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IL-1 receptor blockade restores autophagy and reduces inflammation in chronic granulomatous disease in mice and in humans
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Significance: Chronic granulomatous disease (CGD) has an immunodeficiency component and, in addition, an autoinflammatory component in which autophagy and inflammasome activation are linked and amenable to IL-1 blockade. This study provides a rationale to perform clinical trials to investigate the efficacy of blocking IL-1 in CGD colitis and expands the therapeutic potential of IL-1 antagonists to inflammatory diseases with defective autophagy.
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“Notably, activation of LAP in macrophages also regulates inflammatory signaling pathways (258, 259).”
From Aspergillus fumigatus and Aspergillosis in 2019 (2019) · cites this paper as [258]
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Cites
Autophagy and Viruses: Adversaries or Allies?
Dong, X., & Levine, B. (2013) · Journal of Innate Immunity · doi:10.1159/000346388 · Cited by 4,444
Antimicrobial Autophagy: A Conserved Innate Immune Response in Drosophila
Moy, R. H., & Cherry, S. R. (2013) · Journal of Innate Immunity · doi:10.1159/000350326 · Cited by 3,551
The Wellcome Trust Case Control Consortium, U.K.
Mossman, K. (2008) · Scientific American · doi:10.1038/scientificamerican0108-42a · Cited by 2,714
Mizushima, N., Yamamoto, A., Matsui, M., Yoshimori, T., & Ohsumi, Y. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-09-0704 · Cited by 2,105
Reactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4
Scherz‐Shouval, R., Shvets, E., Fass, E., Shorer, H., Gil, L., & Elazar, Z. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601623 · Cited by 2,101 · cited 1×
“Given the suggested role for ROS in autophagy (29, 30), a defective autophagic process responsible for hyperproduction of IL-1β is consistent with NADPH deficiency.”
BackgroundLoss of the autophagy protein Atg16L1 enhances endotoxin-induced IL-1β production
Saitoh, T., Fujita, N., Jang, M. H., Uematsu, S., Yang, B., Satoh, T., Omori, H., Noda, T., Yamamoto, N., Komatsu, M., et al. (2008) · Nature · doi:10.1038/nature07383 · Cited by 2,064
Hampe, J., Franke, A., Rosenstiel, P. C., Till, A., Teuber, M., Huse, K., Albrecht, M., Mayr, G., Vega, F. M. D. L., Briggs, J. C., et al. (2006) · Nature Genetics · doi:10.1038/ng1954 · Cited by 1,948
Treating inflammation by blocking interleukin-1 in a broad spectrum of diseases
Dinarello, C. A., Simon, A., & van der Meer, J. W. M. (2012) · Nature Reviews Drug Discovery · doi:10.1038/nrd3800 · Cited by 1,812
Self-citationChronic Granulomatous Disease: Report on a National Registry of 368 Patients
Winkelstein, J. A., Marino, M. C., Johnston, R. B., Boyle, J., Curnutte, J., Gallin, J. I., Malech, H. L., Holland, S. M., Ochs, H., Quie, P., et al. (2000) · Medicine · doi:10.1097/00005792-200005000-00003 · Cited by 1,728
Beyond oxidative stress: an immunologist's guide to reactive oxygen species
Nathan, C., & Cunningham-Bussel, A. (2013) · Nature Reviews Immunology · doi:10.1038/nri3423 · Cited by 1,619
Cited by
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Aspergillus fumigatus and Aspergillosis in 2019
