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Alternatively activated macrophages in helminth infections
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“AAMFs are induced during infections with several helminth parasites.33”
From Global issues in allergy and immunology: Parasitic infections and allergy (2017) · cites this paper as [33]
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Cites
The chemokine system in diverse forms of macrophage activation and polarization
MANTOVANI, A., SICA, A., SOZZANI, S., ALLAVENA, P., VECCHI, A., & LOCATI, M. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.09.015 · Cited by 6,534
Inflammatory cells during wound repair: the good, the bad and the ugly
Martin, P., & Leibovich, S. J. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.09.002 · Cited by 1,340 · cited 1×
“AAMΦs can contribute to fibrosis and repair at the site of injury [39], which may be of considerable importance during helminth infection.”
BackgroundBiochemical and functional characterization of three activated macrophage populations
Edwards, J. P., Zhang, X., Frauwirth, K. A., & Mosser, D. M. (2006) · Journal of Leukocyte Biology · doi:10.1189/jlb.0406249 · Cited by 863
Anthony, R. M., Urban, J. F., Alem, F., Hamed, H. A., Rozo, C. T., Boucher, J.-L., Van Rooijen, N., & Gause, W. C. (2006) · Nature Medicine · doi:10.1038/nm1451 · Cited by 522
Self-citation
Research works printed but not linked: 43
- Tato, 2006, Helper T cell differentiation enters a new era: le roi est mort; vive le roi!, J Exp Med, 203, 809, 10.1084/jem.20060522 · DOI
- Herbert, 2004, Alternative macrophage activation is essential for survival during schistosomiasis and downmodulates T helper 1 responses and immunopathology, Immunity, 20, 623, 10.1016/S1074-7613(04)00107-4 · DOI
- Reece, 2006, Innate immune responses to lung-stage helminth infection induce alternatively activated alveolar macrophages, Infect Immun, 74, 4970, 10.1128/IAI.00687-06 · DOI
- Rodriguez-Sosa, 2002, Chronic helminth infection induces alternatively activated macrophages expressing high levels of CCR5 with low interleukin-12 production and Th2-biasing ability, Infect Immun, 70, 3656, 10.1128/IAI.70.7.3656-3664.2002 · DOI
- Dzik, 2004, A non-classical type of alveolar macrophage response to Trichinella spiralis infection, Parasite Immunol, 26, 197, 10.1111/j.0141-9838.2004.00700.x · DOI
- Donnelly, 2005, Thioredoxin peroxidase secreted by Fasciola hepatica induces the alternative activation of macrophages, Infect Immun, 73, 166, 10.1128/IAI.73.1.166-173.2005 · DOI
- Oshiro, 2005, Anti-inflammatory activity of PAS-1, a protein component of Ascaris suum, Inflamm Res, 54, 17, 10.1007/s00011-004-1316-7 · DOI
- Nair, 2003, Macrophages in chronic type 2 inflammation have a novel phenotype characterized by the abundant expression of Ym1 and Fizz1 that can be partly replicated in vitro, Immunol Lett, 85, 173, 10.1016/S0165-2478(02)00225-0 · DOI
- Nair, 2005, Chitinase and Fizz family members are a generalized feature of nematode infection with selective upregulation of Ym1 and Fizz1 by antigen-presenting cells, Infect Immun, 73, 385, 10.1128/IAI.73.1.385-394.2005 · DOI
- Raes, 2002, Differential expression of FIZZ1 and Ym1 in alternatively versus classically activated macrophages, J Leukoc Biol, 71, 597, 10.1189/jlb.71.4.597 · DOI
- Raes, 2005, Macrophage galactose-type C-type lectins as novel markers for alternatively activated macrophages elicited by parasitic infections and allergic airway inflammation, J Leukoc Biol, 77, 321, 10.1189/jlb.0304212 · DOI · Paper page
- Ruckerl, 2006, Alternatively activated macrophages express the IL-27 receptor alpha chain WSX-1, Immunobiology, 211, 427, 10.1016/j.imbio.2006.05.008 · DOI
- Gratchev, 2005, Interleukin-4 and dexamethasone counter-regulate extracellular matrix remodelling and phagocytosis in type-2 macrophages, Scand J Immunol, 61, 10, 10.1111/j.0300-9475.2005.01524.x · DOI
- Stumpo, 2003, IL-10 induces gene expression in macrophages: partial overlap with IL-5 but not with IL-4 induced genes, Cytokine, 24, 46, 10.1016/S1043-4666(03)00270-9 · DOI
