi:10.1007/s00441-021-03514-8 · Cited by 161
Mononuclear phagocytes locally specify and adapt their phenotype in a multiple sclerosis model
Locatelli, G., Theodorou, D., Kendirli, A., Jordão, M. J. C., Staszewski, O., Phulphagar, K., Cantuti-Castelvetri, L., Dagkalis, A., Bessis, A., Simons, M., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0212-3 · Cited by 155
Signals in the pancreatic islet microenvironment influence β‐cell proliferation
Aamodt, K. I., & Powers, A. C. (2017) · Diabetes Obesity and Metabolism · doi:10.1111/dom.13031 · Cited by 166
Development of an in vitro human liver system for interrogating nonalcoholic steatohepatitis
Feaver, R. E., Cole, B. K., Lawson, M. J., Hoang, S. A., Marukian, S., Blackman, B. R., Figler, R. A., Sanyal, A. J., Wamhoff, B. R., & Dash, A. (2016) · JCI Insight · doi:10.1172/jci.insight.90954 · Cited by 153
Chang, H. Y., Lee, H., Kim, W., & Surh, Y. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.10.014 · Cited by 159
Fricker, M., Oliva-Martín, M. J., & Brown, G. C. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-196 · Cited by 137
Macrophage Targeted Theranostics as Personalized Nanomedicine Strategies for Inflammatory Diseases
Patel, S. K., & Janjic, J. M. (2014) · Theranostics · doi:10.7150/thno.9476 · Cited by 155
Nakanishi, H., Kawashima, Y., Kurima, K., Chae, J. J., Ross, A. M., Pinto-Patarroyo, G. P., Patel, S. K., Muskett, J. A., Ratay, J. S., Chattaraj, P., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1702946114 · Cited by 153
Signaling pathways in macrophages: molecular mechanisms and therapeutic targets
Li, M., Wang, M., Wen, Y., Zhang, H., Zhao, G., & Gao, Q. (2023) · MedComm · doi:10.1002/mco2.349 · Cited by 165
Alhouayek, M., Masquelier, J., Cani, P. D., Lambert, D. M., & Muccioli, G. G. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1314017110 · Cited by 152
He, H., Zhang, S., Tighe, S. P., Son, J., & Tseng, S. C. G. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.479584 · Cited by 152
Zhang, W., Cai, Y., Xu, W., Yin, Z., Gao, X., & Xiong, S. (2013) · Journal of Clinical Immunology · doi:10.1007/s10875-013-9881-6 · Cited by 156
Bencze, M., Négroni, E., Vallese, D., Yacoub‐Youssef, H., Chaouch, S., Wolff, A., Aamiri, A., Santo, J. P. D., Chazaud, B., Butler-Browne, G. S., et al. (2012) · Molecular Therapy · doi:10.1038/mt.2012.189 · Cited by 164
Bobinski, F., Teixeira, J. M., Sluka, K. A., & Santos, A. R. S. (2017) · Pain · doi:10.1097/j.pain.0000000000001109 · Cited by 151
Advanced strategies to evade the mononuclear phagocyte system clearance of nanomaterials
Lu, J., Gao, X., Wang, S., He, Y., Ma, X., Zhang, T., & Liu, X. (2023) · Exploration · doi:10.1002/exp.20220045 · Cited by 155
Label-free characterization of white blood cells by measuring 3D refractive index maps
Yoon, J. W., Kim, K., Park, H., Choi, C., Jang, S., & Park, Y. (2015) · Biomedical Optics Express · doi:10.1364/boe.6.003865 · Cited by 152
Organization of the skin immune system and compartmentalized immune responses in infectious diseases
Quaresma, J. A. S. (2019) · Clinical Microbiology Reviews · doi:10.1128/cmr.00034-18 · Cited by 149
