Immune Signaling by RIG-I-like Receptors
Open accessAbstract
The RIG-I-like receptors (RLRs) RIG-I, MDA5, and LGP2 play a major role in pathogen sensing of RNA virus infection to initiate and modulate antiviral immunity. The RLRs detect viral RNA ligands or processed self RNA in the cytoplasm to trigger innate immunity and inflammation and to impart gene expression that serves to control infection. Importantly, RLRs cooperate in signaling crosstalk networks with Toll-like receptors and other factors to impart innate immunity and to modulate the adaptive immune response. RLR regulation occurs at a variety of levels ranging from autoregulation to ligand and cofactor interactions and posttranslational modifications. Abberant RLR signaling or dysregulation of RLR expression is now implicated in the development of autoimmune diseases. Understanding the processes of RLR signaling and response will provide insights to guide RLR-targeted therapeutics for antiviral and immune-modifying applications.
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
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?
Through phosphorylation of the autophagy receptors OPTN, SQSTM1, and CALCOCO2/NDP52, TBK1 regulates macroautophagy, xenophagy and mitophagy.
“Through its phosphorylation of the autophagy receptors OPTN, SQSTM1, and CALCOCO2/NDP52 (calcium binding and coiled-coil domain 2) [58,59,194], TBK1 regulates several aspects of autophagy, including macroautophagy, xenophagy and mitophagy [59,90,148,194–196].”
From Autophagy and ALS: mechanistic insights and therapeutic implications (2022) · cites this paper as [195]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Lysine acetylation targets protein complexes and co-regulates major cellular functions
Choudhary, C., Kumar, C., Gnad, F., Nielsen, M. L., Rehman, M., Walther, T. C., Olsen, J. V., & Mann, M. (2009) · Science · doi:10.1126/science.1175371 · Cited by 4,040 · see citing works
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 3,935 · see citing works
HOW CELLS RESPOND TO INTERFERONS
Stark, G. R., Kerr, I. M., Williams, B. R. G., Silverman, R. H., & Schreiber, R. D. (1998) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.67.1.227 · Cited by 3,932 · see citing works
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 · see citing works
STING is an endoplasmic reticulum adaptor that facilitates innate immune signalling
Ishikawa, H., & Barber, G. N. (2008) · Nature · doi:10.1038/nature07317 · Cited by 3,576 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
NATURAL KILLER CELLS IN ANTIVIRAL DEFENSE: Function and Regulation by Innate Cytokines
Biron, C. A., Nguyen, K. B., Pien, G. C., Cousens, L. P., & Salazar‐Mather, T. P. (1999) · Annual Review of Immunology · doi:10.1146/annurev.immunol.17.1.189 · Cited by 2,110 · see citing works
IFN-λs mediate antiviral protection through a distinct class II cytokine receptor complex
Kotenko, S. V., Gallagher, G. E., Baurin, V. V., Lewis-Antes, A., Shen, M., Shah, N. K., Langer, J. A., Sheikh, F. G., Dickensheets, H. L., & Donnelly, R. P. (2002) · Nature Immunology · doi:10.1038/ni875 · Cited by 1,867 · see citing works
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 · see citing works
Yoneyama, M., Kikuchi, M., Matsumoto, K., Imaizumi, T., Miyagishi, M., Taira, K., Foy, E. M., Loo, Y., Gale, M., Akira, S., et al. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.5.2851 · Cited by 1,691 · see citing works
Self-citationTRIM25 RING-finger E3 ubiquitin ligase is essential for RIG-I-mediated antiviral activity
Gack, M. U., Shin, Y. C., Joo, C.-H., Urano, T., Liang, C., Sun, L., Takeuchi, O., Akira, S., Chen, Z. J., Inoue, S., et al. (2007) · Nature · doi:10.1038/nature05732 · Cited by 1,683 · see citing works
The roles of TLRs, RLRs and NLRs in pathogen recognition
Kawai, T., & Akira, S. (2009) · International Immunology · doi:10.1093/intimm/dxp017 · Cited by 1,666 · see citing works
Kato, H., Takeuchi, O., Mikamo, E., Hirai, R., Kawai, T., Matsushita, K., Hiiragi, A., Dermody, T. S., Fujita, T., & Akira, S. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20080091 · Cited by 1,590 · see citing works
IL-28, IL-29 and their class II cytokine receptor IL-28R
Sheppard, P. O., Kindsvogel, W., Xu, W., Henderson, K., Schlutsmeyer, S., Whitmore, T. E., Kuestner, R. E., Garrigues, U., Birks, C., Roraback, J., et al. (2002) · Nature Immunology · doi:10.1038/ni873 · Cited by 1,563 · see citing works
The Adaptor Protein MITA Links Virus-Sensing Receptors to IRF3 Transcription Factor Activation
Zhong, B., Yang, Y., Li, S., Wang, Y., Li, Y., Diao, F., Lei, C., He, X., Zhang, L., Tien, P., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.09.003 · Cited by 1,513 · see citing works
Cell Type-Specific Involvement of RIG-I in Antiviral Response
