The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.
Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-beta, PGE2, and PAF.
Open accessAbstract
Apoptosis in vivo is followed almost inevitably by rapid uptake into adjacent phagocytic cells, a critical process in tissue remodeling, regulation of the immune response, or resolution of inflammation. Phagocytosis of apoptotic cells by macrophages has been suggested to be a quiet process that does not lead to production of inflammatory mediators. Here we show that phagocytosis of apoptotic neutrophils (in contrast to immunoglobulin G-opsonized apoptotic cells) actively inhibited the production of interleukin (IL)-1beta, IL-8, IL-10, granulocyte macrophage colony-stimulating factor, and tumor necrosis factor-alpha, as well as leukotriene C4 and thromboxane B2, by human monocyte-derived macrophages. In contrast, production of transforming growth factor (TGF)-beta1, prostaglandin E2, and platelet-activating factor (PAF) was increased. The latter appeared to be involved in the inhibition of proinflammatory cytokine production because addition of exogenous TGF-beta1, prostaglandin E2, or PAF resulted in inhibition of lipopolysaccharide-stimulated cytokine production. Furthermore, anti-TGF-beta antibody, indomethacin, or PAF receptor antagonists restored cytokine production in lipopolysaccharide-stimulated macrophages that had phagocytosed apoptotic cells. These results suggest that binding and/or phagocytosis of apoptotic cells induces active antiinflammatory or suppressive properties in human macrophages. Therefore, it is likely that resolution of inflammation depends not only on the removal of apoptotic cells but on active suppression of inflammatory mediator production. Disorders in either could result in chronic inflammatory diseases.
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
“Some of the more common cytokines used in biomaterial‐based research involves the proinflammatory IFN‐γ or IL‐4, which are important effectors in steering the macrophage phenotypes.[ 103 , 232 , 233 , 234 ]”
From Unraveling and Harnessing the Immune Response at the Cell–Biomaterial Interface for Tissue Engineering Purposes (2024) · cites this paper as [234]
In the citing paper
“Interestingly, phagocytosis of neutrophils is also a central element to induce the phenotype switch of macrophages from pro-inflammatory M1 to a reparative M2 phenotype [73].”
From Transition from inflammation to proliferation: a critical step during wound healing (2016) · cites this paper as [73]
In the citing paper
“2-AG increases the number of phagocytosing macrophages, which leads to increased production of anti-inflammatory cytokines, e.g., TGF-β1 and decreased output of pro-inflammatory cytokines, e.g., TNF-α by macrophages [73].”
From Transition from inflammation to proliferation: a critical step during wound healing (2016) · cites this paper as [73]
In the citing paper
“Their apoptosis and engulfment by macrophages (efferocytosis) provides a key signal to the local immune milieu, including macrophages, to transition to an anti-inflammatory, pro-repair state”
From Immunology of Wound Healing (2018) · cites this paper as [47]
In the citing paper
“In physiologic wound repair, neutrophils undergo apoptosis after carrying out their various functions at the site of injury. Local macrophage uptake of apoptotic neutrophils then triggers a transition out of inflammatory phase [47–49].”
From Immunology of Wound Healing (2018) · cites this paper as [47]
In the citing paper
“Macrophages in the wound site are responsible for phagocytosis of apoptotic neutrophils, a process known as efferocytosis [73••]. This action itself induces macrophages to transition from a pro-inflammatory phenotype, to an anti-inflammatory phenotype”
From Immunology of Wound Healing (2018) · cites this paper as [47]
Citations
Cites
Cell Death: The Significance of Apoptosis
Wyllie, A. H., Kerr, J. F. R., & Currie, A. R. (1980) · International review of cytology · doi:10.1016/s0074-7696(08)62312-8 · Cited by 7,151
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
de Waal Malefyt, R., Abrams, J., Bennett, B., Figdor, C. G., & de Vries, J. E. (1991) · The Journal of experimental medicine · doi:10.1084/jem.174.5.1209 · Cited by 3,762
Fadok, V. A., Voelker, D. R., Campbell, P. A., Cohen, J., Bratton, D. L., & Henson, P. M. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.148.7.2207 · Cited by 3,321
Self-citationShull, M. M., Ormsby, I., Kier, A. B., Pawlowski, S., Diebold, R. J., Yin, M., Allen, R., Sidman, C., Proetzel, G., Calvin, D., et al. (1992) · Nature · doi:10.1038/359693a0 · Cited by 2,985
IL-10 inhibits cytokine production by activated macrophages
Fiorentino, D. F., Zlotnik, A., Mosmann, T. R., Howard, M., & O’Garra, A. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.147.11.3815 · Cited by 2,888
