The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
STING is an endoplasmic reticulum adaptor that facilitates innate immune signalling
Open accessAbstract
The cellular innate immune system is essential for recognizing pathogen infection and for establishing effective host defence. But critical molecular determinants responsible for facilitating an appropriate immune response-following infection with DNA and RNA viruses, for example-remain to be identified. Here we report the identification, following expression cloning, of a molecule (STING; stimulator of interferon genes) that appears essential for effective innate immune signalling processes. It comprises five putative transmembrane regions, predominantly resides in the endoplasmic reticulum and is able to activate both NF-kappaB and IRF3 transcription pathways to induce expression of type I interferon (IFN-alpha and IFN-beta ) and exert a potent anti-viral state following expression. In contrast, loss of STING rendered murine embryonic fibroblasts extremely susceptible to negative-stranded virus infection, including vesicular stomatitis virus. Further, STING ablation abrogated the ability of intracellular B-form DNA, as well as members of the herpesvirus family, to induce IFN-beta, but did not significantly affect the Toll-like receptor (TLR) pathway. Yeast two-hybrid and co-immunoprecipitation studies indicated that STING interacts with RIG-I and with SSR2 (also known as TRAPbeta), which is a member of the translocon-associated protein (TRAP) complex required for protein translocation across the endoplasmic reticulum membrane following translation. Ablation by RNA interference of both TRAPbeta and translocon adaptor SEC61beta was subsequently found to inhibit STING's ability to stimulate expression of IFN-beta. Thus, as well as identifying a regulator of innate immune signalling, our results imply a potential role for the translocon in innate signalling pathways activated by select viruses as well as intracellular DNA.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“TBK1 also activates NF‐κB to induce expression of IFN and inflammatory cytokines.65, 66, 67”
From Cellular senescence and senescence-associated secretory phenotype via the cGAS-STING signaling pathway in cancer (2020) · cites this paper as [65]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“cGAMP produced by cGAS activation binds to STING which is located on the membrane of endoplasmic reticulum (ER)391 and leads to the translocation of STING from ER to the Golgi where it is further modified.392”
From Role of neuroinflammation in neurodegeneration development (2023) · cites this paper as [391]
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“the stimulator of interferon genes (STING) has been shown to be a major pathway for the detection of immunogenic tumors and initiation of a spontaneous T cell response18–21.”
From Epigenetic state determines the in vivo efficacy of STING agonist therapy (2023) · cites this paper as [20]
Experimental — accuracy not yet measuredIn the citing paper
“TBK1 associated with STING also facilitates dsDNA-mediated activation of NF-κB to promote proinflammatory gene transcription (Abe and Barber, 2014; Ishikawa and Barber, 2008).”
From Cytoplasmic DNA: sources, sensing, and role in aging and disease (2021) · cites this paper as Ishikawa and Barber, 2008
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