Kato, H., Sato, S., Yoneyama, M., Yamamoto, M., Uematsu, S., Matsui, K., Tsujimura, T., Takeda, K., Fujita, T., Takeuchi, O., et al. (2005) · Immunity · doi:10.1016/j.immuni.2005.04.010 · Cited by 1,368 · see citing works
RNA Polymerase III Detects Cytosolic DNA and Induces Type I Interferons through the RIG-I Pathway
Chiu, Y., MacMillan, J. B., & Chen, Z. J. (2009) · Cell · doi:10.1016/j.cell.2009.06.015 · Cited by 1,185 · see citing works
Gitlin, L., Barchet, W., Gilfillan, S., Cella, M., Beutler, B., Flavell, R. A., Diamond, M., & Colonna, M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0603082103 · Cited by 1,156 · see citing works
Toll-like receptor 3 mediates West Nile virus entry into the brain causing lethal encephalitis
Wang, T., Town, T., Alexopoulou, L., Anderson, J. F., Fikrig, E., & Flavell, R. A. (2004) · Nature Medicine · doi:10.1038/nm1140 · Cited by 1,142 · see citing works
I nterleukin -10 and R elated C ytokines and R eceptors
Pestka, S., Krause, C. D., Sarkar, D., Walter, M. R., Shi, Y., & Fisher, P. B. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104622 · Cited by 1,097 · see citing works
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 · see citing works
Self-citationJego, G., Palucka, A. K., Blanck, J.-P., Chalouni, C., Pascual, V., & Banchereau, J. (2003) · Immunity · doi:10.1016/s1074-7613(03)00208-5 · Cited by 1,067 · see citing works
Marié, I., Durbin, J. E., & Levy, D. E. (1998) · The EMBO Journal · doi:10.1093/emboj/17.22.6660 · Cited by 1,049 · see citing works
Bon, A. L., Schiavoni, G., D’Agostino, G., Gresser, I., Belardelli, F., & Tough, D. F. (2001) · Immunity · doi:10.1016/s1074-7613(01)00126-1 · Cited by 973 · see citing works
Kolumam, G. A., Thomas, S., Thompson, L. J., Sprent, J., & Murali‐Krishna, K. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20050821 · Cited by 967 · see citing works
Specificity in Toll-like receptor signalling through distinct effector functions of TRAF3 and TRAF6
Häcker, H., Redecke, V., Blagoev, B., Kratchmarova, I., Hsu, L.-C., Wang, G. G., Kamps, M. P., Raz, E., Wagner, H., Häcker, G. A., et al. (2005) · Nature · doi:10.1038/nature04369 · Cited by 962 · see citing works
Nejentsev, S., Walker, N., Riches, D., Egholm, M., & Todd, J. A. (2009) · Science · doi:10.1126/science.1167728 · Cited by 958 · see citing works
Sumpter, R., Loo, Y., Foy, E. M., Li, K., Yoneyama, M., Fujita, T., Lemon, S. M., & Gale, M. (2005) · Journal of Virology · doi:10.1128/jvi.79.5.2689-2699.2005 · Cited by 900 · see citing works
Self-citationAblasser, A., Bauernfeind, F. G., Hartmann, G., Latz, E., Fitzgerald, K. A., & Hornung, V. (2009) · Nature Immunology · doi:10.1038/ni.1779 · Cited by 892 · see citing works
Critical role of TRAF3 in the Toll-like receptor-dependent and -independent antiviral response
Oganesyan, G., Saha, S. K., Guo, B., He, J. Q., Shahangian, A., Zarnegar, B. J., Perry, A. K., & Cheng, G. (2005) · Nature · doi:10.1038/nature04374 · Cited by 881 · see citing works
Peroxisomes are signaling platforms for antiviral innate immunity
Dixit, E., Boulant, S., Zhang, Y.-J., Lee, A. S., Odendall, C., Shum, B. O. V., Hacohen, N., Chen, Z.-J. J., Whelan, S. P. J., Fransen, M., et al. (2010) · Cell · doi:10.1016/j.cell.2010.04.018 · Cited by 848 · see citing works
Schlee, M., Roth, A. H. F. J., Hornung, V., Hagmann, C. A., Wimmenauer, V., Barchet, W., Coch, C., Janke, M., Mihailovic, A., Wardle, G. S., et al. (2009) · Immunity · doi:10.1016/j.immuni.2009.05.008 · Cited by 792 · see citing works
Type I Interferons Keep Activated T Cells Alive
Marrack, P., Kappler, J. W., & Mitchell, T. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.189.3.521 · Cited by 763 · see citing works
Sato, S., Hirakata, M., Kuwana, M., Suwa, A., Inada, S., Mimori, T., Nishikawa, T., Oddis, C. V., & Ikeda, Y. (2005) · Arthritis & Rheumatism · doi:10.1002/art.21023 · Cited by 748 · see citing works
Innate immunity induced by composition-dependent RIG-I recognition of hepatitis C virus RNA
Saito, T., Owen, D. M., Jiang, F., Marcotrigiano, J., & Gale, M. (2008) · Nature · doi:10.1038/nature07106 · Cited by 745 · see citing works
Self-citationRegulation of innate antiviral defenses through a shared repressor domain in RIG-I and LGP2
Saito, T., Hirai, R., Loo, Y., Owen, D. M., Johnson, C., Sinha, S. C., Akira, S., Fujita, T., & Gale, M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606699104 · Cited by 743 · see citing works
Self-citationLGP2 is a positive regulator of RIG-I– and MDA5-mediated antiviral responses
Satoh, T., Kato, H., Kumagai, Y., Yoneyama, M., Sato, S., Matsushita, K., Tsujimura, T., Fujita, T., Akira, S., & Takeuchi, O. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912986107 · Cited by 697 · see citing works
Smyth, D. J., Cooper, J. D., Bailey, R., Field, S., Burren, O. S., Smink, L. J., Guja, C., Ionescu-Tirgoviste, C., Widmer, B., Dunger, D. B., et al. (2006) · Nature Genetics · doi:10.1038/ng1800 · Cited by 688 · see citing works