Latgé, J.-P., & Chamilos, G. (2019) · Clinical Microbiology Reviews · doi:10.1128/cmr.00140-18 · Cited by 1,400
Self-citationPathway paradigms revealed from the genetics of inflammatory bowel disease
Graham, D. B., & Xavier, R. J. (2020) · Nature · doi:10.1038/s41586-020-2025-2 · Cited by 801
Self-citationMartinez, J., Malireddi, R. K. S., Lu, Q., Cunha, L. D., Pelletier, S., Gingras, S., Orchard, R., Guan, J.-L., Tan, H., Peng, J., et al. (2015) · Nature Cell Biology · doi:10.1038/ncb3192 · Cited by 758
RetractedNeutrophils: Between Host Defence, Immune Modulation, and Tissue Injury
Krüger, P., Saffarzadeh, M., Weber, A. N. R., Rieber, N. P., Radsak, M. P., von Bernuth, H., Benarafa, C., Roos, D., Skokowa, J., & Hartl, D. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1004651 · Cited by 700
Aspergillus fumigatus morphology and dynamic host interactions
van de Veerdonk, F. L., Gresnigt, M. S., Romani, L., Netea, M. G., & Latgé, J.-P. (2017) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.90 · Cited by 490
Self-citationCOVID-19-associated fungal infections
Hoenigl, M., Seidel, D., Sprute, R., Cunha, C., Oliverio, M., Goldman, G. H., Ibrahim, A. S., & Carvalho, A. (2022) · Nature Microbiology · doi:10.1038/s41564-022-01172-2 · Cited by 482
Crosstalk between autophagy and inflammatory signalling pathways: balancing defence and homeostasis
Cadwell, K. (2016) · Nature reviews. Immunology · doi:10.1038/nri.2016.100 · Cited by 492
Strategies for targeting cytokines in inflammatory bowel disease
Neurath, M. F. (2024) · Nature reviews. Immunology · doi:10.1038/s41577-024-01008-6 · Cited by 444
COVID-19 Associated Pulmonary Aspergillosis (CAPA)—From Immunology to Treatment
Arastehfar, A. A., Carvalho, A., van de Veerdonk, F. L., Jenks, J. D., Koehler, P. A., Krause, R., Cornely, O. A., Perlin, D. S., Lass‐Flörl, C., & Hoenigl, M. (2020) · Journal of Fungi · doi:10.3390/jof6020091 · Cited by 429
Matsuzawa, Y., Hwang, S., & Cadwell, K. (2017) · Annual Review of Immunology · doi:10.1146/annurev-immunol-042617-053253 · Cited by 384
Modulation of inflammation by autophagy: Consequences for human disease
Netea-Maier, R. T., Plantinga, T. S., van de Veerdonk, F. L., Smit, J. W., & Netea, M. G. (2016) · Autophagy · doi:10.1080/15548627.2015.1071759 · Cited by 349
Self-citationInflammasome-independent regulation of IL-1-family cytokines
Netea, M. G., van de Veerdonk, F. L., van der Meer, J. W. M., Dinarello, C. A., & Joosten, L. A. B. (2015) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032414-112306 · Cited by 326
Self-citationEgea, J., Fabregat, I., Frapart, Y., Ghezzi, P., Görlach, A., Kietzmann, T., Kubaichuk, K. I., Knaus, U. G., López, M. G., González, G. O., et al. (2017) · Redox Biology · doi:10.1016/j.redox.2017.05.007 · Cited by 321
Li, H., Zhou, X., Huang, Y., Liao, B., Cheng, L., & Ren, B. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.622534 · Cited by 284
Yang, J., Liu, X., Fan, H., Tang, Q., Shou, Z., Zuo, D.-M., Zou, Z., Xu, M., Chen, Q.-Y., Peng, Y., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0140551 · Cited by 284
A Review of Chronic Granulomatous Disease
Arnold, D. E., & Heimall, J. R. (2017) · Advances in Therapy · doi:10.1007/s12325-017-0636-2 · Cited by 265
The Role of NLRP3 and IL-1β in the Pathogenesis of Inflammatory Bowel Disease
Mao, L., Kitani, A., Strober, W., & Fuss, I. J. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02566 · Cited by 250
