The DOI matches its Crossref record; 53 of the 53 references it cites were found in a registry or an index.
The AIM2 inflammasome is essential for host defense against cytosolic bacteria and DNA viruses
Open accessAbstract
Inflammasomes regulate the activity of caspase-1 and the maturation of interleukin 1beta (IL-1beta) and IL-18. AIM2 has been shown to bind DNA and engage the caspase-1-activating adaptor protein ASC to form a caspase-1-activating inflammasome. Using Aim2-deficient mice, we identify a central role for AIM2 in regulating caspase-1-dependent maturation of IL-1beta and IL-18, as well as pyroptosis, in response to synthetic double-stranded DNA. AIM2 was essential for inflammasome activation in response to Francisella tularensis, vaccinia virus and mouse cytomegalovirus and had a partial role in the sensing of Listeria monocytogenes. Moreover, production of IL-18 and natural killer cell-dependent production of interferon-gamma, events critical in the early control of virus replication, were dependent on AIM2 during mouse cytomegalovirus infection in vivo. Collectively, our observations demonstrate the importance of AIM2 in the sensing of both bacterial and viral pathogens and in triggering innate immunity.
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
“Finally, the authors found no secretion of the proinflammatory cytokine interleukin-1β, a process known to depend on the inflammasome—a caspase-1-containing complex (122).”
From The Impact of Mass Spectrometry–Based Proteomics on Fundamental Discoveries in Virology (2014) · cites this paper as [122]
In the citing paper
“AIM2 has a demonstrated role in immune responses directed against both bacteria51 and DNA viruses52, but it will be important to determine whether there is a physiological role for AIM2 in sterile inflammation, especially in autoimmune diseases such as systemic lupus erythematosus, which is associated with elevated circulating levels of dsDNA.”
From Sterile inflammation: sensing and reacting to damage (2010) · cites this paper as [52]
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
Biologic basis for interleukin-1 in disease.
Dinarello, C. (1996) · Blood · doi:10.1182/blood.v87.6.2095.bloodjournal8762095 · Cited by 4,344
Immunological and inflammatory functions of the interleukin-1 family
Dinarello, C. A. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132612 · Cited by 3,466
Toll-like receptors in innate immunity
Takeda, K. (2004) · International Immunology · doi:10.1093/intimm/dxh186 · Cited by 3,328
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
STING regulates intracellular DNA-mediated, type I interferon-dependent innate immunity
Ishikawa, H., Ma, Z., & Barber, G. N. (2009) · Nature · doi:10.1038/nature08476 · Cited by 2,759 · cited 1×
“The IFN inducing pathway is complex and involves RNA polymerase III, and one or more redundant sensors, which collectively converge on a signaling axis involving STING 38 , TANK Binding Kinase-1 39 and the Interferon Regulatory Factors (IRF3 and IRF7) (reviewed in 37 ).”
