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The AIM2 inflammasome is essential for host defense against cytosolic bacteria and DNA viruses
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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.
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“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]
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“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]
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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
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Sorted by citations
Items 201–300 of 1,001
Dorhoi, A., Nouailles, G., Jörg, S., Hagens, K., Heinemann, E., Pradl, L., Oberbeck‐Müller, D., Correa, M. A. D., Reece, S. T., Ruland, J., et al. (2011) · European Journal of Immunology · doi:10.1002/eji.201141548 · Cited by 172
AIM2 in regulatory T cells restrains autoimmune diseases
Chou, W.-C., Guo, Z., Guo, H., Chen, L., Zhang, G., Liang, K., Xie, L., Tan, X. M., Gibson, S. A., Rampanelli, E., et al. (2021) · Nature · doi:10.1038/s41586-021-03231-w · Cited by 173
Structure, Activation and Regulation of NLRP3 and AIM2 Inflammasomes
Sharma, M., & de Alba, E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22020872 · Cited by 173
Impact of intracellular innate immune receptors on immunometabolism
Chou, W.-C., Rampanelli, E., Li, X., & Ting, J. P. ‐. (2021) · Cellular and Molecular Immunology · doi:10.1038/s41423-021-00780-y · Cited by 173
Inflammasomes as mediators of immunity against influenza virus
Pang, I. K., & Iwasaki, A. (2010) · Trends in Immunology · doi:10.1016/j.it.2010.11.004 · Cited by 176
Unique Loss of the PYHIN Gene Family in Bats Amongst Mammals: Implications for Inflammasome Sensing
Ahn, M., Cui, J., Irving, A. T., & Wang, L. (2016) · Scientific Reports · doi:10.1038/srep21722 · Cited by 176
Li, J., Song, J., Kang, L., Huang, L., Zhou, S., Hu, L., Zheng, J., Li, C., Zhang, X., He, X., et al. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009733 · Cited by 166
The inflammasome in lung diseases
dos Santos, G., Kutuzov, M. A., & Ridge, K. M. (2012) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00225.2012 · Cited by 172
From periphery to center stage: 50 years of advancements in innate immunity
Carpenter, S. B., & O'Neill, L. A. J. (2024) · Cell · doi:10.1016/j.cell.2024.03.036 · Cited by 171
The Inflammasome in Myocardial Injury and Cardiac Remodeling
Toldo, S. A., Mezzaroma, E., Mauro, A. G., Salloum, F. N., Tassell, B. W. V., & Abbate, A. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2014.5989 · Cited by 165
A Mechanistic Understanding of Pyroptosis: The Fiery Death Triggered by Invasive Infection
Liu, X., & Lieberman, J. (2017) · Advances in immunology · doi:10.1016/bs.ai.2017.02.002 · Cited by 167
Jabir, M. S., Hopkins, L., Ritchie, N. D., Ullah, I., Bayes, H. K., Li, D., Tourlomousis, P., Lupton, A., Puleston, D. J., Simon, A. K., et al. (2015) · Autophagy · doi:10.4161/15548627.2014.981915 · Cited by 163
Khare, S., Ratsimandresy, R. A., de Almeida, L., Cuda, C. M., Rellick, S. L., Misharin, A. V., Wallin, M., Gangopadhyay, A., Forte, E., Gottwein, E., et al. (2014) · Nature Immunology · doi:10.1038/ni.2829 · Cited by 172
Cytosolic Recognition of Microbes and Pathogens: Inflammasomes in Action
Hayward, J. A., Mathur, A., Ngo, C., & Man, S. M. (2018) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00015-18 · Cited by 168
Innate immunity to intracellular pathogens: macrophage receptors and responses to microbial entry
Plüddemann, A., Mukhopadhyay, S., & Gordon, S. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2010.00989.x · Cited by 170
Importance of Nucleic Acid Recognition in Inflammation and Autoimmunity
Barrat, F. J., Elkon, K. B., & Fitzgerald, K. A. (2015) · Annual Review of Medicine · doi:10.1146/annurev-med-052814-023338 · Cited by 164
Self-citationBae, J. H., Jo, S. I., Kim, S. J., Lee, J. M., Jeong, J. H., Kang, J. S., Cho, N., Kim, S. S., Lee, E. Y., & Moon, J. (2019) · Cells · doi:10.3390/cells8040328 · Cited by 167
Ratsimandresy, R. A., Indramohan, M., Dorfleutner, A., & Stehlik, C. (2017) · Cellular & Molecular Immunology · doi:10.1038/cmi.2016.35 · Cited by 161