Iannitti, R. G., Napolioni, V., Oikonomou, V., LUCA, A. D., Galosi, C., Pariano, M., Massi-Benedetti, C., Borghi, M., Puccetti, M., Lucidi, V., et al. (2016) · Nature Communications · doi:10.1038/ncomms10791 · Cited by 233
Self-citationAnders, H., Suárez-Álvarez, B., Grigorescu, M., Foresto‐Neto, O., Steiger, S., Desai, J., Marschner, J. A., Honarpisheh, M. M., Shi, C., Jordan, J., et al. (2017) · Kidney International · doi:10.1016/j.kint.2017.09.022 · Cited by 226
Siew, J. J., Chen, H., Chen, H., Chen, H.-L., Chen, C., Soong, B., Wu, Y., Chang, C., Chan, Y., Lin, C., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11441-0 · Cited by 229
NOX2-dependent regulation of inflammation
Singel, K. L., & Segal, B. H. (2016) · Clinical Science · doi:10.1042/cs20150660 · Cited by 224
Roos, D. (2016) · British Medical Bulletin · doi:10.1093/bmb/ldw009 · Cited by 212
Beclin1‐driven autophagy modulates the inflammatory response of microglia via NLRP3
Houtman, J., Freitag, K., Gimber, N., Schmoranzer, J., Heppner, F. L., & Jendrach, M. (2019) · The EMBO Journal · doi:10.15252/embj.201899430 · Cited by 213
Gene therapy targeting haematopoietic stem cells for inherited diseases: progress and challenges
Cavazzana, M., Bushman, F. D., Miccio, A., André‐Schmutz, I., & Six, E. M. (2019) · Nature Reviews Drug Discovery · doi:10.1038/s41573-019-0020-9 · Cited by 205
Chronic Granulomatous Disease: a Comprehensive Review
Yu, H.-H., Yang, Y.-H., & Chiang, B.-L. (2021) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-020-08800-x · Cited by 197
Bode, S. F. N., Ammann, S., Al–Herz, W., Bataneant, M. T., Dvorak, C. C., Gehring, S., Gennery, A. R., Gilmour, K. C., González‐Granado, L. I., Gross‐Wieltsch, U., et al. (2015) · Haematologica · doi:10.3324/haematol.2014.121608 · Cited by 197
Neutrophils in traumatic brain injury (TBI): friend or foe?
Liu, Y., Li, S., & Dai, S.-S. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1173-x · Cited by 197
Cicco, S., Cicco, G., Racanelli, V., & Vacca, A. (2020) · Mediators of Inflammation · doi:10.1155/2020/7527953 · Cited by 195
Autophagy and proinflammatory cytokines: Interactions and clinical implications
Ge, Y., Huang, M., & Yao, Y.-M. (2018) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2018.07.001 · Cited by 191
NADPH Oxidases Are Essential for Macrophage Differentiation
Xu, Q., Choksi, S., Qu, J., Jang, J., Choe, M., Bánfi, B., Engelhardt, J. F., & Liu, Z.-G. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.731216 · Cited by 188
The phagocyte respiratory burst: Historical perspectives and recent advances
Thomas, D. (2017) · Immunology Letters · doi:10.1016/j.imlet.2017.08.016 · Cited by 193
Pathogenic Fungal Infection in the Lung
Li, Z., Lu, G., & Meng, G. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01524 · Cited by 184
The Potential Role of Trained Immunity in Autoimmune and Autoinflammatory Disorders
Arts, R. J. W., Joosten, L. A. B., & Netea, M. G. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00298 · Cited by 183
Self-citationThe roles of NADPH oxidase in modulating neutrophil effector responses
Zeng, M. Y., Miralda, I., Armstrong, C. L., Uriarte, S. M., & Bagaitkar, J. (2019) · Molecular Oral Microbiology · doi:10.1111/omi.12252 · Cited by 184