IKKε and TBK1 are essential components of the IRF3 signaling pathway
Fitzgerald, K. A., McWhirter, S. M., Faia, K. L., Rowe, D. C., Latz, E., Golenbock, D. T., Coyle, A. J., Liao, S.-M., & Maniatis, T. (2003) · Nature Immunology · doi:10.1038/ni921 · Cited by 2,680
Self-citationAIM2 recognizes cytosolic dsDNA and forms a caspase-1-activating inflammasome with ASC
Hornung, V., Ablasser, A., Charrel-Dennis, M., Bauernfeind, F., Horvath, G., Caffrey, D. R., Latz, E., & Fitzgerald, K. A. (2009) · Nature · doi:10.1038/nature07725 · Cited by 2,627
Self-citationThe Inflammasomes: Guardians of the Body
Martinon, F., Mayor, A., & Tschopp, J. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132715 · Cited by 2,436
AIM2 activates the inflammasome and cell death in response to cytoplasmic DNA
Fernandes-Alnemri, T., Yu, J.-W., Datta, P., Wu, J., & Alnemri, E. S. (2009) · Nature · doi:10.1038/nature07710 · Cited by 1,831
DAI (DLM-1/ZBP1) is a cytosolic DNA sensor and an activator of innate immune response
Takaoka, A., Wang, Z., Choi, M. K., Yanai, H., Negishi, H., Ban, T., Lu, Y., Miyagishi, M., Kodama, T., Honda, K., et al. (2007) · Nature · doi:10.1038/nature06013 · Cited by 1,704
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 1,001
Pyroptosis, metabolism, and tumor immune microenvironment
Du, T., Gao, J., Li, P., Wang, Y., Qi, Q., Liu, X., Li, J., Wang, C., & Du, L. (2021) · Clinical and Translational Medicine · doi:10.1002/ctm2.492 · Cited by 335
Sauer, J., Witte, C. E., Zemansky, J., Hanson, B., Lauer, P., & Portnoy, D. A. (2010) · Cell Host & Microbe · doi:10.1016/j.chom.2010.04.004 · Cited by 320
Phosphorylation of NLRC4 is critical for inflammasome activation
Qu, Y., Misaghi, S., Izrael-Tomasevic, A., Newton, K., Gilmour, L. L., Lamkanfi, M., Louie, S., Kayagaki, N., Liu, J., Kömüves, L. G., et al. (2012) · Nature · doi:10.1038/nature11429 · Cited by 330
Vaccari, J. P. D. R., Dietrich, W. D., & Keane, R. W. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.227 · Cited by 319
IRGB10 Liberates Bacterial Ligands for Sensing by the AIM2 and Caspase-11-NLRP3 Inflammasomes
Man, S. M., Karki, R., Sasai, M., Place, D. E., Kesavardhana, S., Temirov, J., Frase, S., Zhu, Q., Malireddi, R. K. S., Kuriakose, T., et al. (2016) · Cell · doi:10.1016/j.cell.2016.09.012 · Cited by 312
The role of inflammasomes in kidney disease
Komada, T., & Muruve, D. A. (2019) · Nature Reviews Nephrology · doi:10.1038/s41581-019-0158-z · Cited by 317
Mechanisms and pathways of innate immune activation and regulation in health and cancer
Cui, J., Chen, Y., Wang, H. Y., & Wang, R. (2014) · Human Vaccines & Immunotherapeutics · doi:10.4161/21645515.2014.979640 · Cited by 327
Mukherjee, A., Morosky, S. A., Delorme‐Axford, E., Dybdahl-Sissoko, N., Oberste, M. S., Wang, T., & Coyne, C. B. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1001311 · Cited by 316
Role of AIM2 inflammasome in inflammatory diseases, cancer and infection
Sharma, B. R., Karki, R., & Kanneganti, T. (2019) · European Journal of Immunology · doi:10.1002/eji.201848070 · Cited by 301
Inflammasomes in cancer: a double-edged sword
Kolb, R. H., Liu, G., Janowski, A. M., Sutterwala, F. S., & Zhang, W. (2013) · Protein & Cell · doi:10.1007/s13238-013-0001-4 · Cited by 300
Listeriolysin O: the Swiss army knife of Listeria
Hamon, M. A., Ribet, D., Stavru, F., & Cossart, P. (2012) · Trends in Microbiology · doi:10.1016/j.tim.2012.04.006 · Cited by 309
Wu, J., Fernandes‐Alnemri, T., & Alnemri, E. S. (2010) · Journal of Clinical Immunology · doi:10.1007/s10875-010-9425-2 · Cited by 300
Which cell death modality wins the contest for photodynamic therapy of cancer?
