Alternative activation of macrophages: Immune function and cellular biology

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

STATs and Gene Regulation

Darnell, 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

Dendritic cells use macropinocytosis and the mannose receptor to concentrate macromolecules in the major histocompatibility complex class II compartment: downregulation by cytokines and bacterial products.

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

Autophagy Is a Defense Mechanism Inhibiting BCG and Mycobacterium tuberculosis Survival in Infected Macrophages

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

Interleukin 4 potently enhances murine macrophage mannose receptor activity: A marker of alternative immunologic macrophage activation

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

Identification 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

From Macrophage Interleukin-13 Receptor to Foam Cell Formation

Yakubenko, V. P., Hsi, L. C., Cathcart, M. K., & Bhattacharjee, A. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.381343 · Cited by 24

Comparison of chosen activation markers of human monocytes/macrophages isolated from the peripheral blood of young and elderly volunteers

Suchy, D., Łabuzek, K., Bułdak, Ł., Szkudłapski, D., & Okopień, B. (2014) · Pharmacological Reports · doi:10.1016/j.pharep.2014.04.008 · Cited by 24

Lnc-M2 controls M2 macrophage differentiation via the PKA/CREB pathway

Chen, Y., Li, H., Ding, T., Li, J., Zhang, Y., Wang, J., Yang, X., Chong, T., Long, Y., Li, X., et al. (2020) · Molecular Immunology · doi:10.1016/j.molimm.2020.06.006 · Cited by 24

A pre-clinical evaluation of silver, iodine and Manuka honey based dressings in a model of traumatic extremity wounds contaminated with Staphylococcus aureus

Guthrie, H., Martin, K. R., Taylor, C., Spear, A. M., Whiting, R., Macildowie, S., Clasper, J. C., & Watts, S. A. (2014) · Injury · doi:10.1016/j.injury.2014.05.007 · Cited by 23

Trypanosomatid Infections: How Do Parasites and Their Excreted–Secreted Factors Modulate the Inducible Metabolism of l-Arginine in Macrophages?

Holzmüller, P., Geiger, A., Nzoumbou‐Boko, R., Pissarra, J., Hamrouni, S., Rodrigues, V., Dauchy, F., Lemesre, J.-L., Vincendeau, P., & Bras‐Gonçalves, R. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00778 · Cited by 23

Alternative activation modifies macrophage resistance to Mycobacterium bovis

Castillo-Velázquez, U., Aranday-Cortés, E., & Gutierrez-Pabello, J. A. (2011) · Veterinary Microbiology · doi:10.1016/j.vetmic.2011.02.025 · Cited by 23

Unexpected immunoregulation effects of D-lactate, different from L-lactate

Yan, Y., Xu, R., Li, X., Yao, Z., Zhang, H., Li, H., & Chen, W. (2022) · Food and Agricultural Immunology · doi:10.1080/09540105.2022.2068508 · Cited by 21

Impact of uterine macrophage phenotype on placental retention in dairy cows

Nelli, R. K., Koster, J. D., Roberts, J. N., de Souza, J., Lock, A. L., Raphael, W., Agnew, D. W., & Contreras, G. A. (2019) · Theriogenology · doi:10.1016/j.theriogenology.2019.01.011 · Cited by 22

TPG-functionalized PLGA/PCL nanofiber membrane facilitates periodontal tissue regeneration by modulating macrophages polarization via suppressing PI3K/AKT and NF-κB signaling pathways

Han, X., Wang, F., Ma, Y., Lv, X., Zhang, K., Wang, Y., Yan, K., Mei, Y., & Wang, X. (2024) · Materials Today Bio · doi:10.1016/j.mtbio.2024.101036 · Cited by 21

Interleukin-19 can enhance angiogenesis by Macrophage Polarization

Gabunia, K., & Autieri, M. V. (2015) · Macrophage · doi:10.14800/macrophage.562 · Cited by 21

Suppression of Chronic Damage in Renal Allografts by Liver X Receptor (LXR) Activation