Yoneyama, M., Kikuchi, M., Natsukawa, T., Shinobu, N., Imaizumi, T., Miyagishi, M., Taira, K., Akira, S., & Fujita, T. (2004) · Nature Immunology · doi:10.1038/ni1087 · Cited by 4,022
Differential roles of MDA5 and RIG-I helicases in the recognition of RNA viruses
Kato, H., Takeuchi, O., Sato, S., Yoneyama, M., Yamamoto, M., Matsui, K., Uematsu, S., Jung, A., Kawai, T., Ishii, K. J., et al. (2006) · Nature · doi:10.1038/nature04734 · Cited by 3,888
Seth, R. B., Sun, L., Ea, C.-K., & Chen, Z. J. (2005) · Cell · doi:10.1016/j.cell.2005.08.012 · Cited by 3,329
IPS-1, an adaptor triggering RIG-I- and Mda5-mediated type I interferon induction
Kawai, T., Takahashi, K., Sato, S., Coban, C., Kumar, H., Kato, H., Ishii, K. J., Takeuchi, O., & Akira, S. (2005) · Nature Immunology · doi:10.1038/ni1243 · Cited by 2,562
5'-Triphosphate RNA Is the Ligand for RIG-I
Hornung, V., Ellegast, J., Kim, S., Brzózka, K., Jung, A., Kato, H., Poeck, H., Akira, S., Conzelmann, K.-K., Schlee, M., et al. (2006) · Science · doi:10.1126/science.1132505 · Cited by 2,474
Cardif is an adaptor protein in the RIG-I antiviral pathway and is targeted by hepatitis C virus
Meylan, E., Curran, J., Hofmann, K., Moradpour, D., Binder, M., Bartenschlager, R., & Tschopp, J. (2005) · Nature · doi:10.1038/nature04193 · Cited by 2,401
RIG-I-mediated antiviral responses to single-stranded RNA bearing 5’-phosphates
Pichlmair, A., Schulz, O., Tan, C. P., Näslund, T. I., Liljeström, P., Weber, F., & Reis e Sousa, C. (2006) · Science · doi:10.1126/science.1132998 · Cited by 2,210
VISA Is an Adapter Protein Required for Virus-Triggered IFN-β Signaling
Xu, L., Wang, Y., Han, K.-J., Li, L., Zhai, Z., & Shu, H. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.08.014 · Cited by 1,849
Distinct RIG-I and MDA5 Signaling by RNA Viruses in Innate Immunity
Loo, Y.-M., Fornek, J., Crochet, N., Bajwa, G., Perwitasari, O., Martinez-Sobrido, L., Akira, S., Gill, M. A., García-Sastre, A., Katze, M. G., et al. (2008) · Journal of Virology · doi:10.1128/jvi.01080-07 · Cited by 1,071
Recognition of Cytosolic DNA Activates an IRF3-Dependent Innate Immune Response
Stetson, D. B., & Medzhitov, R. M. (2006) · Immunity · doi:10.1016/j.immuni.2005.12.003 · Cited by 1,003
Cited by
Sorted by citations
Items 601–700 of 1,005
Recognition of Herpes Simplex Viruses: Toll-Like Receptors and Beyond
Ma, Y., & He, B. (2013) · Journal of Molecular Biology · doi:10.1016/j.jmb.2013.11.012 · Cited by 110
Antigen expression determines adenoviral vaccine potency independent of IFN and STING signaling
Quinn, K. M., Zak, D. E., Costa, A. D. S., Yamamoto, A., Kastenmüller, K., Hill, B. J., Lynn, G. M., Darrah, P. A., Lindsay, R. W. B., Wang, L., et al. (2015) · Journal of Clinical Investigation · doi:10.1172/jci78280 · Cited by 113
Catalytic asymmetric and stereodivergent oligonucleotide synthesis
Featherston, A. L., Kwon, Y., Pompeo, M., Engl, O. D., Leahy, D. K., & Miller, S. J. (2021) · Science · doi:10.1126/science.abf4359 · Cited by 110
Qin, Z., Fang, X., Sun, W., Ma, Z., Dai, T., Wang, S., Zong, Z., Huang, H., Ru, H., Lu, H., et al. (2022) · Nature Immunology · doi:10.1038/s41590-022-01269-0 · Cited by 113
Stimulator of interferon genes (STING) activation exacerbates experimental colitis in mice
Martin, G. R., Blomquist, C. M., Henare, K. L., & Jirik, F. R. (2019) · Scientific Reports · doi:10.1038/s41598-019-50656-5 · Cited by 109