Mishchenko, T. A., Balalaeva, I. V., Gorokhova, A. A., Vedunova, M. V., & Krysko, D. V. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-04851-4 · Cited by 293
Beyond pattern recognition: five immune checkpoints for scaling the microbial threat
Blander, J. M., & Sander, L. E. (2012) · Nature reviews. Immunology · doi:10.1038/nri3167 · Cited by 300
Jin, L., Hill, K. K., Filak, H. C., Mogan, J., Knowles, H. M., Zhang, B., Perraud, A., Cambier, J. C., & Lenz, L. L. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100088 · Cited by 285
The Control of Adaptive Immune Responses by the Innate Immune System
Schenten, D., & Medzhitov, R. M. (2011) · Advances in immunology · doi:10.1016/b978-0-12-387664-5.00003-0 · Cited by 290
Pyroptotic Neuronal Cell Death Mediated by the AIM2 Inflammasome
Adamczak, S. E., Vaccari, J. P. D. R., Dale, G. A., Brand, F. J., Nonner, D., Bullock, M. R. R., Dahl, G., Dietrich, W. D., & Keane, R. W. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.236 · Cited by 289
Caspase-1: The inflammasome and beyond
Sollberger, G., Strittmatter, G. E., Garstkiewicz, M., Sand, J., & Beer, H. (2013) · Innate Immunity · doi:10.1177/1753425913484374 · Cited by 281
Wang, Y., Ning, X., Gao, P., Wu, S., Sha, M., Lv, M., Zhou, X., Gao, J., Fang, R., Meng, G., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.02.011 · Cited by 279
Self-citationKarki, R., Man, S. M., Malireddi, R. K. S., Gurung, P., Vogel, P., Lamkanfi, M., & Kanneganti, T.-D. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.01.006 · Cited by 272
Johnson, K. E., Chikoti, L., & Chandran, B. (2013) · Journal of Virology · doi:10.1128/jvi.00082-13 · Cited by 271
Pierini, R., Juruj, C., Perret, M., Jones, C., Mangeot, P.-E., Weiss, D. S., & Henry, T. (2012) · Cell Death and Differentiation · doi:10.1038/cdd.2012.51 · Cited by 278
Role of pyroptosis in cardiovascular diseases
Jia, C., Chen, H. A., Zhang, J., Zhou, K., Zhuge, Y., Niu, C., Qiu, J., Rong, X., Shi, Z., Xiao, J., et al. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.12.028 · Cited by 268
Gasdermin D Restrains Type I Interferon Response to Cytosolic DNA by Disrupting Ionic Homeostasis
Banerjee, I., Behl, B., Mendonça, M. S. A., Shrivastava, G., Russo, A. J., Ménoret, A., Ghosh, A., Vella, A. T., Vanaja, S. K., Sarkar, S. N., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.07.006 · Cited by 266
Self-citationPerfluoroalkyl substance pollutants activate the innate immune system through the AIM2 inflammasome
Wang, L.-Q., Liu, T., Yang, S., Sun, L., Zhao, Z., Li, L.-Y., She, Y., Zheng, Y.-Y., Ye, X., Bao, Q., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23201-0 · Cited by 270
Listeria monocytogenes induces IFNβ expression through an IFI16‐, cGAS‐ and STING‐dependent pathway
Hansen, K., Prabakaran, T., Laustsen, A., Jørgensen, S. E., Rahbæk, S. H., Jensen, S. B., Nielsen, R., Leber, J. H., Decker, T., Horan, K., et al. (2014) · The EMBO Journal · doi:10.15252/embj.201488029 · Cited by 272
Role of the Inflammasome, IL-1 β , and IL-18 in Bacterial Infections
Sahoo, M., Ceballos‐Olvera, I., del Barrio, L., & Re, F. (2011) · The Scientific World JOURNAL · doi:10.1100/2011/212680 · Cited by 269
Innate Immune Recognition of an AT-Rich Stem-Loop DNA Motif in the Plasmodium falciparum Genome
