The DOI matches its Crossref record; 106 of the 112 references it cites were found in a registry or an index.
Alternative activation of macrophages: Immune function and cellular biology
Abstract
Macrophages are the first line of defense of the organism against pathogens and, in response to the microenvironment, become differentially activated. In the presence of IL-4 and IL-13, cytokines that are produced in a Th-2 type response, particularly during allergy and parasitic infections, macrophages become differentially activated. Alternative activated macrophages play an important role in the protection of the host by decreasing inflammation and promoting tissues repair. However, alternative activation of macrophages also downregulates host protection against selected pathogens. This defect is associated with an altered receptor expression pattern and extensive modulation of intracellular membrane trafficking. This review shows how alternative activation of macrophages induces extensive cellular remodelling of phagocytic, endocytic, signaling and secretory pathways which play an important, but unclear role in the pathogenesis of different disease.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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
“In general, M1s or classically activated MΦs are pro-inflammatory and microbicidal, whereas M2s or alternatively activated MΦs are immunomodulatory, reparative, and poorly microbicidal [7–12].”
From Macrophage functional polarization (M1/M2) in response to varying fiber and pore dimensions of electrospun scaffolds (2013) · cites this paper as [11]
Citations
Cites
Alternative activation of macrophages
Gordon, S. (2003) · Nature Reviews Immunology · doi:10.1038/nri978 · Cited by 6,189
Self-citationMonocyte and macrophage heterogeneity
Gordon, S., & Taylor, P. R. (2005) · Nature Reviews Immunology · doi:10.1038/nri1733 · Cited by 5,190
Self-citationDarnell, J. E. (1997) · Science · doi:10.1126/science.277.5332.1630 · Cited by 3,979
Autophagy in Health and Disease: A Double-Edged Sword
Shintani, T., & Klionsky, D. J. (2004) · Science · doi:10.1126/science.1099993 · Cited by 2,559
Sallusto, F., Cella, M., Danieli, C., & Lanzavecchia, A. (1995) · The Journal of Experimental Medicine · doi:10.1084/jem.182.2.389 · Cited by 2,501
Gutierrez, M. G., Master, S. S., Singh, S. B., Taylor, G. A., Colombo, M. I., & Deretic, V. (2004) · Cell · doi:10.1016/j.cell.2004.11.038 · Cited by 2,252
Multiple defects of immune cell function in mice with disrupted interferon-gamma genes.
Dalton, D., Pitts-Meek, S., Keshav, S., Figari, I., Bradley, A., & Stewart, T. (1993) · Science · doi:10.1126/science.8456300 · Cited by 2,015
Stein, M., Keshav, S., Harris, N., & Gordon, S. (1992) · The Journal of experimental medicine · doi:10.1084/jem.176.1.287 · Cited by 1,960
Self-citationIdentification of the haemoglobin scavenger receptor
Kristiansen, M., Graversen, J. H., Jacobsen, C., Sonne, O., Hoffman, H.-J., Law, S. K. A., & Moestrup, S. K. (2001) · Nature · doi:10.1038/35051594 · Cited by 1,712
Stat6 Is Required for Mediating Responses to IL-4 and for the Development of Th2 Cells
Kaplan, M. H., Schindler, U., Smiley, S. T., & Grusby, M. J. (1996) · Immunity · doi:10.1016/s1074-7613(00)80439-2 · Cited by 1,629
Cited by
Sorted by citations
Alternative activation of macrophages: mechanism and functions
Gordon, S., & Martinez, F. O. (2010) · Immunity · doi:10.1016/j.immuni.2010.05.007 · Cited by 4,197