Chen, X., Yang, J. D., Wang, L., & Liu, B. (2020) · Theranostics · doi:10.7150/thno.38742 · Cited by 112
Stimulator of IFN Gene Is Critical for Induction of IFN-β during Chlamydia muridarum Infection
Prantner, D., Darville, T. L., & Nagarajan, U. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903704 · Cited by 109
Engineering oncolytic viruses to exploit tumor specific defects in innate immune signaling pathways
Naik, S., & Russell, S. J. (2009) · Expert Opinion on Biological Therapy · doi:10.1517/14712590903170653 · Cited by 111
Ohta, A., & Nishiyama, Y. (2010) · Mitochondrion · doi:10.1016/j.mito.2010.08.006 · Cited by 111
The Molecular Basis of Viral Inhibition of IRF- and STAT-Dependent Immune Responses
Chiang, H.-S., & Liu, H. M. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2018.03086 · Cited by 108
Roles of the cGAS-STING Pathway in Cancer Immunosurveillance and Immunotherapy
Yum, S., Li, M., Frankel, A. E., & Chen, Z. J. (2019) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-030518-055636 · Cited by 109
KAT5 acetylates cGAS to promote innate immune response to DNA virus
Song, Z.-M., Lin, H., Yi, X.-M., Guo, W., Hu, M., & Shu, H. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1922330117 · Cited by 109
Regulation of antiviral innate immune signaling and viral evasion following viral genome sensing
Chathuranga, K., Weerawardhana, A., Dodantenna, N., & Lee, J. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00691-y · Cited by 110
Leuzzi, G., Vasciaveo, A., Taglialatela, A., Chen, X., Firestone, T. M., Hickman, A. R., Mao, W., Thakar, T., Vaitsiankova, A., Huang, J., et al. (2024) · Cell · doi:10.1016/j.cell.2024.01.008 · Cited by 113
cGAS-STING pathway mediates activation of dendritic cell sensing of immunogenic tumors
Li, G., Zhao, X., Zheng, Z., Zhang, H., Wu, Y., Shen, Y., & Chen, Q. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05191-6 · Cited by 114
The mechanism of double-stranded DNA sensing through the cGAS-STING pathway
Shu, C., Li, X., & Li, P. (2014) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2014.06.006 · Cited by 110
The role of mitochondria in cellular defense against microbial infection
Arnoult, D., Carneiro, L. A. M., Tattoli, I., & Girardin, S. E. (2009) · Seminars in Immunology · doi:10.1016/j.smim.2009.05.009 · Cited by 107
Galectin-9 promotes a suppressive microenvironment in human cancer by enhancing STING degradation
Zhang, C.-X., Huang, D.-J., Baloche, V. M. D., Zhang, L., Xu, J.-X., Li, B., Zhao, X., He, J., Mai, H., Chen, Q., et al. (2020) · Oncogenesis · doi:10.1038/s41389-020-00248-0 · Cited by 114
Deubiquitylating Enzymes in Cancer and Immunity
Ren, J., Yu, P., Liu, S., Li, R., Niu, X., Chen, Y., Zhang, Z., Zhou, F., & Zhang, L. (2023) · Advanced Science · doi:10.1002/advs.202303807 · Cited by 118
Quan, S., Fu, X., Cai, H., Ren, Z., Xu, Y., & Jia, L. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00815-2 · Cited by 110
Zhang, D., Su, C., & Zheng, C. (2016) · Journal of Virology · doi:10.1128/jvi.00186-16 · Cited by 106
A Nuclear Export Signal Is Required for cGAS to Sense Cytosolic DNA
Sun, H., Huang, Y., Mei, S., Xu, F., Liu, X., Zhao, F., Yin, L., Zhang, D., Wei, L., Wu, C., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2020.108586 · Cited by 105
Brégnard, C., Guerra, J., Déjardin, S., Passalacqua, F., Benkirane, M., & Laguette, N. (2016) · EBioMedicine · doi:10.1016/j.ebiom.2016.05.005 · Cited by 112