Sharma, S., DeOliveira, R. B., Kalantari, P., Parroche, P., Goutagny, N., Jiang, Z., Chan, J., Bartholomeu, D. C., Lauw, F. N., Hall, J. P., et al. (2011) · Immunity · doi:10.1016/j.immuni.2011.05.016 · Cited by 258
Self-citationMolecular mechanisms of inflammasome activation during microbial infections
Brož, P., & Monack, D. M. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01041.x · Cited by 266
The role of inflammasomes in human diseases and their potential as therapeutic targets
Yao, J., Sterling, K., Wang, Z., Zhang, Y., & Song, W. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01687-y · Cited by 260
Mechanisms governing inflammasome activation, assembly and pyroptosis induction
Kesavardhana, S., & Kanneganti, T. (2017) · International Immunology · doi:10.1093/intimm/dxx018 · Cited by 259
The linear ubiquitin assembly complex (LUBAC) is essential for NLRP3 inflammasome activation
Rodgers, M. A., Bowman, J. W., Fujita, H., Orazio, N., Shi, M., Liang, Q., Amatya, R., Kelly, T. J., Iwai, K., Ting, J., et al. (2014) · Journal of Experimental Medicine · doi:10.1084/jem.20132486 · Cited by 247
Chavarría‐Smith, J., & Vance, R. E. (2015) · Immunological Reviews · doi:10.1111/imr.12283 · Cited by 247
Segovia, J. A., Sabbah, A., Mgbemena, V. E., Tsai, S.-Y., Chang, T.-H., Berton, M. T., Morris, I. R., Allen, I. C., Ting, J. P. ‐., & Bose, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029695 · Cited by 247
Zhang, Z., Bao, M., Lu, N., Weng, L., Yuan, B., & Liu, Y. (2012) · Nature Immunology · doi:10.1038/ni.2492 · Cited by 249
Inflammasome-Mediated Inflammation in Liver Ischemia-Reperfusion Injury
Jiménez‐Castro, M. B., Cornide‐Petronio, M. E., Gracia‐Sancho, J., & Peralta, C. (2019) · Cells · doi:10.3390/cells8101131 · Cited by 244
Induction of Pyroptosis and Its Implications in Cancer Management
Wang, Y., Liu, X., & Zhao, R. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.00971 · Cited by 246
Sweeten PAMPs: Role of sugar complexed PAMPs in innate immunity and vaccine biology
Mahla, R. S. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00248 · Cited by 239
The interferon response to intracellular DNA: Why so many receptors?
Unterholzner, L. (2013) · Immunobiology · doi:10.1016/j.imbio.2013.07.007 · Cited by 248
AIM2 in health and disease: Inflammasome and beyond
Kumari, P. H., Russo, A. J., Shivcharan, S., & Rathinam, V. A. K. (2020) · Immunological Reviews · doi:10.1111/imr.12903 · Cited by 250
Self-citationDanger-associated molecular patterns in Alzheimer’s disease
Venegas, C., & Heneka, M. T. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.3mr0416-204r · Cited by 236
Opdenbosch, N. V., Gurung, P., Walle, L. V., Fossoul, A., Kanneganti, T., & Lamkanfi, M. (2014) · Nature Communications · doi:10.1038/ncomms4209 · Cited by 235
Inflammasomes as therapeutic targets in human diseases
Li, Y., Huang, H., Liu, B., Zhang, Y. L., Pan, X., Yu, X., Shen, Z., & Song, Y. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00650-z · Cited by 238
Diverse Activators of the NLRP3 Inflammasome Promote IL-1β Secretion by Triggering Necrosis
Cullen, S. P., Kearney, C. J., Clancy, D. M., & Martin, S. J. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.05.003 · Cited by 234
Role of pyroptosis in spinal cord injury and its therapeutic implications
