The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
Caspase-11 increases susceptibility to Salmonella infection in the absence of caspase-1
Open accessAbstract
Inflammasomes are cytosolic multiprotein complexes assembled by intracellular nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs) and they initiate innate immune responses to invading pathogens and danger signals by activating caspase-1 (ref. 1). Caspase-1 activation leads to the maturation and release of the pro-inflammatory cytokines interleukin (IL)-1β and IL-18, as well as lytic inflammatory cell death known as pyroptosis. Recently, a new non-canonical inflammasome was described that activates caspase-11, a pro-inflammatory caspase required for lipopolysaccharide-induced lethality. This study also highlighted that previously generated caspase-1 knockout mice lack a functional allele of Casp11 (also known as Casp4), making them functionally Casp1 Casp11 double knockouts. Previous studies have shown that these mice are more susceptible to infections with microbial pathogens, including the bacterial pathogen Salmonella enterica serovar Typhimurium (S. typhimurium), but the individual contributions of caspase-1 and caspase-11 to this phenotype are not known. Here we show that non-canonical caspase-11 activation contributes to macrophage death during S. typhimurium infection. Toll-like receptor 4 (TLR4)-dependent and TIR-domain-containing adaptor-inducing interferon-β (TRIF)-dependent interferon-β production is crucial for caspase-11 activation in macrophages, but is only partially required for pro-caspase-11 expression, consistent with the existence of an interferon-inducible activator of caspase-11. Furthermore, Casp1(-/-) mice were significantly more susceptible to infection with S. typhimurium than mice lacking both pro-inflammatory caspases (Casp1(-/-) Casp11(-/-)). This phenotype was accompanied by higher bacterial counts, the formation of extracellular bacterial microcolonies in the infected tissue and a defect in neutrophil-mediated clearance. These results indicate that caspase-11-dependent cell death is detrimental to the host in the absence of caspase-1-mediated innate immunity, resulting in extracellular replication of a facultative intracellular bacterial pathogen.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“type I IFN and IFN gamma (IFNG) also contribute to pyroptosis by promoting: (1) the transactivation of CASP11, through an IFNAR1-dependent or IFNGR1-dependent mechanism initiated by TLR4 or IL18 signaling [620, 643, 644]”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [643]
In the citing paper
“A limitation of our study is that the caspase-1–null mice were also found to be deficient in caspase-11 (46,47)”
From Sustained Inflammasome Activity in Macrophages Impairs Wound Healing in Type 2 Diabetic Humans and Mice (2014) · cites this paper as [47]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Schroder, K., & Tschopp, J. (2010) · Cell · doi:10.1016/j.cell.2010.01.040 · Cited by 5,475
The family of five: TIR-domain-containing adaptors in Toll-like receptor signalling
O'Neill, L. A. J., & Bowie, A. G. (2007) · Nature Reviews Immunology · doi:10.1038/nri2079 · Cited by 2,667
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
Self-citationDifferential activation of the inflammasome by caspase-1 adaptors ASC and Ipaf
Mariathasan, S., Newton, K., Monack, D. M., Vucic, D., French, D. M., Lee, W. P., Roose-Girma, M., Erickson, S. L., & Dixit, V. M. (2004) · Nature · doi:10.1038/nature02664 · Cited by 1,864
Self-citationAltered 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 1,631
Caspase-1-induced pyroptosis is an innate immune effector mechanism against intracellular bacteria
Miao, E. A., Leaf, I. A., Treuting, P. M., Mao, D. P., Dors, M., Sarkar, A., Warren, S. E., Wewers, M. D., & Aderem, A. (2010) · Nature Immunology · doi:10.1038/ni.1960 · Cited by 1,336
The NLRC4 inflammasome receptors for bacterial flagellin and type III secretion apparatus
Zhao, Y., Yang, J., Shi, J., Gong, Y., Lu, Q., Xu, H., Liu, L., & Shao, F. (2011) · Nature · doi:10.1038/nature10510 · Cited by 1,310