Defects in interferon pathways as potential biomarkers of sensitivity to oncolytic viruses
Matveeva, O. V., & Chumakov, P. M. (2018) · Reviews in Medical Virology · doi:10.1002/rmv.2008 · Cited by 113
Going to Bat(s) for Studies of Disease Tolerance
Mandl, J. N., Schneider, C. L., Schneider, D. S., & Baker, M. L. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02112 · Cited by 108
cGAS-STING signaling in cancer immunity and immunotherapy
Du, H., Xu, T., & Cui, M. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110972 · Cited by 106
Ubiquitin-like conjugation by bacterial cGAS enhances anti-phage defence
Jenson, J. M., Li, T., Du, F., Ea, C.-K., & Chen, Z. J. (2023) · Nature · doi:10.1038/s41586-023-05862-7 · Cited by 106
The role of differential expression of human interferon-A genes in antiviral immunity
Génin, P., Vaccaro, A., & Civas, A. (2009) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2009.07.005 · Cited by 105
TBK1, a central kinase in innate immune sensing of nucleic acids and beyond
Zhou, R., Zhang, Q., & Xu, P. (2020) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmaa051 · Cited by 104
Franco, M. M. C., Marim, F. M., Guimarães, E. S., Assis, N. R. G., Cerqueira, D. M., Alves‐Silva, J., Harms, J. S., Splitter, G. A., Smith, J. A., Kanneganti, T., et al. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700725 · Cited by 107
Self-citationFenech, E. J., Lari, F., Charles, P. D., Fischer, R., Laétitia-Thézénas, M., Bagola, K., Paton, A. W., Paton, J. C., Gyrd‐Hansen, M., Kessler, B. M., et al. (2020) · eLife · doi:10.7554/elife.57306 · Cited by 106
Kim, D., Endo, A., Fang, F. G., Huang, K., Bao, X., Choi, H.-W., Majumder, U., Shen, Y., Mathieu, S. R., Zhu, X., et al. (2021) · ChemMedChem · doi:10.1002/cmdc.202100068 · Cited by 108
Wrzesiński, T., Szeląg, M., Cieślikowski, W. A., Ida, A., Giles, R. H., Zodro, E., Szumska, J., Poźniak, J., Kwias, Z., Bluyssen, H. A. R., et al. (2015) · BMC Cancer · doi:10.1186/s12885-015-1530-4 · Cited by 103
Beyond Anti-viral Effects of Chloroquine/Hydroxychloroquine
Gies, V., Bekaddour, N., Dieudonné, Y., Guffroy, A., Frenger, Q., Gros, F., Rodero, M. P., Herbeuval, J., & Korganow, A. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01409 · Cited by 106
Ji, Y., Luo, Y., Wu, Y., Sun, Y., Zhao, L., Xue, Z., Sun, M., Wei, X., He, Z., Wu, S. A., et al. (2023) · Nature Cell Biology · doi:10.1038/s41556-023-01138-4 · Cited by 104
New Insights into the Role of Mitochondria-Associated Endoplasmic Reticulum Membrane
Fujimoto, M., & Hayashi, T. (2011) · International review of cytology · doi:10.1016/b978-0-12-386033-0.00002-5 · Cited by 106
Emerging Role of Ubiquitination in Antiviral RIG-I Signaling
Maelfait, J., & Beyaert, R. (2012) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.05012-11 · Cited by 105
Poxviruses Evade Cytosolic Sensing through Disruption of an mTORC1-mTORC2 Regulatory Circuit
Meade, N., Furey, C., Li, H., Verma, R., Chai, Q., Rollins, M. G., DiGiuseppe, S., Naghavi, M. H., & Walsh, D. (2018) · Cell · doi:10.1016/j.cell.2018.06.053 · Cited by 107
Chikungunya virus antagonizes cGAS-STING mediated type-I interferon responses by degrading cGAS
Webb, L. G., Veloz, J., Silva, J. P., Zhu, T., Rangel, M. V., Mutetwa, T., Zhang, L., Bernal‐Rubio, D., Figueroa, D., Carrau, L., et al. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008999 · Cited by 105