Mamun, A. A., Wu, Y., Monalisa, I., Jia, C., Zhou, K., Munir, F., & Xiao, J. (2020) · Journal of Advanced Research · doi:10.1016/j.jare.2020.08.004 · Cited by 232
Nucleoside reverse transcriptase inhibitors possess intrinsic anti-inflammatory activity
Fowler, B. J., Gelfand, B. D., Kim, Y., Kerur, N., Tarallo, V., Hirano, Y., Amarnath, S., Fowler, D. H., Radwan, M., Young, M. T., et al. (2014) · Science · doi:10.1126/science.1261754 · Cited by 225
Adenovirus Detection by the cGAS/STING/TBK1 DNA Sensing Cascade
Lam, E., Stein, S. C., & Falck-Pedersen, E. (2013) · Journal of Virology · doi:10.1128/jvi.02702-13 · Cited by 236
Recognition of bacterial infection by innate immune sensors
Kumar, S., Ingle, H., Prasad, D. V. R., & Kumar, H. (2012) · Critical Reviews in Microbiology · doi:10.3109/1040841x.2012.706249 · Cited by 232
The PYHIN protein family as mediators of host defenses
Schattgen, S., & Fitzgerald, K. A. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01053.x · Cited by 224
Self-citationAIM2 inflammasome surveillance of DNA damage shapes neurodevelopment
Lammert, C. R., Frost, E. L., Bellinger, C. E., Bolte, A. C., McKee, C. A., Hurt, M. E., Paysour, M. J., Ennerfelt, H. E., & Lukens, J. R. (2020) · Nature · doi:10.1038/s41586-020-2174-3 · Cited by 223
Extensive evolutionary and functional diversity among mammalian AIM2-like receptors
Brunette, R. L., Young, J. M., Whitley, D. G., Brodsky, I. E., Malik, H. S., & Stetson, D. B. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20121960 · Cited by 230
Host specificity of the gut microbiome
Mallott, E. K., & Amato, K. R. (2021) · Nature Reviews Microbiology · doi:10.1038/s41579-021-00562-3 · Cited by 222
Verway, M. J., Bouttier, M., Wang, T. T., Carrier, M., Calderon, M. R., An, B., Devemy, E., McIntosh, F. A., Divangahi, M., Behr, M. A., et al. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003407 · Cited by 222
Modulation of Inflammasome Pathways by Bacterial and Viral Pathogens
Lamkanfi, M., & Dixit, V. M. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100229 · Cited by 217
Recognition of nucleic acids by pattern‐recognition receptors and its relevance in autoimmunity
Kawasaki, T., Kawai, T., & Akira, S. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01048.x · Cited by 226
Innate immune recognition of DNA: A recent history
Dempsey, A., & Bowie, A. (2015) · Virology · doi:10.1016/j.virol.2015.03.013 · Cited by 229
Honda, H., Nagai, Y., Matsunaga, T., Okamoto, N., Watanabe, Y., Tsuneyama, K., Hayashi, H., Fujii, I., Ikutani, M., Hirai, Y., et al. (2014) · Journal of Leukocyte Biology · doi:10.1189/jlb.3a0114-005rr · Cited by 215
DNA Sensing in the Innate Immune Response
Briard, B., Place, D. E., & Kanneganti, T. (2020) · Physiology · doi:10.1152/physiol.00022.2019 · Cited by 222
Hasan, U. A., Zannetti, C., Parroche, P., Goutagny, N., Malfroy, M., Roblot, G., Carreira, C., Hussain, I., Müller, M. B. D., Taylor‐Papadimitriou, J., et al. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20122394 · Cited by 219
Immune System, Cell Senescence, Aging and Longevity - Inflamm-Aging Reappraised
Salvioli, S., Monti, D., Lanzarini, C., Conte, M., Pirazzini, C., Bacalini, M. G., Garagnani, P., Giuliani, C., Fontanesi, E., Ostan, R., et al. (2013) · Current Pharmaceutical Design · doi:10.2174/138161213805219531 · Cited by 209
