The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
An endogenous caspase-11 ligand elicits interleukin-1 release from living dendritic cells
Open accessAbstract
Immune activation in context: Dendritic cells (DCs) initiate protective immunity upon binding molecules derived from microbes or released from dying cells. Zanoni et al. examined how microbial and endogenous signals interact to shape the course of the ensuing immune response (see the Perspective by Napier and Monack). They found that oxPAPC, an oxidized phospholipid released from dying cells, binds to a protein called caspase-11 in DCs, activating an inflammatory program in these cells. Whereas caspase-11 binding to oxPAPC and bacterial lipopolysaccharide causes DCs to produce the cytokine interleukin-1 (IL-1) and undergo cell death, binding to oxPAPC alone triggers DCs to secrete IL-1 and induce strong adaptive immunity. Thus, context-dependent signals can shape the ensuing immune response. Science , this issue p. 1232 ; see also p. 1173
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
“at least in some cell types including DCs, CASP11 activation can drive IL-1β secretion in the absence of cell death [628].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [628]
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
Cleavage of GSDMD by inflammatory caspases determines pyroptotic cell death
Shi, J., Zhao, Y., Wang, K., Shi, X., Wang, Y., Huang, H., Zhuang, Y., Cai, T., Wang, F., & Shao, F. (2015) · Nature · doi:10.1038/nature15514 · Cited by 6,659
Self-citationMartinon, F., Burns, K., & Tschopp, J. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00599-3 · Cited by 6,066
Caspase-11 cleaves gasdermin D for non-canonical inflammasome signalling
Kayagaki, N., Stowe, I. B., Lee, B. L., O’Rourke, K., Anderson, K., Warming, S., Cuellar, T., Haley, B., Roose-Girma, M., Phung, Q. T., et al. (2015) · Nature · doi:10.1038/nature15541 · Cited by 3,686
Inflammatory caspases are innate immune receptors for intracellular LPS
Shi, J., Zhao, Y., Wang, Y., Gao, W., Ding, J., Li, P., Hu, L., & Shao, F. (2014) · Nature · doi:10.1038/nature13683 · Cited by 2,285
Self-citationControl of adaptive immunity by the innate immune system
Iwasaki, A., & Medzhitov, R. (2015) · Nature Immunology · doi:10.1038/ni.3123 · Cited by 2,160
How dying cells alert the immune system to danger
Kono, H., & Rock, K. L. (2008) · Nature Reviews Immunology · doi:10.1038/nri2215 · Cited by 1,737
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
The IL-1 family: regulators of immunity
Sims, J. E., & Smith, D. E. (2010) · Nature reviews. Immunology · doi:10.1038/nri2691 · Cited by 1,459
Imai, Y., Kuba, K., Neely, G. G., Yaghubian-Malhami, R., Perkmann, T., van Loo, G., Ermolaeva, M., Veldhuizen, R., Leung, Y. H. C., Wang, H., et al. (2008) · Cell · doi:10.1016/j.cell.2008.02.043 · Cited by 1,356
Pyroptotic cell death defends against intracellular pathogens
Jorgensen, I., & Miao, E. A. (2015) · Immunological Reviews · doi:10.1111/imr.12287 · Cited by 1,021
Cited by
Sorted by citations
Items 301–400 of 593
DNGR-1-mediated cross-presentation of dead cell-associated antigens
Henry, C. M., Castellanos, C. A., & Sousa, C. R. E. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101726 · Cited by 28
Caspase-5: Structure, Pro-Inflammatory Activity and Evolution
Eckhart, L., & Fischer, H. (2024) · Biomolecules · doi:10.3390/biom14050520 · Cited by 26