- Atochina, 2001, A schistosome-expressed immunomodulatory glycoconjugate expands peritoneal Gr1(+) macrophages that suppress naive CD4(+) T cell proliferation via an IFN-gamma and nitric oxide-dependent mechanism, J Immunol, 167, 4293, 10.4049/jimmunol.167.8.4293 · DOI
- Brys, 2005, Reactive oxygen species and 12/15-lipoxygenase contribute to the antiproliferative capacity of alternatively activated myeloid cells elicited during helminth infection, J Immunol, 174, 6095, 10.4049/jimmunol.174.10.6095 · DOI
- Pesce, 2006, The IL-21 receptor augments Th2 effector function and alternative macrophage activation, J Clin Invest, 116, 2044, 10.1172/JCI27727 · DOI
- Frohlich, 2007, IL-21 receptor signaling is integral to the development of Th2 effector responses in vivo, Blood, 109, 2023, 10.1182/blood-2006-05-021600 · DOI
- Omori, 2007, Induction of IL-4 expression in CD4(+) T cells by thymic stromal lymphopoietin, J Immunol, 178, 1396, 10.4049/jimmunol.178.3.1396 · DOI
- Taylor, 2006, F4/80+ alternatively activated macrophages control CD4+ T cell hyporesponsiveness at sites peripheral to filarial infection, J Immunol, 176, 6918, 10.4049/jimmunol.176.11.6918 · DOI
- Rodriguez-Sosa, 2006, Acute cysticercosis favours rapid and more severe lesions caused by Leishmania major and Leishmania mexicana infection, a role for alternatively activated macrophages, Cell Immunol, 242, 61, 10.1016/j.cellimm.2006.09.006 · DOI
- Reese, 2007, Chitin induces accumulation in tissue of innate immune cells associated with allergy, Nature, 10.1038/nature05746 · DOI
- Hesse, 2001, Differential regulation of nitric oxide synthase-2 and arginase-1 by type 1/type 2 cytokines in vivo: granulomatous pathology is shaped by the pattern of l-arginine metabolism, J Immunol, 167, 6533, 10.4049/jimmunol.167.11.6533 · DOI
- Hesse, 2000, NOS-2 mediates the protective anti-inflammatory and antifibrotic effects of the Th1-inducing adjuvant, IL-12, in a Th2 model of granulomatous disease, Am J Pathol, 157, 945, 10.1016/S0002-9440(10)64607-X · DOI
- Hayashi, 1999, Kupffer cells from Schistosoma mansoni-infected mice participate in the prompt type 2 differentiation of hepatic T cells in response to worm antigens, J Immunol, 163, 6702, 10.4049/jimmunol.163.12.6702 · DOI
- Mantovani, 2002, Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes, Trends Immunol, 23, 549, 10.1016/S1471-4906(02)02302-5 · DOI · Paper page
- Liu, 2004, Requirements for the development of IL-4-producing T cells during intestinal nematode infections: what it takes to make a Th2 cell in vivo, Immunol Rev, 201, 57, 10.1111/j.0105-2896.2004.00186.x · DOI
- Barner, 1998, Differences between IL-4R alpha-deficient and IL-4-deficient mice reveal a role for IL-13 in the regulation of Th2 responses, Curr Biol, 8, 669, 10.1016/S0960-9822(98)70256-8 · DOI
- Urban, 2000, IL-13-mediated worm expulsion is B7 independent and IFN-gamma sensitive, J Immunol, 164, 4250, 10.4049/jimmunol.164.8.4250 · DOI
- Rutitzky, 2003, Disruption of the ICOS-B7RP-1 costimulatory pathway leads to enhanced hepatic immunopathology and increased gamma interferon production by CD4 T cells in murine schistosomiasis, Infect Immun, 71, 4040, 10.1128/IAI.71.7.4040-4044.2003 · DOI
- Greenwald, 1997, Effects of blocking B7-1 and B7-2 interactions during a type 2 in vivo immune response, J Immunol, 158, 4088, 10.4049/jimmunol.158.9.4088 · DOI
- Greenwald, 2001, CTLA-4 regulates induction of anergy in vivo, Immunity, 14, 145, 10.1016/S1074-7613(01)00097-8 · DOI · Paper page
- Liang, 2003, Regulation of PD-1, PD-L1, and PD-L2 expression during normal and autoimmune responses, Eur J Immunol, 33, 2706, 10.1002/eji.200324228 · DOI
- Smith, 2004, Schistosoma mansoni worms induce anergy of T cells via selective upregulation of programmed death ligand 1 on macrophages, J Immunol, 173, 1240, 10.4049/jimmunol.173.2.1240 · DOI
- Terrazas, 2005, Role of the programmed Death-1 pathway in the suppressive activity of alternatively activated macrophages in experimental cysticercosis, Int J Parasitol, 35, 1349, 10.1016/j.ijpara.2005.06.003 · DOI