Small self-RNA generated by RNase L amplifies antiviral innate immunity
Malathi, K., Dong, B., Gale, M., & Silverman, R. H. (2007) · Nature · doi:10.1038/nature06042 · Cited by 636 · see citing works
Self-citationCurtsinger, J., Valenzuela, J. O., Agarwal, P., Lins, D. C., & Mescher, M. F. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.8.4465 · Cited by 633 · see citing works
Zeng, W., Sun, L., Jiang, X., Chen, X., Hou, F., Adhikari, A., Xu, M., & Chen, Z. J. (2010) · Cell · doi:10.1016/j.cell.2010.03.029 · Cited by 613 · see citing works
Sato, S., Hoshino, K., Satoh, T., Fujita, T., Kawakami, Y., Fujita, T., & Kuwana, M. (2009) · Arthritis & Rheumatism · doi:10.1002/art.24621 · Cited by 601 · see citing works
Ank, N., West, H., Bartholdy, C., Eriksson, K., Thomsen, A. R., & Paludan, S. R. (2006) · Journal of Virology · doi:10.1128/jvi.80.9.4501-4509.2006 · Cited by 598 · see citing works
NLRX1 is a regulator of mitochondrial antiviral immunity
Moore, C. B., Bergstralh, D. T., Duncan, J. A., Lei, Y. L., Morrison, T. E., Zimmermann, A. G., Accavitti-Loper, M. A., Madden, V. J., Sun, L., Ye, Z., et al. (2008) · Nature · doi:10.1038/nature06501 · Cited by 586 · see citing works
Dotta, F., Censini, S., van Halteren, A. G. S., Marselli, L., Masini, M., Dionisi, S., Mosca, F., Boggi, U., Muda, A. O., Prato, S. D., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700442104 · Cited by 569 · see citing works
The Atg5–Atg12 conjugate associates with innate antiviral immune responses
Jounai, N., Takeshita, F., Kobiyama, K., Sakaue-Sawano, A., Miyawaki, A., Xin, K.-Q., Ishii, K. J., Kawai, T., Akira, S., Suzuki, K., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704014104 · Cited by 562 · see citing works
Positive feedback regulation of type I IFN genes by the IFN‐inducible transcription factor IRF‐7
Sato, M., Hata, N., Asagiri, M., Nakaya, T., Taniguchi, T., & Tanaka, N. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)01514-2 · Cited by 553 · see citing works
Poeck, H., Bscheider, M., Groß, O., Finger, K., Roth, S., Rebsamen, M., Hannesschläger, N., Schlee, M., Rothenfußer, S., Barchet, W., et al. (2009) · Nature Immunology · doi:10.1038/ni.1824 · Cited by 518 · see citing works
Essential role of IPS-1 in innate immune responses against RNA viruses
Kumar, H., Kawai, T., Kato, H., Sato, S., Takahashi, K., Coban, C., Yamamoto, M., Uematsu, S., Ishii, K. J., Takeuchi, O., et al. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20060792 · Cited by 503 · see citing works
The C-Terminal Regulatory Domain Is the RNA 5′-Triphosphate Sensor of RIG-I
Cui, S., Eisenächer, K., Kirchhofer, A., Brzózka, K. D., Lammens, A., Lammens, K., Fujita, T., Conzelmann, K., Krug, A., & Hopfner, K. (2008) · Molecular Cell · doi:10.1016/j.molcel.2007.10.032 · Cited by 495 · see citing works
Coccia, E. M., Severa, M., Giacomini, E., Monneron, D., Remoli, M. E., Julkunen, I., Cella, M., Lande, R., & Uzé, G. (2004) · European Journal of Immunology · doi:10.1002/eji.200324610 · Cited by 489 · see citing works
Negative regulation of the RIG-I signaling by the ubiquitin ligase RNF125
Arimoto, K., Takahashi, H., Hishiki, T., Konishi, H., Fujita, T., & Shimotohno, K. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611551104 · Cited by 472 · see citing works
Activation of MDA5 Requires Higher-Order RNA Structures Generated during Virus Infection
Pichlmair, A., Schulz, O., Tan, C.-P., Rehwinkel, J., Kato, H., Takeuchi, O., Akira, S., Way, M., Schiavo, G., & Sousa, C. R. E. (2009) · Journal of Virology · doi:10.1128/jvi.00770-09 · Cited by 469 · see citing works
A Deubiquitinase That Regulates Type I Interferon Production
Kayagaki, N., Phung, Q. T., Chan, S. B., Chaudhari, R., Quan, C., O’Rourke, K. M., Eby, M. T., Pietras, E. M., Cheng, G., Bazán, J. F., et al. (2007) · Science · doi:10.1126/science.1145918 · Cited by 452 · see citing works
NLRC5 Negatively Regulates the NF-κB and Type I Interferon Signaling Pathways
Cui, J., Zhu, L., Xia, X., Wang, H. Y., Legras, X. D., Hong, J. K., Ji, J., Shen, P., Zheng, S. S., Chen, Z. J., et al. (2010) · Cell · doi:10.1016/j.cell.2010.03.040 · Cited by 449 · see citing works
Interferon-Lambda: A New Addition to an Old Family
Donnelly, R. P., & Kotenko, S. V. (2010) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2010.0078 · Cited by 427 · see citing works
Baum, A., Sachidanandam, R., & García‐Sastre, A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005077107 · Cited by 424 · see citing works
Loss of DExD/H Box RNA Helicase LGP2 Manifests Disparate Antiviral Responses
Venkataraman, T., Valdes, M., Elsby, R., Kakuta, S., Cáceres, G., Saijo, S., Iwakura, Y., & Barber, G. N. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.10.6444 · Cited by 400 · see citing works
Richardson, S. J., Willcox, A., Bone, A. J., Foulis, A. K., & Morgan, N. G. (2009) · Diabetologia · doi:10.1007/s00125-009-1276-0 · Cited by 384 · see citing works