Kiss, É., Popovic, Z., Bedke, J., Wang, S., Bonrouhi, M., Gretz, N., Stettner, P., Teupser, D., Thiery, J., Porubský, Š., et al. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.03.019 · Cited by 21

Activation of RAW264.7 macrophages by an acidic polysaccharide derived from Citrus grandis ‘Tomentosa’

Fan, R., Zhu, C., Qiu, D., Mao, G., & Zeng, J. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.11.172 · Cited by 21

The Role of Microglial Depletion Approaches in Pathological Condition of CNS

Tahmasebi, F., & Barati, S. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01326-8 · Cited by 21

Macrophages.com: An on-line community resource for innate immunity research

Robert, C., Lu, X., Law, A., Freeman, T. C., & Hume, D. A. (2011) · Immunobiology · doi:10.1016/j.imbio.2011.07.025 · Cited by 22

Genes associated with alternatively activated macrophages discretely regulate helminth infection and pathogenesis in experimental mouse models

Horsnell, W. G. C., & Brombacher, F. (2010) · Immunobiology · doi:10.1016/j.imbio.2010.05.011 · Cited by 20

OMIP‐041: Optimized multicolor immunofluorescence panel rat microglial staining protocol

Furman, N. E. T., Prabhakara, K. S., Bedi, S. S., Cox, C. S., & Olson, S. D. (2017) · Cytometry Part A · doi:10.1002/cyto.a.23267 · Cited by 20

Free radical scavenging and antioxidant activity of D-pinitol against 7, 12 dimethylbenz (a) anthracene induced breast cancer in sprague dawley rats

Rengarajan, T., Rajendran, P., Nandakumar, N., Balasubramanian, M. P., & Nishigaki, I. (2014) · Asian Pacific Journal of Tropical Disease · doi:10.1016/s2222-1808(14)60592-2 · Cited by 20

Reprogramming of lysosomal gene expression by interleukin-4 and Stat6

Brignull, L. M., Czimmerer, Z., Saidi, H., Dániel, B., Villela, I. V., Bartlett, N. W., Johnston, S. L., Meira, L. B., Nagy, L., & Nohturfft, A. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-853 · Cited by 22

Modulation of cellular innate immunity by Lepeophtheirus salmonis secretory products

Lewis, D. L., Barker, D. E., & McKinley, R. S. (2014) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2014.03.014 · Cited by 18

Exopolysaccharide from Paecilomyces lilacinus modulates macrophage activities through the TLR4/NF‑κB/MAPK pathway

He, C., Lin, H., Wang, C., Zhang, M., Lin, Y., Huang, F., Lin, Y., & Tan, G. (2019) · Molecular Medicine Reports · doi:10.3892/mmr.2019.10746 · Cited by 17

The CD 20 homolog M s4a8a integrates pro‐ and anti‐inflammatory signals in novel M 2‐like macrophages and is expressed in parasite infection

Schmieder, A., Schledzewski, K., Michel, J., Schönhaar, K., Morias, Y., Bosschaerts, T., den Bossche, J. V., Dorny, P., Sauer, A., Sticht, C., et al. (2012) · European Journal of Immunology · doi:10.1002/eji.201142331 · Cited by 16

Influence of functional genetic polymorphism (−590C/T) in non-small cell lung cancer (NSCLC) development: The paradoxal role of IL-4

Gomes, M. P., Coelho, A., Araújo, A., Teixeira, A. L., Catarino, R., & Medeiros, R. (2012) · Gene · doi:10.1016/j.gene.2012.05.008 · Cited by 16

Resolution of inflammation in periodontitis: a review.