Martin, S. J., Reutelingsperger, C. P., McGahon, A. J., Rader, J. A., van Schie, R. C., LaFace, D. M., & Green, D. R. (1995) · The Journal of experimental medicine · doi:10.1084/jem.182.5.1545 · Cited by 2,824
Koopman, G., Reutelingsperger, C. P. M., Kuijten, G., Keehnen, R. M. J., Pals, S. T., & van Oers, M. H. J. (1994) · Blood · doi:10.1182/blood.v84.5.1415.1415 · Cited by 2,687
Kulkarni, A. B., Huh, C. G., Becker, D., Geiser, A., Lyght, M., Flanders, K. C., Roberts, A. B., Sporn, M. B., Ward, J. M., & Karlsson, S. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.2.770 · Cited by 1,967
Savill, J. S., Wyllie, A. H., Henson, J. E., Walport, M. J., Henson, P. M., & Haslett, C. (1989) · Journal of Clinical Investigation · doi:10.1172/jci113970 · Cited by 1,536
Self-citation
Cited by
Sorted by citations
Items 901–1,000 of 1,020
Intestinal Macrophages in Resolving Inflammation
Hine, A. M., & Loke, P. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900345 · Cited by 85
Complement: coming full circle
Friec, G. L., & Kemper, C. (2009) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-009-0047-4 · Cited by 85
“Binding of these complement components induces cell uptake via two routes: C1q, MBL/ficolins, and properdin are either recognized by the respective receptors on the phagocytes (Fadok et al. 1998; Kemper et al. 2008; Savill et al. 2002) or they induce complement activation on the apoptotic cell surface and initiate the…”
BackgroundThe Hsp110 and Grp170 stress proteins: newly recognized relatives of the Hsp70s
Easton, D. P., Kaneko, Y., & Subjeck, J. R. (2000) · Cell Stress and Chaperones · doi:10.1379/1466-1268(2000)005 · Cited by 328
Alemán, M., Schierloh, P., de la Barrera, S., Musella, R. M., Saab, M. A., Baldini, M., Abbate, E. H., & Sasiain, M. D. C. (2004) · Infection and Immunity · doi:10.1128/iai.72.9.5150-5158.2004 · Cited by 84
Apoptosis in systemic lupus erythematosus
Kaplan, M. J. (2004) · Clinical Immunology · doi:10.1016/j.clim.2004.04.007 · Cited by 85
The many ways tissue phagocytes respond to dying cells
Blander, J. M. (2017) · Immunological Reviews · doi:10.1111/imr.12537 · Cited by 84
Vickman, R. E., Aaron, L., Zhang, R., Lanman, N. A., Lapin, B. R., Gil, V., Greenberg, M., Sasaki, T., Cresswell, G. M., Broman, M. M., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-29719-1 · Cited by 89
Anti-Inflammatory Neutrophil Functions in the Resolution of Inflammation and Tissue Repair
Loh, W., & Vermeren, S. (2022) · Cells · doi:10.3390/cells11244076 · Cited by 92
IL‐13 induces expression of CD36 in human monocytes through PPARγ activation
Berry, A., Balard, P., Coste, A., Olagnier, D. P., Lagane, C., Authier, H., Benoit‐Vical, F., Lepert, J., Séguéla, J. P., Magnaval, J., et al. (2007) · European Journal of Immunology · doi:10.1002/eji.200636625 · Cited by 88
Mathematical Modelling of Immune Response in Tissues
Su, B., Zhou, W., Dorman, K. S., & Jones, D. E. (2008) · Computational and Mathematical Methods in Medicine · doi:10.1080/17486700801982713 · Cited by 84
Opsonization of Apoptotic Cells and Its Effect on Macrophage and T Cell Immune Responses
Kim, S. J., Gershov, D., Ma, X., Brot, N., & Elkon, K. B. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb06034.x · Cited by 84
Pathways mediating resolution of inflammation: when enough is too much
Fullerton, J. N., O'Brien, A. J., & Gilroy, D. W. (2013) · The Journal of Pathology · doi:10.1002/path.4232 · Cited by 83
New Insights and Novel Therapeutic Potentials for Macrophages in Myocardial Infarction
Zhang, Z., Tang, J., Cui, X., Qin, B., Zhang, J., Zhang, H., Zhang, H., Liu, G., Wang, W., & Zhang, J. (2021) · Inflammation · doi:10.1007/s10753-021-01467-2 · Cited by 86
Tsioumpekou, M., Krijgsman, D., Leusen, J. H. W., & Olofsen, P. A. (2023) · Cells · doi:10.3390/cells12151981 · Cited by 100
Milk Fat Globule-EGF Factor VIII in Sepsis and Ischemia-Reperfusion Injury
Matsuda, A., Jacob, A., Wu, R., Zhou, M., Nicastro, J. M., Coppa, G. F., & Wang, P. (2010) · Molecular Medicine · doi:10.2119/molmed.2010.00135 · Cited by 83
Ectosomes of polymorphonuclear neutrophils activate multiple signaling pathways in macrophages
Eken, C., Sadallah, S., Martin, P. J., Treves, S., & Schifferli, J. A. (2012) · Immunobiology · doi:10.1016/j.imbio.2012.05.021 · Cited by 89
Hamdy, N. A., & Gamal‐Eldeen, A. M. (2009) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2009.06.023 · Cited by 83
Apoptotic Genes are Differentially Expressed in Aged Gingival Tissue
González, O. A., Stromberg, A. J., Huggins, P. M., González‐Martínez, J., Novak, M. J., & Ebersole, J. L. (2011) · Journal of Dental Research · doi:10.1177/0022034511403744 · Cited by 83
“…supports an important role for apoptosis as an essential mechanism that regulates the inflammatory response through the generation of anti-inflammatory signals affecting phagocytes at the site of the infection, originally recruited to clear the infection (Fadok et al., 1998; Kim et al., 2004).”