Gao, P., Zillinger, T., Wang, W., Ascano, M., Dai, P., Hartmann, G., Tuschl, T., Deng, L., Barchet, W., & Patel, D. J. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.08.010 · Cited by 105
Intracellular Innate Immune Cascades and Interferon Defenses That Control Hepatitis C Virus
Horner, S. M., & Gale, M. (2009) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2009.0063 · Cited by 101
Severe combined immunodeficiency in stimulator of interferon genes (STING) V154M/wild-type mice
Bouis, D., Kirstetter, P., Arbogast, F., Lamon, D., Delgado, V., Jung, S., Ebel, C., Jacobs, H., Knapp, A., Jeremiah, N., et al. (2018) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2018.04.034 · Cited by 107
STING Operation at the ER/Golgi Interface
Taguchi, T., Mukai, K., Takaya, E., & Shindo, R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.646304 · Cited by 104
From Design to Clinic: Engineered Nanobiomaterials for Immune Normalization Therapy of Cancer
Saeed, M., Chen, F., Ye, J., Shi, Y., Lammers, T., Geest, B. G. D., Xu, Z. P., & Yu, H. (2021) · Advanced Materials · doi:10.1002/adma.202008094 · Cited by 102
Wei, X., Zhang, L., Yang, Y., Hou, Y., Xu, Y., Wang, Z., Su, H., Han, F., Han, J., Liu, P., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110880 · Cited by 103
Fang, R., Jiang, Q., Jia, X., & Jiang, Z. (2023) · Immunity · doi:10.1016/j.immuni.2023.02.004 · Cited by 101
Molecular and Structural Basis of DNA Sensors in Antiviral Innate Immunity
Zahid, A., Ismail, H., Li, B., & Jin, T. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.613039 · Cited by 100
Tumor-infiltrating CD8+ T cell antitumor efficacy and exhaustion: molecular insights
Kumar, S., Singh, S. K., Rana, B., & Rana, A. (2021) · Drug Discovery Today · doi:10.1016/j.drudis.2021.01.002 · Cited by 101
The mechanism of STING autoinhibition and activation
Liu, S., Yang, B., Hou, Y., Cui, K., Yang, X., Li, X., Chen, L., Liu, S., Zhang, Z., Jia, Y., et al. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.03.029 · Cited by 102
Luthra, P., Aguirre, S., Yen, B. C., Pietzsch, C. A., Sánchez-Aparicio, M. T., Tigabu, B., Morlock, L., García‐Sastre, A., Leung, D. W., Williams, N. S., et al. (2017) · mBio · doi:10.1128/mbio.00368-17 · Cited by 101
TRIM13 Is a Negative Regulator of MDA5-Mediated Type I Interferon Production
Narayan, K., Waggoner, L., Pham, S. T., Hendricks, G. L., Waggoner, S. N., Conlon, J. E., Wang, J. P., Fitzgerald, K. A., & Kang, J. (2014) · Journal of Virology · doi:10.1128/jvi.02593-13 · Cited by 101
Multifaceted roles of TRIM38 in innate immune and inflammatory responses
Hu, M., & Shu, H. (2017) · Cellular and Molecular Immunology · doi:10.1038/cmi.2016.66 · Cited by 99
Regulating STING in health and disease
Li, Y., Wilson, H. L., & Kiss‐Toth, E. (2017) · Journal of Inflammation · doi:10.1186/s12950-017-0159-2 · Cited by 104
Hua, X., Li, B., Song, L., Hu, C., Li, X., Wang, D., Xiong, Y., Zhao, P., He, H., Xia, Q., et al. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra117.000194 · Cited by 101
Elion, D. L., & Cook, R. S. (2018) · Oncotarget · doi:10.18632/oncotarget.25626 · Cited by 99
STING Promotes Homeostasis via Regulation of Cell Proliferation and Chromosomal Stability
Rañoa, D. R. E., Widau, R. C., Mallon, S., Parekh, A. D., Nicolae, C. M., Huang, X., Bolt, M. J., Arina, A., Parry, R., Kron, S. J., et al. (2018) · Cancer Research · doi:10.1158/0008-5472.can-18-1972 · Cited by 103
A STING to inflammation and autoimmunity