Wei, R., Li, S., Yu, G., Guan, X., Liu, H., Quan, J., Jiang, Z., & Wang, X. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.755384 · Cited by 26
p204 Is Required for Canonical Lipopolysaccharide-induced TLR4 Signaling in Mice
Yi, Y., Jian, J., González-Gugel, E., Shi, Y., Tian, Q., Fu, W., Hettinghouse, A., Song, W., Liu, R., He, M., et al. (2018) · EBioMedicine · doi:10.1016/j.ebiom.2018.02.012 · Cited by 26
Diverse functions of NLRP3 inflammasome in PANoptosis and diseases
Jiang, Y., Qiang, Z., Liu, Y., Zhu, L., Xiao, L., Du, Z., Cai, R., & Qiang, S. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02689-1 · Cited by 25
López‐Haber, C., Netting, D. J., Hutchins, Z., Ma, X., Hamilton, K. E., & Mantegazza, A. R. (2022) · The EMBO Journal · doi:10.15252/embj.2022111161 · Cited by 25
Zhou, B., Ryder, C. B., Dubyak, G., & Abbott, D. W. (2022) · Science Signaling · doi:10.1126/scisignal.abl6781 · Cited by 25
A detailed molecular network map and model of the NLRP3 inflammasome
Krantz, M., Eklund, D., Särndahl, E., & Hedbrant, A. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1233680 · Cited by 25
Sartorius, R., D’Apice, L., Barba, P., Cipria, D., Grauso, L., Cutignano, A., & Berardinis, P. D. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01496 · Cited by 25
Pyroptosis Induction and Detection
den Hartigh, A. B., & Fink, S. L. (2018) · Current Protocols in Immunology · doi:10.1002/cpim.52 · Cited by 25
Interplay between Mitophagy and Inflammasomes in Neurological Disorders
Kesharwani, R., Sarmah, D., Kaur, H., Mounika, L., Verma, G., Veeresh, P., Kotian, V., Kalia, K., Borah, A., Dave, K. R., et al. (2019) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.9b00117 · Cited by 25
de Carvalho, R. A., Silva, A. L. N., dos Santos, L. L., Andrade, W. A., de Sá, K. S. G., & Zamboni, D. S. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.ma1118-471r · Cited by 25
Kim, Y. S., Choi, S., Kim, K.-Y., Pelaez, J. M. N., Perkins, G. A., Choi, S., Kim, J., Nazarenkov, N., Rissman, R. A., Ju, W., et al. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03214-4 · Cited by 24
New insights into the noncanonical inflammasome point to caspase-4 as a druggable target
Elkayam, E., Gervais, F. G., Wu, H., Crackower, M. A., & Lieberman, J. (2025) · Nature reviews. Immunology · doi:10.1038/s41577-025-01142-9 · Cited by 24
Self-citationZhao, X., Lempke, S. L., Arroyo, J., Brown, I. G., Yin, B., Magaj, M. M., Holness, N. K., Smiley, J., Redemann, S., & Ewald, S. E. (2024) · Nature Communications · doi:10.1038/s41467-024-46790-y · Cited by 24
Noncanonical inflammasomes: Antimicrobial defense that does not play by the rules
Crowley, S. M., Vallance, B. A., & Knodler, L. A. (2017) · Cellular Microbiology · doi:10.1111/cmi.12730 · Cited by 24
Inflammasome-independent pyroptosis
Liu, X., & Lieberman, J. (2024) · Current Opinion in Immunology · doi:10.1016/j.coi.2024.102432 · Cited by 25
Research progress of mitochondrial dysfunction induced pyroptosis in acute lung injury
Yang, L., Ren, Q., Wang, Y., Zheng, Y., Du, F., Wang, F., Zhou, J., Gui, L., Chen, S., Chen, X., et al. (2024) · Respiratory Research · doi:10.1186/s12931-024-03028-1 · Cited by 23
Atrial cardiomyocyte-restricted cleavage of gasdermin D promotes atrial arrhythmogenesis
Yuan, Y., Martsch, P., Chen, X., Martinez, E., Li, L., Song, J., Poppenborg, T., Bruns, F., Kim, J. H., Kamler, M., et al. (2025) · European Heart Journal · doi:10.1093/eurheartj/ehaf024 · Cited by 23