Huang, J., Cai, X., Ou, Y., Zhou, Y., & Wang, Y. (2018) · Europe PMC (PubMed Central) · Cited by 16

Supramolecular structure features and immunomodulatory effects of exopolysaccharide from Paecilomyces cicadae TJJ1213 in RAW264.7 cells through NF-κB/MAPK signaling pathways

Tian, J., Tang, C., Wang, X., Zhang, X., Xiao, L., & Li, W. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.03.029 · Cited by 16

Interleukin-25 fails to activate STAT6 and induce alternatively activated macrophages

Stolfi, C., Caruso, R., Franzè, E., Sarra, M., Nitto, D. D., Rizzo, A., Pallone, F., & Monteleone, G. (2010) · Immunology · doi:10.1111/j.1365-2567.2010.03340.x · Cited by 16

A second combinatorial immune receptor in monocytes/macrophages is based on the TCRγδ

Fuchs, T., Püellmann, K., Hahn, M., Dollt, C., Pechlivanidou, I., Ovsiy, I., Kzhyshkowska, J. G., Gratchev, A. N., Fleig, J., Emmert, A., et al. (2012) · Immunobiology · doi:10.1016/j.imbio.2012.11.005 · Cited by 16

HAT/HDAC: The epigenetic regulators of inflammatory gene expression (Review)

Swaroop, S., Batabyal, A., & Bhattacharjee, A. (2021) · International Journal of Epigenetics · doi:10.3892/ije.2021.5 · Cited by 12

Aspects immunologiques de la grossesse

Hanssens, S., Salzet, M., & Vinatier, D. (2012) · Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément/Journal de gynécologie obstétrique et biologie de la reproduction · doi:10.1016/j.jgyn.2012.07.001 · Cited by 17

Effect of hexane fraction of leaves of Cinnamomum tamala Linn on macrophage functions

Chaurasia, J. K., Pandey, N., & Tripathi, Y. B. (2010) · Inflammopharmacology · doi:10.1007/s10787-009-0029-5 · Cited by 15

Activation of RAW264.7 macrophages by oxidized galectin-1

Echigo, Y., Sugiki, H., Koizumi, Y., Hikitsuchi, S., & Inoue, H. (2010) · Immunology Letters · doi:10.1016/j.imlet.2010.03.010 · Cited by 15

Inhibition of immunotoxicity of Pb2+-induced RAW264.7 macrophages by selenium species in selenium-enriched rice

Wu, J., Ding, J. H., Shi, Y., Fang, Y., Li, P., Fan, F., Zhao, E., Sun, X., Shen, X., & Hu, Q. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111943 · Cited by 15

NOTCH4 potentiates the IL-13 induced genetic program in M2 alternative macrophages through the AP1 and IRF4–JMJD3 axis

López‐López, S., de Ávila, M. J. R., González-Gómez, M.-J., Nueda, M., Baladrón, V., Monsalve, E. M., Garcı́a-Ramı́rez, J. J., & Díaz-Guerrá, M. J. M. (2023) · International Immunology · doi:10.1093/intimm/dxad028 · Cited by 14

Lymphocyte proliferation stimulated by activated Cebus apella macrophages treated with a complex homeopathic immune response modifiers

Moreira, C. O. C., da Costa, J. D. F. F. B., Leal, M. F., Andrade, E., Rezende, A. P., Imbeloni, A. A., Muniz, J. A. P. C., Smith, M. D. A. C., Burbano, R. M. R., & de Assumpção, P. P. (2012) · Homeopathy · doi:10.1016/j.homp.2011.09.001 · Cited by 14

Gene Therapy for Noninfectious Uveitis

Chu, C. J., Barker, S. E., Dick, A. D., & Ali, R. R. (2012) · Ocular Immunology and Inflammation · doi:10.3109/09273948.2012.726392 · Cited by 14

Role of Host and Parasite MIF Cytokines during Leishmania Infection

Holowka, T., & Bucala, R. (2020) · Tropical Medicine and Infectious Disease · doi:10.3390/tropicalmed5010046 · Cited by 14

Nanosensor Chemical Cytometry for Characterizing the Efflux Heterogeneity of Nitric Oxide from Macrophages

Cho, S., Koman, V. B., Gong, X., Moon, S. J., Gordiichuk, P. I., & Strano, M. S. (2021) · ACS Nano · doi:10.1021/acsnano.1c04958 · Cited by 14

Proteasome inhibitor immunotherapy for the epithelial to mesenchymal transition: assessing the A549 lung cancer cell microenvironment and the role of M1, M2a and M2c ‘hydrocortisone-polarised’ macrophages

Engür, S., & Dikmen, M. (2022) · Molecular Biology Reports · doi:10.1007/s11033-022-07329-w · Cited by 14

The role of macrophages in thermal injury.