Fang, R., Tsuchiya, K., Kawamura, I., Shen, Y., Hara, H., Sakai, S., Yamamoto, T., Fernandes‐Alnemri, T., Yang, R., Hernández-Cuellar, E., et al. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100381 · Cited by 166
Jounai, N., Kobiyama, K., Takeshita, F., & Ishii, K. J. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2012.00168 · Cited by 169
Interferon-induced guanylate-binding proteins in inflammasome activation and host defense
Kim, B.-H., Chee, J., Bradfield, C. J., Park, E., Kumar, P., & MacMicking, J. D. (2016) · Nature Immunology · doi:10.1038/ni.3440 · Cited by 171
The pathological features of regulated necrosis
Tonnus, W., Meyer, C., Paliege, A., Belavgeni, A., von Mäßenhausen, A., Bornstein, S. R., Hugo, C., Becker, J. U., & Linkermann, A. (2019) · The Journal of Pathology · doi:10.1002/path.5248 · Cited by 168
Innate immune inflammatory cell death: PANoptosis and PANoptosomes in host defense and disease
Chen, W., Gullett, J. M., Tweedell, R. E., & Kanneganti, T. (2023) · European Journal of Immunology · doi:10.1002/eji.202250235 · Cited by 161
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 161
Current understanding of the gut microbiota shaping mechanisms
Chang, C., & Kao, C. (2019) · Journal of Biomedical Science · doi:10.1186/s12929-019-0554-5 · Cited by 166
The Therapeutic Potential of Modifying Inflammasomes and NOD-Like Receptors
Virgilio, F. D. (2013) · Pharmacological Reviews · doi:10.1124/pr.112.006171 · Cited by 168
Localization and Functionality of the Inflammasome in Neutrophils
Bakele, M., Joos, M., Burdi, S., Allgaier, N., Pöschel, S., Fehrenbacher, B., Schaller, M., Marcos, V., Kümmerle-Deschner, J., Rieber, N., et al. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.505636 · Cited by 157
Bröms, J. E., Sjöstedt, A. B., & Lavander, M. (2010) · Frontiers in Microbiology · doi:10.3389/fmicb.2010.00136 · Cited by 172
Type I interferons: diversity of sources, production pathways and effects on immune responses
Swiecki, M. K., & Colonna, M. (2011) · Current Opinion in Virology · doi:10.1016/j.coviro.2011.10.026 · Cited by 162
Deregulated inflammasome signaling in disease
Lamkanfi, M., Walle, L. V., & Kanneganti, T. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01042.x · Cited by 154
Inflammasomes, the eye and anti-inflammasome therapy
Yerramothu, P., Vijay, A. K., & Willcox, M. D. P. (2017) · Eye · doi:10.1038/eye.2017.241 · Cited by 155
Mechanisms of Francisella tularensis Intracellular PathogenesisPreprint
Celli, J., & Zahrt, T. C. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a010314 · Cited by 153
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
Komada, T., Chung, H., Lau, A. N., Platnich, J. M., Beck, P. L., Benediktsson, H., Duff, H. J., Jenne, C. N., & Muruve, D. A. (2018) · Journal of the American Society of Nephrology · doi:10.1681/asn.2017080863 · Cited by 152
Antagonism of the STING Pathway via Activation of the AIM2 Inflammasome by Intracellular DNA
Corrales, L. P., Woo, S., Williams, J. B., McWhirter, S. M., Dubensky, T. W., & Gajewski, T. F. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502538 · Cited by 155
How Inflammasomes Inform Adaptive Immunity
Evavold, C. L., & Kagan, J. C. (2017) · Journal of Molecular Biology · doi:10.1016/j.jmb.2017.09.019 · Cited by 155
A noncanonical function of cGAMP in inflammasome priming and activation
Swanson, K. V., Junkins, R. D., Kurkjian, C. J., Holley-Guthrie, E., Pendse, A. A., Morabiti, R. E., Petrucelli, A., Barber, G. N., Benedict, C. A., & Ting, J. P. ‐. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20171749 · Cited by 148
Maruzuru, Y., Ichinohe, T., Sato, R., Miyake, K., Okano, T., Suzuki, T., Koshiba, T., Koyanagi, N., Tsuda, S., Watanabe, M., et al. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2017.12.014 · Cited by 150
Induction of type I interferons by bacteria
Monroe, K. M., McWhirter, S. M., & Vance, R. E. (2010) · Cellular Microbiology · doi:10.1111/j.1462-5822.2010.01478.x · Cited by 149
AIM2 inflammasome is activated by pharmacological disruption of nuclear envelope integrity
Di Micco, A., Frera, G., Lugrin, J., Jamilloux, Y., Hsu, E.-T., Tardivel, A., De Gassart, A., Zaffalon, L., Bujisic, B., Siegert, S., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1602419113 · Cited by 143
Inflammasomes and the fine line between defense and disease