Cytosolic DNA sensors regulating type I interferon induction
Keating, S. E., Baran, M., & Bowie, A. (2011) · Trends in Immunology · doi:10.1016/j.it.2011.08.004 · Cited by 212
Mayer-Barber, K. D., & Yan, B. (2016) · Cellular and Molecular Immunology · doi:10.1038/cmi.2016.25 · Cited by 210
Horan, K., Hansen, K., Jakobsen, M. R., Holm, C. K., Søby, S., Unterholzner, L., Thompson, M., West, J. A., Iversen, M. B., Rasmussen, S. B., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202749 · Cited by 212
Self-citationArtlett, C. M., Sassi‐Gaha, S., Rieger, J., Boesteanu, A. C., Feghali‐Bostwick, C. A., & Katsikis, P. D. (2011) · Arthritis & Rheumatism · doi:10.1002/art.30568 · Cited by 210
NOD-like receptors and the innate immune system: Coping with danger, damage and death
Kersse, K., Bertrand, M. J. M., Lamkanfi, M., & Vandenabeele, P. (2011) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2011.09.003 · Cited by 214
Critical role of AIM2 in Mycobacterium tuberculosis infection
Saiga, H., Kitada, S., Shimada, Y., Kamiyama, N., Okuyama, M., Makino, M., Yamamoto, M., & Takeda, K. (2012) · International Immunology · doi:10.1093/intimm/dxs062 · Cited by 202
Mechanistic insights into gasdermin-mediated pyroptosis
Bai, Y., Pan, Y., & Liu, X. (2025) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-025-00837-0 · Cited by 218
The mammalian PYHIN gene family: Phylogeny, evolution and expression
Cridland, J. A., Curley, E. Z., Wykes, M., Schroder, K., Sweet, M. J., Roberts, T. L., Ragan, M. A., Kassahn, K. S., & Stacey, K. J. (2012) · BMC Evolutionary Biology · doi:10.1186/1471-2148-12-140 · Cited by 200
Liu, Y., Li, J., Chen, J., Li, Y., Wang, W., Du, X., Song, W., Zhang, W., Lin, L., & Yuan, Z. (2014) · Journal of Virology · doi:10.1128/jvi.02760-14 · Cited by 207
Kalantari, P., DeOliveira, R. B., Chan, J., Corbett, Y., Rathinam, V. A. K., Stutz, A., Latz, E., Gazzinelli, R. T., Golenbock, D. T., & Fitzgerald, K. A. (2014) · Cell Reports · doi:10.1016/j.celrep.2013.12.014 · Cited by 198
Self-citationWang, Y., Lian, Q., Yang, B., Yan, S., Zhou, H., He, L., Lin, G., Lian, Z., Jiang, Z., & Sun, B. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005012 · Cited by 197
Self-citationAdvances in mechanism and regulation of PANoptosis: Prospects in disease treatment
Zhu, P., Ke, Z.-R., Chen, J.-X., Li, S., Ma, T., & Fan, X.-L. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1120034 · Cited by 200
Inflammasome, Inflammation, and Tissue Homeostasis
Rathinam, V. A. K., & Chan, F. K.-M. (2018) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2018.01.004 · Cited by 199
Self-citationThe innate and adaptive immune system of fish
Secombes, C. J., & Wang, T. (2012) · Elsevier eBooks · doi:10.1533/9780857095732.1.3 · Cited by 199
Of inflammasomes and pathogens – sensing of microbes by the inflammasome
Bauernfeind, F. G., & Hornung, V. (2013) · EMBO Molecular Medicine · doi:10.1002/emmm.201201771 · Cited by 198
Self-citationLian, Q., Xu, J., Yan, S., Huang, M., Ding, H., Sun, X., Bi, A., Ding, J., Sun, B., & Geng, M. (2017) · Cell Research · doi:10.1038/cr.2017.54 · Cited by 191
Response of host inflammasomes to viral infection
Chen, I.-Y., & Ichinohe, T. (2014) · Trends in Microbiology · doi:10.1016/j.tim.2014.09.007 · Cited by 198