Penatzer, J. A., Srinivas, S., & Thakkar, R. K. (2022) · PubMed Central · Cited by 15

The Protection of Midazolam Against Immune Mediated Liver Injury Induced by Lipopolysaccharide and Galactosamine in Mice

Li, J., Tan, H., Zhou, X., Zhang, C., Jin, H., Tian, Y., Zhao, X., Li, X., Sun, X., Duan, M., et al. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.01528 · Cited by 14

Imaging Macrophage Phagocytosis Using AIE Luminogen‐Labeled E. coli

Gu, M., Zeng, Z., Wu, M., Leung, J., Zhao, E., Wang, S., & Chen, S. (2019) · Chemistry - An Asian Journal · doi:10.1002/asia.201801859 · Cited by 14

Molecular Characteristics and Potent Immunomodulatory Activity of Fasciola hepatica Cystatin

Zhang, K., Liu, Y., Zhang, G., Wang, X., Li, Z., Shang, Y., Ning, C., Ji, C., Cai, X., Xia, X., et al. (2022) · Korean Journal of Parasitology · doi:10.3347/kjp.2022.60.2.117 · Cited by 13

Insulin-like growth factor 1 in heat stress-induced neuroinflammation: novel perspective about the neuroprotective role of chromium

Wang, S., Hou, K., Gui, S., Ma, Y., Wang, S., Zhao, S., & Zhu, X. (2023) · Stress Biology · doi:10.1007/s44154-023-00105-1 · Cited by 13

On the horizon: Flexible immune recognition outside lymphocytes

Kaminski, W. E., Beham, A. W., Kzhyshkowska, J. G., Gratchev, A. N., & Püellmann, K. (2012) · Immunobiology · doi:10.1016/j.imbio.2012.05.024 · Cited by 13

Recurrent Airway Obstruction and Summer Pasture‐Associated Obstructive Pulmonary Disease

Bullone, M., & Lavoie, J. (2015) · doi:10.1002/9781119086512.ch16 · Cited by 13

Nanoparticulate Systems for Controlling Monocyte/Macrophage Behavior

Pentecost, A., Lurier, E. B., & Spiller, K. L. (2015) · Springer eBooks · doi:10.1007/978-3-319-20726-1_14 · Cited by 12

Microglia and status epilepticus in the immature brain

López‐Meraz, M. L., & Álvarez‐Croda, D. (2022) · Epilepsia Open · doi:10.1002/epi4.12610 · Cited by 10

Antineoplastic drug NSC631570 modulates functions of hypoxic macrophages

Skivka, L. M., Федорчук, О. Г., Rudyk, M. P., Позур, В. В., Khranovska, N., Grom, M. Y., & Jw, N. (2013) · Cytology and Genetics · doi:10.3103/s0095452713050095 · Cited by 12

Dietary arginine and citrulline supplementation modulates the immune condition and inflammatory response of European seabass

Azeredo, R., Machado, M., Fontinha, F., Fernández-Boo, S., Conceição, L. E. C., Dias, J. P., & Costas, B. (2020) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2020.07.060 · Cited by 12

Recognition and uptake of free and nanoparticle‐bound betalactoglobulin – a food allergen – by human monocytes

Marengo, M., Bonomi, F., Iametti, S., Prinz, E., Hempelmann, R., Boyé, M., & Frøkiær, H. (2011) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201100386 · Cited by 12

Integrated Metabolomics and Network Pharmacology Study on Immunoregulation Mechanisms ofPanax ginsengthrough Macrophages