Xia, Y., Liu, N., Xie, X., Bi, G., Ba, H., Li, L., Zhang, J., Deng, X., Yao, Y., Tang, Z., et al. (2019) · Autophagy · doi:10.1080/15548627.2019.1569916 · Cited by 177
Uric acid priming in human monocytes is driven by the AKT–PRAS40 autophagy pathway
Crișan, T. O., Cleophas, M. C. P., Novakovic, B., Erler, K., van de Veerdonk, F. L., Stunnenberg, H. G., Netea, M. G., Dinarello, C. A., & Joosten, L. A. B. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1620910114 · Cited by 168
Self-citationGenetic disorders coupled to ROS deficiency
O’Neill, S., Brault, J., Stasia, M.-J., & Knaus, U. G. (2015) · Redox Biology · doi:10.1016/j.redox.2015.07.009 · Cited by 164
Pathogenesis of Respiratory Viral and Fungal Coinfections
Salazar, F., Bignell, E., Brown, G. D., Cook, P. C., & Warris, A. (2021) · Clinical Microbiology Reviews · doi:10.1128/cmr.00094-21 · Cited by 164
Ritvo, P.-G., Churlaud, G., Quiniou, V., Flórez, L. V., Brimaud, F., Fourcade, G., Mariotti‐Ferrandiz, E., & Klatzmann, D. (2017) · Science Immunology · doi:10.1126/sciimmunol.aan0368 · Cited by 156
Gazendam, R. P., van de Geer, A., Roos, D., van den Berg, T. K., & Kuijpers, T. W. (2016) · Immunological Reviews · doi:10.1111/imr.12454 · Cited by 151
Moderate Hypoxia Potentiates Interleukin-1β Production in Activated Human Macrophages
Folco, E. J. E., Sukhova, G. K., Quillard, T., & Libby, P. (2014) · Circulation Research · doi:10.1161/circresaha.115.304437 · Cited by 148
Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects
Chiriaco, M., Salfa, I., Matteo, G. D., Rossi, P., & Finocchi, A. (2015) · Pediatric Allergy and Immunology · doi:10.1111/pai.12527 · Cited by 147
Mechanisms of Pediatric Inflammatory Bowel Disease
Peloquin, J. M., Goel, G., Villablanca, E. J., & Xavier, R. J. (2016) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032414-112151 · Cited by 141
Self-citationKelsen, J. R., Sullivan, K. E., Rabizadeh, S., Singh, N., Snapper, S. B., Elkadri, A. A., & Grossman, A. B. (2020) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000002567 · Cited by 142
From Flies to Men: ROS and the NADPH Oxidase in Phagocytes
Moghadam, Z. M., Henneke, P., & Kolter, J. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.628991 · Cited by 146
Immunotherapeutic approaches to treatment of fungal diseases
Armstrong-James, D., Brown, G. D., Netea, M. G., Zelante, T., Gresnigt, M. S., van de Veerdonk, F. L., & Levitz, S. M. (2017) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(17)30442-5 · Cited by 135
Self-citationBuvelot, H., Jaquet, V., & Krause, K. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9424-3_2 · Cited by 136
Caffrey, A. K., Lehmann, M. M., Zickovich, J. M., Espinosa, V., Shepardson, K. M., Watschke, C. P., Hilmer, K. M., Thammahong, A., Barker, B. M., Rivera, A., et al. (2015) · PLOS Pathogens · doi:10.1371/journal.ppat.1004625 · Cited by 132
Genetics of inflammatory bowel disease from multifactorial to monogenic forms
Bianco, A. M. (2015) · World Journal of Gastroenterology · doi:10.3748/wjg.v21.i43.12296 · Cited by 127
Phagocyte NADPH oxidase, chronic granulomatous disease and mycobacterial infections
Deffert, C., Cachat, J., & Krause, K. (2014) · Cellular Microbiology · doi:10.1111/cmi.12322 · Cited by 126
Helyes, Z., Tékus, V., Szentes, N., Pohóczky, K., Botz, B., Kiss, T., Kemény, Á., Környei, Z., Tóth, K., Lénárt, N., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820168116 · Cited by 122