Franchi, L., Amer, A., Body-Malapel, M., Kanneganti, T.-D., Özören, N., Jagirdar, R., Inohara, N., Vandenabeele, P., Bertin, J., Coyle, A., et al. (2006) · Nature Immunology · doi:10.1038/ni1346 · Cited by 1,131
Cytoplasmic flagellin activates caspase-1 and secretion of interleukin 1β via Ipaf
Miao, E. A., Alpuche-Aranda, C. M., Dors, M., Clark, A. E., Bader, M. W., Miller, S. I., & Aderem, A. (2006) · Nature Immunology · doi:10.1038/ni1344 · Cited by 1,127
Sensing and reacting to microbes through the inflammasomes
Franchi, L., Muñoz-Planillo, R., & Núñez, G. (2012) · Nature Immunology · doi:10.1038/ni.2231 · Cited by 1,046
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 539
Epithelial cell extrusion: Pathways and pathologies
Gudipaty, S. A., & Rosenblatt, J. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.05.010 · Cited by 163
Differential roles of caspase-1 and caspase-11 in infection and inflammation
Man, S. M., Karki, R., Briard, B., Burton, A. R., Gingras, S., Pelletier, S. W., & Kanneganti, T. (2017) · Scientific Reports · doi:10.1038/srep45126 · Cited by 155
Chen, G., Brown, N. K., Wu, W., Khedri, Z., Yu, H., Chen, X., van de Vlekkert, D., d’Azzo, A., Zheng, P., & Liu, Y. (2014) · eLife · doi:10.7554/elife.04066 · Cited by 153
Complement pathway amplifies caspase-11–dependent cell death and endotoxin-induced sepsis severity
Napier, B. A., Brubaker, S. W., Sweeney, T. E., Monette, P., Rothmeier, G. H., Gertsvolf, N. A., Puschnik, A., Carette, J. E., Khatri, P., & Monack, D. M. (2016) · Journal of Experimental Medicine · doi:10.1084/jem.20160027 · Cited by 149
Self-citationDoerflinger, M., Deng, Y., Whitney, P. G., Salvamoser, R., Engel, S., Kueh, A. J., Tai, L., Bachem, A., Gressier, E., Geoghegan, N. D., et al. (2020) · Immunity · doi:10.1016/j.immuni.2020.07.004 · Cited by 147
Now you see me, now you don't: the interaction of Salmonella with innate immune receptors
Keestra, A. M., Tsolis, R. M., & Bäumler, A. J. (2015) · Nature Reviews Microbiology · doi:10.1038/nrmicro3428 · Cited by 148
Zhou, C., & Fang, J. (2019) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2019.05.001 · Cited by 143
Outer Membrane Lipid Secretion and the Innate Immune Response to Gram-Negative Bacteria
Giordano, N. P., Cian, M. B., & Dalebroux, Z. D. (2020) · Infection and Immunity · doi:10.1128/iai.00920-19 · Cited by 144
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
Exploiting host immunity: the Salmonella paradigm
Behnsen, J., Pérez-López, A., Nuccio, S., & Raffatellu, M. (2015) · Trends in Immunology · doi:10.1016/j.it.2014.12.003 · Cited by 138
Growth inhibition of cytosolic Salmonella by caspase-1 and caspase-11 precedes host cell death
Thurston, T. L. M., Matthews, S. A., Jennings, E. R., Alix, E., Shao, F., Shenoy, A. R., Birrell, M. A., & Holden, D. W. (2016) · Nature Communications · doi:10.1038/ncomms13292 · Cited by 142
Epithelial Cell Inflammasomes in Intestinal Immunity and Inflammation
Lei, A., Murphy, A. G., & Maloy, K. J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01168 · Cited by 141
Bacterial recognition pathways that lead to inflammasome activation
Storek, K. M., & Monack, D. M. (2015) · Immunological Reviews · doi:10.1111/imr.12289 · Cited by 132
Self-citationA long-awaited merger of the pathways mediating host defence and programmed cell death
Blander, J. M. (2014) · Nature reviews. Immunology · doi:10.1038/nri3720 · Cited by 127
Aachoui, Y., Kajiwara, Y., Leaf, I. A., Mao, D., Ting, J. P.-Y., Coers, J., Aderem, A., Buxbaum, J. D., & Miao, E. A. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.07.016 · Cited by 125
IL-1α Signaling Initiates the Inflammatory Response to Virulent Legionella pneumophila In Vivo
Barry, K. C., Fontana, M. F., Portman, J. L., Dugan, A. S., & Vance, R. E. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300100 · Cited by 128
Inflammasomes and intestinal inflammation
Zmora, N., Levy, M., Pevsner-Fishcer, M., & Elinav, E. (2017) · Mucosal Immunology · doi:10.1038/mi.2017.19 · Cited by 130
Gullett, J. M., Tweedell, R. E., & Kanneganti, T. (2022) · Cells · doi:10.3390/cells11091495 · Cited by 129
Yuan, Y., Xie, K.-X., Wang, S.-L., & Yuan, L. (2018) · Gastroenterology report · doi:10.1093/gastro/goy011 · Cited by 127
Ambiguities in NLRP3 inflammasome regulation: Is there a role for mitochondria?