BackgroundComplement deficiencies in humans and animals: Links to autoimmunity
Lewis, M., & Botto, M. (2006) · Autoimmunity · doi:10.1080/08916930600739233 · Cited by 83
“[99] Fadok VA, Bratton DL, Konowal A, Freed PW, Westcott JY,”
BackgroundJohann, A. M., von Knethen, A., Lindemann, D., & Brüne, B. (2005) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401832 · Cited by 85
Köröskényi, K., Duró, E., Pallai, A., Sarang, Z., Kloor, D., Ucker, D. S., Beceiro, S., Castrillo, A., Chawla, A., Ledent, C. A., et al. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1002284 · Cited by 83
“Because previous studies indicated that in longterm (1 d) experiments TGF-b1 and IL-10 might mediate the anti-inflammatory effects of apoptotic cells (4, 5, 10), we checked whether TGF-b1 or IL-10 release is altered in macrophages lacking A2AR.”
BackgroundResultInfluentialThe Melanocortin Agonist AP214 Exerts Anti-Inflammatory and Proresolving Properties
Montero‐Melendez, T., Patel, H., Seed, M. P., Nielsen, S. D.-H., Jonassen, T. E. N., & Perretti, M. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.03.042 · Cited by 83
Defining therapeutic targets for liver fibrosis: Exploiting the biology of inflammation and repair
Iredale, J. P. (2008) · Pharmacological Research · doi:10.1016/j.phrs.2008.06.011 · Cited by 80
Thymocyte apoptosis drives the intrathymic generation of regulatory T cells
Konkel, J. E., Jin, W., Abbatiello, B., Grainger, J. R., & Chen, W. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1320319111 · Cited by 92
“As it is well established that uptake of apoptotic cells by phagocytes induces TGFβ secretion from phagocytes (20, 21), we hypothesized that thymocyte apoptosis, and consequent TGFβ production, might be the initiation steps in tTreg generation.”
BackgroundMethodInfluentialMonocytes and macrophages in cardiac injury and repair
Sager, H. B., Kessler, T., & Schunkert, H. (2017) · Journal of Thoracic Disease · doi:10.21037/jtd.2016.11.17 · Cited by 85
“Ly6Clow macrophages facilitate wound healing and regeneration by (I) promoting transdifferentiation of fibroblasts into secretory and contractile myofibroblast (α-smooth muscle actin-positive fibroblast that are the major source of collagen for extracellular matrix deposition) through TGFβ secretion; (II) promoting an…”
BackgroundInterferon-γ Directly Inhibits TRANCE-Induced Osteoclastogenesis
Fox, S. W., & Chambers, T. J. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.3577 · Cited by 82
Ottonello, L. C. (2002) · British journal of rheumatology · doi:10.1093/rheumatology/41.11.1249 · Cited by 84
The Cardiac Microenvironment Instructs Divergent Monocyte Fates and Functions in Myocarditis
Hou, X., Chen, G., Bracamonte-Baran, W., Choi, H. S., Diny, N. L., Sung, J., Hughes, D., Won, T., Wood, M. K., Talor, M. V., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.007 · Cited by 83
“Moreover, efferocytosis triggers a shift in macrophage activation, making them phenotypically less proinflammatory (Camenisch et al., 1999; Fadok et al., 1998; Healy et al., 2016).”