An Expanding Role for Interleukin-1 Blockade from Gout to Cancer
Dinarello, C. A. (2014) · Molecular Medicine · doi:10.2119/molmed.2014.00232 · Cited by 127
Self-citationObesity-induced inflammation exacerbates clonal hematopoiesis
Pasupuleti, S. K., Ramdas, B., Burns, S. S., Palam, L. R., Kanumuri, R., Kumar, R., Pandhiri, T. R., Davé, U. P., Yellapu, N. K., Zhou, X., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci163968 · Cited by 125
Loss-of-function CARD8 mutation causes NLRP3 inflammasome activation and Crohn’s disease
Mao, L., Kitani, A., Similuk, M. N., Oler, A. J., Albenberg, L. G., Kelsen, J. R., Aktay, A., Quezado, M., Yao, M. D., Montgomery-Recht, K., et al. (2018) · Journal of Clinical Investigation · doi:10.1172/jci98642 · Cited by 111
Elder, M. J., Webster, S. J., Chee, R., Williams, D. L., Gaston, H., & GOODALL, J. C. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00791 · Cited by 116
mTOR Mediates IL-23 Induction of Neutrophil IL-17 and IL-22 Production
Chen, F., Cao, A., Yao, S., Evans‐Marin, H., Liu, H., Wu, W. H., Carlsen, E. D., Dann, S. M., Soong, L., Sun, J., et al. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1501541 · Cited by 107
Blocking IL-1 to prevent respiratory failure in COVID-19
van de Veerdonk, F. L., & Netea, M. G. (2020) · Critical Care · doi:10.1186/s13054-020-03166-0 · Cited by 106
Self-citationLc3-associated phagocytosis—The highway to hell for phagocytosed microbes
Herb, M., Gluschko, A., & Schramm, M. (2020) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2019.04.016 · Cited by 103
An Integrated Taxonomy for Monogenic Inflammatory Bowel Disease
Bolton, C., Smillie, C. S., Pandey, S., Elmentaite, R., Wei, G., Argmann, C., Aschenbrenner, D., James, K. R., McGovern, D. P. B., Macchi, M., et al. (2021) · Gastroenterology · doi:10.1053/j.gastro.2021.11.014 · Cited by 99
Self-citationKyrmizi, I., Ferreira, H., Carvalho, A., Figueroa, J. A. L., Zarmpas, P., Cunha, C., Akoumianaki, T., Stylianou, K., Deepe, G. S., Samonis, G., et al. (2018) · Nature Microbiology · doi:10.1038/s41564-018-0167-x · Cited by 96
Self-citationLi, H., Zhou, X., Huang, Y., Liao, B., Cheng, L., & Ren, B. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.685133 · Cited by 91
Denson, L. A., Jurickova, I., Karns, R. A., Shaw, K. A., Cutler, D. J., Okou, D. T., Dodd, A., Quinn, K., Mondal, K., Aronow, B. J., et al. (2018) · Gastroenterology · doi:10.1053/j.gastro.2018.02.016 · Cited by 90
Self-citationRoudbary, M., Kumar, S., Kumar, A., Černáková, L., Nikoomanesh, F., & Rodrigues, C. F. (2021) · Journal of Fungi · doi:10.3390/jof7090720 · Cited by 89
Staphylococcus aureus, phagocyte NADPH oxidase and chronic granulomatous disease
Buvelot, H., Posfay-Barbe, K. M., Linder, P., Schrenzel, J., & Krause, K. (2016) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuw042 · Cited by 92
Autoinflammatory diseases: update on classification diagnosis and management
Pathak, S., McDermott, M., & Savic, S. (2016) · Journal of Clinical Pathology · doi:10.1136/jclinpath-2016-203810 · Cited by 87
Antifungal innate immunity: recognition and inflammatory networks
Becker, K. L., Ifrim, D. C., Quintin, J., Netea, M. G., & van de Veerdonk, F. L. (2015) · Seminars in Immunopathology · doi:10.1007/s00281-014-0467-z · Cited by 86