- Sandler, 2003, Global gene expression profiles during acute pathogen-induced pulmonary inflammation reveal divergent roles for Th1 and Th2 responses in tissue repair, J Immunol, 171, 3655, 10.4049/jimmunol.171.7.3655 · DOI
- Liu, 2004, FIZZ1 stimulation of myofibroblast differentiation, Am J Pathol, 164, 1315, 10.1016/S0002-9440(10)63218-X · DOI
- Gratchev, 2001, Alternatively activated macrophages differentially express fibronectin and its splice variants and the extracellular matrix protein betaIG-H3, Scand J Immunol, 53, 386, 10.1046/j.1365-3083.2001.00885.x · DOI · Paper page
- Gause, 2003, The immune response to parasitic helminths: insights from murine models, Trends Immunol, 24, 269, 10.1016/S1471-4906(03)00101-7 · DOI
- Finkelman, 2004, Interleukin-4- and interleukin-13-mediated host protection against intestinal nematode parasites, Immunol Rev, 201, 139, 10.1111/j.0105-2896.2004.00192.x · DOI · Paper page
- Voehringer, 2007, Eosinophils develop in distinct stages and are recruited to peripheral sites by alternatively activated macrophages, J Leukoc Biol, 10.1189/jlb.1106686 · DOI · Paper page
- Owhashi, 2000, Identification of a novel eosinophil chemotactic cytokine (ECF-L) as a chitinase family protein, J Biol Chem, 275, 1279, 10.1074/jbc.275.2.1279 · DOI
- Zhu, 2004, Acidic mammalian chitinase in asthmatic Th2 inflammation and IL-13 pathway activation, Science, 304, 1678, 10.1126/science.1095336 · DOI
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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
Diversity and dialogue in immunity to helminths
Allen, J. E., & Maizels, R. M. (2011) · Nature reviews. Immunology · doi:10.1038/nri2992 · Cited by 831
Macrophages, Foreign Body Giant Cells and Their Response to Implantable Biomaterials
Sheikh, Z., Brooks, P., Barzilay, O., Fine, N., & Glogauer, M. (2015) · Materials · doi:10.3390/ma8095269 · Cited by 701
Ferrante, C. J., Pinhal-Enfield, G., Elson, G., Cronstein, B. N., Hasko, G., Outram, S., & Leibovich, S. J. (2013) · Inflammation · doi:10.1007/s10753-013-9621-3 · Cited by 375
Coakley, G., McCaskill, J. L., Borger, J. G., Simbari, F., Robertson, E., Millar, M., Harcus, Y., McSorley, H. J., Maizels, R. M., & Buck, A. H. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.05.001 · Cited by 219
Filbey, K. J., Grainger, J. R., Smith, K. A., Boon, L., van Rooijen, N., Harcus, Y., Jenkins, S., Hewitson, J. P., & Maizels, R. M. (2014) · Immunology & Cell Biology · doi:10.1038/icb.2013.109 · Cited by 130
Vereyken, E. J., Heijnen, P. D., Baron, W., de Vries, E. H., Dijkstra, C. D., & Teunissen, C. E. (2011) · Journal of Neuroinflammation · doi:10.1186/1742-2094-8-58 · Cited by 108
“Due to activation of arginase, arginine is converted to ornithine, a precursor for collagen, which contributes to the production of extracellular matrix molecules (ECM) [8-11] and promotes cell growth [10,12].”
BackgroundInfluentialMaternal immune activation leads to activated inflammatory macrophages in offspring
Onore, C. E., Schwartzer, J. J., Careaga, M., Berman, R. F., & Ashwood, P. (2014) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.02.007 · Cited by 106
Global issues in allergy and immunology: Parasitic infections and allergy
Cruz, A. A., Cooper, P. J., Figueiredo, C. A., Alcantara-Neves, N. M., Rodrigues, L. C., & Barreto, M. L. (2017) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2017.09.005 · Cited by 82
Sulaiman, A. A., Zolnierczyk, K., Japa, O., Owen, J. P., Maddison, B. C., Emes, R. D., Hodgkinson, J. E., Gough, K. C., & Flynn, R. J. (2016) · PLOS Pathogens · doi:10.1371/journal.ppat.1005991 · Cited by 60
Metadata
- Authors
- Kreider, T., Anthony, R. M., Urban, J. F., & Gause, W. C.
- Venue
- Current Opinion in Immunology
- Publisher
- Elsevier BV
- Published
- 2007-08
- Volume
- 19
- Issue
- 4
- Pages
- 448-453
- ISSN
- 0952-7915
- Cited by
- 304
- References
- 4
- Language
- en
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