Kumar, V. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.4mir1018-397rr · Cited by 100
Polycarbonate-based ultra-pH sensitive nanoparticles improve therapeutic window
Wang, X., Wilhelm, J., Li, W., Li, S., Wang, Z., Huang, G., Wang, J., Tang, H., Khorsandi, S., Sun, Z., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19651-7 · Cited by 99
Unraveling the Link Between Mitochondrial Dynamics and Neuroinflammation
de Oliveira, L. G., Angelo, Y. D. S., Iglesias, A. H., & Peron, J. P. S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.624919 · Cited by 100
Lipid Nanoparticle Spherical Nucleic Acids for Intracellular DNA and RNA Delivery
Sinegra, A. J., Evangelopoulos, M., Park, J., Huang, Z. N., & Mirkin, C. A. (2021) · Nano Letters · doi:10.1021/acs.nanolett.1c01973 · Cited by 100
Nucleic Acid Sensors and Type I Interferon Production in Systemic Lupus Erythematosus
Shrivastav, M., & Niewold, T. B. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00319 · Cited by 99
Zinzula, L., & Tramontano, E. (2013) · Antiviral Research · doi:10.1016/j.antiviral.2013.10.002 · Cited by 101
Innate Immune Signaling and Its Role in Metabolic and Cardiovascular Diseases
Xu, M. M., Liu, P. P., & Li, H. (2018) · Physiological Reviews · doi:10.1152/physrev.00065.2017 · Cited by 100
STING palmitoylation as a therapeutic target
Hansen, A. L., Mukai, K., Schopfer, F. J., Taguchi, T., & Holm, C. K. (2019) · Cellular and Molecular Immunology · doi:10.1038/s41423-019-0205-5 · Cited by 102
cGAS-STING pathway in oncogenesis and cancer therapeutics
Hoong, B. Y. D., Gan, Y., Liu, H., & Chen, E. S. (2020) · Oncotarget · doi:10.18632/oncotarget.27673 · Cited by 106
IRF3 activates RB to authorize cGAS-STING–induced senescence and mitigate liver fibrosis
Wu, Q., Leng, X., Zhang, Q., Zhu, Y., Zhou, R., Liu, Y., Chen, M., Zhang, D., Liu, S., Chen, S., et al. (2024) · Science Advances · doi:10.1126/sciadv.adj2102 · Cited by 101
The binding of TBK1 to STING requires exocytic membrane traffic from the ER
Ogawa, E., Mukai, K., Saito, K., Arai, H., & Taguchi, T. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.05.199 · Cited by 101
Jeon, S., Jeon, Y., Lim, J.-Y., Kim, Y., Cha, B., & Kim, W. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-02070-1 · Cited by 105
Impact of COVID-19 on Mitochondrial-Based Immunity in Aging and Age-Related Diseases
Ganji, R., & Reddy, P. H. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.614650 · Cited by 96
MITA/STING: A central and multifaceted mediator in innate immune response
Ran, Y., Shu, H., & Wang, Y. (2014) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2014.05.003 · Cited by 96
STING Signaling in Melanoma Cells Shapes Antigenicity and Can Promote Antitumor T-cell Activity
Falahat, R., Perez-Villarroel, P., Mailloux, A. W., Zhu, G., Pilon-Thomas, S., Barber, G. N., & Mulé, J. J. (2019) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-19-0229 · Cited by 95
Self-citationRAB11-mediated trafficking in host–pathogen interactions
Guichard, A., Nizet, V., & Bier, E. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3325 · Cited by 105
Sunthamala, N., Thierry, F., Teissier, S., Pientong, C., Kongyingyoes, B., Tangsiriwatthana, T., Sangkomkamhang, U. S., & Ekalaksananan, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091473 · Cited by 95
Exploration of Pattern Recognition Receptor Agonists as Candidate Adjuvants