Molecular mechanisms of inflammasome signaling
Mathur, A., Hayward, J. A., & Man, S. M. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.3mr0617-250r · Cited by 192
The E3 ubiquitin ligase Pellino2 mediates priming of the NLRP3 inflammasome
Humphries, F., Bergin, R., Jackson, R. P., Delagic, N., Wang, B., Yang, S., Dubois, A. V., Ingram, R. J., & Moynagh, P. N. (2018) · Nature Communications · doi:10.1038/s41467-018-03669-z · Cited by 197
Li, Y., Shen, Y., Jin, K., Wen, Z., Cao, W., Wu, B., Wen, R. M., Tian, L., Berry, G. J., Goronzy, J. J., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.06.016 · Cited by 190
Tang, J., Tu, S., Lin, G., Guo, H., Yan, C., Liu, Q., Huang, L., Tang, N., Xiao, Y., Pope, R. M., et al. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20182091 · Cited by 191
β-amyloid, microglia, and the inflammasome in Alzheimer’s disease
Gold, M., & El Khoury, J. (2015) · Seminars in Immunopathology · doi:10.1007/s00281-015-0518-0 · Cited by 187
Antiviral immune responses in the genital tract: clues for vaccines
Iwasaki, A. (2010) · Nature reviews. Immunology · doi:10.1038/nri2836 · Cited by 195
Gorp, H. V., Saavedra, P. H. V., de Vasconcelos, N. M., Opdenbosch, N. V., Walle, L. V., Matusiak, M., Prencipe, G., Insalaco, A., Hauwermeiren, F. V., Demon, D., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1613156113 · Cited by 185
DHX9 Pairs with IPS-1 To Sense Double-Stranded RNA in Myeloid Dendritic Cells
Zhang, Z., Yuan, B., Lu, N., Facchinetti, V., & Liu, Y. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1101307 · Cited by 184
The AIM2-like Receptors Are Dispensable for the Interferon Response to Intracellular DNA
Gray, E. E., Winship, D., Snyder, J. M., Child, S. J., Geballe, A. P., & Stetson, D. B. (2016) · Immunity · doi:10.1016/j.immuni.2016.06.015 · Cited by 197
DNA-stimulated cell death: implications for host defence, inflammatory diseases and cancer
Paludan, S. R., Reinert, L. S., & Hornung, V. (2019) · Nature reviews. Immunology · doi:10.1038/s41577-018-0117-0 · Cited by 187
Self-citationThe future of human DNA vaccines
Li, L., Saadé, F., & Petrovsky, N. (2012) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2012.08.012 · Cited by 183
Innate and adaptive immune responses to viral infection and vaccination
Aoshi, T., Koyama, S., Kobiyama, K., Akira, S., & Ishii, K. J. (2011) · Current Opinion in Virology · doi:10.1016/j.coviro.2011.07.002 · Cited by 179
Tumor Necrosis Factor-α in Heart Failure: an Updated Review
Schumacher, S. M., & Prasad, S. V. N. (2018) · Current Cardiology Reports · doi:10.1007/s11886-018-1067-7 · Cited by 179
Novel Roles for Caspase-8 in IL-1β and Inflammasome Regulation
Gurung, P., & Kanneganti, T. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.08.025 · Cited by 185
RIG‐I detects infection with live Listeria by sensing secreted bacterial nucleic acids
Abdullah, Z., Schlee, M., Roth, S., Mraheil, M. A., Barchet, W., Böttcher, J. P., Hain, T., Geiger, S., Hayakawa, Y., Fritz, J. H., et al. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.274 · Cited by 183
Multi-receptor detection of individual bacterial products by the innate immune system
Kieser, K. J., & Kagan, J. C. (2017) · Nature reviews. Immunology · doi:10.1038/nri.2017.25 · Cited by 184