Self-citationAutophagy and microbial pathogenesis
Keller, M. D., Torres, V. J., & Cadwell, K. (2020) · Cell Death and Differentiation · doi:10.1038/s41418-019-0481-8 · Cited by 86
Symington, J., Wang, C., Twentyman, J., Owusu‐Boaitey, N., Schwendener, R. A., Núñez, G., Schilling, J. D., & Mysorekar, I. U. (2015) · Mucosal Immunology · doi:10.1038/mi.2015.7 · Cited by 82
Webster, S. J., Brode, S., Ellis, L., Fitzmaurice, T. J., Elder, M. J., Gekara, N. O., Tourlomousis, P., Bryant, C. E., Clare, S., Chee, R., et al. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006383 · Cited by 85
How neutrophil extracellular traps orchestrate the local immune response in gout
Maueröder, C., Kienhöfer, D., Hahn, J., Schauer, C., Manger, B., Schett, G. A., i, M. H., & Hoffmann, M. H. (2015) · Journal of Molecular Medicine · doi:10.1007/s00109-015-1295-x · Cited by 85
Zhao, J., Sun, Y., Shi, P., Dong, J.-N., Zuo, L.-G., Wang, H.-G., Gong, J.-F., Li, Y., Gu, L.-L., Li, N., et al. (2015) · International Immunopharmacology · doi:10.1016/j.intimp.2015.03.033 · Cited by 80
Noninfectious Manifestations and Complications of Chronic Granulomatous Disease
Henrickson, S. E., Jongco, A. M., Thomsen, K. F., Garabedian, E., & Thomsen, I. P. (2018) · Journal of the Pediatric Infectious Diseases Society · doi:10.1093/jpids/piy014 · Cited by 78
The cellular autophagy/apoptosis checkpoint during inflammation
Messer, J. S. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2403-y · Cited by 79
Weisser, M., Demel, U. M., Stein, S., Chen-Wichmann, L., Touzot, F., Santilli, G., Sujer, S., Brendel, C., Siler, U., Cavazzana, M., et al. (2016) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2015.11.028 · Cited by 77
Autophagy protects C. elegans against necrosis during Pseudomonas aeruginosa infection
Zou, C., Ma, Y., Dai, L.-L., & Zhang, K. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1405032111 · Cited by 76
Aspergillosis in Chronic Granulomatous Disease
King, J., Henriet, S., & Warris, A. (2016) · Journal of Fungi · doi:10.3390/jof2020015 · Cited by 76
Role of Inflammasomes in Intestinal Inflammation and Crohnʼs Disease
Opipari, A. W., & Franchi, L. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000230 · Cited by 75
The Inflammasome and IL-1β: Implications for the Treatment of Inflammatory Diseases
Satoh, T. K., Otsuka, A., Contassot, E., & French, L. E. (2015) · Immunotherapy · doi:10.2217/imt.14.106 · Cited by 77
Primary immune deficiencies with defects in neutrophil function
Dinauer, M. C. (2016) · Hematology · doi:10.1182/asheducation-2016.1.43 · Cited by 74
Intestinal Autophagy and Its Pharmacological Control in Inflammatory Bowel Disease
Ke, P., Shao, B., Xu, Z., Chen, X., & Liu, C. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00695 · Cited by 71
The Multifaceted Role of T-Helper Responses in Host Defense against Aspergillus fumigatus
Dewi, I., Van de Veerdonk, F., & Gresnigt, M. (2017) · Journal of Fungi · doi:10.3390/jof3040055 · Cited by 69
Self-citationCole, J., Aberdein, J., Jubrail, J., & Dockrell, D. H. (2014) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/bs.ampbs.2014.08.004 · Cited by 71
Inflammatory consequences of inherited disorders affecting neutrophil function
Dinauer, M. C. (2019) · Blood · doi:10.1182/blood-2018-11-844563 · Cited by 72
