Simultaneous Targeting of IL-1 and IL-18 Is Required for Protection against Inflammatory and Septic Shock
Open accessAbstract
Rationale: Sepsis is one of the leading causes of death around the world. The failure of clinical trials to treat sepsis demonstrates that the molecular mechanisms are multiple and are still insufficiently understood. Objectives: To clarify the long disputed hierarchical contribution of several central inflammatory mediators (IL-1β, IL-18, caspase [CASP] 7, CASP1, and CASP11) in septic shock and to explore their therapeutic potential. Methods: LPS- and tumor necrosis factor (TNF)-induced lethal shock, and cecal ligation and puncture (CLP) were performed in genetically or pharmacologically targeted mice. Body temperature and survival were monitored closely, and plasma was analyzed for several markers of cellular disintegration and inflammation. Measurements and Main Results: Interestingly, deficiency of both IL-1β and IL-18 additively prevented LPS-induced mortality. The detrimental role of IL-1β and IL-18 was confirmed in mice subjected to a lethal dose of TNF, or to a lethal CLP procedure. Although their upstream activator, CASP1, and its amplifier, CASP11, are considered potential therapeutic targets because of their crucial involvement in endotoxin-induced toxicity, CASP11- or CASP1/11-deficient mice were not, or hardly, protected against a lethal TNF or CLP challenge. In line with our results obtained in genetically deficient mice, only the combined neutralization of IL-1 and IL-18, using the IL-1 receptor antagonist anakinra and anti–IL-18 antibodies, conferred complete protection against endotoxin-induced lethality. Conclusions: Our data point toward the therapeutic potential of neutralizing IL-1 and IL-18 simultaneously in sepsis, rather than inhibiting the upstream inflammatory caspases.
Integrity signals
Registry
Cites
Statistics
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?
Pyroptosis is etiologically involved in pathological conditions such as lethal septic shock at least as induced by LPS.
“(4) is etiologically involved in pathological conditions such as lethal septic shock (at least as induced by LPS) [610, 611].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [611]
Cites
Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in <i>Tlr4</i> Gene
Poltorak, A., He, X., Smirnova, I., Liu, M.-Y., Huffel, C. V., Du, X., Birdwell, D., Alejos, E., Silva, M., Galanos, C., et al. (1998) · Science · doi:10.1126/science.282.5396.2085 · Cited by 7,631 · see citing works
Hoshino, K., Takeuchi, O., Kawai, T., Sanjo, H., Ogawa, T., Takeda, Y., Takeda, K., & Akira, S. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.7.3749 · Cited by 3,374 · see citing works
Pyroptosis: host cell death and inflammation
Bergsbaken, T., Fink, S. L., & Cookson, B. T. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2070 · Cited by 3,185 · see citing works
Cryopyrin activates the inflammasome in response to toxins and ATP
Mariathasan, S., Weiss, D. S., Newton, K., McBride, J., O'Rourke, K., Roose-Girma, M., Lee, W. P., Weinrauch, Y., Monack, D. M., & Dixit, V. M. (2006) · Nature · doi:10.1038/nature04515 · Cited by 3,080 · see citing works
Non-canonical inflammasome activation targets caspase-11
Kayagaki, N., Warming, S., Lamkanfi, M., Walle, L. V., Louie, S., Dong, J., Newton, K., Qu, Y., Liu, J., Heldens, S., et al. (2011) · Nature · doi:10.1038/nature10558 · Cited by 2,530 · see citing works
Unresponsiveness of MyD88-deficient mice to endotoxin.
Kawai, T., Adachi, O., Ogawa, T., Takeda, K., & Akira, S. (1999) · Immunity · doi:10.1016/s1074-7613(00)80086-2 · Cited by 2,367 · see citing works
Immunodesign of experimental sepsis by cecal ligation and puncture
Rittirsch, D., Huber-Lang, M. S., Flierl, M. A., & Ward, P. A. (2009) · Nature Protocols · doi:10.1038/nprot.2008.214 · Cited by 2,209 · see citing works
Franchi, L., Eigenbrod, T., Muñoz-Planillo, R., & Nuñez, G. (2009) · Nature Immunology · doi:10.1038/ni.1703 · Cited by 1,834 · see citing works
Altered Cytokine Export and Apoptosis in Mice Deficient in Interleukin-1β Converting Enzyme
Kuida, K., Lippke, J. A., Ku, G., Harding, M. W., Livingston, D. J., Su, M. S. S., & Flavell, R. A. (1995) · Science · doi:10.1126/science.7535475 · Cited by 1,606 · see citing works
Noncanonical Inflammasome Activation by Intracellular LPS Independent of TLR4
Kayagaki, N., Wong, M. T., Stowe, I. B., Ramani, S. R., Gonzalez, L. C., Akashi‐Takamura, S., Miyake, K., Zhang, J., Lee, W. P., Muszyński, A., et al. (2013) · Science · doi:10.1126/science.1240248 · Cited by 1,545 · see citing works
Endotoxin-tolerant Mice Have Mutations in Toll-like Receptor 4 ( Tlr4 )
Qureshi, S. T., Larivière, L., Leveque, G., Clermont, S., Moore, K. J., Gros, P., & Malo, D. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.189.4.615 · Cited by 1,525 · see citing works
Pannexin‐1 mediates large pore formation and interleukin‐1β release by the ATP‐gated P2X7 receptor
Pelegrı́n, P., & Surprenant, A. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601378 · Cited by 1,428 · see citing works
Li, P., Allen, H., Banerjee, S., Franklin, S., Herzog, L., Johnston, C. G., McDowell, J., Paskind, M. P., Rodman, L., Salfeld, J. G., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90490-5 · Cited by 1,408 · see citing works
Cytoplasmic LPS Activates Caspase-11: Implications in TLR4-Independent Endotoxic Shock
Hagar, J. A., Powell, D. A., Aachoui, Y., Ernst, R. K., & Miao, E. A. (2013) · Science · doi:10.1126/science.1240988 · Cited by 1,261 · see citing works
Caspase-1 processes IFN-γ-inducing factor and regulates LPS-induced IFN- γ production
Ghayur, T., Banerjee, S., Hugunin, M., Butler, D., Herzog, L., Carter, A. B., Quintal, L. J., Sekut, L., Talanian, R. V., Paskind, M. P., et al. (1997) · Nature · doi:10.1038/386619a0 · Cited by 1,204 · see citing works
Activation of Interferon-γ Inducing Factor Mediated by Interleukin-1β Converting Enzyme
Gu, Y., Kuida, K., Tsutsui, H., Ku, G., Hsiao, K., Fleming, M. A., Hayashi, N., Higashino, K., Okamura, H., Nakanishi, K., et al. (1997) · Science · doi:10.1126/science.275.5297.206 · Cited by 1,159 · see citing works
Caspase‐1‐induced pyroptotic cell death
Miao, E. A., Rajan, J. V., & Aderem, A. A. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01044.x · Cited by 1,139 · see citing works
The P2X7 Receptor: A Key Player in IL-1 Processing and Release
Ferrari, D., Pizzirani, C., Adinolfi, E., Lemoli, R. M., Curti, A., Idzko, M., Panther, E., & Di Virgilio, F. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.7.3877 · Cited by 1,025 · see citing works
Inflammasomes and Their Roles in Health and Disease
Lamkanfi, M., & Dixit, V. M. (2012) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-101011-155745 · Cited by 935 · cited 1× · see citing works
“This result questions the possibility of targeting inflammatory caspases as a strategy to treat patients with sepsis (46), which was recently proposed based on the central role of CASP11 in intracellular sensing of bacteria (47–49).”