Self-citationNeuroinflammation and M2 Microglia: The Good, the Bad, and the Inflamed
Cherry, J. D., Olschowka, J. A., & O’Banion, M. K. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-98 · Cited by 1,748
Overview of General and Discriminating Markers of Differential Microglia Phenotypes
Jurga, A. M., Paleczna, M., & Kuter, K. Z. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00198 · Cited by 1,000
Microglia in Alzheimer's disease
Sarlus, H., & Heneka, M. T. (2017) · Journal of Clinical Investigation · doi:10.1172/jci90606 · Cited by 911
Radiation-induced fibrosis: mechanisms and implications for therapy
Straub, J. M., New, J., Hamilton, C. D., Lominska, C., Shnayder, Y., & Thomas, S. M. (2015) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-015-1974-6 · Cited by 677
Strzelak, A., Ratajczak, A., Adamiec, A., & Feleszko, W. (2018) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph15051033 · Cited by 557
Esposito, G., Irons, P. C., Webb, E. C., & Chapwanya, A. (2013) · Animal Reproduction Science · doi:10.1016/j.anireprosci.2013.11.007 · Cited by 587
Wang, Y., He, F., Feng, F., Liu, X., Dong, G., Qin, H., Hu, X., Zheng, M., Liang, L., Feng, L., et al. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-0269 · Cited by 483
Ly6Chi monocytes direct alternatively activated profibrotic macrophage regulation of lung fibrosis
Gibbons, M. A., MacKinnon, A. C., Ramachandran, P., Dhaliwal, K., Duffin, R., Phythian-Adams, A. T., van Rooijen, N., Haslett, C., Howie, S. E., Simpson, A. J., et al. (2011) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201010-1719oc · Cited by 466
Human macrophage polarization in vitro: maturation and activation methods compared.
Vogel, D., Glim, J. E., Stavenuiter, A. W., Breur, M., Heijnen, P., Amor, S., Dijkstra, C., & Beelen, R. (2014) · Immunobiology · doi:10.1016/j.imbio.2014.05.002 · Cited by 431
Garg, K., Pullen, N. A., Oskeritzian, C. A., Ryan, J. J., & Bowlin, G. L. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.02.065 · Cited by 457
“Scaffold pore size can also alter the MF response and subsequent angiogenic functions [10,11].”
Mung Bean (Vigna radiata L.): Bioactive Polyphenols, Polysaccharides, Peptides, and Health Benefits
Hou, D., Yousaf, L., Xue, Y., Hu, J., Wu, J., Hu, X., Feng, N., & Shen, Q. (2019) · Nutrients · doi:10.3390/nu11061238 · Cited by 485
M1 and M2 Macrophages: The Chicken and the Egg of Immunity
Mills, C. D., & Ley, K. F. (2014) · Journal of Innate Immunity · doi:10.1159/000364945 · Cited by 422
Mikita, J., Dubourdieu-Cassagno, N., Deloire, M. S., Vekris, A., Biran, M., Raffard, G., Brochet, B., Canron, M.-H., Franconi, J.-M., Boiziau, C., et al. (2011) · Multiple Sclerosis Journal · doi:10.1177/1352458510379243 · Cited by 358
Inflammation in Alzheimer’s disease: Lessons learned from microglia-depletion models
Spangenberg, E. E., & Green, K. N. (2017) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2016.07.003 · Cited by 352
Zhou, Z., Yang, Y.-X., Ding, J., Li, Y., & Miao, Z. (2012) · Natural Product Reports · doi:10.1039/c2np00088a · Cited by 313
CXC Chemokine Ligand 4 Induces a Unique Transcriptome in Monocyte-Derived Macrophages
Gleissner, C. A., Shaked, I., Little, K. M., & Ley, K. F. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0901368 · Cited by 300
Mesenchymal stem cell therapy for attenuation of scar formation during wound healing
Jackson, W. M., Nesti, L. J., & Tuan, R. S. (2012) · Stem Cell Research & Therapy · doi:10.1186/scrt111 · Cited by 282