Hao, J., Hu, H., Liu, J., Wang, X., Liu, X., Wang, J., Niu, M., Zhao, Y., & Xiao, X. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/3630260 · Cited by 11

Dendrimer-Based N-Acetyl Cysteine Maternal Therapy Ameliorates Placental Inflammation via Maintenance of M1/M2 Macrophage Recruitment

Liu, Y., Na, Q., Liu, J., Liu, A., Oppong, A. Y., Lee, J. Y., Chudnovets, A., Lei, J., Sharma, R. B., Kannan, S., et al. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.819593 · Cited by 10

Polarized Tissue-Derived Macrophages Display Enhanced M2d Phenotype after Prolonged Stimulation with Adenosine A2A Receptor Agonist in the Presence of LPS

Barilo, J., Ratsimor, M., Chan, A., Hembruff, H., & Basta, S. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl27638 · Cited by 10

Anti-Inflammatory Effects of Cannabinoids in Therapy of Neurodegenerative Disorders and Inflammatory Diseases of the CNS

Tomaszewska-Zaremba, D., Gajewska, A., & Misztal, T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26146570 · Cited by 12

Administration of TGF-ß Inhibitor Mitigates Radiation-induced Fibrosis in a Mouse Model

Gans, I., Abiad, J. M. E., James, A. W., Levin, A. S., & Morris, C. D. (2020) · Clinical Orthopaedics and Related Research · doi:10.1097/corr.0000000000001286 · Cited by 10

Potentilla anserina L. polysaccharide ameliorates LPS-induced acute lung injury and relevant intestinal mucosal barrier impairment

Liu, H., Wang, J., Zhao, J., Gu, S., Chen, S., Jia, W., Huang, S., & Wu, J. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.140667 · Cited by 9

FuFangChangTai Decoction Activates Macrophages via Inducing Autophagy

Li, L., Wang, H., Qian, J., Wei, G., Ding, R., Hu, C., Fang, D., Jiang, Z., Bi, L., Song, J., et al. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/5657035 · Cited by 9

The Biological Applications of Two Aggregation‐Induced Emission Luminogens

Gu, M., Zeng, Z., Mai, X., Xiong, Y., Deng, Z., Chen, S., & Wang, L. (2019) · Biotechnology Journal · doi:10.1002/biot.201900212 · Cited by 9

Heterogalactan WPEP-N-b from Pleurotus eryngii enhances immunity in immunocompromised mice

Chen, L., Ren, A., Wang, Y., Qu, Y., Gong, H., Mayo, K. H., Zhou, Y., & Cheng, H. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.11.163 · Cited by 9

In vitro initial immune response against Leishmania amazonensis infection is characterized by an increased production of IL-10 and IL-13

Coêlho, Z. C. B., Teixeira, M. J., Mota, É. F., Frutuoso, M. S., Silva, J. S., Barral, A. M. P., Barral‐Netto, M., & Pompeu, M. M. L. (2010) · The Brazilian Journal of Infectious Diseases · doi:10.1016/s1413-8670(10)70096-9 · Cited by 9

An ultrastructural study, effects of Proteus vulgaris OX19 on the rabbit spleen cells

Gül, N., Özkorkmaz, E. G., Keleşoğlu, İ., & Özlük, A. (2012) · Micron · doi:10.1016/j.micron.2012.05.010 · Cited by 9

Deciphering the Cell-Specific Effect of Osteoblast-Macrophage Crosstalk in Periodontitis

Jacho, D., Babaniamansour, P., Osorio, R., Toledano, M., Rabino, A., García‐Mata, R., & Yildirim-Ayan, E. D. (2023) · Tissue Engineering Part A · doi:10.1089/ten.tea.2023.0104 · Cited by 8

Olive (Olea europaea) leaf extract alters the cytokine profile of Leishmania major‐infected macrophages: New insight into the underlying mechanism

Kheirandish, F., Mosaffa, N., Tarrahi, M. J., & Fallahi, S. (2018) · Parasite Immunology · doi:10.1111/pim.12520 · Cited by 8