BackgroundConfirmatory interleukin-1 receptor antagonist trial in severe sepsis
Opal, S. M., Fisher, C. J., Dhainaut, J.-F., Vincent, J., Brase, R., Lowry, S. F., SADOFF, J. C., Slotman, G. J., Levy, H. A., BALK, R. A., et al. (1997) · Critical Care Medicine · doi:10.1097/00003246-199707000-00010 · Cited by 867 · see citing works
Interleukin-1 receptor antagonist reduces mortality from endotoxin shock
OHLSSON, K., Björk, P., Bergenfeldt, M., Hageman, R. J. J., & Thompson, R. C. (1990) · Nature · doi:10.1038/348550a0 · Cited by 852 · see citing works
Cecal ligation and puncture: the gold standard model for polymicrobial sepsis?
Dejager, L., Pinheiro, I., Dejonckheere, E., & Libert, C. (2011) · Trends in Microbiology · doi:10.1016/j.tim.2011.01.001 · Cited by 789 · see citing works
RIP Kinase-Dependent Necrosis Drives Lethal Systemic Inflammatory Response Syndrome
Duprez, L., Takahashi, N., Hauwermeiren, F. V., Vandendriessche, B., Goossens, V., Berghe, T. V., Declercq, W., Libert, C., Cauwels, A., & Vandenabeele, P. (2011) · Immunity · doi:10.1016/j.immuni.2011.09.020 · Cited by 591 · see citing works
Self-citationCaspase-11 Protects Against Bacteria That Escape the Vacuole
Aachoui, Y., Leaf, I. A., Hagar, J. A., Fontana, M. F., Campos, C. G., Zak, D. E., Tan, M. H., Cotter, P. A., Vance, R. E., Aderem, A. A., et al. (2013) · Science · doi:10.1126/science.1230751 · Cited by 544 · see citing works
Kanneganti, T., Lamkanfi, M., Kim, Y., Chen, G., Park, J., Franchi, L., Vandenabeele, P., & Núñez, G. (2007) · Immunity · doi:10.1016/j.immuni.2007.03.008 · Cited by 526 · see citing works
Self-citationEfficient gene modulation in mouse epiblast using a Sox2Cre transgenic mouse strain
Hayashi, S., Lewis, P. M., Pevny, L., & McMahon, A. P. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(03)00099-6 · Cited by 492 · see citing works
Inflammasome-Dependent Release of the Alarmin HMGB1 in Endotoxemia
Lamkanfi, M., Sarkar, A., Walle, L. V., Vitari, A. C., Amer, A. O., Wewers, M. D., Tracey, K. J., Kanneganti, T., & Dixit, V. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000803 · Cited by 468 · see citing works
Phenotypic and functional characterization of mice that lack the type I receptor for IL-1.
Glaccum, M. B., Stocking, K., Charrier, K., Smith, J., Willis, C., Maliszewski, C., Livingston, D., Peschon, J., & Morrissey, P. (1997) · Journal of Immunology · doi:10.4049/jimmunol.159.7.3364 · Cited by 418 · see citing works
Zheng, H., Fletcher, D., Kozak, W., Jiang, M., Hofmann, K. J., Corn, C., Soszynski, D., Grabiec, C., Trumbauer, M., Shaw, A. R., et al. (1995) · Immunity · doi:10.1016/1074-7613(95)90154-x · Cited by 404 · see citing works
Immunotherapy for Sepsis — A New Approach against an Ancient Foe
Hotchkiss, R. S., & Opal, S. M. (2010) · New England Journal of Medicine · doi:10.1056/nejmcibr1004371 · Cited by 367 · see citing works
Targeted Peptidecentric Proteomics Reveals Caspase-7 as a Substrate of the Caspase-1 Inflammasomes
Lamkanfi, M., Kanneganti, T., Damme, P. V., Berghe, T. V., Vanoverberghe, I., Vandekerckhove, J., Vandenabeele, P., Gevaert, K., & Nuénñez, G. (2008) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m800132-mcp200 · Cited by 341 · see citing works
Self-citationFischer, E., Marano, M. A., Zee, K. J. V., Rock, C. S., Hawes, A. S., Thompson, W. A., DeForge, L. E., Kenney, J. S., Remick, D. G., & Bloedow, D. C. (1992) · Journal of Clinical Investigation · doi:10.1172/jci115748 · Cited by 333 · see citing works
Enhanced bacterial clearance and sepsis resistance in caspase-12-deficient mice
Saleh, M., Mathison, J. C., Wolinski, M. K., Bensinger, S. J., Fitzgerald, P., Droin, N. M., Ulevitch, R. J., Green, D. R., & Nicholson, D. W. (2006) · Nature · doi:10.1038/nature04656 · Cited by 323 · see citing works
Functions of interleukin 1 receptor antagonist in gene knockout and overproducing mice.