Marques, J. T., Devosse, T., Wang, D., Zamanian-Daryoush, M., Serbinowski, P., Hartmann, R., Fujita, T., Behlke, M. A., & Williams, B. R. G. (2006) · Nature Biotechnology · doi:10.1038/nbt1205 · Cited by 380 · see citing works
Toll-Like Receptor 3 Has a Protective Role against West Nile Virus Infection
Daffis, S., Samuel, M. A., Suthar, M. S., Gale, M., & Diamond, M. (2008) · Journal of Virology · doi:10.1128/jvi.00935-08 · Cited by 359 · see citing works
Self-citationViral Infections Activate Types I and III Interferon Genes through a Common Mechanism
Onoguchi, K., Yoneyama, M., Takemura, A., Akira, S., Taniguchi, T., Namiki, H., & Fujita, T. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m608618200 · Cited by 354 · see citing works
Oshiumi, H., Matsumoto, M., Hatakeyama, S., & Seya, T. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m804259200 · Cited by 353 · see citing works
The tumour suppressor CYLD is a negative regulator of RIG‐I‐mediated antiviral response
Friedman, C. S., O’Donnell, M. A., Legarda, D., Ng, A., Cardenas, W. B., Yount, J. S., Moran, T. M., Basler, C. F., Komuro, A., Horvath, C. M., et al. (2008) · EMBO Reports · doi:10.1038/embor.2008.136 · Cited by 334 · see citing works
Nakashima, R., Imura, Y., Kobayashi, S., Yukawa, N., Yoshifuji, H., Nojima, T., Kawabata, D., Ohmura, K., Usui, T., Fujii, T., et al. (2009) · Lara D. Veeken · doi:10.1093/rheumatology/kep375 · Cited by 334 · see citing works
Habjan, M., Andersson, I., Klingström, J., Schümann, M., Arnold, M., Zimmermann, P., Wagner, V., Pichlmair, A., Schneider, U., Mühlberger, E., et al. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002032 · Cited by 331 · see citing works
Fredericksen, B. L., Keller, B. C., Fornek, J. L., Katze, M. G., & Gale, M. (2007) · Journal of Virology · doi:10.1128/jvi.01305-07 · Cited by 328 · see citing works
Self-citationGono, T., Kawaguchi, Y., Satoh, T., Kuwana, M., Katsumata, Y., Takagi, K., Masuda, I., Tochimoto, A., Baba, S., Okamoto, Y., et al. (2010) · Lara D. Veeken · doi:10.1093/rheumatology/keq149 · Cited by 319 · see citing works
The NEMO adaptor bridges the nuclear factor-κB and interferon regulatory factor signaling pathways
Zhao, T., Yang, L., Sun, Q., Arguello, M., Ballard, D. W., Hiscott, J. B., & Lin, R. (2007) · Nature Immunology · doi:10.1038/ni1465 · Cited by 317 · see citing works
Mitochondrial dynamics regulate the RIG-I-like receptor antiviral pathway
Castanier, C., Garcin, D., Vazquez, A., & Arnoult, D. (2010) · The EMBO Reports · doi:10.1038/embor.2009.258 · Cited by 316 · see citing works
EB virus‐encoded RNAs are recognized by RIG‐I and activate signaling to induce type I IFN
Samanta, M., Iwakiri, D., Kanda, T., Imaizumi, T., & Takada, K. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601314 · Cited by 313 · see citing works
Koyama, S., Ishii, K. J., Kumar, H., Tanimoto, T., Coban, C., Uematsu, S., Kawai, T., & Akira, S. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.7.4711 · Cited by 309 · see citing works
TRADD Protein Is an Essential Component of the RIG-like Helicase Antiviral Pathway
Michallet, M., Meylan, E., Ermolaeva, M., Vázquez, J., Rebsamen, M., Curran, J. A., Poeck, H., Bscheider, M., Hartmann, G., König, M. F., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.03.013 · Cited by 304 · see citing works
Ylipaasto, P., Klingel, K., Lindberg, A., Otonkoski, T., Kandolf, R., Hovi, T., & Roivainen, M. (2004) · Diabetologia · doi:10.1007/s00125-003-1297-z · Cited by 294 · see citing works
Type I interferons: crucial participants in disease amplification in autoimmunity
Hall, J. C., & Rosen, A. (2010) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2009.237 · Cited by 266 · see citing works
Oshiumi, H., Miyashita, M., Inoue, N., Okabe, M., Matsumoto, M., & Seya, T. (2010) · Cell Host & Microbe · doi:10.1016/j.chom.2010.11.008 · Cited by 264 · see citing works
Gack, M. U., Kirchhofer, A., Shin, Y. C., Inn, K., Liang, C., Cui, S., Myong, S., Ha, T., Hopfner, K., & Jung, J. U. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804947105 · Cited by 258 · see citing works
Mitochondrial Membrane Potential Is Required for MAVS-Mediated Antiviral Signaling
Koshiba, T., Yasukawa, K., Yanagi, Y., & Kawabata, S.-I. (2011) · Science Signaling · doi:10.1126/scisignal.2001147 · Cited by 257 · see citing works
Panne, D. (2008) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2007.12.002 · Cited by 257 · see citing works
Mitofusin 2 Inhibits Mitochondrial Antiviral Signaling
Yasukawa, K., Oshiumi, H., Takeda, M., Ishihara, N., Yanagi, Y., Seya, T., Kawabata, S.-I., & Koshiba, T. (2009) · Science Signaling · doi:10.1126/scisignal.2000287 · Cited by 255 · see citing works
Kim, M.-J., Hwang, S., Imaizumi, T., & Yoo, J.-Y. (2007) · Journal of Virology · doi:10.1128/jvi.01650-07 · Cited by 239 · see citing works