Graphene Oxide Induces Toll-like Receptor 4 (TLR4)-Dependent Necrosis in Macrophages
Qu, G., Liu, S., Zhang, S., Wang, L., Wang, X., Sun, B., Yin, N., Gao, X., Xia, T., Chen, J.-J., et al. (2013) · ACS Nano · doi:10.1021/nn402330b · Cited by 273
Functional polarization of neuroglia: Implications in neuroinflammation and neurological disorders
Jha, M. K., Lee, W., & Suk, K. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.11.003 · Cited by 267
Aging‐dependent changes of microglial cells and their relevance for neurodegenerative disorders
Von Bernhardi, R., Tichauer, J. E., & Eugenín, J. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06537.x · Cited by 258
Rey-Giraud, F., Hafner, M., & Ries, C. H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042656 · Cited by 269
Ageing and the immune system: focus on macrophages
Linehan, E., & Fitzgerald, D. (2015) · European Journal of Microbiology and Immunology · doi:10.1556/eujmi-d-14-00035 · Cited by 234
Advanced Age Impairs Macrophage Polarization
Mahbub, S., Deburghgraeve, C. R., & Kovacs, E. J. (2012) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2011.0058 · Cited by 222
Phenotypic and functional switch of macrophages induced by regulatory CD4 + CD25 + T cells in mice
Liu, G., Ma, H., Qiu, L., Li, L., Cao, Y., Ma, J., & Zhao, Y. X. (2010) · Immunology and Cell Biology · doi:10.1038/icb.2010.70 · Cited by 223
Lively, S. S., & Schlichter, L. C. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-75 · Cited by 208
Molecular Mechanisms and Treatment of Radiation-Induced Lung Fibrosis
Ding, N.-H., Li, J. J., & Sun, L.-Q. (2013) · Current Drug Targets · doi:10.2174/13894501113149990198 · Cited by 214
Vallée, A., Lecarpentier, Y., Guillevin, R., & Vallée, J.-N. (2017) · Oncotarget · doi:10.18632/oncotarget.21234 · Cited by 211
Shirey, K. A., Pletneva, L. M., Puche, A. C., Keegan, A. D., Prince, G. A., Blanco, J. C. G., & Vogel, S. N. (2010) · Mucosal Immunology · doi:10.1038/mi.2010.6 · Cited by 209
The macrophage in HIV-1 infection: From activation to deactivation?
Herbein, G., & Varin, A. (2010) · Retrovirology · doi:10.1186/1742-4690-7-33 · Cited by 203
Self-citationChen, M., Zhang, Y., Zhou, P., Liu, X., Zhao, H., Zhou, X., Gu, Q., Li, B., Zhu, X., & Shi, Q. (2020) · Bioactive Materials · doi:10.1016/j.bioactmat.2020.05.004 · Cited by 229
“As a part of the innate immune system, macrophages are relevant to defense against invading pathogens [18,19].”
BackgroundThe innate and adaptive immune system of fish
Secombes, C. J., & Wang, T. (2012) · Elsevier eBooks · doi:10.1533/9780857095732.1.3 · Cited by 199
Benner, B. N., Scarberry, L., Suarez‐Kelly, L. P., Duggan, M. C., Campbell, A. R., Smith, E., Lapurga, G., Jiang, K., Butchar, J. P., Tridandapani, S., et al. (2019) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-019-0622-0 · Cited by 188
Modulation of macrophage activation and programming in immunity
Liu, G., & Yang, H. (2012) · Journal of Cellular Physiology · doi:10.1002/jcp.24157 · Cited by 171
Viral infection of the lung: Host response and sequelae
Yoo, J., Kim, T. S., Hufford, M. M., & Braciale, T. J. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2013.06.006 · Cited by 170
Microglia activation states and cannabinoid system: Therapeutic implications
Mecha, M., Carrillo-Salinas, F. J., Feliú, A., Mestre, L., & Guaza, C. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.06.011 · Cited by 165