Christgen, S. L., & Kanneganti, T. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.11.007 · Cited by 145
Pateras, I. S., Havaki, S., Nikitopoulou, X., Vougas, K. N., Townsend, P. A., Panayiotidis, M. I., Georgakilas, A. G., & Gorgoulis, V. G. (2015) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2015.06.011 · Cited by 147
Pattern recognition receptors: sentinels in innate immunity and targets of new vaccine adjuvants
Olive, C. (2012) · Expert Review of Vaccines · doi:10.1586/erv.11.189 · Cited by 152
Cutting Edge: Cytosolic Bacterial DNA Activates the Inflammasome via Aim2
Warren, S. E., Armstrong, A. M., Hamilton, M. K., Mao, D. P., Leaf, I. A., Miao, E. A., & Aderem, A. A. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000724 · Cited by 142
Vanhove, W., Peeters, P. M., Staelens, D., Schraenen, A., der Goten, J. V., Cleynen, I., Schepper, S. D., Lommel, L. V., Reynaert, N. L., Schuit, F. C., et al. (2015) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000535 · Cited by 144
Viruses and the Diversity of Cell Death
Danthi, P. (2016) · Annual Review of Virology · doi:10.1146/annurev-virology-110615-042435 · Cited by 144
Toll-Like Receptor Polymorphisms, Inflammatory and Infectious Diseases, Allergies, and Cancer
Medvedev, A. E. (2013) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2012.0140 · Cited by 140
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
Rad50-CARD9 interactions link cytosolic DNA sensing to IL-1β production
Roth, S., Rottach, A., Lotz-Havla, A. S., Laux, V., Muschaweckh, A., Gersting, S. W., Muntau, A. C., Hopfner, K., Jin, L., Vanness, K., et al. (2014) · Nature Immunology · doi:10.1038/ni.2888 · Cited by 147
Inflammasome control of viral infection
Lupfer, C. R., Malik, A., & Kanneganti, T. (2015) · Current Opinion in Virology · doi:10.1016/j.coviro.2015.02.007 · Cited by 142
Strategies Used by Bacteria to Grow in Macrophages
Mitchell*, G., Chen*, C., & Portnoy, D. A. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0012-2015 · Cited by 137
Innate Sensing of DNA Virus Genomes
Ma, Z., Ni, G., & Damania, B. (2018) · Annual Review of Virology · doi:10.1146/annurev-virology-092917-043244 · Cited by 140
Biochemical regulation of the inflammasome
Dowling, J. K., & O'Neill, L. A. J. (2012) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409238.2012.694844 · Cited by 139
Vidal, S. M., Khakoo, S. I., & Biron, C. A. (2011) · Current Opinion in Virology · doi:10.1016/j.coviro.2011.10.017 · Cited by 136
Differential Requirements for NAIP5 in Activation of the NLRC4 Inflammasome
Lightfield, K. L., Persson, J., Trinidad, N. J., Brubaker, S. W., Kofoed, E. M., Sauer, J., Dunipace, E. A., Warren, S. E., Miao, E. A., & Vance, R. E. (2011) · Infection and Immunity · doi:10.1128/iai.01187-10 · Cited by 139
Inflammasomes: Their Role in Normal and Complicated Pregnancies
Gomez‐Lopez, N., Motomura, K., Miller, D., Garcia‐Flores, V., Galaz, J., & Romero, R. J. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900901 · Cited by 136
Song, X., Ma, F., & Herrup, K. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.0774-19.2019 · Cited by 133
Innate Immunity and Biomaterials at the Nexus: Friends or Foes
Christo, S. N., Diener, K. R., Bachhuka, A., Vasilev, K. A., & Hayball, J. D. (2015) · BioMed Research International · doi:10.1155/2015/342304 · Cited by 138
The NLRP3 Inflammasome Detects Encephalomyocarditis Virus and Vesicular Stomatitis Virus Infection
Rajan, J. V., Rodriguez, D. J., Miao, E. A., & Aderem, A. A. (2011) · Journal of Virology · doi:10.1128/jvi.01687-10 · Cited by 133
Emerging Role of Mitochondrial DNA as a Major Driver of Inflammation and Disease Progression
Zhong, F., Liang, S., & Zhong, Z. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.10.008 · Cited by 135
HPV16 activates the AIM2 inflammasome in keratinocytes
Reinholz, M., Kawakami, Y., Salzer, S., Kreuter, A., Dombrowski, Y., Koglin, S., Kresse, S., Ruzicka, T., & Schauber, J. (2013) · Archives of Dermatological Research · doi:10.1007/s00403-013-1375-0 · Cited by 132
Subversion of Host Recognition and Defense Systems by Francisella spp
Jones, C. L., Napier, B. A., Sampson, T. R., Llewellyn, A. C., Schroeder, M. R., & Weiss, D. S. (2012) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.05027-11 · Cited by 135