BackgroundTherapeutic applications of TRAIL receptor agonists in cancer and beyond
Amarante-Mendes, G. P., & Griffith, T. S. (2015) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2015.09.001 · Cited by 83
“…by apoptotic cells has been attributed to a number of mechanisms, including the production of immunosuppressive cytokines from phagocytic cells (Fadok et al., 1998), production of inhibitors from the dead cell itself (Gao et al., 1998; W. Chen et al., 2001), and effects on the maturation of DC…”
Schwartsburd, P. M. (2003) · Cancer and Metastasis Reviews · doi:10.1023/a:1022220219975 · Cited by 81
“Reciprocal regulation of the NOS/COX-2/HO-1 balance between cytotoxic and regenerative inflammatory stages can also be controled by tumor growth factor (TGF-b) and PGE2 which are released by phagocytosis of apoptotic cells from adjacent macrophages [13].”
BackgroundChemerin Peptides Promote Phagocytosis in a ChemR23- and Syk-Dependent Manner
Cash, J. L., Christian, A., & Greaves, D. R. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903378 · Cited by 81
“MF phagocytosis of apoptotic cells is the classic example of phagocytic clearance without the provocation of an inflammatory response and is an important determinant of the resolution of inflammation (7, 9, 28).”
Apoptotic mechanisms in the pathogenesis of COPD
Plataki, M. E., Tzortzaki, E. G., Rytilä, P. H., Demosthenes, M., Koutsopoulos, A. V., & Siafakas, N. M. (2006) · International Journal of COPD · doi:10.2147/copd.2006.1.2.161 · Cited by 81
“…release of proinflammatory agents, such as interleukin (IL)-1β, GM-CSF, IL-8, and TNF, but increase macrophage release of agents, such as transforming growth factor β (TGF-β), and prostaglandin E 2 , that have suppressive infl uences on the infl ammatory response (Fadok et al 1998; Haslett 1999).”
Phagocytosis of apoptotic cells
Hart, S. P., Dransfield, I., & Rossi, A. G. (2008) · Methods · doi:10.1016/j.ymeth.2007.11.009 · Cited by 84
Inflammation and polyamine catabolism: the good, the bad and the ugly
Babbar, N., Stewart, T. M., & Casero, R. A. (2007) · Biochemical Society Transactions · doi:10.1042/bst0350300 · Cited by 81
CD200 is a novel p53-target gene involved in apoptosis-associated immune tolerance
Rosenblum, M. D., Olasz, E. B., Woodliff, J. E., Johnson, B. D., Konkol, M. C., Gerber, K. A., Orentas, R. J., Sandford, G. R., & Truitt, R. L. (2003) · Blood · doi:10.1182/blood-2003-09-3184 · Cited by 80
How Does TGF-β Mediate Tubulointerstitial Fibrosis?
Gewin, L. S., & Zent, R. (2012) · Seminars in Nephrology · doi:10.1016/j.semnephrol.2012.04.001 · Cited by 81
T CELLS ARE POTENT EARLY MEDIATORS OF THE HOST RESPONSE TO SEPSIS
Kasten, K. R., Tschöp, J., Adediran, S., Hildeman, D. A., & Caldwell, C. C. (2010) · Shock · doi:10.1097/shk.0b013e3181e14c2e · Cited by 82
“Phagocytosis of apoptotic cells was shown to decrease macrophage production of granulocyte macrophage colony-stimulating factor, IL-1, IL-8, IL-10, and TNF-!, while increasing the production of transforming growth factor-" (TGF-"), prostaglandin E2, and platelet activating factor (92).”
BackgroundPersson, A., Blomgran, R., Rahman, S., Zheng, L., & Stendahl, O. I. (2007) · Microbes and Infection · doi:10.1016/j.micinf.2007.11.007 · Cited by 81
Gauthier‐Kemper, A., Fisch, A., Seuwen, K., Baumgarten, B. U., Ruffner, H., Aebi, A., Rausch, M., Kiessling, F. M., Bartneck, M., Weiskirchen, R., et al. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.04.006 · Cited by 80
Cunningham, C. M., Boche, D., & Perry, V. H. (2002) · Neuropathology and Applied Neurobiology · doi:10.1046/j.1365-2990.2002.00383.x · Cited by 80
Akahoshi, T., Namai, R., Murakami, Y., Watanabe, M., Matsui, T., Nishimura, A., Kitasato, H., Kameya, T., & Kondo, H. (2003) · Arthritis & Rheumatism · doi:10.1002/art.10709 · Cited by 82
Rossaint, J., Thomas, K., Mersmann, S., Skupski, J., Margraf, A., Tekath, T., Jouvene, C. C., Dalli, J., Hidalgo, A., Meuth, S. G., et al. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20201353 · Cited by 80
Douglass, T. G., Driggers, L., Zhang, J. G., Hoa, N. T., Delgado, C., Williams, C. C., Dan, Q., Sanchez, R., Jeffes, E. W. B., Wepsic, H. T., et al. (2008) · International Immunopharmacology · doi:10.1016/j.intimp.2008.04.016 · Cited by 81
Welin, A., Raffetseder, J., Eklund, D., Stendahl, O. I., & Lerm, M. (2011) · Journal of Innate Immunity · doi:10.1159/000325297 · Cited by 81
Using an agent-based model to analyze the dynamic communication network of the immune response
Folcik, V. A., Broderick, G., Mohan, S., Block, B., Ekbote, C., Doolittle, J., Khoury, M., Davis, L., & Marsh, C. B. (2011) · Theoretical Biology and Medical Modelling · doi:10.1186/1742-4682-8-1 · Cited by 81
“An immune response most effectively protects the body when the leukocytes rapidly eliminate pathogens and then naturally diminish in numbers (via apoptosis), avoiding damaging chronic inflammation [2-5].”