Foth, B. J., Tsai, I. J., Reid, A. J., Bancroft, A. J., Nichol, S., Tracey, A., Holroyd, N. E., Cotton, J. A., Stanley, E., Zarowiecki, M., et al. (2014) · Nature Genetics · doi:10.1038/ng.3010 · Cited by 153
Immunomodulatory activity of andrographolide on macrophage activation and specific antibody response
Wang, W., Wang, J., Dong, S.-F., Liu, C., Italiani, P., Sun, S.-H., Xu, J., Boraschi, D., Ma, S., & Qu, D. (2010) · Acta Pharmacologica Sinica · doi:10.1038/aps.2009.205 · Cited by 143
The stimulation of an osteogenic response by classical monocyte activation
Omar, O., Granéli, C., Ekström, K. M., Karlsson, C., Johansson, A., Lausmaa, J., Wexell, C. L., & Thomsen, P. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.07.055 · Cited by 136
Postprandial lipoproteins and the molecular regulation of vascular homeostasis
Botham, K. M., & Wheeler-Jones, C. P. D. (2013) · Progress in Lipid Research · doi:10.1016/j.plipres.2013.06.001 · Cited by 137
Balce, D. R., Li, B., Allan, E. R. O., Rybicka, J. M., Krohn, R. M., & Yates, R. M. (2011) · Blood · doi:10.1182/blood-2011-01-328906 · Cited by 134
MMP28 promotes macrophage polarization toward M2 cells and augments pulmonary fibrosis
Gharib, S. A., Johnston, L. K., Huizar, I., Birkland, T. P., Hanson, J. F., Wang, Y., Parks, W. C., & Manicone, A. M. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.1112587 · Cited by 133
Macrophage immunoregulatory pathways in tuberculosis
Rajaram, M. V. S., Ni, B., Dodd, C. E., & Schlesinger, L. S. (2014) · Seminars in Immunology · doi:10.1016/j.smim.2014.09.010 · Cited by 131
Targeting innate immunity for neurodegenerative disorders of the central nervous system
Andreasson, K. I., Bachstetter, A. D., Colonna, M., Ginhoux, F., Holmes, C., Lamb, B., Landreth, G., Lee, D. C., Low, D., Lynch, M. A., et al. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13667 · Cited by 126
Peptide-based materials for cancer immunotherapy
Zhang, L., Huang, Y., Lindstrom, A. R., Lin, T., Lam, K. S., & Li, Y. (2019) · Theranostics · doi:10.7150/thno.37194 · Cited by 125
Sharma, R. B., Kambhampati, S. P., Zhang, Z., Sharma, A., Chen, S., Duh, E. I., Kannan, S., Tso, M. O. M., & Kannan, R. M. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.04.036 · Cited by 126
Moliné-Velázquez, V., Cuervo, H., Sol, V. V., Ortega, M. C., Clemente, D., & de Castro, F. (2011) · Brain Pathology · doi:10.1111/j.1750-3639.2011.00495.x · Cited by 124
M2 Polarized Macrophages and Giant Cells Contribute to Myofibrosis in Neuromuscular Sarcoidosis
Prokop, S., Heppner, F. L., Goebel, H. H., & Stenzel, W. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2010.11.065 · Cited by 119
Leng, T., Shi, Y., Xiong, Z., & Sun, D. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.12.008 · Cited by 123
Wu, M., Li, W., Zhang, Y., Shi, L., Xu, Z., Xia, W., & Zhang, W. (2020) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2020.117190 · Cited by 120
Use of In Vitro Assays to Assess Immunogenicity Risk of Antibody-Based Biotherapeutics
Joubert, M. K., Deshpande, M., Yang, J., Reynolds, H., Bryson, C. J., Fogg, M. H., Baker, M., Herskovitz, J., Goletz, T. J., Zhou, L., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0159328 · Cited by 118
Krneta, T., Gillgrass, A. E., Poznanski, S. M., Chew, M. V., Lee, A. J., Kolb, M. R. J., & Ashkar, A. A. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.3a1215-552r · Cited by 120
Radiation-Induced Lung Fibrosis: Preclinical Animal Models and Therapeutic Strategies