Ong, G. H., Lian, B. S. X., Kawasaki, T., & Kawai, T. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.745016 · Cited by 100
Epigenetic state determines the in vivo efficacy of STING agonist therapy
Falahat, R., Berglund, A., Perez-Villarroel, P., Putney, R. M., Hamaidi, I., Kim, S., Pilon-Thomas, S., Barber, G. N., & Mulé, J. J. (2023) · Nature Communications · doi:10.1038/s41467-023-37217-1 · Cited by 94
Self-citationStempel, M., Chan, B., Lisnić, V. J., Krmpotić, A., Hartung, J., Paludan, S. R., Füllbrunn, N., Lemmermann, N. A. W., & Brinkmann, M. M. (2019) · The EMBO Journal · doi:10.15252/embj.2018100983 · Cited by 96
Acetylation-Dependent Deubiquitinase OTUD3 Controls MAVS Activation in Innate Antiviral Immunity
Zhang, Z., Fang, X., Wu, X., Li, L., Chu, F., Li, J., Wang, S., Zang, J., Zhang, B., Ye, S., et al. (2020) · Molecular Cell · doi:10.1016/j.molcel.2020.06.020 · Cited by 96
Innate immune sensing of lysosomal dysfunction drives multiple lysosomal storage disorders
Wang, A., Chen, C., Chen, M., Liu, S., Xiang, C., Fang, W., Zhang, F., Xu, Y., Chen, S., Zhang, Q., et al. (2024) · Nature Cell Biology · doi:10.1038/s41556-023-01339-x · Cited by 97
Mitochondria: commanders of innate immunity and disease?
Cloonan, S. M., & Choi, A. M. K. (2011) · Current Opinion in Immunology · doi:10.1016/j.coi.2011.11.001 · Cited by 95
Interfaces between cellular responses to DNA damage and cancer immunotherapyPreprint
Pilger, D., Seymour, L. W., & Jackson, S. P. (2021) · Genes & Development · doi:10.1101/gad.348314.121 · Cited by 96
Diner, B. A., Lum, K. K., Javitt, A., & Cristea, I. M. (2015) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m114.047068 · Cited by 93
The Trinity of cGAS, TLR9, and ALRs Guardians of the Cellular Galaxy Against Host-Derived Self-DNA
Kumar, V. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.624597 · Cited by 95
Polymeric STING Pro‐agonists for Tumor‐Specific Sonodynamic Immunotherapy
Yu, J., He, S., Zhang, C., Xu, C., Huang, J., Xu, M., & Pu, K. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202307272 · Cited by 93
Kemmoku, H., Takahashi, K., Mukai, K., Mori, T., Hirosawa, K. M., Kiku, F., Uchida, Y., Kuchitsu, Y., Nishioka, Y., Sawa, M., et al. (2024) · Nature Communications · doi:10.1038/s41467-023-44317-5 · Cited by 95
TRIM59 interacts with ECSIT and negatively regulates NF-κB and IRF-3/7-mediated signal pathways
Kondo, T., Watanabe, M., & Hatakeyama, S. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.05.028 · Cited by 94
Chicken STING Mediates Activation of the IFN Gene Independently of the RIG-I Gene
Cheng, Y., Sun, Y., Wang, H., Yan, Y., Ding, C., & Sun, J. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1500638 · Cited by 93
Prantner, D., Perkins, D. J., & Vogel, S. N. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.763268 · Cited by 95
Innate Immune Responses to Avian Influenza Viruses in Ducks and Chickens
Evseev, D., & Magor, K. E. (2019) · Veterinary Sciences · doi:10.3390/vetsci6010005 · Cited by 97
The functional interactome of PYHIN immune regulators reveals IFIX is a sensor of viral DNA
Diner, B. A., Li, T., Greco, T. M., Crow, M. S., Fuesler, J., Wang, J. P., & Cristea, I. M. (2015) · Molecular Systems Biology · doi:10.15252/msb.20145808 · Cited by 95
Identification of α‐Mangostin as an Agonist of Human STING
Zhang, Y., Sun, Z., Pei, J., Luo, Q., Zeng, X. Y., Li, Q., Yang, Z., & Quan, J. (2018) · ChemMedChem · doi:10.1002/cmdc.201800481 · Cited by 92