Versatility of gasdermin D beyond pyroptosis
Zhao, T., Chi, Z., & Wang, D. (2025) · Trends in Cell Biology · doi:10.1016/j.tcb.2025.02.011 · Cited by 23
Targeting inflammasomes as an immunotherapeutic strategy for cancer
Huang, L., Chen, X., Liu, R., Nan, D., Bao, W., Yang, L., Dai, X., Tang, J., Zhang, H., & Lu, Y. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06665-2 · Cited by 23
DAMP signaling networks: from receptors to diverse pathophysiological functions
Chen, R., Zou, J., Zhong, X. Y., Liu, J., Kang, R., & Tang, D. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.07.047 · Cited by 26
Clinical development of cancer vaccines
Haanen, J. B. A. G., Schumacher, T. N., Kagan, J. C., Fritsch, E. F., & Wu, C. J. (2026) · Nature Medicine · doi:10.1038/s41591-026-04241-9 · Cited by 23
Self-citationPrather, E. R., Gavrilin, M. A., & Wewers, M. D. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102024 · Cited by 23
Tang, J., Yang, Y., Qu, J., Ban, W., Song, H., Gu, Z., Yang, Y., Cai, L., Theivendran, S., Wang, Y., et al. (2022) · Chemical Science · doi:10.1039/d1sc05319a · Cited by 23
The Therapeutic Potential of Pyroptosis in Melanoma
Zaffaroni, N., & Beretta, G. L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021285 · Cited by 23
Oxidized phospholipid damage signals as modulators of immunity
Choi, J. H., & Kagan, J. C. (2025) · Open Biology · doi:10.1098/rsob.240391 · Cited by 22
Self-citationPhospholipid metabolism in innate immunity and inflammation: from basic to clinic
Liu, J., Chen, Y., & O'Neill, L. A. J. (2025) · Immunity & Inflammation · doi:10.1007/s44466-025-00001-5 · Cited by 23
Inactivation of inflammasomes by pathogens regulates inflammation
Garib, F. Y., Ризопулу, А. П., Kuchmiy, A. A., & Garib, V. (2016) · Biochemistry (Moscow) · doi:10.1134/s0006297916110109 · Cited by 22
Fiction and Facts about BCG Imparting Trained Immunity against COVID-19
Kaur, G., Singh, S., Nanda, S., Zafar, M. A., Malik, J. A., Arshi, M. U., Lamba, T., & Agrewala, J. N. (2022) · Vaccines · doi:10.3390/vaccines10071006 · Cited by 22
Yi, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147580 · Cited by 22
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 23
Cleavage-Mediated Regulation of Myd88 Signaling by Inflammasome-Activated Caspase-1
Avbelj, M., Hafner‐Bratkovič, I., Lainšček, D., Manček‐Keber, M., Peternelj, T. T., Panter, G., Treon, S. P., Gole, B., Potočnik, U., & Jerala, R. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.790258 · Cited by 21
Bucket lists must be completed during cell death
Nozaki, K., & Miao, E. A. (2023) · Trends in Cell Biology · doi:10.1016/j.tcb.2023.02.008 · Cited by 21
Structural and mechanistic elucidation of inflammasome signaling by cryo-EM
Shen, C., Sharif, H., Xia, S., & Wu, H. (2019) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2019.03.033 · Cited by 21
Self-citationLima, C., Falcão, M. A. P., Andrade‐Barros, A. I., Seni-Silva, A. C., Grund, L. Z., Balogh, E., Conceição, K., Queniaux, V. F., Ryffel, B., & Lopes‐Ferreira, M. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.107287 · Cited by 21
Great balls of fire: activation and signalling of inflammatory caspases
Bateman, G., Hill, B., Knight, R., & Boucher, D. (2021) · Biochemical Society Transactions · doi:10.1042/bst20200986 · Cited by 21
Alendronate augments lipid A-induced IL-1β release and Smad3/NLRP3/ASC-dependent cell death