Lawlor, K. E., & Vince, J. E. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.08.014 · Cited by 124
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
Deng, Q., Wang, Y., Zhang, Y., Li, M., Li, D., Huang, X., Wu, Y., Pu, J., & Wu, M. (2015) · Infection and Immunity · doi:10.1128/iai.00945-15 · Cited by 121
Innate Sensors Trigger Regulated Cell Death to Combat Intracellular Infection
Nozaki, K., Li, L., & Miao, E. A. (2022) · Annual Review of Immunology · doi:10.1146/annurev-immunol-101320-011235 · Cited by 121
Hausmann, A., Böck, D., Geiser, P., Berthold, D. L., Fattinger, S. A., Furter, M., Bouman, J. A., Barthel, M., Lang, C. M., Bakkeren, E., et al. (2020) · Mucosal Immunology · doi:10.1038/s41385-019-0247-0 · Cited by 121
Caspase-11 interaction with NLRP3 potentiates the noncanonical activation of the NLRP3 inflammasome
Moretti, J., Jia, B., Hutchins, Z., Roy, S., Yip, H., Wu, J., Shan, M., Jaffrey, S. R., Coers, J., & Blander, J. M. (2022) · Nature Immunology · doi:10.1038/s41590-022-01192-4 · Cited by 121
Cypryk, W., Nyman, T. A., & Matikainen, S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02188 · Cited by 121
Intra-amniotic inflammation induces preterm birth by activating the NLRP3 inflammasome†
Faro, J. P., Romero, R. J., Schwenkel, G., Garcia‐Flores, V., Arenas‐Hernandez, M., Leng, Y., Xu, Y., Miller, D., Hassan, S. S., & Gomez‐Lopez, N. (2018) · Biology of Reproduction · doi:10.1093/biolre/ioy261 · Cited by 115
Toll-like receptor co-receptors as master regulators of the immune response
Gioia, M. D., & Zanoni, I. (2014) · Molecular Immunology · doi:10.1016/j.molimm.2014.05.008 · Cited by 113
Role of inflammasomes in inflammatory autoimmune rheumatic diseases
Yi, Y. (2017) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.2018.22.1.1 · Cited by 111
An Update on PYRIN Domain-Containing Pattern Recognition Receptors: From Immunity to Pathology
Ratsimandresy, R. A., Dorfleutner, A., & Stehlik, C. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00440 · Cited by 114
Man, S. M., Place, D. E., Kuriakose, T., & Kanneganti, T. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.4mr0516-223r · Cited by 111
A Role for the Inflammasome in Spontaneous Preterm Labor With Acute Histologic Chorioamnionitis
Gomez‐Lopez, N., Romero, R. J., Xu, Y., Plazyo, O., Unkel, R., Leng, Y., Than, N. G., Chaiworapongsa, T., Panaitescu, B., Dong, Z., et al. (2017) · Reproductive Sciences · doi:10.1177/1933719116687656 · Cited by 108
A Role for the Inflammasome in Spontaneous Labor at Term
Romero, R. J., Xu, Y., Plazyo, O., Chaemsaithong, P., Chaiworapongsa, T., Unkel, R., Than, N. G., Chiang, P. J., Dong, Z., Xu, Z., et al. (2016) · American Journal of Reproductive Immunology · doi:10.1111/aji.12440 · Cited by 110
Salmonella enterica Serovar Typhimurium Strategies for Host Adaptation
Anderson, C. J., & Kendall, M. M. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01983 · Cited by 115
Actin polymerization as a key innate immune effector mechanism to control Salmonella infection
Man, S. M., Ekpenyong, A. E., Tourlomousis, P., Achouri, S., Cammarota, E., Hughes, K., Rizzo, A., Ng, G., Wright, J. A., Cicuta, P., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1419925111 · Cited by 106
Oxidative metabolism enables Salmonella evasion of the NLRP3 inflammasome