The Structural Basis of 5′ Triphosphate Double-Stranded RNA Recognition by RIG-I C-Terminal Domain
Lu, C. C., Xu, H., Ranjith-Kumar, C. T., Brooks, M. T., Hou, T. Y., Hu, F., Herr, A. B., Strong, R. K., Kao, C. C., & Li, P. (2010) · Structure · doi:10.1016/j.str.2010.05.007 · Cited by 233 · see citing works
MDA-5 Recognition of a Murine Norovirus
McCartney, S. A., Thackray, L. B., Gitlin, L., Gilfillan, S., Virgin, H. W., & Colonna, M. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.1000108 · Cited by 229 · see citing works
Roth-Cross, J. K., Bender, S. J., & Weiss, S. R. (2008) · Journal of Virology · doi:10.1128/jvi.01199-08 · Cited by 228 · see citing works
IPS-1 Is Essential for the Control of West Nile Virus Infection and Immunity
Suthar, M. S., Ma, D. Y., Thomas, S., Lund, J. M., Zhang, N., Daffis, S., Rudensky, A. Y., Bevan, M. J., Clark, E. A., Murali‐Krishna, K., et al. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000757 · Cited by 224 · see citing works
Self-citationModulation of the Interferon Antiviral Response by the TBK1/IKKi Adaptor Protein TANK
Guo, B., & Cheng, G. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m700017200 · Cited by 221 · see citing works
Town, T., Bai, F., Wang, T., Kaplan, A. T., Qian, F., Montgomery, R. R., Anderson, J. F., Flavell, R. A., & Fikrig, E. (2009) · Immunity · doi:10.1016/j.immuni.2008.11.012 · Cited by 217 · see citing works
Lin, R., Lacoste, J., Nakhaei, P., Sun, Q., Yang, L., Paz, S., Wilkinson, P. A., Julkunen, I., Vitour, D., MEURS, E. F., et al. (2006) · Journal of Virology · doi:10.1128/jvi.02495-05 · Cited by 216 · see citing works
Lin, R., Yang, L., Nakhaei, P., Sun, Q., Sharif‐Askari, E., Julkunen, I., & Hiscott, J. B. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m510326200 · Cited by 215 · see citing works
Ryzhakov, G., & Randow, F. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601743 · Cited by 196 · see citing works
Kang, D., Gopalkrishnan, R. V., Lin, L., Randolph, A. L., Valerie, K. C., Pestka, S., & Fisher, P. B. (2003) · Oncogene · doi:10.1038/sj.onc.1207300 · Cited by 196 · see citing works
Solution Structures of Cytosolic RNA Sensor MDA5 and LGP2 C-terminal Domains
Takahasi, K., Kumeta, H., Tsuduki, N., Narita, R., Shigemoto, T., Hirai, R., Yoneyama, M., Horiuchi, M., Ogura, K., Fujita, T., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.007179 · Cited by 196 · see citing works
Fredericksen, B. L., & Gale, M. (2006) · Journal of Virology · doi:10.1128/jvi.80.6.2913-2923.2006 · Cited by 194 · see citing works
Self-citationMonroe, K. M., McWhirter, S. M., & Vance, R. E. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000665 · Cited by 190 · see citing works
Plumet, S., Herschke, F., Bourhis, J., Valentin, H., Longhi, S., & Gerlier, D. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000279 · Cited by 185 · see citing works
Österlund, P., Veckman, V., Sirén, J., Klucher, K. M., Hiscott, J. B., Matikainen, S., & Julkunen, I. (2005) · Journal of Virology · doi:10.1128/jvi.79.15.9608-9617.2005 · Cited by 183 · see citing works
Onoguchi, K., Onomoto, K., Takamatsu, S., Jogi, M., Takemura, A., Morimoto, S., Julkunen, I., Namiki, H., Yoneyama, M., & Fujita, T. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001012 · Cited by 180 · see citing works
Li, S., Zheng, H., Mao, A., Zhong, B., Li, Y., Liu, Y., Gao, Y., Ran, Y., Tien, P., & Shu, H. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.074971 · Cited by 179 · see citing works
Dysregulation of TLR3 Impairs the Innate Immune Response to West Nile Virus in the Elderly
Kong, K., Delroux, K., Wang, X., Qian, F., Arjona, A., Malawista, S. E., Fikrig, E., & Montgomery, R. R. (2008) · Journal of Virology · doi:10.1128/jvi.00618-08 · Cited by 179 · see citing works
Kubota, T., Matsuoka, M., Chang, T.-H., Tailor, P. B., Sasaki, T., Tashiro, M., Kato, A., & Ozato, K. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m804479200 · Cited by 174 · see citing works
Nakhaei, P., Mésplède, T., Solis, M., Sun, Q., Zhao, T., Yang, L., Chuang, T., Ware, C. F., Lin, R., & Hiscott, J. B. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000650 · Cited by 173 · see citing works
Tom70 mediates activation of interferon regulatory factor 3 on mitochondria
Liu, X.-Y., Wei, B., Shi, H.-X., Shan, Y.-F., & Wang, C. (2010) · Cell Research · doi:10.1038/cr.2010.103 · Cited by 171 · see citing works
The regulatory domain of the RIG-I family ATPase LGP2 senses double-stranded RNA
Pippig, D. A., Hellmuth, J. C., Cui, S., Kirchhofer, A., Lammens, K., Lammens, A., Schmidt, A., Rothenfußer, S., & Hopfner, K. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp059 · Cited by 167 · see citing works
The RIG-I-like Receptor LGP2 Recognizes the Termini of Double-stranded RNA