Jin, H. K., Yoo, Y., Kim, Y.-H., Kim, Y., Cho, J., & Lee, Y. (2020) · Cancers · doi:10.3390/cancers12061561 · Cited by 115
TSPO Modulates IL-4-Induced Microglia/Macrophage M2 Polarization via PPAR-γ Pathway
Zhou, D., Ji, L., & Chen, Y. (2019) · Journal of Molecular Neuroscience · doi:10.1007/s12031-019-01454-1 · Cited by 110
Liu, A.-J., Yu, J., Ji, H., Zhang, H.-C., Zhang, Y., & Liu, H. (2017) · Molecules · doi:10.3390/molecules23010062 · Cited by 108
Nuclear factor‐kappa‐B signaling in lung development and disease: One pathway, numerous functions
Alvira, C. M. (2014) · Birth Defects Research Part A Clinical and Molecular Teratology · doi:10.1002/bdra.23233 · Cited by 107
Wang, J., Zhu, R., Gao, B., Wu, B., Li, K., Sun, X., Liu, H., & Wang, S. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.09.060 · Cited by 108
Erbel, C., Tyka, M., Helmes, C. M., Akhavanpoor, M., Rupp, G., Domschke, G., Linden, F., Wolf, A., Doesch, A. O., Lasitschka, F., et al. (2014) · Innate Immunity · doi:10.1177/1753425914526461 · Cited by 115
Tian, L., Li, W., Yang, L., Chang, N., Fan, X., Ji, X., Xie, J., Yang, L., & Li, L. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01214 · Cited by 103
Sharma, A., Porterfield, J. E., Smith, E., Sharma, R. B., Kannan, S., & Kannan, R. M. (2018) · Journal of Controlled Release · doi:10.1016/j.jconrel.2018.06.003 · Cited by 100
NLRP3 Inflammasome Activation: A Therapeutic Target for Cerebral Ischemia–Reperfusion Injury
Wang, L., Ren, W., Wu, Q., Liu, T., Wei, Y. L., Ding, J., Zhou, C., Xu, H., & Yang, S. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.847440 · Cited by 105
The cannabinoid system and microglia in health and disease
Duffy, S. S., Hayes, J. P., Fiore, N. T., & Moalem‐Taylor, G. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108555 · Cited by 103
Synthetic Cationic Peptide IDR-1018 Modulates Human Macrophage Differentiation
Pena, O. M., Afacan, N. J., Pistolic, J., Chen, C. C. L., Madera, L., Falsafi, R., Fjell, C. D., & Hancock, R. E. W. (2013) · PLoS ONE · doi:10.1371/journal.pone.0052449 · Cited by 99
Bruce, K. D., Gorkhali, S., Given, K., Coates, A. M., Boyle, K. E., Macklin, W. B., & Eckel, R. H. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00057 · Cited by 94
Jaworska, J., Ziemka-Nalecz, M., Sypecka, J., & Zalewska, T. (2017) · Journal of Neuroinflammation · doi:10.1186/s12974-017-0807-8 · Cited by 93
Profibrotic Activities for Matrix Metalloproteinase-8 during Bleomycin-Mediated Lung Injury
Craig, V. J., Quintero, P. A., Fyfe, S. E., Patel, A. S., Knolle, M. D., Kobzik, L., & Owen, C. A. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1201043 · Cited by 91
The Dynamic Role of Microglia and the Endocannabinoid System in Neuroinflammation
Young, A. P., & Denovan‐Wright, E. M. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.806417 · Cited by 92
Similarity and Diversity in Macrophage Activation by Nematodes, Trematodes, and Cestodes
Jenkins, S. J., & Allen, J. E. (2010) · BioMed Research International · doi:10.1155/2010/262609 · Cited by 95
Sherry, C. L., Kim, S. S., Dilger, R. N., Bauer, L. L., Moon, M. L., Tapping, R. I., Fahey, G. C., Jr., Tappenden, K. A., & Freund, G. G. (2010) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2010.01.015 · Cited by 88
Clinical reviews in allergy and immunology
Leung, D. Y. M., Ledford, D. K., Wechsler, M. E., Fulkerson, P. C., Bochner, B. S., Gauvreau, G. M., Gleich, G. J., Henkel, T., Kolbeck, R., Mathur, S. K., et al. (2012) · Cited by 87