Hirsch, E., Irikura, V. M., Paul, S. M., & Hirsh, D. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.20.11008 · Cited by 317 · see citing works
Interleukin‐18 and Host Defense against Infection
Dinarello, C. A., & Fantuzzi, G. (2003) · The Journal of Infectious Diseases · doi:10.1086/374751 · Cited by 287 · see citing works
A NOVEL IL-18BP ELISA SHOWS ELEVATED SERUM IL-18BP IN SEPSIS AND EXTENSIVE DECREASE OF FREE IL-18
Novick, D., Schwartsburd, B. I., Pinkus, R., Suissa, D., Belzer, I., Sthoeger, Z. M., Keane, W. F., Chvatchko, Y., Kim, S. H., Fantuzzi, G., et al. (2001) · Cytokine · doi:10.1006/cyto.2001.0914 · Cited by 278 · see citing works
Shock and Multiple-Organ Dysfunction after Self-Administration of Salmonella Endotoxin
da Silva, A. M. T., Kaulbach, H. C., Chuidian, F. S., Lambert, D. R., Suffredini, A. F., & Danner, R. L. (1993) · New England Journal of Medicine · doi:10.1056/nejm199305203282005 · Cited by 276 · see citing works
Endotoxins and Other Sepsis Triggers
Opal, S. M. (2010) · Contributions to nephrology · doi:10.1159/000315915 · Cited by 258 · see citing works
Raupach, B., Peuschel, S.-K., Monack, D. M., & Zychlinsky, A. (2006) · Infection and Immunity · doi:10.1128/iai.00417-06 · Cited by 255 · see citing works
Netea, M. G., Fantuzzi, G., Kullberg, B. J., Stuyt, R. J. L., Pulido, E. J., McIntyre, R. C., Joosten, L. A. B., van der Meer, J. W. M., & Dinarello, C. A. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.5.2644 · Cited by 210 · see citing works
Effect of endotoxin in IL-1 β-deficient mice
Fantuzzi, G., Zheng, H., Faggioni, R., Benigni, F., Ghezzi, P., Sipe, J. D., SHAW, A. R., & Dinarello, C. A. (1996) · The Journal of Immunology · doi:10.4049/jimmunol.157.1.291 · Cited by 190 · see citing works
The P2X7 receptor–pannexin connection to dye uptake and IL-1β release
Pelegrı́n, P., & Surprenant, A. (2009) · Purinergic Signalling · doi:10.1007/s11302-009-9141-7 · Cited by 169 · see citing works
Fantuzzi, G., & Dinarello, C. A. (1996) · Journal of Leukocyte Biology · doi:10.1002/jlb.59.4.489 · Cited by 156 · see citing works
Inflammasomes as microbial sensors
Franchi, L., Muñoz-Planillo, R., Reimer, T., Eigenbrod, T., & Núñez, G. (2010) · European Journal of Immunology · doi:10.1002/eji.200940180 · Cited by 121 · see citing works
Hillenbrand, A., Knippschild, U., Weiß, M., Schrezenmeier, H., Henne‐Bruns, D., Huber-Lang, M. S., & Wolf, A. M. (2010) · BMC Surgery · doi:10.1186/1471-2482-10-26 · Cited by 113 · see citing works
Hochholzer, P., Lipford, G. B., Wagner, H., Pfeffer, K., & Heeg, K. M. (2000) · Infection and Immunity · doi:10.1128/iai.68.6.3502-3508.2000 · Cited by 73 · see citing works
Update on biologicals for treatment of juvenile idiopathic arthritis
Horneff, G. (2013) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.2013.735657 · Cited by 68 · see citing works
Caspase-7 deficiency protects from endotoxin-induced lymphocyte apoptosis and improves survival
Lamkanfi, M., Moreira, L. O., Makena, P. S., Spierings, D. C. J., Boyd, K. L., Murray, P. J., Green, D. R., & Kanneganti, T. (2009) · Blood · doi:10.1182/blood-2008-09-178038 · Cited by 65 · see citing works
Genetic Background Determines Susceptibility during Murine Septic Peritonitis
Godshall, C. J., Scott, M. J., Peyton, J. C., Gardner, S. A., & Cheadle, W. G. (2002) · Journal of Surgical Research · doi:10.1006/jsre.2001.6319 · Cited by 58 · see citing works
Kenneth, N. S., Younger, J. M., Hughes, E. D., Marcotte, D., Barker, P. A., Saunders, T. L., & Duckett, C. S. (2012) · Biochemical Journal · doi:10.1042/bj20120249 · Cited by 56 · see citing works
Interleukin 18 (IL-18) levels in patients with sepsis.