A novel polysaccharide from plant fermentation extracts and its immunomodulatory activity in macrophage RAW264.7 cells

Yan, L., Liu, C., Yan, S., Pu, W., Wu, B., Jiang, C., Li, X., Liu, Y., & Li, X. (2021) · Food and Agricultural Immunology · doi:10.1080/09540105.2021.1874884 · Cited by 8

Immunostimulatory activity of stem bark of Kalopanax pictus in RAW 264.7 macrophage

Kim, S., Lee, C. H., Yeo, J.-Y., Hwang, K. W., & Park, S. (2021) · Journal of Herbal Medicine · doi:10.1016/j.hermed.2021.100504 · Cited by 8

Neuronal melatonin type 1 receptor overexpression promotes M2 microglia polarization in cerebral ischemia/reperfusion-induced injury

Suofu, Y., Jauhari, A., Nirmala, E. S., Mullins, W. A., Wang, X., Li, F., Carlisle, D. L., & Friedlander, R. M. (2022) · Neuroscience Letters · doi:10.1016/j.neulet.2022.137043 · Cited by 8

Bacteroides thetaiotaomicron and its inactivated bacteria ameliorate colitis by inhibiting macrophage activation

Sikong, Y., Li, L., Yan, L., Xiang, G., Yanqing, L., & Zuo, X. (2023) · Clinics and Research in Hepatology and Gastroenterology · doi:10.1016/j.clinre.2023.102276 · Cited by 8

The influence of ezetimibe on classical and alternative activation pathways of monocytes/macrophages isolated from patients with hypercholesterolemia

Suchy, D., Łabuzek, K., Machnik, G., & Okopień, B. (2014) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-014-0982-4 · Cited by 8

A20 Controls Macrophage to Elicit Potent Cytotoxic CD4+ T Cell Response

Wang, L., Hong, B., Jiang, X., Jones, L. E., Chen, S., & Huang, X. F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048930 · Cited by 8

FcγRIIb Exacerbates LPS-Induced Neuroinflammation by Binding with the Bridging Protein DAP12 and Promoting the Activation of PI3K/AKT Signaling Pathway in Microglia

Han, Y., Wang, L., Ye, X., Gong, X., & Shao, X. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s428093 · Cited by 7

Effects of mannan oligosaccharide on immune function and disease resistance in pigs

Minh, T. (2010) · Cited by 7

Deacetylation of IRF8 inhibits iNOS expression and inflammation via SIRT1 in macrophages

Jia, Y., Shen, K., Yang, Y., Cai, W., Wang, K., Zhang, Y., Zhao, M., Luo, L., Su, L., Guan, H., et al. (2022) · Immunobiology · doi:10.1016/j.imbio.2022.152300 · Cited by 7

Antibody binding to porcine sialoadhesin reduces phagocytic capacity without affecting other macrophage effector functions

Baere, M. D., Gorp, H. V., Nauwynck, H., & Delputte, P. (2011) · Cellular Immunology · doi:10.1016/j.cellimm.2011.08.016 · Cited by 7

Evaluation of the inflammatory responses to sol–gel coatings with distinct biocompatibility levels

Cerqueira, A., Araújo‐Gomes, N., Zhang, Y., van den Beucken, J. J. J. P., Martínez‐Ramos, C., Ozturan, S., Izquierdo, R., Muriach, M., Romero‐Cano, R., Baliño, P., et al. (2021) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.37149 · Cited by 7

Fractionated irradiations lead to chronic allergic airway inflammation through increasing the influx of macrophages

Park, H., Jo, S., Yu, D.-K., & Jung, U. (2012) · Inflammation Research · doi:10.1007/s00011-012-0547-2 · Cited by 7

Early Macrophage Activation in Preterm Newborns and Respiratory Disease

Milan, À., Priante, E., Nardo, D., Tosato, F., Pantano, G., Baraldi, E., & Zaramella, P. (2017) · Journal of Child Science · doi:10.1055/s-0037-1605579 · Cited by 6