Programmed Necrosis and Disease:We interrupt your regular programming to bring you necroinflammation
Kim, E. H., Wong, S., & Martinez, J. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0179-3 · Cited by 181
Inflammasomes and Metabolic Disease
Henao‐Mejia, J., Elinav, E., Thaiss, C. A., & Flavell, R. A. (2013) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021113-170324 · Cited by 176
The cytoskeleton in cell-autonomous immunity: structural determinants of host defence
Mostowy, S., & Shenoy, A. R. (2015) · Nature reviews. Immunology · doi:10.1038/nri3877 · Cited by 190
Jin, T., Perry, A., Smith, P. T., Jiang, J., & Xiao, T. S. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.468033 · Cited by 174
Liang, J., Wang, Q., Li, J.-Q., Guo, T., & Yu, D. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113139 · Cited by 174
Inflammasomes and host defenses against bacterial infections
Vladimer, G. I., Marty-Roix, R., Ghosh, S., Weng, D., & Lien, E. (2013) · Current Opinion in Microbiology · doi:10.1016/j.mib.2012.11.008 · Cited by 173
Chen, L., Wang, L., Tsang, N., Ojcius, D. M., Chen, C., OuYang, C., Hsueh, C., Liang, Y. J., Chang, K., Chen, C., et al. (2012) · EMBO Molecular Medicine · doi:10.1002/emmm.201201569 · Cited by 176
Metadata
- Authors
- Rathinam, V. A. K., Jiang, Z., Waggoner, S. N., Sharma, S., Cole, L. E., Waggoner, L., Vanaja, S. K., Monks, B. G., Ganesan, S., Latz, E., Hornung, V., Vogel, S. N., Szomolanyi-Tsuda, E., & Fitzgerald, K. A.
- Affiliations
- University of Massachusetts Chan Medical School (US)
- University of Maryland, Baltimore (US)
- University of Bonn (DE)
- Corresponding author
- Fitzgerald, Katherine A
- ORCID
- Venue
- Nature Immunology
- Published
- 2010-03-28
- Volume
- 11
- Issue
- 5
- Pages
- 395-402
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- PMC
- PMC2887480
- OpenAlex
- W2104195963
- Cited by
- 1,331
- References
- 53
- Citations by year
- 2026: 42 · 2025: 52 · 2024: 74 · 2023: 64 · 2022: 66 · 2021: 68 · 2020: 80 · 2019: 89 · 2018: 70 · 2017: 89 · 2016: 95 · 2015: 90 · 2014: 103 · 2013: 108 · 2012: 72
- FWCI
- 44.92
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- eScholarship@UMassChan (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- National Cancer Institute (CA 66644, R01CA066644, CA034461, R01CA034461)
- National Institute of Allergy and Infectious Diseases (AI-07349, U54 AI157168, AI083713, R01AI083713, T32AI007349)
- 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 › interferon and immune responses
- Keywords
- AIM2 inflammasome, caspase-1, IL-1β maturation, pyroptosis, innate immunity, cytosolic bacteria, DNA viruses, Francisella tularensis, vaccinia virus, murine cytomegalovirus, Listeria monocytogenes, interferon-gamma, natural killer cells, double-stranded DNA sensing
- MeSH terms
- Animals, Cell Line, Cytoskeletal Proteins, DNA, DNA Virus Infections, DNA Viruses, DNA-Binding Proteins, Francisella tularensis, Humans, Immunity, Innate, Killer Cells, Natural, Listeriosis, Lymphocyte Activation, Macrophages, Mice, Inbred C57BL, Nuclear Proteins, Transcription Factors, Tularemia, Signal Transduction, Cytokines, Mice, Knockout, Viral Load, Caspase 1, Multiprotein Complexes, Apoptosis Regulatory Proteins, Mice, CARD Signaling Adaptor Proteins
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