Endo, S., Inada, K., Yamada, Y., Wakabayashi, G., Ishikura, H., Tanaka, T., & Sato, S. (2000) · PubMed · Cited by 45 · see citing works
DIFFERENTIAL EFFECT OF CASPASE INHIBITION ON PROINFLAMMATORY CYTOKINE RELEASE IN SEPTIC PATIENTS
Oberholzer, A., Härter, L., Feilner, A., Steckholzer, U., Trentz, O., & Ertel, W. (2000) · Shock · doi:10.1097/00024382-200014030-00002 · Cited by 33 · see citing works
Joosten, L. A. B., van de Veerdonk, F. L., Vonk, A. G., Boerman, O. C., Keuter, M., Fantuzzi, G., Verschueren, I., van der Poll, T., Dinarello, C. A., Kullberg, B. J., et al. (2010) · Apmis · doi:10.1111/j.1600-0463.2010.02684.x · Cited by 29 · see citing works
Lochner, M., Wagner, H., Classen, M., & Förster, I. (2002) · Journal of Immunological Methods · doi:10.1016/s0022-1759(01)00505-1 · Cited by 23 · see citing works
An Inactivating Caspase-11 Passenger Mutation Muddles Sepsis Research
Berghe, T. V., Goethals, A., Demon, D., Bogaert, P., Mak, T. W., Cauwels, A., & Vandenabeele, P. (2013) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201210-1775le · Cited by 19 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Galluzzi, L., Vitale, I., Aaronson, S. A., Abrams, J. M., Adam, D., Agostinis, P., Alnemri, E. S., Altucci, L., Amelio, I., Andrews, D. W., et al. (2018) · Cell Death & Differentiation · doi:10.1038/s41418-017-0012-4 · Cited by 6,680 · see citing works
Pyroptosis: Mechanisms and Diseases
Yu, P., Zhang, X., Liu, N., Tang, L., Peng, C., & Chen, X. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00507-5 · Cited by 2,353 · see citing works
Caspases in Cell Death, Inflammation, and Disease
Opdenbosch, N. V., & Lamkanfi, M. (2019) · Immunity · doi:10.1016/j.immuni.2019.05.020 · Cited by 1,230 · see citing works
Pyroptosis versus necroptosis: similarities, differences, and crosstalk
Frank, D., & Vince, J. E. (2019) · Cell Death & Differentiation · doi:10.1038/s41418-018-0212-6 · Cited by 1,062 · see citing works
Genomic landscape of the individual host response and outcomes in sepsis: a prospective cohort study
Davenport, E. E., Burnham, K. L., Radhakrishnan, J., Humburg, P., Hutton, P., Mills, T. C., Rautanen, A., Gordon, A. C., Garrard, C. S., Hill, A. V. S., et al. (2016) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(16)00046-1 · Cited by 866 · see citing works
Lipid Peroxidation Drives Gasdermin D-Mediated Pyroptosis in Lethal Polymicrobial Sepsis
Kang, R., Zeng, L., Zhu, S., Xie, Y., Liu, J., Wen, Q., Cao, L., Xie, M., Ran, Q., Kroemer, G., et al. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.05.009 · Cited by 620 · see citing works
Interleukin‐18: Biological properties and role in disease pathogenesis
Kaplanski, G. (2017) · Immunological Reviews · doi:10.1111/imr.12616 · Cited by 609 · see citing works
Regulated cell death and inflammation: an auto-amplification loop causes organ failure
Linkermann, A., Stockwell, B. R., Krautwald, S., & Anders, H.-J. (2014) · Nature Reviews Immunology · doi:10.1038/nri3743 · Cited by 522 · see citing works
Self-citationSepsis therapies: learning from 30 years of failure of translational research to propose new leads
Cavaillon, J., Singer, M., & Skirecki, T. (2020) · EMBO Molecular Medicine · doi:10.15252/emmm.201810128 · Cited by 318 · see citing works
Mechanism and regulation of pyroptosis-mediated in cancer cell death
Ruan, J., Wang, S., & Wang, J. (2020) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2020.109052 · Cited by 274 · see citing works
Extracellular ATP drives systemic inflammation, tissue damage and mortality
Cauwels, A., Rogge, E., Vandendriessche, B., Shiva, S., & Brouckaert, P. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.70 · Cited by 275 · see citing works
Self-citationDemarco, B., Grayczyk, J. P., Bjånes, E., Roy, D. L., Tonnus, W., Assenmacher, C., Radaelli, E., Fettrelet, T., Mack, V., Linkermann, A., et al. (2020) · Science Advances · doi:10.1126/sciadv.abc3465 · Cited by 237 · see citing works
Biological and clinical roles of IL-18 in inflammatory diseases
Landy, E., Carol, H. A., Ring, A. M., & Canna, S. (2023) · Nature Reviews Rheumatology · doi:10.1038/s41584-023-01053-w · Cited by 206 · see citing works
Neutrophil pyroptosis: new perspectives on sepsis
Liu, L., & Sun, B. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03060-1 · Cited by 197 · see citing works
Targeting ferroptosis protects against experimental (multi)organ dysfunction and death
Van Coillie, S., Van San, E., Goetschalckx, I., Wiernicki, B., Mukhopadhyay, B., Tonnus, W., Choi, S. M., Roelandt, R., Dumitrascu, C., Lamberts, L., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28718-6 · Cited by 186 · see citing works
Self-citationNecroptosis Promotes Staphylococcus aureus Clearance by Inhibiting Excessive Inflammatory Signaling
Kitur, K., Wachtel, S., Brown, A. O., Wickersham, M., Paulino, F. E., Peñaloza, H. F., Soong, G., Bueno, S. M., Parker, D., & Prince, A. S. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.039 · Cited by 180 · see citing works
NLRP3 Inflammasome Deficiency Protects Against Microbial Sepsis Via Increased Lipoxin B4 Synthesis
Lee, S., Nakahira, K., Dalli, J., Siempos, I. Ι., Norris, P. C., Colas, R. A., Moon, J., Shinohara, M., Hisata, S., Howrylak, J. A., et al. (2017) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201604-0892oc · Cited by 159 · see citing works
ABRO1 promotes NLRP3 inflammasome activation through regulation of NLRP3 deubiquitination
Ren, G., Zhang, X., Xiao, Y., Zhang, W., Wang, Y., Ma, W., Wang, X., Song, P., Lai, L., Chen, H., et al. (2019) · The EMBO Journal · doi:10.15252/embj.2018100376 · Cited by 154 · see citing works
Immunotherapy in sepsis - brake or accelerate?