Wynosky-Dolfi, M. A., Snyder, A. G., Philip, N. H., Doonan, P. J., Poffenberger, M. C., Avizonis, D. Z., Zwack, E. E., Riblett, A. M., Hu, B., Strowig, T., et al. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20130627 · Cited by 105
Protease signaling in animal and plant‐regulated cell death
Salvesen, G. S., Hempel, A., & Coll, N. S. (2015) · FEBS Journal · doi:10.1111/febs.13616 · Cited by 109
The NAIP/NLRC4 inflammasome in infection and pathology
Bauer, R., & Rauch, I. (2020) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2020.100863 · Cited by 107
Demon, D., Kuchmiy, A. A., Fossoul, A., Zhu, Q., Kanneganti, T., & Lamkanfi, M. (2014) · Mucosal Immunology · doi:10.1038/mi.2014.36 · Cited by 103
Increasing complexity of NLRP3 inflammasome regulation
Moretti, J., & Blander, J. M. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.3mr0520-104rr · Cited by 107
Interferons in health and disease
Boehmer, D. F. R., & Zanoni, I. (2025) · Cell · doi:10.1016/j.cell.2025.06.044 · Cited by 112
Jabir, M. S., Ritchie, N. D., Li, D., Bayes, H. K., Tourlomousis, P., Puleston, D. J., Lupton, A., Hopkins, L., Simon, A. K., Bryant, C. E., et al. (2014) · Cell Host & Microbe · doi:10.1016/j.chom.2014.01.010 · Cited by 101
Inflammatory caspases: key regulators of inflammation and cell death
Fernández, D. J., & Lamkanfi, M. (2014) · Biological Chemistry · doi:10.1515/hsz-2014-0253 · Cited by 101
Inhibition of inflammasome activation by Coxiella burnetii type IV secretion system effector IcaA
Cunha, L. D., Ribeiro, J. M., Fernandes, T. D., Massis, L. M., Khoo, C. A., Moffatt, J. H., Newton, H. J., Roy, C. R., & Zamboni, D. S. (2015) · Nature Communications · doi:10.1038/ncomms10205 · Cited by 101
Malireddi, R. K. S., & Kanneganti, T. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00077 · Cited by 101
Genetic susceptibility to invasive Salmonella disease
Gilchrist, J. J., MacLennan, C. A., & Hill, A. V. S. (2015) · Nature reviews. Immunology · doi:10.1038/nri3858 · Cited by 100
Lupfer, C. R., Anand, P., Liu, Z., Stokes, K. L., Vogel, P., Lamkanfi, M., & Kanneganti, T. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004410 · Cited by 97
Dubey, S. R., Turnbull, C., Pandey, A., Zhao, A., Kurera, M., Al-Zidan, R. N., Shen, C. X., Gautam, M., Mahajan, S., Jadhav, P. S., et al. (2025) · Cellular and Molecular Immunology · doi:10.1038/s41423-025-01354-y · Cited by 101
Cerqueira, D. M., Gomes, M. T. R., Silva, A. L. N., Rungue, M., Assis, N. R. G., Guimarães, E. S., Morais, S. B., Brož, P., Zamboni, D. S., & Oliveira, S. C. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1007519 · Cited by 98
Weinheimer-Haus, E. M., Mirza, R. E., & Koh, T. J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119106 · Cited by 95
Role of Inflammasomes in Kidney Diseases via Both Canonical and Non-canonical Pathways
Xiang, H., Zhu, F., Xu, Z., & Xiong, J. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00106 · Cited by 96
Caspase-11 Controls Interleukin-1β Release through Degradation of TRPC1
Py, B. F., Jin, M., Desai, B. N., Penumaka, A., Zhu, H., Kober, M., Dietrich, A., Lipinski, M. M., Henry, T., Clapham, D. E., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.02.015 · Cited by 93
Huang, X., Feng, Y., Xiong, G., Whyte, S. K., Duan, J., Yang, Y., Wang, K., Yang, S., Geng, Y., Ou, Y., et al. (2019) · Cell & Bioscience · doi:10.1186/s13578-019-0292-0 · Cited by 95