Tamai, R., & Kiyoura, Y. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.02.014 · Cited by 21
Gasdermin Pore Forming Activities that Promote Inflammation from Living and Dead Cells
Cao, A., & Kagan, J. C. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167427 · Cited by 20
Self-citationIto, M., Ducasa, G. M., Molina, J., Santos, J. V., Mallela, S. K., Kim, J., Ge, M., Mitrofanova, A. V., Sloan, A. J., Merscher, S., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-35499-5 · Cited by 20
Induction of Trained Immunity by Recombinant Vaccines
Covián, C., Ríos, M., Berríos-Rojas, R. V., Bueno, S. M., & Kalergis, A. M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.611946 · Cited by 20
Imaging Approaches to Monitor Inflammasome Activation
Nandi, D., Farid, N. S. S., Karuppiah, H. A. R., & Kulkarni, A. A. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167251 · Cited by 20
Hou, J., Li, T., Hsu, J.-M., Zhang, X., & Hung, M. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101833 · Cited by 20
Inflammasomes and Cardiovascular Disease: Linking Inflammation to Cardiovascular Pathophysiology
Saadh, M. J., Muhammad, F. A., Albadr, R. J., Sanghvi, G. V., Jyothi, S. R., Kundlas, M., Joshi, K. K., Rakhmatullaev, A., Taher, W. M., Alwan, M., et al. (2025) · Scandinavian Journal of Immunology · doi:10.1111/sji.70020 · Cited by 19
Human cytomegalovirus infection triggers a paracrine senescence loop in renal epithelial cells
Raviola, S., Griffante, G., Iannucci, A., Chandel, S., Cigno, I. L., Lacarbonara, D., Caneparo, V., Pasquero, S., Favero, F., Corà, D., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-05957-5 · Cited by 18
Blocking TIR Domain Interactions in TLR9 Signaling
Javmen, A., Szmacinski, H., Lakowicz, J. R., & Toshchakov, V. Y. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1800194 · Cited by 18
Borriello, F., van Haren, S. D., & Levy, O. (2018) · mSphere · doi:10.1128/msphere.00214-18 · Cited by 18
Tyrkalska, S. D., Candel, S., & Mulero, V. (2020) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2020.103874 · Cited by 18
Inflammasome Activation and Neutrophil Extracellular Traps in Atherosclerosis
Karasawa, T., & Takahashi, M. (2025) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.rv22033 · Cited by 19
Mitochondrial DNA in Exercise-Mediated Innate Immune Responses
Wen, X., Fan, J., Duan, X., Zhu, X., Bai, J., & Zhang, T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26073069 · Cited by 17
Saeki, A., Tsuchiya, K., Suda, T., Into, T., Hasebe, A., Suzuki, T., & Shibata, K. (2020) · Immunology · doi:10.1111/imm.13230 · Cited by 17
Zou, B., Goodwin, M., Saleem, D., Jiang, W., Tang, J., Chu, Y., Munford, R., & Lu, M. (2021) · eLife · doi:10.7554/elife.70938 · Cited by 17
Activation, Amplification, and Ablation as Dynamic Mechanisms of Dendritic Cell Maturation
Bourque, J., & Hawiger, D. (2023) · Biology · doi:10.3390/biology12050716 · Cited by 17
Inflammasome activation by SARS-CoV-2 and its participation in COVID-19 exacerbation
Rodrigues, T. S., & Zamboni, D. S. (2023) · Current Opinion in Immunology · doi:10.1016/j.coi.2023.102387 · Cited by 17
Hurtado‐Navarro, L., Cuenca‐Zamora, E. J., Zamora, L., Bellosillo, B., Such, E., Soler‐Espejo, E., Martínez‐Banaclocha, H., Hernández‐Rivas, J. M., Marco, J., Martínez-Alarcón, L., et al. (2023) · Cell Reports Medicine · doi:10.1016/j.xcrm.2023.101329 · Cited by 17
Flis, W., & Socha, M. W. (2024) · Cells · doi:10.3390/cells13070600 · Cited by 17