Steinhagen, F., Schmidt, S. V., Schewe, J., Peukert, K., Klinman, D. M., & Bode, C. (2020) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107476 · Cited by 150 · see citing works
Recent Insights on Inflammasomes, Gasdermin Pores, and PyroptosisPreprint
de Vasconcelos, N. M., & Lamkanfi, M. (2019) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a036392 · Cited by 139 · see citing works
Caspase-8 Collaborates with Caspase-11 to Drive Tissue Damage and Execution of Endotoxic Shock
Mandal, P., Feng, Y., Lyons, J. D., Berger, S. B., Otani, S., DeLaney, A. A., Tharp, G. K., Maner-Smith, K. M., Burd, E. M., Schaeffer, M. C., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.06.011 · Cited by 130 · see citing works
The biology of natural killer cells during sepsis
Guo, Y., Patil, N. K., Luan, L., Bohannon, J. K., & Sherwood, E. R. (2017) · Immunology · doi:10.1111/imm.12854 · Cited by 128 · see citing works
Aziz, M., Jacob, A., & Wang, P. (2014) · Cell Death & Disease · doi:10.1038/cddis.2014.488 · Cited by 125 · see citing works
Transcriptomic correlates of organ failure extent in sepsis
Almansa, R., Heredia‐Rodríguez, M., Gómez‐Sánchez, E., Andaluz‐Ojeda, D., Iglesias, V., Rico, L., Ortega, A., Gómez‐Pesquera, E., Liu, P., Aragón, M. F., et al. (2014) · Journal of Infection · doi:10.1016/j.jinf.2014.12.010 · Cited by 122 · see citing works
A Critical Role for Human Caspase-4 in Endotoxin Sensitivity
Kajiwara, Y., Schiff, T., Voloudakis, G., Sosa, M. A. G., Elder, G. A., Bozdagi, O., & Buxbaum, J. D. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1303424 · Cited by 119 · see citing works
The in vivo evidence for regulated necrosis
Tonnus, W., & Linkermann, A. (2017) · Immunological Reviews · doi:10.1111/imr.12551 · Cited by 109 · see citing works
Targeting IL-17A attenuates neonatal sepsis mortality induced by IL-18
Wynn, J. L., Wilson, C., Hawiger, J., Scumpia, P. O., Marshall, A. F., Liu, J.-H., Zharkikh, I. L., Wong, H. R., Lahni, P. M., Benjamin, J. T., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1515793113 · Cited by 107 · see citing works
Zhou, R., Yang, X., Li, X., Qu, Y., Huang, Q., Sun, X., & Mu, D. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1651-9 · Cited by 100 · see citing works
Dysregulation of neutrophil death in sepsis
Zhu, C., Wang, Y., Liu, Q., Li, H.-R., Yu, C.-M., Li, P., Deng, X., & Wang, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.963955 · Cited by 104 · see citing works
Acute downregulation of miR-199a attenuates sepsis-induced acute lung injury by targeting SIRT1
Liu, Y., Guan, H., Zhang, J., Zheng, Z., Wang, H.-T., Tao, K., Han, S., Su, L., & Hu, D. (2018) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00173.2017 · Cited by 99 · see citing works
Yang, X., Li, W., Zhang, S., Wu, D., Jiang, X., Tan, R., Niu, X., Wang, Q., Wu, X., Liu, Z., et al. (2019) · The EMBO Journal · doi:10.15252/embj.2019102201 · Cited by 94 · see citing works
RIP kinase 1–dependent endothelial necroptosis underlies systemic inflammatory response syndrome
Zelic, M., Roderick, J. E., O’Donnell, J. A., Lehman, J. W., Lim, S. E., Janardhan, H. P., Trivedi, C. M., Pasparakis, M., & Kelliher, M. A. (2018) · Journal of Clinical Investigation · doi:10.1172/jci96147 · Cited by 92 · see citing works
Wu, K. K. L., Long, K., Lin, H., Siu, P. M., Hoo, R. L. C., Ye, D., Xu, A., & Cheng, K. K. Y. (2021) · Nature Communications · doi:10.1038/s41467-021-26987-1 · Cited by 93 · see citing works
Restoring the infected powerhouse: Mitochondrial quality control in sepsis
Chavez, F. L., Gartzke, L. P., van Beuningen, F. E., Wink, S. E., Henning, R. H., Krenning, G., & Bouma, H. R. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102968 · Cited by 97 · see citing works
ROS‐Mediated NLRP3 Inflammasome Activity Is Essential for Burn‐Induced Acute Lung Injury
Han, S., Cai, W., Yang, X., Jia, Y., Zheng, Z., Wang, H., Li, J., Li, Y., Gao, J., Fan, L., et al. (2015) · Mediators of Inflammation · doi:10.1155/2015/720457 · Cited by 86 · see citing works
Toll-like receptor-induced cytokines as immunotherapeutic targets in cancers and autoimmune diseases
Patra, M. C., Shah, M., & Choi, S. (2019) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2019.05.002 · Cited by 84 · see citing works
Self-citationDondelinger, Y., Priem, D., Huyghe, J., Delanghe, T., Vandenabeele, P., & Bertrand, M. J. M. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06284-z · Cited by 91 · see citing works
Self-citationGe, Y., Huang, M., & Yao, Y.-M. (2018) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2018.12.004 · Cited by 85 · see citing works
Geniposide protects against sepsis-induced myocardial dysfunction through AMPKα-dependent pathway
Song, P. K., She, Z., Meng, Y., Kong, C., Zhang, X., Yuan, Y., Yan, L., Tang, Q., & Ma, Z. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.02.011 · Cited by 77 · see citing works
The role of regulated necrosis in endocrine diseases
Tonnus, W., Belavgeni, A., Beuschlein, F., Eisenhofer, G., Faßnacht, M., Kroiß, M., Krone, N. P., Reincke, M., Bornstein, S. R., & Linkermann, A. (2021) · Nature Reviews Endocrinology · doi:10.1038/s41574-021-00499-w · Cited by 72 · see citing works