Carden, S., Walker, G. T., Honeycutt, J. D., Lugo, K., Pham, T. H. M., Jacobson, A. R., Bouley, D. M., Idoyaga, J., Tsolis, R. M., & Monack, D. M. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.01.009 · Cited by 92
Self-citationStructures of the Gasdermin D C-Terminal Domains Reveal Mechanisms of Autoinhibition
Liu, Z., Wang, C., Rathkey, J. K., Yang, J., Dubyak, G., Abbott, D. W., & Xiao, T. S. (2018) · Structure · doi:10.1016/j.str.2018.03.002 · Cited by 96
Insights into phagocytosis-coupled activation of pattern recognition receptors and inflammasomes
Moretti, J., & Blander, J. M. (2013) · Current Opinion in Immunology · doi:10.1016/j.coi.2013.11.003 · Cited by 97
The role of type I interferons in intestinal infection, homeostasis, and inflammation
Cho, H., & Kelsall, B. L. (2014) · Immunological Reviews · doi:10.1111/imr.12195 · Cited by 94
Subversion of inflammasome activation and pyroptosis by pathogenic bacteria
Cunha, L. D., & Zamboni, D. S. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00076 · Cited by 93
The Regulation and Modification of GSDMD Signaling in Diseases
Li, Z., Ji, S., Jiang, M., Xu, Y., & Zhang, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.893912 · Cited by 95
Advances in the molecular mechanisms of NLRP3 inflammasome activators and inactivators
Liu, D., Zeng, X., Li, X., Cui, C., Hou, R., Guo, Z., Mehta, J. L., & Wang, X. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.113863 · Cited by 88
Activation and Function of NLRP3 Inflammasome in Bone and Joint-Related Diseases
Murakami, T., Nakaminami, Y., Takahata, Y., Hata, K., & Nishimura, R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105365 · Cited by 89
Ion channels in regulated cell death
Kunzelmann, K. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2208-z · Cited by 93
Protective Role for Caspase-11 during Acute Experimental Murine Colitis
Oficjalska, K., Raverdeau, M., Aviello, G., Wade, S. C., Hickey, A., Sheehan, K. M., Corr, S. C., Kay, E. W., O'Neill, L. A. J., Mills, K. H. G., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1400501 · Cited by 86
What role does pyroptosis play in microbial infection?
Xia, X., Wang, X., Zheng, Y., Jiang, J., & Hu, J. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27909 · Cited by 86
Noncanonical Inflammasomes: Caspase-11 Activation and Effector Mechanisms
Brož, P., & Monack, D. M. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003144 · Cited by 85
Self-citationThe role of glycine in regulated cell death
Weinberg, J. M., Bienholz, A., & Venkatachalam, M. A. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2201-6 · Cited by 85
Naseer, N., Egan, M. S., Ruiz, V. M. R., Scott, W. P., Hunter, E. N., Demissie, T., Rauch, I., Brodsky, I. E., & Shin, S. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1009718 · Cited by 86
The pathogenesis and potential therapeutic targets in sepsis
Zhang, W., Jiang, H., Wu, G., Huang, P., Wang, H., An, H., Liu, S., & Zhang, W. (2023) · MedComm · doi:10.1002/mco2.418 · Cited by 85
Litwiniuk, A., Bik, W., Kalisz, M., & Baranowska-Bik, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115603 · Cited by 82
Caspase‐11: The driving factor for noncanonical inflammasomes
Viganò, E., & Mortellaro, A. (2013) · European Journal of Immunology · doi:10.1002/eji.201343800 · Cited by 82
Pyroptosis in Cancer: Friend or Foe?