Li, X., Ranjith-Kumar, C. T., Brooks, M. T., Dharmaiah, S., Herr, A. B., Kao, C. C., & Li, P. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m900818200 · Cited by 167 · see citing works
Bamming, D., & Horvath, C. M. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m807365200 · Cited by 164 · see citing works
Identification of Loss of Function Mutations in Human Genes Encoding RIG-I and MDA5
Shigemoto, T., Kageyama, M., Hirai, R., Zheng, J., Yoneyama, M., & Fujita, T. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m809449200 · Cited by 161 · see citing works
Liu, S., Wang, H., Jin, Y., Podolsky, R. H., Reddy, M. P. L., Pedersen, J. V., Bode, B. W., Reed, J., Steed, D., Anderson, S. W., et al. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn342 · Cited by 160 · see citing works
SIKE is an IKKε/TBK1‐associated suppressor of TLR3‐ and virus‐triggered IRF‐3 activation pathways
Huang, J., Liu, T., Xu, L., Chen, D., Zhai, Z., & Shu, H. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600863 · Cited by 155 · see citing works
Nucleotide Sequences and Modifications That Determine RIG-I/RNA Binding and Signaling Activities
Uzri, D., & Gehrke, L. (2009) · Journal of Virology · doi:10.1128/jvi.02449-08 · Cited by 155 · see citing works
Regulation of the innate immune response by threonine-phosphatase of Eyes absent
Okabe, Y., Sano, T., & Nagata, S. (2009) · Nature · doi:10.1038/nature08138 · Cited by 154 · see citing works
Bhoj, V. G., Sun, Q., Bhoj, E. J. K., Somers, C., Chen, X., Torres, J. P., Mejías, A., Gomez, A. M., Jafri, H. S., Ramilo, O., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804717105 · Cited by 150 · see citing works
Szretter, K. J., Samuel, M. A., Gilfillan, S., Fuchs, A. G., Colonna, M., & Diamond, M. S. (2009) · Journal of Virology · doi:10.1128/jvi.00836-09 · Cited by 149 · see citing works
Paz, S., Vilasco, M., Werden, S. J., Arguello, M., Joseph-Pillai, D., Zhao, T., Nguyên, T. L.-A., Sun, Q., MEURS, E. F., Lin, R., et al. (2011) · Cell Research · doi:10.1038/cr.2011.2 · Cited by 148 · see citing works
REUL Is a Novel E3 Ubiquitin Ligase and Stimulator of Retinoic-Acid-Inducible Gene-I
Gao, D., Yang, Y., Wang, R., Zhou, X., Diao, F., Li, M., Zhai, Z., Jiang, Z., & Chen, D. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005760 · Cited by 141 · see citing works
Sasai, M., Shingai, M., Funami, K., Yoneyama, M., Fujita, T., Matsumoto, M., & Seya, T. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.12.8676 · Cited by 138 · see citing works
Zhou, S., Cerny, A., Zacharia, A., Fitzgerald, K. A., Kurt‐Jones, E. A., & Finberg, R. W. (2010) · Journal of Virology · doi:10.1128/jvi.00155-10 · Cited by 138 · see citing works
RNase L releases a small RNA from HCV RNA that refolds into a potent PAMP
Malathi, K., Saito, T., Crochet, N., Barton, D. J., Gale, M., & Silverman, R. H. (2010) · RNA · doi:10.1261/rna.2244210 · Cited by 136 · see citing works
Self-citationDaffis, S., Suthar, M. S., Szretter, K. J., Gale, M., & Diamond, M. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000607 · Cited by 133 · see citing works
Self-citationRegulation of IκB Kinase-related Kinases and Antiviral Responses by Tumor Suppressor CYLD
Zhang, M., Wu, X., Lee, A. J., Jin, W., Chang, M., Wright, A., Imaizumi, T., & Sun, S. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m801451200 · Cited by 131 · see citing works
A Human Type 1 Diabetes Susceptibility Locus Maps to Chromosome 21q22.3
CONCANNON, P. J., Önengüt-Gümüşcü, S., Todd, J. A., Smyth, D. J., Pociot, F., Bergholdt, R., Akolkar, B., Erlich, H. A., Hilner, J. E., Julier, C., et al. (2008) · Diabetes · doi:10.2337/db08-0753 · Cited by 130 · see citing works
Diao, F., Li, S., Tian, Y., Zhang, M., Xu, L., Zhang, Y., Wang, R., Chen, D., Zhai, Z., Zhong, B., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700544104 · Cited by 129 · see citing works
Rig-I−/− mice develop colitis associated with downregulation of Gαi2
Wang, Y., Zhang, H., Sun, Y., Liu, Z.-X., Liu, X., Wang, L., Lu, S., Kong, H., Liu, Q., Li, X., et al. (2007) · Cell Research · doi:10.1038/cr.2007.81 · Cited by 125 · see citing works
Structural basis of double-stranded RNA recognition by the RIG-I like receptor MDA5
Li, X., Lu, C. C., Stewart, M. D., Xu, H., Strong, R. K., Igumenova, T. I., & Li, P. (2009) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2009.06.008 · Cited by 113 · see citing works
Phosphorylation of RIG-I by Casein Kinase II Inhibits Its Antiviral Response
Sun, Z., Ren, H., Liu, Y., et al. (2010) · Journal of Virology · doi:10.1128/jvi.01734-10 · Cited by 111 · see citing works
Szretter, K. J., Daffis, S., Patel, J. R., Suthar, M. S., Klein, R. S., Gale, M., & Diamond, M. (2010) · Journal of Virology · doi:10.1128/jvi.01026-10 · Cited by 110 · see citing works
Self-citationPothlichet, J., Niewold, T., Vitour, D., Solhonne, B., Crow, M., & Si-Tahar, M. (2011) · EMBO Molecular Medicine · doi:10.1002/emmm.201000120 · Cited by 110 · see citing works