Hu, Z., Murakami, T., Suzuki, K., Tamura, H., Reich, J., Kuwahara‐Arai, K., Iba, T., & Nagaoka, I. (2016) · International Immunology · doi:10.1093/intimm/dxv113 · Cited by 73 · see citing works
Caspase‐11: arming the guards against bacterial infection
Stowe, I. B., Lee, B. L., & Kayagaki, N. (2015) · Immunological Reviews · doi:10.1111/imr.12292 · Cited by 73 · see citing works
Wang, Y., Mao, X., Chen, H., Feng, J., Yan, M., Wang, Y., & Yu, Y. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.05.027 · Cited by 71 · see citing works
Jia, X., Cao, B., An, Y., Zhang, X., & Wang, C. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.12.017 · Cited by 70 · see citing works
Copper Regulates the Canonical NLRP3 Inflammasome
Deigendesch, N., Zychlinsky, A., & Meissner, F. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1700712 · Cited by 66 · see citing works
Peli1 facilitates NLRP3 inflammasome activation by mediating ASC ubiquitination
Zhang, L., Ko, C., Li, Y., Jie, Z., Zhu, L., Zhou, X., Xie, X., Gao, T., Liu, T., Cheng, X., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109904 · Cited by 68 · see citing works
Risk Factors for Stroke in Patients With Sepsis and Bloodstream Infections
Shao, I. Y., Elkind, M. S. V., & Boehme, A. K. (2019) · Stroke · doi:10.1161/strokeaha.118.023443 · Cited by 65 · see citing works
Verweyen, E. L., Holzinger, D., Weinhage, T., Hinze, C. H., Wittkowski, H., Pickkers, P., Albeituni, S., Verbist, K., Nichols, K. E., Schulert, G. S., et al. (2019) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201903-0659oc · Cited by 65 · see citing works
Inner sensors of endotoxin – implications for sepsis research and therapy
Skirecki, T., & Cavaillon, J. (2019) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuz004 · Cited by 64 · see citing works
Mechanisms of radiation‐induced tissue damage and response
Zhou, L., Zhu, J., Liu, Y., Zhou, P., & Gu, Y. (2024) · MedComm · doi:10.1002/mco2.725 · Cited by 71 · see citing works
New strategies for treatment of infectious sepsis
Ward, P. A., & Fattahi, F. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.4mir1118-425r · Cited by 62 · see citing works
Acute Lung Injury and the NLRP3 Inflammasome
Gu, W., Zeng, Q., Wang, X., Jasem, H., & Ma, L. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s464838 · Cited by 60 · see citing works
Impellizzeri, D., Siracusa, R., Cordaro, M., Peritore, A. F., Gugliandolo, E., Mancuso, G., Midiri, A., Paola, R. D., & Cuzzocrea, S. (2018) · Biochemical Pharmacology · doi:10.1016/j.bcp.2018.06.029 · Cited by 59 · see citing works
Zhang, P., Liu, Y., Hu, L., Huang, K., Hong, M., Wang, Y., Fan, X., Ulevitch, R. J., & Han, J. (2021) · Science Advances · doi:10.1126/sciadv.abi9471 · Cited by 55 · see citing works
Role of the nucleotide‐binding domain‐like receptor protein 3 inflammasome in acute kidney injury
Cao, Y., Fei, D., Chen, M., Sun, M., Xu, J., Kang, K., Jiang, L., & Zhao, M. (2015) · FEBS Journal · doi:10.1111/febs.13379 · Cited by 55 · see citing works
Eidt, M. V., Nunes, F. B., Pedrazza, L., Caeran, G., Pellegrin, G., Melo, D. A. S., Possuelo, L. G., Jost, R. T., Dias, H. B., Donadio, M. V. F., et al. (2015) · Clinica Chimica Acta · doi:10.1016/j.cca.2015.12.009 · Cited by 50 · see citing works
Detection of Serum Interleukin‐6/10/18 Levels in Sepsis and Its Clinical Significance
Feng, M., Sun, T., Zhao, Y., & Zhang, H. (2016) · Journal of Clinical Laboratory Analysis · doi:10.1002/jcla.21977 · Cited by 50 · see citing works
Chen, X.-L., Wang, N., Zhu, Y.-F., Lu, Y.-L., Liu, X., & Zheng, J. (2017) · Mediators of Inflammation · doi:10.1155/2017/6543237 · Cited by 45 · see citing works
A Functional Synonymous Coding Variant in the IL1RN Gene Is Associated with Survival in Septic Shock
Meyer, N. J., Ferguson, J. F., Feng, R., Wang, F., Patel, P. N., Li, M., Xue, C., Qu, L., Liu, Y., Boyd, J. H., et al. (2014) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201403-0586oc · Cited by 50 · see citing works
Granzyme A inhibition reduces inflammation and increases survival during abdominal sepsis
Garzón-Tituaña, M., Sierra-Monzón, J. L., Comas, L., Santiago, L., Ushakova, T. K., Uranga-Murillo, I., Ramírez-Labrada, A., Tapia, E., Morte-Romea, E., Algarate, S., et al. (2021) · Theranostics · doi:10.7150/thno.49288 · Cited by 49 · see citing works
IRF-7 Mediates Type I IFN Responses in Endotoxin-Challenged Mice
Sin, W., Yeong, J. P.-S., Lim, T. J. F., Su, I.-H., Connolly, J. E., & Chin, K.-C. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00640 · Cited by 41 · see citing works
Tonnus, W., Gembardt, F., Latk, M., Parmentier, S. P., Hugo, C., Bornstein, S. R., & Linkermann, A. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0193-5 · Cited by 42 · see citing works
Naji, A., Suganuma, N., Espagnolle, N., Yagyu, K.-I., Baba, N., Sensebé, L., & Deschaseaux, F. (2016) · Stem Cells Translational Medicine · doi:10.5966/sctm.2016-0289 · Cited by 41 · see citing works
Wang, Y.-C., Liu, Y., Liu, Q., Zheng, Q., Dong, X., Liu, X., Gao, W., Bai, X., & Li, Z. (2020) · BioMed Research International · doi:10.1155/2020/9152140 · Cited by 41 · see citing works
Ferroptosis and pyroptosis signatures in critical COVID-19 patients
Peleman, C., Coillie, S. V., Ligthart, S., Choi, S. M., Waele, J. J. D., Depuydt, P. O., Benoît, D., Schaubroeck, H., Francque, S., Dams, K., et al. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01204-2 · Cited by 38 · see citing works