BackgroundKomura, H., Miksa, M., Wu, R., Goyert, S. M., & Wang, P. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.182.1.581 · Cited by 80
The Many Roles of the Class A Macrophage Scavenger Receptor
Platt, N., Haworth, R., Darley, L., & Gordon, S. (2002) · International review of cytology · doi:10.1016/s0074-7696(01)12002-4 · Cited by 81
Lipoxins Induce Actin Reorganization in Monocytes and Macrophages But Not in Neutrophils
MADERNA, P., Cottell, D. C., Berlasconi, G., Petasis, N. A., Brady, H. R., & Godson, C. (2002) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)61175-3 · Cited by 80
“ated with the production of quiescing intermediates such as transforming growth factor- that actively suppress cytokine release.(14) Thus LXs are not only braking signals for PMN-mediated inflammation(5) but also actively promote the resolution of inflammatory processes on monocytes and M .”
BackgroundMonocyte CD14: a multifunctional receptor engaged in apoptosis from both sides
Heidenreich, S. (1999) · Journal of Leukocyte Biology · doi:10.1002/jlb.65.6.737 · Cited by 84
“First, it has been proposed that phagocytosis of apoptotic cells is a neutral event without cytokine release but recent data have convincingly shown that secondary secretory responses occur at least in cell culture and that apoptotic cell tethering may even actively suppress release of inflammatory mediators [9–11].”
BackgroundAdvances in the Immunobiology of Eosinophils and Their Role in Disease
Walsh, G. M. (1999) · Critical Reviews in Clinical Laboratory Sciences · doi:10.1080/10408369991239277 · Cited by 81
Immunotherapy of melanoma: Present options and future promises
Rotte, A., Bhandaru, M., Zhou, Y., & McElwee, K. J. (2015) · Cancer and Metastasis Reviews · doi:10.1007/s10555-014-9542-0 · Cited by 80
“PS exposing cells can suppress the immune and inflammatory response by binding to PS receptors of antigen presenting cells and inhibit their maturation, leading to the production of anti-inflammatory cytokines such as TGFβ and interleukin-10 (IL-10) [45].”
Maimon, A., Levi-Yahid, V., Ben‐Meir, K., Halpern, A., Talmi, Z., Priya, S., Mizraji, G., Mistriel-Zerbib, S., Berger, M., Baniyash, M., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci126089 · Cited by 84
“Apoptotic cell clearance not only eliminates further inflammation by secondary necrosis of uncleared dying cells (18, 69) but also actively stimulates antiinflammatory signaling (14, 15, 70, 71).”
Neutrophilic inflammation in bronchiectasis
Chalmers, J. D., Metersky, M. L., Aliberti, S., Morgan, L. C., Fucile, S., LAUTERIO, M., & McDonald, P. P. (2025) · European Respiratory Review · doi:10.1183/16000617.0179-2024 · Cited by 84
“Pro-resolving macrophages produce anti-inflammatory cytokines and mediators, including transforming growth factor-β 1 and prostaglandin E2 [72].”