Kuo, H., Tsai, M., Huang, M., Chiu, C.-W., Tsai, C.-Y., Lee, M.-J., Huang, W., Lin, Y.-L., Kuo, W.-C., & Cheng, H. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2592-10.2011 · Cited by 87
Impact of age-related neuroglial cell responses on hippocampal deterioration
Ojo, J. O., Rezaie, P., Gabbott, P. L. A., & Stewart, M. G. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00057 · Cited by 83
Hanke, M. L., Angle, A., & Kielian, T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042476 · Cited by 79
Sarkar, S., Song, Y., Sarkar, S., Kipen, H. M., Laumbach, R. J., Zhang, J. J., Ohman‐Strickland, P., Gardner, C. R., & Schwander, S. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1101380 · Cited by 79
Boytard, L., Spear, R., Chinetti, G., Acosta‐Martin, A. E., Vanhoutte, J., Lamblin, N., Staels, B., Amouyel, P., Haulon, S., & Pinet, F. (2012) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.112.300663 · Cited by 78
Derlindati, E., Dei, A., Montanini, B., Spigoni, V., Curella, V., Aldigeri, R., Ardigò, D., Zavaroni, I., & Bonadonna, R. C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119751 · Cited by 78
The role of macrophages in healing the wounded lung
Alber, A., Howie, S., Wallace, W. A., & Hirani, N. (2012) · International Journal of Experimental Pathology · doi:10.1111/j.1365-2613.2012.00833.x · Cited by 77
Bone marrow-derived macrophages from aged rats are more responsive to inflammatory stimuli
Barrett, J. P., Costello, D. A., O’Sullivan, J., Cowley, T. R., & Lynch, M. A. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0287-7 · Cited by 76
Bułdak, Ł., Machnik, G., Bułdak, R. J., Łabuzek, K., Bołdys, A., Belowski, D., Basiak, M., & Okopień, B. (2015) · Pharmacological Reports · doi:10.1016/j.pharep.2015.10.008 · Cited by 79
Cameron, B., Tse, W., Lamb, R., Li, X., Lamb, B. T., & Landreth, G. E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1729-12.2012 · Cited by 76
Neonatal binge alcohol exposure increases microglial activation in the developing rat hippocampus
Boschen, K. E., Ruggiero, M., & Klintsova, A. Y. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.03.033 · Cited by 72
Akt2 Affects Periodontal Inflammation via Altering the M1/M2 Ratio
Wu, X., Chen, H., Wang, Y., & Gu, Y. (2020) · Journal of Dental Research · doi:10.1177/0022034520910127 · Cited by 70
Role of NADPH Oxidase in Formation and Function of Multinucleated Giant Cells
Quinn, M. T., & Schepetkin, I. A. (2009) · Journal of Innate Immunity · doi:10.1159/000228158 · Cited by 72
Glim, J. E., Niessen, F. B., Everts, V. E., van Egmond, M., & Beelen, R. H. J. (2012) · Immunobiology · doi:10.1016/j.imbio.2012.10.004 · Cited by 74
Exopolysaccharide from Trichoderma pseudokoningii induces macrophage activation
Wang, G., Zhu, L., Yu, B., Chen, K., Liu, B., Liu, J., Qin, G., Liu, C., Liu, H., & Chen, K. (2016) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2016.04.093 · Cited by 70
Mamilos, A., Winter, L., Schmitt, V. H., Barsch, F., Grevenstein, D., Wagner, W. L., Babel, M., Keller, K., Schmitt, C., Gürtler, F., et al. (2023) · Cells · doi:10.3390/cells12020276 · Cited by 75
Lively, S. S., & Schlichter, L. C. (2012) · Translational Stroke Research · doi:10.1007/s12975-012-0151-3 · Cited by 68
Lastra, G., & Manrique, C. M. (2015) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2015-0010 · Cited by 70