Lu, X., Guo, T., & Zhang, X. (2021) · Cancers · doi:10.3390/cancers13143620 · Cited by 81
The Endotoxin Hypothesis of Parkinson's Disease
Brown, G. C., Camacho, M., & Williams‐Gray, C. H. (2023) · Movement Disorders · doi:10.1002/mds.29432 · Cited by 85
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
Yi, Y. (2019) · Immunology · doi:10.1111/imm.13134 · Cited by 85
Liu, B. C., Sarhan, J., Panda, A., Muendlein, H. I., Ilyukha, V., Coers, J., Yamamoto, M., Isberg, R. R., & Poltorak, A. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.06.012 · Cited by 82
NLRP3 inflammasome: Pathogenic role and potential therapeutic target for IgA nephropathy
Tsai, Y., Hua, K., Chen, A., Wei, C.-W., Chen, W., Wu, C.-Y., Chu, C., Yu, Y., Lo, C., & Ka, S. (2017) · Scientific Reports · doi:10.1038/srep41123 · Cited by 79
Roles of ginsenosides in inflammasome activation
Yi, Y. (2017) · Journal of Ginseng Research · doi:10.1016/j.jgr.2017.11.005 · Cited by 78
Cerqueira, D. M., Pereira, M. S. F., Silva, A. L. N., Cunha, L. D., & Zamboni, D. S. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1501223 · Cited by 78
Uropathogenic Escherichia coli strain CFT073 disrupts NLRP3 inflammasome activation
Waldhuber, A., Puthia, M., Wieser, A., Cirl, C., Dürr, S., Neumann-Pfeifer, S., Albrecht, S., Römmler, F., Müller, T., Zheng, Y., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci81916 · Cited by 76
Interferons and inflammasomes: Cooperation and counterregulation in disease
Labzin, L. I., Lauterbach, M., & Latz, E. (2016) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2016.05.010 · Cited by 77
Babamale, A. O., & Chen, S.-T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111398 · Cited by 78
Regulated necrosis, a proinflammatory cell death, potentially counteracts pathogenic infections
Zhang, G., Wang, J., Zhao, Z., Xin, T., Fan, X., Shen, Q., Raheem, A., Lee, C. R., Jiang, H., & Ding, J. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05066-3 · Cited by 75
Pyroptosis in development, inflammation and disease
Pan, Y., Cai, W., Huang, J., Cheng, A., Wang, M., Yin, Z., & Jia, R. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.991044 · Cited by 74
A Role for Stefin B (Cystatin B) in Inflammation and Endotoxemia
Maher, K., Kokelj, B. J., Butinar, M., Mikhaylov, G., Manček‐Keber, M., Stoka, V., Vasiljeva, O. S., Turk, B., Grigoryev, S. A., & Kopitar‐Jerala, N. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.609396 · Cited by 73
Wilson, N. S., Duewell, P., Yang, B., Li, Y., Marsters, S. A., Koernig, S., Latz, E., Maraskovsky, E., Morelli, A. B., Schnurr, M. M., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302011 · Cited by 74
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 76
Self-citationThe 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 74
Yang, D., Zheng, X., Chen, S., Wang, Z., Xu, W., Tan, J., Hu, T., Hou, M., Wang, W., Gu, Z., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04984-1 · Cited by 72
Host Cell Death Responses to Non-typhoidal Salmonella Infection
Wemyss, M. A., & Pearson, J. S. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01758 · Cited by 72
Regulatory Roles of the Caspase-11 Non-Canonical Inflammasome in Inflammatory Diseases
Yi, Y. (2018) · Immune Network · doi:10.4110/in.2018.18.e41 · Cited by 71
Insights Into Mucosal Innate Immune Responses in House Dust Mite-Mediated Allergic Asthma