Toki, D., Zhang, W., Hor, K., Liuwantara, D., Alexander, S. I., Yi, Z., Sharma, R. N., Chapman, J. R., Nankivell, B. J., Murphy, B. T., et al. (2014) · American Journal of Transplantation · doi:10.1111/ajt.12803 · Cited by 150
Targeting macrophage immunometabolism: Dawn in the darkness of sepsis
Kumar, V. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.03.005 · Cited by 150
Lipocalin 2 deactivates macrophages and worsens pneumococcal pneumonia outcomes
Warszawska, J. M., Gawish, R., Sharif, O., Sigel, S., Doninger, B., Lakovits, K., Mesteri, I., Nairz, M., Boon, L., Spiel, A., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci67911 · Cited by 148
Risk factors and outcome of bacterial infections in cirrhosis
Bruns, T. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i10.2542 · Cited by 148
The Skin-Resident Immune Network
Tay, S. S., Roediger, B., Tong, P. L., Tikoo, S., & Weninger, W. (2014) · Current Dermatology Reports · doi:10.1007/s13671-013-0063-9 · Cited by 147
IL-34 mediates acute kidney injury and worsens subsequent chronic kidney disease
Baek, J.-H., Zeng, R., Weinmann‐Menke, J., Valerius, M. T., Wada, Y., Ajay, A. K., Colonna, M., & Kelley, V. R. (2015) · Journal of Clinical Investigation · doi:10.1172/jci81166 · Cited by 147
Immune Activation in Irritable Bowel Syndrome: Can Neuroimmune Interactions Explain Symptoms?
Hughes, P. A., Zola, H., Penttila, I., Blackshaw, L. A., Andrews, J. M., & Krumbiegel, D. (2013) · The American Journal of Gastroenterology · doi:10.1038/ajg.2013.120 · Cited by 147
Jones, C. V., & Ricardo, S. D. (2013) · Organogenesis · doi:10.4161/org.25676 · Cited by 152
Wu, C., Xue, Y., Wang, P., Lin, L., Liu, Q., Li, N., Xu, J., & Cao, X. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302379 · Cited by 147
Wang, X., Ji, Y., Feng, P., Liu, R., Li, G., Zheng, J., Xue, Y., Wei, Y., Ji, C., Chen, D., et al. (2021) · Advanced Science · doi:10.1002/advs.202100209 · Cited by 147
Macrophage arginase-1 controls bacterial growth and pathology in hypoxic tuberculosis granulomas
Duque-Correa, M. A., Kühl, A. A., Rodriguez, P. C., Zedler, U., Schommer-Leitner, S., Rao, M., Weiner, J., Hurwitz, R., Qualls, J. E., Kosmiadi, G. A., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1408839111 · Cited by 146
Self-citationRybka, J., Kędziora-Kornatowska, K., Banaś-Leżańska, P., Majsterek, I., Carvalho, L. A., Cattaneo, A., Anacker, C., & Kędziora, J. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.05.019 · Cited by 146
The importance of microglia in the development of the vasculature in the central nervous system
Arnold, T., & Betsholtz, C. (2013) · Vascular Cell · doi:10.1186/2045-824x-5-4 · Cited by 157
Song, W., Li, Q., Ryu, M., Ahn, J., Bhang, D. H., Jung, Y. C., & Youn, H. (2017) · Scientific Reports · doi:10.1038/s41598-017-04766-7 · Cited by 146
Tumor-associated macrophages in cancers
Hu, W., Li, X., Zhang, C., Yang, Y., Jiang, J., & Wu, C. (2015) · Clinical & Translational Oncology · doi:10.1007/s12094-015-1373-0 · Cited by 147
Chu, H. X., Broughton, B. R. S., Kim, H. A., Lee, S., Drummond, G. R., & Sobey, C. G. (2015) · Stroke · doi:10.1161/strokeaha.115.009426 · Cited by 149
Changes in macrophage phenotype as the immune response evolves
Lichtnekert, J., Kawakami, T., Parks, W. C., & Duffield, J. S. (2013) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2013.05.013 · Cited by 151