Self-citationImmune Homeostasis in Epithelial Cells: Evidence and Role of Inflammasome Signaling Reviewed
Peeters, P. M., Wouters, E. F. �., & Reynaert, N. L. (2015) · Journal of Immunology Research · doi:10.1155/2015/828264 · Cited by 38 · see citing works
Anderko, R. R., Gómez, H., Canna, S., Shakoory, B., Angus, D. C., Yealy, D. M., Huang, D. T., Kellum, J. A., Carcillo, J. A., For the ProCESS Investigators, et al. (2022) · Intensive Care Medicine Experimental · doi:10.1186/s40635-022-00433-y · Cited by 38 · see citing works
Schaack, D., Siegler, B. H., Tamulyte, S., Weigand, M. A., & Uhle, F. (2018) · PLoS ONE · doi:10.1371/journal.pone.0198555 · Cited by 34 · see citing works
Li, X., Xiao, G.-Y., Guo, T., Song, Y., & Li, Q. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.986565 · Cited by 37 · see citing works
Regulation of the Tec family of non-receptor tyrosine kinases in cardiovascular disease
Yin, Z., Zou, Y., Wang, D., Huang, X., Xiong, S., Cao, L., Zhang, Y., Sun, Y., & Zhang, N. (2022) · Cell Death Discovery · doi:10.1038/s41420-022-00927-4 · Cited by 36 · see citing works
O’Riordan, C. E., Purvis, G. S. D., Collotta, D., Chiazza, F., Wissuwa, B., Zoubi, S. A., Stiehler, L., Märtin, L., Coldewey, S. M., Collino, M., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02129 · Cited by 36 · see citing works
RetractedLuan, L., Patil, N. K., Guo, Y., Hernandez, A., Bohannon, J. K., Fensterheim, B. A., Wang, J., Xu, Y., Enkhbaatar, P., Stark, R. J., et al. (2017) · Scientific Reports · doi:10.1038/srep40050 · Cited by 35 · see citing works
Neuroprotective effect of ketamine against TNF‐α‐induced necroptosis in hippocampal neurons
Wang, L., Deng, B., Yan, P., Wu, H., Li, C., Zhu, H., Du, J., & Hou, L. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16426 · Cited by 36 · see citing works
Betulin attenuates lung and liver injuries in sepsis
Zhao, H., Liu, Z., Liu, W., Han, X., & Zhao, M. (2015) · International Immunopharmacology · doi:10.1016/j.intimp.2015.11.028 · Cited by 35 · see citing works
Cutting Edge: IL-1α and Not IL-1β Drives IL-1R1–Dependent Neonatal Murine Sepsis Lethality
Benjamin, J. T., Moore, D. J., Bennett, C., van der Meer, R., Royce, A., Loveland, R., & Wynn, J. L. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1801089 · Cited by 34 · see citing works
Non-canonical Caspase-1 Signaling Drives RIP2-Dependent and TNF-α-Mediated Inflammation In Vivo
Reinke, S., Linge, M., Diebner, H. H., Luksch, H., Glage, S., Gocht, A., Robertson, A. A. B., Cooper, M. A., Hofmann, S. R., Naumann, R., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.090 · Cited by 33 · see citing works
Delvaeye, T., Smet, M. A. J. D., Verwaerde, S., Decrock, E., Czekaj, A., Vandenbroucke, R. E., Lemeire, K., Gonçalves, A. C., Declercq, W., Vandenabeele, P., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-52900-4 · Cited by 32 · see citing works
Self-citationCyanidin-3-O-glucoside attenuates acute lung injury in sepsis rats
Yan, X., Wu, L., Li, B., Meng, X., Dai, H., Zheng, Y., & Fu, J. (2015) · Journal of Surgical Research · doi:10.1016/j.jss.2015.06.013 · Cited by 32 · see citing works
Rump, K., Unterberg, M., Bergmann, L., Bánkfalvi, Á., Menon, A. G., Schäfer, S. T., Scherag, A., Bazzi, Z., Siffert, W., Peters, J., et al. (2016) · Journal of Translational Medicine · doi:10.1186/s12967-016-1079-2 · Cited by 32 · see citing works
Does Viral Hemorrhagic Fever Represent Reactive Hemophagocytic Syndrome?
Cron, R. Q., Behrens, E. M., Shakoory, B., Ramanan, A. V., & Chatham, W. W. (2015) · The Journal of Rheumatology · doi:10.3899/jrheum.150108 · Cited by 30 · see citing works
The double sides of NLRP3 inflammasome activation in sepsis
Vigneron, C., Py, B. F., Monneret, G., & Venet, F. (2023) · Clinical Science · doi:10.1042/cs20220556 · Cited by 33 · see citing works
An Essential Role for SHARPIN in the Regulation of Caspase 1 Activity in Sepsis
Nastase, M.-V., Zeng-Brouwers, J., Frey, H., Hsieh, L. T.-H., Poluzzi, C., Beckmann, J., Schroeder, N., Pfeilschifter, J. M., López-Mosqueda, J., Mersmann, J., et al. (2016) · American Journal Of Pathology · doi:10.1016/j.ajpath.2015.12.026 · Cited by 30 · see citing works
Vahkal, B., Altosaar, I., Ariana, A., Jabbour, J., Pantieras, F., Daniel, R., Tremblay, É., Sad, S., Beaulieu, J., Côté, M., et al. (2024) · Pediatric Research · doi:10.1038/s41390-024-03757-5 · Cited by 32 · see citing works
Emerging therapeutic targets for sepsis
Tindal, E. W., Armstead, B. E., Monaghan, S. F., Heffernan, D. S., & Ayala, A. (2021) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2021.1897107 · Cited by 30 · see citing works
Haschka, D., Tymoszuk, P., Petzer, V., Hilbe, R., Heeke, S., Dichtl, S., Skvortsov, S., Demetz, E., Berger, S., Seifert, M., et al. (2021) · JCI Insight · doi:10.1172/jci.insight.141760 · Cited by 29 · see citing works
Cytokine Storm and Sepsis-Induced Multiple Organ Dysfunction Syndrome
Carcillo, J. A., & Shakoory, B. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-59815-9_30 · Cited by 28 · see citing works
Hu, Z., Gu, Z., Sun, M., Zhang, K., Gao, P., Yang, Q., & Yuan, Y. (2014) · Journal of Surgical Research · doi:10.1016/j.jss.2014.10.027 · Cited by 28 · see citing works