Thoracic Irradiation Recruit M2 Macrophage into the Lung, Leading to Pneumonitis and Pulmonary Fibrosis

Park, H., Jo, S., & Jung, U. (2017) · Journal of Radiation Protection and Research · doi:10.14407/jrpr.2017.42.4.177 · Cited by 6

Immunomodulatory Effects of Lidocaine: Mechanisms of Actions and Therapeutic Applications

Wu, J., Chen, Q., He, Z., Yang, B., Dai, Z., & Qiu, F. (2026) · Pharmaceuticals · doi:10.3390/ph19010134 · Cited by 5

Peptide based vesicles for cancer immunotherapy: design, construction and applications

Yu, Y., Lyu, J., Muhadaisi, Y., Shi, C., & Wang, D. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1609162 · Cited by 5

Vitamin D and Macrophage Functions in Tuberculosis

Selvaraj, P. (2015) · Macrophage · doi:10.14800/macrophage.756 · Cited by 5

Oral Paracoccidioidomycosis Granulomas are Predominantly Populated by CD163+ Multinucleated Giant Cells

Pedreira, R. D. P. G., de Carli, M. L., Beijo, L. A., Nonogaki, S., Pereira, A. A. C., Ribeiro, N. V., Sperandio, F. F., & Hanemann, J. A. C. (2016) · Mycopathologia · doi:10.1007/s11046-016-0016-5 · Cited by 5

Anti-inflammatory Activity of Veronica peregrina

Jeon, H. (2012) · Natural Product Sciences · Cited by 5

Cervus nippon var. mantchuricus water extract treated with digestive enzymes (CE) modulates M1 macrophage polarization through TLR4/MAPK/NF-κB signaling pathways on murine macrophages

Hong, S. H., Ku, J. M., Lim, Y. S., Kim, H. I., Shin, Y. C., & Ko, S. (2021) · European Journal of Inflammation · doi:10.1177/20587392211000898 · Cited by 5

Maresin-like 1 Ameliorates Neuropathology of Alzheimer’s Disease in Brains of a Transgenic Mouse Model

Shrivastava, P., Lu, Y., Su, S., Kobayashi, Y., Zhao, Y., Lien, N., Masoud, A., Lukiw, W. J., & Hong, S. (2024) · Biomedicines · doi:10.3390/biomedicines12122865 · Cited by 5

Argemone oil, an edible oil adulterant, induces systemic immunosuppression in Balb/c mice in an oral 28 days repeated dose toxicity study

Mandal, P., Tewari, P., Kumar, S., Yadav, S., Ayanur, A., Chaturvedi, R. K., Das, M., & Tripathi, A. (2018) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2018.04.013 · Cited by 4

Temperature induces brain-intake shift of recombinant high-density lipoprotein after traumatic brain injury

Huang, J., Peng, Y., Wang, X., Gu, X., Yao, Y., Wang, W., He, Z., Ma, Z., Feng, Q., Qi, W., et al. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-03016-z · Cited by 5

Inflammation and White Matter Injury in Animal Models of Ischemic Stroke

Schlichter, L. C., Hutchings, S., & Lively, S. S. (2013) · Springer eBooks · doi:10.1007/978-1-4614-9123-1_19 · Cited by 4

Chronicles of Cell Death Foretold: Specificities in the Mechanism of Disposal

Hughes, L. D., Bosurgi, L., Ghosh, S., & Rothlin, C. V. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01743 · Cited by 4

Modulation of Neuroinflammation via Selective Nanoparticle‐Mediated Drug Delivery to Activated Microglia/Macrophages in Spinal Cord Injury

Stigliano, C., Frazier, A. M., & Horner, P. J. (2022) · Advanced Therapeutics · doi:10.1002/adtp.202200083 · Cited by 4

Impaired Autophagic Degradation of Transforming Growth Factor-β-Induced Protein by Macrophages in Lattice Corneal Dystrophy