Obesity Causes Abrupt Changes in the Testicular Microbiota and Sperm Motility of Zebrafish
Su, Y., He, L., Hu, Z., Li, Y., Zhang, Y., Fan, Z., Zhao, K., Zhang, H., & Liu, C. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.639239 · Cited by 17
Buscetta, M., Cristaldi, M., Cimino, M., Mensa, A. L., Dino, P., Bucchieri, F., Rappa, F., Amato, S., Aronica, T. S., Pace, E., et al. (2022) · The FASEB Journal · doi:10.1096/fj.202200837r · Cited by 17
Guidelines for mouse and human DC functional assays
Clausen, B. E., Amon, L., Backer, R. A., Berod, L., Bopp, T., Brand, A., Burgdorf, S., Chen, L., Da, M., Distler, U., et al. (2022) · European Journal of Immunology · doi:10.1002/eji.202249925 · Cited by 16
To die or not to die: Gasdermins in intestinal health and disease
Lin, Z., Chen, Q., & Ruan, H. (2024) · Seminars in Immunology · doi:10.1016/j.smim.2024.101865 · Cited by 16
Wong, M. P., Juan, E. Y. W., Chelluri, S. S., Wang, P., Pahmeier, F., Castillo-Rojas, B., Blanc, S. F., Biering, S. B., Vance, R. E., & Harris, E. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012167 · Cited by 17
Frank, M. G., Baratta, M. V., Zhang, K., Fallon, I. P., Pearson, M. A., Liu, G., Hutchinson, M. R., Watkins, L. R., Goldys, E. M., & Maier, S. F. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.07.042 · Cited by 16
Davies, C., Stowe, I. B., Phung, Q. T., Ho, H., Bakalarski, C. E., Gupta, A., Zhang, Y., Lill, J. R., Payandeh, J., Kayagaki, N., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2018024118 · Cited by 16
Functions of IFNλs in Anti-Bacterial Immunity at Mucosal Barriers
Alphonse, N., Dickenson, R. E., Alrehaili, A., & Odendall, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.857639 · Cited by 16
CASP4/11 Contributes to NLRP3 Activation and COVID-19 Exacerbation
Rodrigues, T. S., Caetano, C. C. D. S., de Sá, K. S. G., de Almeida, L., Becerra, A., Gonçalves, A. V., Lopes, L. D. S., Oliveira, S., Mascarenhas, D. P. A., Batah, S. S., et al. (2023) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiad037 · Cited by 16
Serum-borne lipids amplify TLR-activated inflammatory responses
Sharma, N., Akhade, A. S., Ismaeel, S., & Qadri, A. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.3ab0720-241rr · Cited by 16
Lei, B., Wang, S., Yu, L., & Ma, Q. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1673643 · Cited by 15
Mutagenic Consequences of Sublethal Cell Death Signaling
Hawkins, C. J., & Miles, M. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22116144 · Cited by 15
Nanda, S. K., Vollmer, S., & Pérez‐Oliva, A. B. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.887533 · Cited by 15
Deryabin, P. I., Shatrova, A. N., & Borodkina, A. V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232214251 · Cited by 15
Alipour, S., Mardi, A., Shajari, N., Kazemi, T., Sadeghi, M. R., Heris, J. A., Masoumi, J., & Baradaran, B. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.122686 · Cited by 15
Ge, S., Qiu, B., Liu, R., Sun, L., Yang, L., Chen, X., Tao, H., Yang, W., Yu, Y., & Wang, D. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.116879 · Cited by 15
Dissociation of TRIF bias and adjuvanticity
Richard, K., Perkins, D. J., Harberts, E. M., Song, Y., Gopalakrishnan, A., Shirey, K. A., Lai, W., Vlk, A., Mahurkar, A., Nallar, S. C., et al. (2020) · Vaccine · doi:10.1016/j.vaccine.2020.04.042 · Cited by 15