Khweek, A. A., Kim, E., Joldrichsen, M. R., Amer, A. O., & Boyaka, P. N. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.534501 · Cited by 73
Zwack, E. E., Snyder, A. G., Wynosky-Dolfi, M. A., Ruthel, G. T., Philip, N. H., Marketon, M. M., Francis, M. S., Bliska, J. B., & Brodsky, I. E. (2015) · mBio · doi:10.1128/mbio.02095-14 · Cited by 69
Pyroptotic and non‐pyroptotic effector functions of caspase‐11
Khweek, A. A., & Amer, A. O. (2020) · Immunological Reviews · doi:10.1111/imr.12910 · Cited by 71
Pyroptosis in defense against intracellular bacteria
Li, L., Dickinson, M. S., Coers, J., & Miao, E. A. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101805 · Cited by 73
Thomas, D., Clare, S., Sowerby, J. M., Pardo, M., Juss, J. K., Goulding, D., van der Weyden, L., Storisteanu, D. M. L., Prakash, A., Espéli, M., et al. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20161382 · Cited by 69
Death Be Not Proud—Cell Death Control in Plant Fungal Interactions
Dickman, M. B., & de Figueiredo, P. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003542 · Cited by 67
Naseer, N., Zhang, J., Bauer, R., Constant, D. A., Nice, T. J., Brodsky, I. E., Rauch, I., & Shin, S. (2022) · Infection and Immunity · doi:10.1128/iai.00663-21 · Cited by 67
Emerging Significance of NLRs in Inflammatory Bowel Disease
Davis, B. K., Philipson, C. W., Hontecillas, R., Eden, K. B., Bassaganya-Riera, J., & Allen, I. C. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000151 · Cited by 69
Gram’s Stain Does Not Cross the Bacterial Cytoplasmic Membrane
Wilhelm, M. J., Sheffield, J. B., Gh., M. S., Wu, Y., Spahr, C., Gonella, G., Xu, B., & Dai, H. (2015) · ACS Chemical Biology · doi:10.1021/acschembio.5b00042 · Cited by 71
Questions and controversies in innate immune research: what is the physiological role of NLRP3?
Coll, R. C., O'Neill, L. A. J., & Schroder, K. (2016) · Cell Death Discovery · doi:10.1038/cddiscovery.2016.19 · Cited by 69
Metadata
- Authors
- Broz, P., Ruby, T., Belhocine, K., Bouley, D. M., Kayagaki, N., Dixit, V. M., & Monack, D. M.
- Affiliations
- Stanford Medicine (US)
- Genentech (US)
- Corresponding author
- Monack, Denise M.
- Venue
- Nature
- Published
- 2012-08-15
- Volume
- 490
- Issue
- 7419
- Pages
- 288-291
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3470772
- OpenAlex
- W2024591203
- Cited by
- 535
- References
- 23
- Citations by year
- 2026: 13 · 2025: 25 · 2024: 20 · 2023: 35 · 2022: 33 · 2021: 31 · 2020: 47 · 2019: 40 · 2018: 38 · 2017: 40 · 2016: 51 · 2015: 49 · 2014: 53 · 2013: 53 · 2012: 6
- FWCI
- 20.71
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (F32AI008972, AI095396, R01AI089722, AI08972, R01AI095396)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Agricultural and Biological Sciences › Food Science › Salmonella and Campylobacter epidemiology
- Keywords
- caspase-11, caspase-1, Salmonella typhimurium, non-canonical inflammasome, macrophage cell death, pyroptosis, bacterial dissemination, innate immunity, TLR4, TRIF, NOD2, NOD-like receptors, IL-1β, IL-18
- MeSH terms
- Adjuvants, Immunologic, Animals, Cells, Cultured, Disease Susceptibility, Gene Expression Regulation, Interferon-gamma, Lipopolysaccharides, Macrophages, Salmonella Infections, Animal, Salmonella typhimurium, Signal Transduction, Cell Death, Mice, Knockout, Caspases, Mice, Caspases, Initiator, Inflammasomes
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