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
Huang, L., Xu, W., Liu, H., Xue, M., Liu, X., Zhang, K., Hu, L., Li, J., Liu, X., Xiang, Z., et al. (2021) · The Journal of Immunology · doi:10.4049/jimmunol.2100320 · Cited by 91
Ran, Y., Li, D., Xiong, M.-G., Liu, H., Feng, T., Shi, Z., Li, Y., Wu, H.-N., Wang, S., Zheng, H., et al. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010270 · Cited by 91
cGAS-STING pathway as a potential trigger of immunosenescence and inflammaging
Schmitz, C. R. R., Maurmann, R. M., Guma, F. T. C. R., Bauer, M. E., & Barbé‐Tuana, F. M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1132653 · Cited by 95
STING agonist-based ER-targeting molecules boost antigen cross-presentation
Wang, X., Huang, Z., Xing, L., Shang, L., Jiang, J., Deng, C., Yu, W., Peng, L., Yang, H., Zheng, X., et al. (2025) · Nature · doi:10.1038/s41586-025-08758-w · Cited by 99
Dynamic Structural Differences between Human and Mouse STING Lead to Differing Sensitivity to DMXAA
Shih, A. Y., Damm‐Ganamet, K. L., & Mirzadegan, T. (2018) · Biophysical Journal · doi:10.1016/j.bpj.2017.10.027 · Cited by 93
Evasion of the STING DNA-Sensing Pathway by VP11/12 of Herpes Simplex Virus 1
Deschamps, T., & Kalamvoki, M. (2017) · Journal of Virology · doi:10.1128/jvi.00535-17 · Cited by 90
Sun, M., Zhang, J., Jiang, L., Pan, Y.-X., Tan, J.-Y., Yu, F., Guo, L., Yin, L., Shen, C., Shu, H., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.11.048 · Cited by 92
Targeting STING oligomerization with small-molecule inhibitors
Humphries, F., Shmuel-Galia, L., Jiang, Z., Zhou, J. Y., Barasa, L., Mondal, S., Wilson, R., Sultana, N., Shaffer, S. A., Ng, S., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2305420120 · Cited by 91
Message in a bottle: lessons learned from antagonism of STING signalling during RNA virus infection
Maringer, K., & Fernández-Sesma, A. (2014) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2014.08.004 · Cited by 90
Metadata
- Authors
- Ishikawa, H., & Barber, G. N.
- Affiliations
- University of Miami (US)
- Corresponding author
- Barber, Glen N.
- Venue
- Nature
- Published
- 2008-08-24
- Volume
- 455
- Issue
- 7213
- Pages
- 674-678
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC2804933
- OpenAlex
- W2060004514
- Semantic Scholar
- cd831bfb6fd9847baedbe5161ddd21d405728bee
- Cited by
- 3,576
- References
- 29
- Citations by year
- 2026: 310 · 2025: 394 · 2024: 359 · 2023: 332 · 2022: 322 · 2021: 315 · 2020: 270 · 2019: 195 · 2018: 163 · 2017: 161 · 2016: 115 · 2015: 118 · 2014: 112 · 2013: 123 · 2012: 83
- FWCI
- 28.23
- Type
- journal article
- Language
- en
- Update notices
- erratum (2008-11-13)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (R01AI079336)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Endoplasmic Reticulum Stress and Disease
- Keywords
- STING, endoplasmic reticulum, innate immunity, interferon-beta, IRF3, NF-κB, RIG-I, Sec61β, translocon, TRAP complex, vesicular stomatitis virus, herpesvirus, negative-strand RNA viruses, viral DNA sensing, antiviral defense, protein translocation, pattern recognition receptors
- MeSH terms
- STING Protein, Animals, Cell Line, Endoplasmic Reticulum, Fibroblasts, Humans, Immunity, Innate, Interferons, Membrane Proteins, Mice, Inbred C57BL, Signal Transduction, Mice, Knockout, Mice
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