A 3-O-methylated heterogalactan from Pleurotus eryngii activates macrophages
Yan, J., Meng, Y., Zhang, M., Zhou, X., Cheng, H., Sun, L., & Zhou, Y. (2018) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2018.11.063 · Cited by 67
Mawhinney, L., Thawer, S. G., Lu, W.-Y., van Rooijen, N., Weaver, L. C., Brown, A. M., & Dekaban, G. A. (2012) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3182479b41 · Cited by 73
Park, H., Jo, S., & Jung, U. (2019) · In Vivo · doi:10.21873/invivo.11668 · Cited by 72
Xu, Y., Qian, L., Zong, G., Ma, K., Zhu, X., Zhang, H., Li, N., Yang, Q., Bai, H., Ben, J., et al. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.05.036 · Cited by 66
Ferreira, R., Lively, S. S., & Schlichter, L. C. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00183 · Cited by 67
Xia, Q., Wei, L., Zhang, Y. L., Kong, H., Shi, Y., Wang, X. B., Chen, X., Han, L., & Liu, K. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.01457 · Cited by 65
Macrophage Heterogeneity and Plasticity: Impact of Macrophage Biomarkers on Atherosclerosis
Rojas, J., Salazar, J. J., Martínez, M. S., Palmar, J., Bautista, J., Chávez-Castillo, M., Gómez, A., & Bermúdez, V. (2015) · Scientifica · doi:10.1155/2015/851252 · Cited by 65
Ryu, M., Kulkarni, O. P., Radomska, E., Miosge, N., Groß, O., & Anders, H. (2010) · Kidney International · doi:10.1038/ki.2010.373 · Cited by 61
Selective liposome targeting of folate receptor positive immune cells in inflammatory diseases
Poh, S., Chelvam, V., Ayala-López, W., Putt, K. S., & Low, P. S. (2018) · Nanomedicine Nanotechnology Biology and Medicine · doi:10.1016/j.nano.2018.01.009 · Cited by 61
Chang, L.-H., Huang, H., Wu, P., Jou, I., Pan, M., Chang, W., Wang, D. D. H., & Wang, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045378 · Cited by 58
Hamilton, M. J., Ho, V. W., Kuroda, E., Rüschmann, J., Antignano, F., Lam, V., & Krystal, G. (2010) · Experimental Hematology · doi:10.1016/j.exphem.2010.11.002 · Cited by 61
Involvement of IGF-1 and Akt in M1/M2 activation state in bone marrow-derived macrophages
Barrett, J. P., Minogue, A. M., Falvey, A., & Lynch, M. A. (2015) · Experimental Cell Research · doi:10.1016/j.yexcr.2015.05.015 · Cited by 59
Metadata
- Authors
- Varin, A., & Gordon, S.
- Affiliations
- University of Oxford (GB)
- Corresponding author
- Gordon, Siamon
- Venue
- Immunobiology
- Publisher
- Elsevier BV
- Published
- 2009-07
- Volume
- 214
- Issue
- 7
- Pages
- 630-641
- ISSN
- 0171-2985 (ISSN-L)
- OpenAlex
- W2091360431
- Cited by
- 361
- References
- 112
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 7 · 2023: 13 · 2022: 32 · 2021: 15 · 2020: 23 · 2019: 22 · 2018: 20 · 2017: 21 · 2016: 14 · 2015: 27 · 2014: 24 · 2013: 35 · 2012: 43
- FWCI
- 2.43
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Immunobiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Fondation pour la Recherche Médicale
- Medical Research Council
- 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
- alternative macrophage activation, M2 macrophages, IL-4, IL-13, Th2 immune response, parasitic infection, allergy, inflammation, tissue repair, receptor expression, membrane trafficking, phagocytosis, endocytosis, secretory pathway, host-pathogen interaction
- MeSH terms
- Animals, Endocytosis, Humans, Hypersensitivity, Immune Tolerance, Macrophage Activation, Membrane Fusion, Parasitic Diseases, Wound Healing, Signal Transduction, Interleukin-4, Th2 Cells
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