Gratchev, A. N., Schledzewski, K., Guillot, P., & Goerdt, S. (2001) · Skin Pharmacology and Physiology · doi:10.1159/000056357 · Cited by 79
Specific Recognition of Apoptotic Cells Reveals a Ubiquitous and Unconventional Innate Immunity
Cvetanović, M., Mitchell, J. E., Patel, V. A., Avner, B. S., Su, Y. A., van der Saag, P. T., Witte, P. L., Fiore, S., Levine, J. S., & Ucker, D. S. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m603920200 · Cited by 79
Hoa, N. T., Myers, M. P., Douglass, T. G., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004631 · Cited by 79
Reznikov, L. L., Kim, S. H., Westcott, J. Y., Frishman, J. I., Fantuzzi, G., Novick, D., Rubinstein, M., & Dinarello, C. A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.040582597 · Cited by 79
Self-citationFerracini, M., Rios, F. J. O., Pecenin, M. F., & Jancar, S. (2013) · Mediators of Inflammation · doi:10.1155/2013/950273 · Cited by 86
Negreiros-Lima, G. L., Lima, K. M., Moreira, I. Z., Jardim, B. L. O., Vago, J. P., Galvão, I., Teixeira, L. C. R., Pinho, V., Teixeira, M. M., Sugimoto, M. A., et al. (2020) · Cells · doi:10.3390/cells9010128 · Cited by 80
Prostanoids and Resolution of Inflammation – Beyond the Lipid-Mediator Class Switch
Schmid, T., & Brüne, B. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.714042 · Cited by 79
Glaubitz, J., Asgarbeik, S., Lange, R., Mazloum, H., Elsheikh, H., Weiß, F. U., & Sendler, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1279539 · Cited by 81
Autoimmunity versus tolerance: Can dying cells tip the balance?
Viorritto, I. C. B., Nikolov, N. P., & Siegel, R. M. (2006) · Clinical Immunology · doi:10.1016/j.clim.2006.07.012 · Cited by 78
“[21] Vioritto et al.”
Macrophages in neovascular age-related macular degeneration: friends or foes?
Skeie, J. M., & Mullins, R. F. (2008) · Eye · doi:10.1038/eye.2008.206 · Cited by 80
Airway immune homeostasis and implications for influenza-induced inflammation
Snelgrove, R. J., Godlee, A., & Hussell, T. (2011) · Trends in Immunology · doi:10.1016/j.it.2011.04.006 · Cited by 80
Aberrant Wound Healing and TGF-β Production in the Autoimmune-Prone MRL/+ Mouse
Kench, J. A., Russell, D. M., Fadok, V. A., Young, S. K., Worthen, G. S., Jones‐Carson, J., Henson, J. E., Henson, P. M., & Nemazee, D. A. (1999) · Clinical Immunology · doi:10.1006/clim.1999.4754 · Cited by 78
Self-citationLeitch, A. E., Haslett, C., & Rossi, A. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00402.x · Cited by 77
Ultraviolet light and cutaneous lupus
Bijl, M., & Kallenberg, C. G. M. (2006) · Lupus · doi:10.1177/0961203306071705 · Cited by 78
Maeda, Y., Shiratsuchi, A., Namiki, M., & Nakanishi, Y. (2002) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401046 · Cited by 78
Nickoloff, B. J., Bonish, B. K., Marble, D. J., Schriedel, K. A., DiPietro, L. A., Gordon, K. B., & Lingen, M. W. (2006) · Journal of Investigative Dermatology Symposium Proceedings · doi:10.1038/sj.jidsymp.5650010 · Cited by 78
“Macrophages and neutrophils exhibit cross-talk and the ingestion of neutrophils by macrophages may serve as an anti-inflammatory process (Fadok et al., 1998; Murai et al., 2003; Daley et al., 2005).”
BackgroundA paradox of immunodeficiency and inflammation in human aging: lessons learned from apoptosis
Gupta, S., Agrawal, A., Agrawal, S., Su, H., & Gollapudi, S. (2006) · Immunity & Ageing · doi:10.1186/1742-4933-3-5 · Cited by 77
Endothelial Apoptosis and Chronic Transplant Vasculopathy: Recent Results, Novel Mechanisms
Cailhier, J., Laplante, P., & Hébert, M. (2005) · American Journal of Transplantation · doi:10.1111/j.1600-6143.2005.01165.x · Cited by 77
“Phosphatidylserinedependent recognition and engulfment of apoptotic cells trigger the release of cytokines and growth factors of central importance for the control of vascular wall cellularity such as TGF-b1 (Figure 2) (47).”
BackgroundCheung, W.-Y., Simmons, C. A., & You, L. (2011) · Bone · doi:10.1016/j.bone.2011.09.052 · Cited by 76
“However, recent evidence suggests that apoptosis is a key regulator of inflammatory responses [29,30].”
BackgroundPal, S., Dolai, S., Yadav, R. K., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011271 · Cited by 77
“We cannot exclude that differences in TNF-a or TGF-b production could be responsible for different rates of infection observed between OE and KO strains.”
BackgroundInfluentialKajbafzadeh, A. M., Payabvash, S., Salmasi, A., et al. (2006) · The Journal of Urology · doi:10.1016/j.juro.2006.03.041 · Cited by 77
Manipulation of Host Cholesterol by Obligate Intracellular Bacteria
Samanta, D., Mulye, M., Clemente, T. M., Justis, A. V., & Gilk, S. D. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00165 · Cited by 78
“…V β 3 normally functions during macrophage phagocytosis of apoptotic cells (Wu et al., 2005), a process that suppresses the immune response by inhibiting macrophage production of interleukin (IL)-1 β , IL-8, tumor necrosis factor (TNF)- α , leukotriene C 4 , and thromboxane B2 (Fadok et al., 1998).”