Negative Role of RIG-I Serine 8 Phosphorylation in the Regulation of Interferon-β Production
Nistal‐Villán, E., Gack, M. U., Martínez-Delgado, G., Maharaj, N. P., Inn, K., Yang, H., Wang, R., Aggarwal, A. K., Jung, J. U., & García‐Sastre, A. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.089912 · Cited by 105 · see citing works
Structure and Function of LGP2, a DEX(D/H) Helicase That Regulates the Innate Immunity Response
Murali, A., Li, X., Ranjith-Kumar, C. T., Bhardwaj, K., Holzenburg, A., Li, P., & Kao, C. C. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m800542200 · Cited by 104 · see citing works
Colli, M. L., Moore, F., Gurzov, E. N., Ortis, F., & Eizirik, D. L. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp474 · Cited by 103 · see citing works
Polo-like Kinase 1 (PLK1) Regulates Interferon (IFN) Induction by MAVS
Vitour, D., Dabo, S., Pour, M. A., Vilasco, M., Vidalain, P., Jacob, Y., Mesel‐Lemoine, M., Paz, S., Arguello, M., Lin, R., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.018275 · Cited by 101 · see citing works
Retinoic Acid-Inducible Gene-I-Like Receptors
Onoguchi, K., Yoneyama, M., & Fujita, T. (2010) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2010.0057 · Cited by 101 · see citing works
Reduced Expression of IFIH1 Is Protective for Type 1 Diabetes
Downes, K., Pękalski, M. Ł., Angus, K. L., Hardy, M. P., Nutland, S. L., Smyth, D. J., Walker, N. M., Wallace, C., & Todd, J. A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012646 · Cited by 100 · see citing works
The Chase for the RIG-I Ligand—Recent Advances
Schlee, M., & Hartmann, G. (2010) · Molecular Therapy · doi:10.1038/mt.2010.90 · Cited by 98 · see citing works
Wang, F., Gao, X., Barrett, J. W., Shao, Q., Bartee, E., Mohamed, M. R., Rahman, M. M., Werden, S. J., Irvine, T. S., Cao, J., et al. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.1000099 · Cited by 98 · see citing works
Negative Regulation of MAVS-Mediated Innate Immune Response by PSMA7
Jia, Y., Song, T., Wei, C., Ni, C., Zheng, Z., Xu, Q., Ma, H., Li, L., Zhang, Y., He, X., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901646 · Cited by 97 · see citing works
Öhman, T., Rintahaka, J., Kalkkinen, N., Matikainen, S., & Nyman, T. A. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803093 · Cited by 96 · see citing works
Crystal structure of human IPS-1/MAVS/VISA/Cardif caspase activation recruitment domain
Potter, J. A., Randall, R. E., & Taylor, G. L. (2008) · BMC Structural Biology · doi:10.1186/1472-6807-8-11 · Cited by 96 · see citing works
Caspase-12 controls West Nile virus infection via the viral RNA receptor RIG-I
Wang, P., Arjona, A., Zhang, Y., Sultana, H., Dai, J., Yang, L., LeBlanc, P. M., Doiron, K., Saleh, M., & Fikrig, E. (2010) · Nature Immunology · doi:10.1038/ni.1933 · Cited by 96 · see citing works
Toll-like receptor 7-induced immune response to cutaneous West Nile virus infection
Welte, T., Reagan, K. L., Fang, H., Machaín-Williams, C., Zheng, X., Mendell, N. L., Chang, G. J., Wu, P., Blair, C. D., & Wang, T. (2009) · Journal of General Virology · doi:10.1099/vir.0.011783-0 · Cited by 93 · see citing works
Induction of IRF-3 and IRF-7 phosphorylation following activation of the RIG-I pathway.
Paz, S., Sun, Q., Nakhaei, P., Romieu, R., Goubau, D., Julkunen, I., Lin, R., & Hiscott, J. B. (2006) · PubMed · Cited by 92 · see citing works
Coexpressed RIG-I Agonist Enhances Humoral Immune Response to Influenza Virus DNA Vaccine
Luke, J. M., Simon, G. G., Söderholm, J., Errett, J. S., August, J. T., Gale, M., Hodgson, C. P., & Williams, J. A. (2010) · Journal of Virology · doi:10.1128/jvi.01250-10 · Cited by 89 · see citing works
Self-citationActivation of IFN-β expression by a viral mRNA through RNase L and MDA5
Luthra, P., Sun, D., Silverman, R. H., & He, B. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1012409108 · Cited by 87 · see citing works
Enteroviruses and type 1 diabetes: towards a better understanding of the relationship
Jaïdane, H., Sauter, P., Sané, F., Goffard, A., Gharbi, J., & Hober, D. (2010) · Reviews in Medical Virology · doi:10.1002/rmv.647 · Cited by 85 · see citing works
Ubiquitin-Regulated Recruitment of IκB Kinase ε to the MAVS Interferon Signaling Adapter
Paz, S., Vilasco, M., Arguello, M., Sun, Q., Lacoste, J., Nguyên, T. L.-A., Zhao, T., Shestakova, E. A., Zaari, S., Bibeau-Poirier, A., et al. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.00880-08 · Cited by 84 · see citing works
RNA sensor–induced type I IFN prevents diabetes caused by a β cell–tropic virus in mice
McCartney, S. A., Vermi, W., Lonardi, S., Rossini, C., Otero, K., Calderón, B., Gilfillan, S., Diamond, M., Unanue, E. R., & Colonna, M. (2011) · Journal of Clinical Investigation · doi:10.1172/jci44005 · Cited by 78 · see citing works
Approaching the RNA ligand for RIG‐I?