Han, J. K., Zhang, M., Lin, H., Huang, F., Lin, Y., Tan, G., & Zheng, Z.-Y. (2019) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.18-25838 · Cited by 4

Le trophoblaste : chef d’orchestre de la tolérance immunologique maternelle

Mesdag, V., Salzet, M., & Vinatier, D. (2014) · Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément/Journal de gynécologie obstétrique et biologie de la reproduction · doi:10.1016/j.jgyn.2014.06.008 · Cited by 4

Interaction Between Mesenchymal Stem Cells and Immune Cells in Tissue Engineering

Huang, R. S., Zhou, Y., & Xiao, Y. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.99877-5 · Cited by 4

Controlled release of pioglitazone from biodegradable hydrogels to modify macrophages phenotype

Sato, K., Sakai, S., Kishi, K., & Tabata, Y. (2015) · Inflammation and Regeneration · doi:10.2492/inflammregen.35.086 · Cited by 3

Effets immunomodulateurs des macrolides au cours des pathologies respiratoires chroniques

Guillon, A., Jouan, Y., Petit, A., & Gueugnon, F. (2013) · Réanimation · doi:10.1007/s13546-012-0639-6 · Cited by 3

Alternative Activation of Macrophages: Concepts and Prospects

Gordon, S., Helming, L., & Martínez, F. O. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1311-4_3 · Cited by 4

Is There a Biological Basis for Treatment of Fibrodysplasia Ossificans Progressiva with Rosiglitazone? Potential Benefits and Undesired Effects

Bocciardi, R., & Ravazzolo, R. (2010) · PPAR Research · doi:10.1155/2010/541927 · Cited by 3

Immune-enhancing screening of fourteen plants on murine macrophage RAW 264.7 cells

Kim, S., Jo, E.-S., Kim, N.-Y., Hwang, K. W., & Park, S. (2019) · Tropical Journal of Pharmaceutical Research · doi:10.4314/tjpr.v18i1.13 · Cited by 4

Analysis of macrophage transcriptome in atherogenesis

Kubekina, M. V., Nikiforov, N. G., Карагодин, В. П., Sobenin, I. A., & Orekhov, A. N. (2019) · Russian Journal of Cardiology · doi:10.15829/1560-4071-2019-2-92-98 · Cited by 2

Persistent immune injury induced by short-term decabromodiphenyl ether (BDE-209) exposure to female middle-aged Balb/c mice

Ding, Y., Chen, Y., Feng, W., Huang, G., Dong, M., Zhao, T. K., Chen, N., Yang, L., Mao, G., & Wu, X. (2023) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-30148-w · Cited by 2

Use of Primary Macrophages for Searching Novel Immunocorrectors

Nikiforov, N. G., Elizova, N. V., Bukrinsky, M., Dubrovsky, L., Makeev, V. J., Wakabayashi, Y., Liu, P., Foxx, K. K., Kruth, H. S., Jin, X., et al. (2017) · Current Pharmaceutical Design · doi:10.2174/1381612823666170125110128 · Cited by 2

Toll-like receptor 10 has a role in human macrophage response against Streptococcus pneumoniae

Balachandran, Y., & Singh, B. (2022) · Cell and Tissue Research · doi:10.1007/s00441-022-03671-4 · Cited by 2

Structure of the IL4 receptor and signal transduction mechanism of IL4

Izuhara, K., Yang, G., Miyajima, A., Howard, M., & Harada, N. (1993) · Research in Immunology · doi:10.1016/s0923-2494(05)80007-0 · Cited by 13

Interleukin-4- and Interleukin-13-Mediated Alternatively Activated Macrophages: Roles in Homeostasis and Disease

Dyken, S. J. V., & Locksley, R. M. (2013) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-095906 · Cited by 743

Alternative Activation of Macrophages: An Immunologic Functional Perspective

Martinez, F. O., Helming, L., & Gordon, S. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132532 · Cited by 2,745

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

Alternative activation of macrophages

Gordon, S. (2003) · Nature Reviews Immunology · doi:10.1038/nri978 · Cited by 6,189