Noncanonical Fungal Autophagy Inhibits Inflammation in Response to IFN-γ via DAPK1
Oikonomou, V., Moretti, S., Renga, G., Galosi, C., Borghi, M., Pariano, M., Puccetti, M., Palmerini, C. A., Amico, L., Carotti, A., et al. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.10.012 · Cited by 68
Self-citationAbdelaziz, D. H., Khalil, H., Cormet‐Boyaka, E., & Amer, A. O. (2015) · Immunological Reviews · doi:10.1111/imr.12288 · Cited by 68
Recent advances in chronic granulomatous disease
Anjani, G., Vignesh, P., Joshi, V., Shandilya, J. K., Bhattarai, D., Sharma, J., & Rawat, A. K. (2019) · Genes & Diseases · doi:10.1016/j.gendis.2019.07.010 · Cited by 71
Marsh, R. A., Leiding, J. W., Logan, B. R., Griffith, L. M., Arnold, D. E., Haddad, É., Falcone, E. L., Yin, Z., Patel, K., Arbuckle, E. P., et al. (2019) · Journal of Clinical Immunology · doi:10.1007/s10875-019-00659-8 · Cited by 65
Tegtmeyer, D., Seidl, M., Gerner, P., Baumann, U., & Klemann, C. (2017) · Pediatric Allergy and Immunology · doi:10.1111/pai.12734 · Cited by 63
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Metadata
- Authors
- de Luca, A., Smeekens, S. P., Casagrande, A., Iannitti, R., Conway, K. L., Gresnigt, M. S., Begun, J., Plantinga, T. S., Joosten, L. A. B., van der Meer, J. W. M., Chamilos, G., Netea, M. G., Xavier, R. J., Dinarello, C. A., Romani, L., & van de Veerdonk, F. L.
- Affiliations
- Department of Experimental Medicine and Biochemical Sciences, University of Perugia, 06122 Perugia, Italy;
- Radboud University Medical Center (NL)
- University of Perugia (IT)
- Harvard University (US)
- Department of Medicine, Radboud University Medical Centre, 6500 HB, Nijmegen, The Netherlands;
- University of Crete (GR)
- Corresponding author
- Dinarello, Charles A.
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2014-02-18
- Volume
- 111
- Issue
- 9
- Pages
- 3526-3531
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3948220
- OpenAlex
- W2153164696
- Cited by
- 313
- References
- 49
- Citations by year
- 2026: 13 · 2025: 16 · 2024: 10 · 2023: 16 · 2022: 22 · 2021: 32 · 2020: 24 · 2019: 34 · 2018: 26 · 2017: 41 · 2016: 35 · 2015: 26 · 2014: 18
- FWCI
- 18.28
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Radboud Repository (Radboud University) (submittedVersion)
- Funders
- Crohn's and Colitis Foundation
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (AI‑15614, AI-62773, R56AI015614, R01AI062773, R01AI015614)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK083756, DK-60049, DK 83756, R01DK097485, DK 43351, R01DK060049, P30DK043351)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- chronic granulomatous disease, IL-1 receptor blockade, anakinra, autophagy, inflammasome activation, IL-1β, NADPH oxidase deficiency, colitis, invasive aspergillosis, macrophages, monocytes, neutrophil recruitment, Th17 response, reactive oxygen species
- MeSH terms
- Animals, Anti-Inflammatory Agents, Aspergillus fumigatus, Autophagy, Colitis, Enzyme-Linked Immunosorbent Assay, Granulomatous Disease, Chronic, Humans, Mice, Inbred C57BL, Mice, Mutant Strains, Microtubule-Associated Proteins, Phagosomes, Receptors, Interleukin-1, Statistics, Nonparametric, NADPH Oxidases, Mice, Interleukin-1beta, Interleukin 1 Receptor Antagonist Protein, Real-Time Polymerase Chain Reaction
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