Terlizzi, M., Antonio, M., Colarusso, C., Somma, P., Rosa, I. D., Troisi, J., Scala, G., Salvi, R., Pinto, A., & Sorrentino, R. (2020) · Oncotarget · doi:10.18632/oncotarget.27724 · Cited by 15
Wang, S., Moreau, F., & Chadee, K. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010415 · Cited by 15
Targeting the NLRP3 Inflammasome-Gasdermin D Axis to Combat Cardiovascular Diseases
Choi, J. S. Y., Pervin, M., Vince, J. E., Sharma, A., & de Haan, J. B. (2025) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2025.09.006 · Cited by 15
Gasdermins, Executors of Pyroptosis: A Decade in Perspective
Zhou, B., & Abbott, D. W. (2025) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-042624-121548 · Cited by 14
The landscape of regulated cell death: It’s all downhill from here
Aufschnaiter, A., Oh, T., & Oberst, A. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.11.013 · Cited by 15
Inflammasomes as regulators of non-infectious disease
Okin, D. A., & Kagan, J. C. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101815 · Cited by 14
Self-citationEpigenetic and transcriptional control of gasdermins
Cadena, C., Kornfeld, O. S., Lee, B. L., & Kayagaki, N. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101841 · Cited by 15
Adipose triglyceride lipase suppresses noncanonical inflammasome by hydrolyzing LPS
Li, W., Liu, Q., Qian, Y., Wang, C., Kong, C., Sun, L., Sun, L., Liu, H., Zhang, Y., Jiang, D., et al. (2024) · Nature Chemical Biology · doi:10.1038/s41589-024-01569-6 · Cited by 14
Strategies of bacterial detection by inflammasomes
Jastrab, J. B., & Kagan, J. C. (2024) · Cell chemical biology · doi:10.1016/j.chembiol.2024.03.009 · Cited by 14
Self-citationHuang, L., Li, X., Zhang, H., Liu, F., Dai, Z., Xiao, F., Wang, L., & Wang, Z. (2025) · ACS Nano · doi:10.1021/acsnano.4c17491 · Cited by 14
Inflammasome involvement in CS-induced damage in HaCaT keratinocytes
Prieux, R., Ferrara, F., Cervellati, F., Guiotto, A., Benedusi, M., & Valacchi, G. (2022) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-022-00658-x · Cited by 14
Mantegazza, A. R., Wynosky-Dolfi, M. A., Casson, C. N., Lefkovith, A. J., Shin, S., Brodsky, I. E., & Marks, M. S. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006785 · Cited by 14
Bauer, D. L., Bachnak, L., Limbert, V. M., Horowitz, R. M., Baudier, R. L., D’Souza, S. J., Immethun, V. E., Kurtz, J. R., Grant, S. B., & McLachlan, J. B. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2200221 · Cited by 13
Heyman, O., Yehezkel, D., Mattioli, C. C., Blumberger, N., Rosenberg, G., Solomon, A., Hoffman, D., Moshe, N. B. B., & Avraham, R. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2218812120 · Cited by 13
Bruce, J. K., Li, L. Y., Tang, Y., Forster, E., Winsor, N. J., Bi, P. Y., Krustev, C., Keely, S., Lee, J. E., Rohde, J. R., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-08183-9 · Cited by 13
Gioia, M. D., Poli, V., Tan, P. J., Spreafico, R., Chu, A., Cuenca, A. G., Wu, Z., Benamar, M., Pandolfi, L., Meloni, F., et al. (2025) · Immunity · doi:10.1016/j.immuni.2025.06.017 · Cited by 13
Self-citationRocha, F. R. G., Delitto, A. E., de Souza, J. A. C., Gonzalez-Maldonado, L., Wallet, S. M., & Rossa, C. (2019) · Immunobiology · doi:10.1016/j.imbio.2019.10.004 · Cited by 13
Ox-inflammasome involvement in neuroinflammation
Vallese, A., Cordone, V., Pecorelli, A., & Valacchi, G. (2023) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2023.07.010 · Cited by 13