Inflammasomes and its importance in viral infections
Shrivastava, G., León‐Juárez, M., García‐Cordero, J., Meza-Sánchez, D. E., & Cedillo‐Barrón, L. (2016) · Immunologic Research · doi:10.1007/s12026-016-8873-z · Cited by 135
Wang, X., Hua, P., He, C., & Chen, M. (2022) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2022.03.020 · Cited by 131
Sauer, J., Pereyre, S., Archer, K. A., Burke, T., Hanson, B., Lauer, P., & Portnoy, D. A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1019041108 · Cited by 130
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
The Antisocial Network: Cross Talk Between Cell Death Programs in Host Defense
Snyder, A. G., & Oberst, A. (2021) · Annual Review of Immunology · doi:10.1146/annurev-immunol-112019-072301 · Cited by 129
Emerging mechanisms of pyroptosis and its therapeutic strategy in cancer
Lu, L., Zhang, Y., Tan, X., Merkher, Y., Leonov, S. V., Zhu, L., Deng, Y., zhang, H., Zhu, D., Tan, Y., et al. (2022) · Cell Death Discovery · doi:10.1038/s41420-022-01101-6 · Cited by 131
Shin, M. S., Kang, Y., Lee, N., Wahl, E. R., Kim, S., Kang, K. S., Lazova, R. Z., & Kang, I. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1201195 · Cited by 127
Cellular Sensing of Viral DNA and Viral Evasion Mechanisms
Orzalli, M. H., & Knipe, D. M. (2014) · Annual Review of Microbiology · doi:10.1146/annurev-micro-091313-103409 · Cited by 128
Thompson, M., Sharma, S., Atianand, M., Jensen, S. B., Carpenter, S. B., Knipe, D. M., Fitzgerald, K. A., & Kurt‐Jones, E. A. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.554147 · Cited by 129
Self-citationIntracellular sensing of microbes and danger signals by the inflammasomes
Horvath, G. L., Schrum, J. E., Nardo, C. M. D., & Latz, E. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01050.x · Cited by 127
Self-citationPyroptosis in the Initiation and Progression of Atherosclerosis
Qian, Z., Zhao, Y., Wan, C., Deng, Y., Zhuang, Y., Xu, Y., Zhu, Y., Lu, S., & Bao, Z. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.652963 · Cited by 127
Cross-regulation between the IL-1β/IL-18 processing inflammasome and other inflammatory cytokines
Barker, B. R., Taxman, D. J., & Ting, J. P. ‐. (2011) · Current Opinion in Immunology · doi:10.1016/j.coi.2011.07.005 · Cited by 124
Gonçalves, V. M., Matteucci, K. C., Buzzo, C. L., Miollo, B. H., Ferrante, D., Torrecilhas, A. C., Rodrigues, M. M., Alvarez, J. M., & Bortoluci, K. R. (2013) · PLoS Neglected Tropical Diseases · doi:10.1371/journal.pntd.0002469 · Cited by 123
Shah, S., Bohsali, A., Ahlbrand, S. E., Srinivasan, L., Rathinam, V. A. K., Vogel, S. N., Fitzgerald, K. A., Sutterwala, F. S., & Briken, V. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1301331 · Cited by 123
Self-citationMolecular mechanism for NLRP6 inflammasome assembly and activation
Shen, C., Lu, A. Z., Xie, W. J., Ruan, J., Negro, R., Egelman, E. H., Fu, T., & Wu, H. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1817221116 · Cited by 124
Activation and Regulation of DNA-Driven Immune Responses
Paludan, S. R. (2015) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00061-14 · Cited by 128
AIM2 Inflammasome Is Critical for Influenza-Induced Lung Injury and Mortality
Zhang, H., Luo, J., Alcorn, J. F., Chen, K., Fan, S., Pilewski, J. M., Liu, A., Chen, W., Kolls, J. K., & Wang, J. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1600714 · Cited by 122
IFITs: Emerging Roles as Key Anti-Viral Proteins
Vladimer, G. I., Górna, M. W., & Superti‐Furga, G. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00094 · Cited by 134
Hu, S., Peng, L., Kwak, Y.-T., McElvania, E., Pasare, C., Malter, J. S., Hooper, L. V., & Zaki, H. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.040 · Cited by 123
Activation of the Pyrin Inflammasome by Intracellular Burkholderia cenocepacia
Gavrilin, M. A., Abdelaziz, D. H., Mostafa, M., Abdulrahman, B., Grandhi, J., Akhter, A., Khweek, A. A., Aubert, D., Valvano, M. A., Wewers, M. D., et al. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1102272 · Cited by 123
Oxylipins and metabolites from pyroptotic cells act as promoters of tissue repair
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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
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