Sakaguchi, N., Sasai, M., Bando, H., Lee, Y., Pradipta, A., Su, J., & Yamamoto, M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.561948 · Cited by 28 · see citing works
Update in Sepsis and Acute Kidney Injury 2014
Schortgen, F., & Asfar, P. (2015) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201502-0307up · Cited by 27 · see citing works
Geniposide ameliorated sepsis-induced acute kidney injury by activating PPARγ
Liu, J., Zhao, N., Shi, G., & Wang, H. (2020) · Aging · doi:10.18632/aging.103902 · Cited by 27 · see citing works
TYK2 licenses non-canonical inflammasome activation during endotoxemia
Poelzl, A., Lassnig, C., Tangermann, S., Hromadová, D., Reichart, U., Gawish, R., Mueller, K. M., Moriggl, R., Linkermann, A., Glösmann, M., et al. (2020) · Cell Death and Differentiation · doi:10.1038/s41418-020-00621-x · Cited by 26 · see citing works
Flaherty, R. A., Donahue, D. L., Carothers, K. E., Ross, J. N., Ploplis, V. A., Castellino, F., & Lee, S. W. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00211 · Cited by 26 · see citing works
Bu, W., Li, S.-S., Liu, C. X., Wang, Y., Lu, J., Dong, C.-R., Zheng, D.-J., Fan, Z.-Y., Yu, Y., Zhang, W., et al. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.12.027 · Cited by 25 · see citing works
Delvaeye, T., Wyffels, L., Deleye, S., Lemeire, K., Gonçalves, A. C., Decrock, E., Staelens, S. G., Leybaert, L., Vandenabeele, P., & Krysko, D. V. (2018) · Journal of Nuclear Medicine · doi:10.2967/jnumed.117.205815 · Cited by 25 · see citing works
Self-citationMeprin and ADAM proteases as triggers of systemic inflammation in sepsis
Rahn, S., & Becker‐Pauly, C. (2021) · FEBS Letters · doi:10.1002/1873-3468.14225 · Cited by 23 · see citing works
Regulation of inflammatory processes by caspases
Beltrán‐Visiedo, M., Soler-Agesta, R., Sarosiek, K. A., Green, D. R., & Galluzzi, L. (2025) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-025-00869-6 · Cited by 21 · see citing works
Scophthalmus maximus interleukin-1β limits Edwardsiella piscicida colonization in vivo
Chen, S., Ma, X., Wu, D., Yang, D., Zhang, Y., & Liu, Q. (2019) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2019.10.050 · Cited by 21 · see citing works
Wang, Y., Guan, Q.-N., Zhang, Z.-J., & Zhang, Y. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2025.1627008 · Cited by 26 · see citing works
Biological relevance of Granzymes A and K during E. coli sepsis
Uranga-Murillo, I., Tapia, E., Garzón-Tituaña, M., Ramírez-Labrada, A., Santiago, L., Pesini, C., Esteban, P., Roig, F. J., Gálvez, E. M., Bird, P. I., et al. (2021) · Theranostics · doi:10.7150/thno.59418 · Cited by 20 · see citing works
The Role of Programmed Necrosis in Colorectal Cancer
Yu, Y., Gámez‐Belmonte, R., Patankar, J. V., Liebing, E., & Becker, C. (2022) · Cancers · doi:10.3390/cancers14174295 · Cited by 20 · see citing works
- Authors
- Berghe, T. V., Demon, D., Bogaert, P., Vandendriessche, B., Goethals, A., Depuydt, B., Vuylsteke, M., Roelandt, R., Van Wonterghem, E., Vandenbroecke, J., Choi, S. M., Meyer, E., Krautwald, S., Declercq, W., Takahashi, N., Cauwels, A., & Vandenabeele, P.
- Affiliations
- VIB-UGent Center for Inflammation Research (BE)
- Ghent University (BE)
- Inflammation Research Center, VIB, Ghent, Belgium
- Department of Pharmacology, Toxicology and Biochemistry, Faculty of Veterinary Medicine, and
- University Hospital Schleswig-Holstein (DE)
- ORCID
- Venue
- American Journal of Respiratory and Critical Care Medicine
- Publisher
- Oxford University Press (OUP)
- Published
- 2014-02-01
- Volume
- 189
- Issue
- 3
- Pages
- 282-291
- ISSN
- 1073-449X (ISSN-L)
- 1535-4970
- OpenAlex
- W1971998620
- Cited by
- 173
- References
- 55
- Citations by year
- 2026: 3 · 2025: 13 · 2024: 16 · 2023: 7 · 2022: 16 · 2021: 16 · 2020: 14 · 2019: 20 · 2018: 17 · 2017: 10 · 2016: 13 · 2015: 16 · 2014: 10
- FWCI
- 12.33
- Type
- journal article
- Language
- en
- Open access
- green
- zenodo.org
- Locations
- American Journal of Respiratory and Critical Care Medicine (publishedVersion)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion)
- Zenodo (CERN European Organization for Nuclear Research) (submittedVersion, other-oa)
- Funders
- European Commission (200767)
- Fonds Wetenschappelijk Onderzoek (G.0875.11, FWO G.0973.11, G.0973.11, FWO G.0875.11)
- Universiteit Gent (01M00709)
- Vlaams Instituut voor Biotechnologie (BOF09/01M00709)
- Vlaamse regering (BOF09/01M00709)
- Fondation contre le Cancer
- Leibniz-Gemeinschaft
- Topics
- Health Sciences › Medicine › Epidemiology › Sepsis Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Inflammation biomarkers and pathways
- Keywords
- sepsis, septic shock, IL-1β, IL-18, caspase-1, caspase-11, caspase-7, TNF-α, cecal ligation and puncture, anakinra, inflammatory mediators
- MeSH terms
- Animals, Anti-Inflammatory Agents, Autoantibodies, Cecum, Drug Therapy, Combination, Lipopolysaccharides, Mice, Inbred C57BL, Shock, Septic, Tumor Necrosis Factor-alpha, Biomarkers, Mice, Knockout, Caspases, Caspase 1, Interleukin-18, Mice, Caspase 7, Caspases, Initiator, Interleukin-1beta, Interleukin 1 Receptor Antagonist Protein
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