Mechanism of oxidized phospholipid-related inflammatory response in vascular ageing
Wang, T., Wang, Y., Zhang, X., Xu, W., Jin, K., Pang, Y., Wu, Y., Luo, J., Xu, R., Jiao, L., et al. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101888 · Cited by 12
Pandori, W., Matsuno, S. Y., Shin, J., Kim, S. C., Kao, T. H., Mallya, S., Batarseh, S. N., & Lodoen, M. B. (2024) · The Journal of Immunology · doi:10.4049/jimmunol.2200513 · Cited by 12
Colaço, M., Cruz, M. T., de Almeida, L. P., & Borges, O. (2024) · Pharmaceutics · doi:10.3390/pharmaceutics16101308 · Cited by 12
Huang, Y., Xie, X., Huang, G., Hong, X., Lu, W., Fu, W., & Wang, L. (2025) · Science Progress · doi:10.1177/00368504251328754 · Cited by 12
From damage signals to immune modulators: oxidized lipids in immunometabolic inflammation
Srivastava, N., & Wan, X. (2026) · Journal of Lipid Research · doi:10.1016/j.jlr.2026.100990 · Cited by 14
NLRP3 Inflammasome as a Therapeutic Target for Atherosclerosis: A Focus on Potassium Outflow
Jin, Y.-J., An, Z., Sun, Z., & Liu, X.-C. (2022) · Reviews in Cardiovascular Medicine · doi:10.31083/j.rcm2308268 · Cited by 12
The noncanonical inflammasome in health and disease
Cahoon, J. G., Yang, D., & Wang, P. (2022) · Infectious Medicine · doi:10.1016/j.imj.2022.09.001 · Cited by 12
The role of regulated necrosis in inflammation and ocular surface diseases
Guo, X.-X., Pu, Q., Hu, J., Chang, X., Li, A.-L., & Li, X. (2023) · Experimental Eye Research · doi:10.1016/j.exer.2023.109537 · Cited by 12
Ernandes, M. J., & Kagan, J. C. (2021) · mBio · doi:10.1128/mbio.00584-21 · Cited by 12
Self-citation
Metadata
- Authors
- Zanoni, I., Tan, Y., Di Gioia, M., Broggi, A., Ruan, J., Shi, J., Donado, C. A., Shao, F., Wu, H., Springstead, J. R., & Kagan, J. C.
- Affiliations
- Boston Children's Hospital (US)
- Harvard Medical School and Division of Gastroenterology, Boston Children’s Hospital, Boston, MA, USA.
- Harvard University (US)
- National Institute of Biological Sciences, Beijing (CN)
- Western Michigan University (US)
- Corresponding author
- Kagan, Jonathan C.
- ORCID
- Venue
- Science
- Published
- 2016-06-03
- Volume
- 352
- Issue
- 6290
- Pages
- 1232-1236
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC5111085
- OpenAlex
- W2340046691
- Cited by
- 583
- References
- 30
- Citations by year
- 2026: 34 · 2025: 69 · 2024: 58 · 2023: 76 · 2022: 69 · 2021: 62 · 2020: 61 · 2019: 51 · 2018: 49 · 2017: 38 · 2016: 14
- FWCI
- 26.34
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- BOA (University of Milano-Bicocca) (submittedVersion)
- Funders
- Mead Johnson & Company
- Burroughs Wellcome Fund
- Harvard Digestive Diseases Center (P30 DK34854)
- Cariplo Foundation
- Jane Coffin Childs Fund
- NIH (AI093589, AI072955, P30 DK34854, 1R01AI121066-01A1, 1R15HL121770-01A1)
- 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 › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- caspase-11, dendritic cells, OxPAPC, lipopolysaccharide, pyroptosis, inflammasome, dendritic cell activation, pattern recognition receptors, innate immunity, adaptive immune response
- MeSH terms
- NLR Family, Pyrin Domain-Containing 3 Protein, Animals, Carrier Proteins, Dendritic Cells, Immunity, Innate, Lipopolysaccharides, Phospholipids, Cell Death, Mice, Knockout, Caspases, Receptors, Pattern Recognition, Toll-Like Receptor 4, Mice, Caspases, Initiator, Interleukin-1beta, Adaptive Immunity, 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