Tseng, S. C. G. (2016) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.15-17637 · Cited by 145
Fang, W., Zhai, X., Han, D., Xiong, X., Wang, T., Zeng, X., He, S., Liu, R., Miyata, M., Xu, B., et al. (2018) · Theranostics · doi:10.7150/thno.24475 · Cited by 148
Exercise Attenuates M1 Macrophages and CD8+ T Cells in the Adipose Tissue of Obese Mice
Kawanishi, N., Mizokami, T., Yano, H., & Suzuki, K. (2013) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e31828ff9c6 · Cited by 146
Nath, S., Obaid, G., & Hasan, T. G. (2019) · Photochemistry and Photobiology · doi:10.1111/php.13173 · Cited by 146
Progression of liver fibrosis in post-transplant hepatitis C: Mechanisms, assessment and treatment
Berenguer, M., & Schuppan, D. (2012) · Journal of Hepatology · doi:10.1016/j.jhep.2012.12.014 · Cited by 146
Riquelme, P., Tomiuk, S., Kammler, A., Fändrich, F., Schlitt, H. J., Geissler, E. K., & Hutchinson, J. A. (2012) · Molecular Therapy · doi:10.1038/mt.2012.168 · Cited by 145
Pateras, I. S., Havaki, S., Nikitopoulou, X., Vougas, K. N., Townsend, P. A., Panayiotidis, M. I., Georgakilas, A. G., & Gorgoulis, V. G. (2015) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2015.06.011 · Cited by 147
Mechanisms Linking Excess Adiposity and Carcinogenesis Promotion
Pérez-Hernández, A. I., Catalán, V., Gómez‐Ambrosi, J., RodrÃguez, A., & Frühbeck, G. (2014) · Frontiers in Endocrinology · doi:10.3389/fendo.2014.00065 · Cited by 148
Dale, M. A., Xiong, W., Carson, J. S., Suh, M. K., Karpisek, A., Meisinger, T. M., Casale, G. P., & Baxter, B. T. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502454 · Cited by 147
Wang, Y., Yu, J., Luo, Z., Shi, Q., Liu, G., Wu, F., Wang, Z., Huang, Y., & Zhou, D. (2021) · Advanced Materials · doi:10.1002/adma.202103497 · Cited by 143
Metadata
- Authors
- Murray, P. J., & Wynn, T. A.
- Affiliations
- St. Jude Children's Research Hospital (US)
- National Institutes of Health (US)
- Corresponding author
- Murray, Peter J.
- Wynn, Thomas A.
- Venue
- Nature Reviews Immunology
- Published
- 2011-10-14
- Volume
- 11
- Issue
- 11
- Pages
- 723-737
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- PMC
- PMC3422549
- OpenAlex
- W1985859986
- Cited by
- 5,269
- References
- 178
- Citations by year
- 2026: 300 · 2025: 355 · 2024: 374 · 2023: 403 · 2022: 423 · 2021: 421 · 2020: 379 · 2019: 353 · 2018: 336 · 2017: 363 · 2016: 381 · 2015: 395 · 2014: 362 · 2013: 265 · 2012: 147
- FWCI
- 22.32
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Cancer Institute (P 30CA 21765, P30CA021765)
- National Institute of Allergy and Infectious Diseases (Z01AI001019, ZIAAI001019, ZIAAI000829, Z01AI000829)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
- Keywords
- macrophage heterogeneity, macrophage plasticity, macrophage polarization, tissue homeostasis, inflammation, macrophage recruitment, antimicrobial defense, antitumor immunity, obesity, allergy, asthma, carcinogenesis, autoimmunity, atherosclerosis, fibrosis, wound healing
- MeSH terms
- Bacterial Infections, Humans, Inflammation, Macrophage Activation, Macrophages, Neoplasms, Phagocytosis, Signal Transduction, Models, Immunological, Cell Proliferation
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review