BackgroundPoxviruses Utilize Multiple Strategies to Inhibit Apoptosis
Nichols, D., Martini, W. D., & Cottrell, J. A. (2017) · Viruses · doi:10.3390/v9080215 · Cited by 78
“During apoptotic clearance, transforming growth factor-β (TGF-β) and IL-10 are produced to prevent inflammatory responses [85,272,289,290].”
BackgroundFarhood, B., Goradel, N. H., Mortezaee, K., Khanlarkhani, N., Salehi, E., Nashtaei, M. S., Shabeeb, D., Musa, A. E., Fallah, H., & Najafi, M. (2018) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-018-0473-3 · Cited by 78
Nucleosomes in the pathogenesis of systemic lupus erythematosus
Koutouzov, S., Jerônimo, A. L. C., Campos, H., & Amoura, Z. (2004) · Rheumatic Disease Clinics of North America · doi:10.1016/j.rdc.2004.04.001 · Cited by 77
“This process actively suppresses an inflammatory response through downregulation of proinflammatory cytokine production (tumor necrosis factor [TNF]-a, interleukin (IL)-1, and IL-12) by macrophages, whereas it increases the secretion of anti-inflammatory and immunoregulatory cytokines, such as transforming growth fact…”
BackgroundKaliyaperumal, A., Michaels, M. A., & Datta, S. K. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.5.2530 · Cited by 77
Blood derivatives awaken in regenerative medicine strategies to modulate wound healing
Mendes, B. B., Gómez‐Florit, M., Babo, P. S., Domingues, R. M. A., Reis, R. L., & Gomes, M. E. (2017) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2017.12.018 · Cited by 75
Patel, V., Dial, K., Wu, J., Gauthier, A. G., Wu, W., Lin, M., Espey, M. G., Thomas, D. D., Ashby, C. R., & Mantell, L. L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21030977 · Cited by 76
“The failure to phagocytose apoptotic neutrophils can lead to spontaneous secondary necrosis, thereby further stimulating the production of pro-inflammatory cytokines [54,56], establishing a cycle of excessive inflammatory responses.”
BackgroundPharmacological targets of metabolism in disease: Opportunities from macrophages
Castegna, A., Gissi, R., Menga, A., Montopoli, M., Favia, M., Viola, A., & Canton, M. (2020) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107521 · Cited by 75
Infarct in the Heart: What’s MMP-9 Got to Do with It?
Becirovic‐Agic, M., Chalise, U., Daseke, M. J., Konfrst, S. R., Salomon, J., Mishra, P. K., & Lindsey, M. L. (2021) · Biomolecules · doi:10.3390/biom11040491 · Cited by 81
Ma, S., Zhang, J., Liu, H., Li, S., & Wang, Q. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.896591 · Cited by 81
Clayton, A. R., Prue, R. L., Harper, L., Drayson, M. T., & Savage, C. O. S. (2003) · Arthritis & Rheumatism · doi:10.1002/art.11130 · Cited by 76
Immuno-modulation and anti-inflammatory benefits of antibiotics: the example of tilmicosin.
Buret, A. G. (2010) · Europe PMC (PubMed Central) · Cited by 76
Davis, K. I., Banerjee, S., Friggeri, A., Bell, C. P., Abraham, E. H., & Zerfaoui, M. (2011) · Molecular Medicine · doi:10.2119/molmed.2011.00203 · Cited by 78
Improved survival in experimental sepsis with an orally administered inhibitor of apoptosis
Weaver, J., Rouse, M. S., Steckelberg, J. M., & Badley, A. D. (2004) · The FASEB Journal · doi:10.1096/fj.03-1230com · Cited by 75
Efferocytosis drives a tryptophan metabolism pathway in macrophages to promote tissue resolution
Sukka, S. R., Ampomah, P. B., Darville, L. N. F., Ngai, D., Wang, X., Kuriakose, G., Xiao, Y., Shi, J., Koomen, J. M., McCusker, R. H., et al. (2024) · Nature Metabolism · doi:10.1038/s42255-024-01115-7 · Cited by 82
“Efferocytosis stimulates the production of pro-resolving mediators, notably TGF-β1 and IL-10, which are important in tissue repair 14,30 .”
Altered structure of autoantigens during apoptosis
Hall, J. C., Casciola-Rosen, L. A., & Rosen, A. (2004) · Rheumatic Disease Clinics of North America · doi:10.1016/j.rdc.2004.04.012 · Cited by 75
“Apoptotic cell death occurs throughout development and during tissue homeostasis; in these circumstances, the immune consequences are predominantly noninflammatory and tolerogenic [5–8].”
BackgroundT helper 17 cells: discovery, function, and physiological trigger
Torchinsky, M. B., & Blander, J. M. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0248-3 · Cited by 79
“It has been known for some time that phagocytosis of apoptotic cells by macrophages induces synthesis of TGF-b [138, 139], presumably in order to maintain a state of tolerance towards self-antigens present in dead and dying cells that are cleared by phagocytes.”
BackgroundRobin, M., Demeilliers, C., Sutton, A., Paradis, V., Maisonneuve, C., Dubois, S., Poirel, O., Lettéron, P., Pessayre, D., & Fromenty, B. (2005) · Hepatology · doi:10.1002/hep.20949 · Cited by 80
Rahman, M., Sing, S., Golabkesh, Z., Fiskesund, R., Gustafsson, T. P., Jogestrand, T., Frostegård, A. G., Hafström, I., Liu, A., & Frostegård, J. (2016) · Clinical Immunology · doi:10.1016/j.clim.2016.04.007 · Cited by 75
TGF-β: Receptors, Signaling Pathways and Autoimmunity
Chen, W., & Wahl, S. M. (2001) · KARGER eBooks · doi:10.1159/000060548 · Cited by 75
Hart, S. P., Alexander, K. M., & Dransfield, I. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.3.1882 · Cited by 75
Sindrilaru, A., Peters, T., Schymeinsky, J., Oreshkova, T., Wang, H., Gompf, A., Mannella, F., Wlaschek, M., Sunderkötter, C., Rudolph, K. L., et al. (2009) · Blood · doi:10.1182/blood-2008-07-166702 · Cited by 73
“After cleaning the wound from invading pathogens, PMN undergo apoptosis and are removed by M by adhesion-dependent phagocytosis, which stimulates M to release large amounts of TGF1.(3,4) M activation to release active TGF- 1 (Figure S2B) preferentially depends on 2-integrin–mediated adhesion to and phagocytosis of apo…”
ResultPhagocytosis of apoptotic cells by liver: A morphological study
Dini, L., Pagliara, P., & Carlà, E. C. (2002) · Microscopy Research and Technique · doi:10.1002/jemt.10107 · Cited by 87
“…manipulation of phagocyte responses to apoptotic cell stimuli and the development of novel therapeutic strategies (for example, during tissue repair) as an effective antiinflammatory and immunosuppressive strategy (Voll et al., 1997; Fadok et al., 1998; Botto et al., 1998; Herrmann et al., 1998).”
BackgroundEating the dead to keep atherosclerosis at bay
Brophy, M. L., Dong, Y., Wu, H., Rahman, H. N. A., Song, K., & Chen, H. (2017) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2017.00002 · Cited by 68
ten Brink, T., Damanik, F., Rotmans, J. I., & Moroni, L. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202301939 · Cited by 71
Metadata
- Authors
- Fadok, V. A., Bratton, D. L., Konowal, A., Freed, P. W., Westcott, J. Y., & Henson, P. M.
- Affiliations
- National Jewish Health (US)
- ORCID
- Henson, P M
- Venue
- Journal of Clinical Investigation
- Published
- 1998-02-15
- Volume
- 101
- Issue
- 4
- Pages
- 890-898
- ISSN
- 0021-9738 (ISSN-L)
- PMC
- PMC508637
- OpenAlex
- W2095537212
- Semantic Scholar
- 3e88d8a52759097d481b92ec0d06606afbadafab
- Cited by
- 3,166
- References
- 50
- Citations by year
- 2026: 60 · 2025: 74 · 2024: 91 · 2023: 82 · 2022: 91 · 2021: 129 · 2020: 114 · 2019: 125 · 2018: 106 · 2017: 113 · 2016: 117 · 2015: 109 · 2014: 116 · 2013: 130 · 2012: 133
- FWCI
- 29.16
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Clinical Investigation (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL34303, P01HL034303)
- National Institute of General Medical Sciences (GM48211, R01GM048211)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Keywords
- phagocytosis of apoptotic cells, macrophages, inflammation resolution, anti-inflammatory macrophages, inflammatory cytokines, TGF-β1, prostaglandin E2, platelet-activating factor, autocrine and paracrine signaling, neutrophil apoptosis, monocyte-derived macrophages, indomethacin, PAF receptor antagonists
- MeSH terms
- Humans, Inflammation, Macrophages, Neutrophils, Phagocytosis, Platelet Activating Factor, Solubility, Thromboxane B2, Dinoprostone, Cytokines, Transforming Growth Factor beta, Apoptosis, Leukotriene C4, Jurkat 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