Schlee, M., Hartmann, E., Coch, C., Wimmenauer, V., Janke, M., Barchet, W., & Hartmann, G. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00724.x · Cited by 78 · see citing works
Lu, C. C., Ranjith-Kumar, C. T., Hao, L., Kao, C. C., & Li, P. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq974 · Cited by 76 · see citing works
The role of mitochondria in the mammalian antiviral defense system
Scott, I. (2010) · Mitochondrion · doi:10.1016/j.mito.2010.02.005 · Cited by 71 · see citing works
Sanada, T., Takaesu, G., Mashima, R., Yoshida, R., Kobayashi, T., & Yoshimura, A. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m806923200 · Cited by 66 · see citing works
Mashima, R., Saeki, K., Aki, D., Minoda, Y., Takaki, H., Sanada, T., Kobayashi, T., Aburatani, H., Yamanashi, Y., & Yoshimura, A. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m508221200 · Cited by 66 · see citing works
Molecular basis for an attenuated cytoplasmic dsRNA response in human embryonic stem cells
Chen, L., Yang, L. C., & Carmichael, G. (2010) · Cell Cycle · doi:10.4161/cc.9.17.12792 · Cited by 65 · see citing works
Ovsyannikova, I. G., Haralambieva, I. H., Dhiman, N., O’Byrne, M. M., Pankratz, V. S., Jacobson, R. M., & Poland, G. A. (2009) · The Journal of Infectious Diseases · doi:10.1086/649588 · Cited by 62 · see citing works
Agonist and Antagonist Recognition by RIG-I, a Cytoplasmic Innate Immunity Receptor
Ranjith-Kumar, C. T., Murali, A., Dong, W., Dharmaiah, S., Vaughan, R. C., Ortiz-Alcántara, J. M., Bhardwaj, K., Li, X., Li, P., & Kao, C. C. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m806219200 · Cited by 61 · see citing works
The non-canonical role of Atg family members as suppressors of innate antiviral immune signaling
Takeshita, F., Kobiyama, K., Miyawaki, A., Jounai, N., & Okuda, K. (2008) · Autophagy · doi:10.4161/auto.5055 · Cited by 61 · see citing works
Immunostimulatory RNA Blocks Suppression by Regulatory T Cells
Anz, D., Koelzer, V. H., Moder, S., Thaler, R., Schwerd, T., Lahl, K., Sparwasser, T. D., Besch, R., Poeck, H., Hornung, V., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901245 · Cited by 57 · see citing works
UbcH8 regulates ubiquitin and ISG15 conjugation to RIG-I
Arimoto, K., Konishi, H., & Shimotohno, K. (2007) · Molecular Immunology · doi:10.1016/j.molimm.2007.07.021 · Cited by 57 · see citing works
Pothlichet, J., Burtey, A., Kubarenko, A. V., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007582 · Cited by 53 · see citing works
Cytokine-Independent Upregulation of MDA5 in Viral Infection
Yount, J. S., Moran, T. M., & López, C. B. (2007) · Journal of Virology · doi:10.1128/jvi.00545-07 · Cited by 52 · see citing works
Hu, J., Nistal‐Villán, E., Voho, A., Ganee, A., Kumar, M., Ding, Y., García‐Sastre, A., & Wetmur, J. G. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903291 · Cited by 50 · see citing works
Novel splice variants of human IKKε negatively regulate IKKε‐induced IRF3 and NF‐kB activation
Koop, A. C., Lepenies, I., Braum, O., et al. (2010) · European Journal of Immunology · doi:10.1002/eji.201040814 · Cited by 47 · see citing works
Zanone, M. M., Favaro, E., Ferioli, E., Huang, G. C., Klein, N. J., Perin, P. C., Peakman, M., Conaldi, P. G., & Camussi, G. (2007) · The FASEB Journal · doi:10.1096/fj.06-7905com · Cited by 43 · see citing works
Regulation of immune cell homeostasis by type I interferons
Mattei, F., Schiavoni, G., & Tough, D. F. (2010) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2010.05.002 · Cited by 42 · see citing works
Williams, Ç. H., Oikarinen, S., Tauriainen, S., Salminen, K., Hyöty, H., & Stanway, G. (2006) · Journal of Clinical Microbiology · doi:10.1128/jcm.44.2.441-448.2006 · Cited by 39 · see citing works
Johnsen, I. B., Nguyen, T. T., Bergstrøm, B., Fitzgerald, K. A., & Anthonsen, M. W. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m808233200 · Cited by 36 · see citing works
c‐Abl tyrosine kinase interacts with MAVS and regulates innate immune response
Song, T., Wei, C., Zheng, Z., Xu, Y., Cheng, X., Yuan, Y., Guan, K., Zhang, Y., Ma, Q., Shi, W., et al. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.11.025 · Cited by 32 · see citing works
Hiscott, J., Lacoste, J., & Lin, R. (2006) · Biochemical Pharmacology · doi:10.1016/j.bcp.2006.06.030 · Cited by 31 · see citing works
Pathogenic mechanisms of disease in myositis: autoantigens as clues
Betteridge, Z., Gunawardena, H., & McHugh, N. J. (2009) · Current Opinion in Rheumatology · doi:10.1097/bor.0b013e328331638a · Cited by 30 · see citing works
Funke, B., Lasitschka, F., Roth, W., et al. (2011) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21572 · Cited by 30 · see citing works
Involvement of retinoic acid-inducible gene-I in the IFN-γ/STAT1 signalling pathway in BEAS-2B cells
Imaizumi, T., Kumagai, M., Taima, K., et al. (2005) · European Respiratory Journal · doi:10.1183/09031936.05.00102104 · Cited by 30 · see citing works
Short-hairpin RNAs synthesized by T7 phage polymerase do not induce interferon
Gondai, T., Yamaguchi, K., Miyano‐Kurosaki, N., et al. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm1043 · Cited by 28 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Toll-like receptors and their crosstalk with other innate receptors in infection and immunity
Kawai, T., & Akira, S. (2011) · Immunity · doi:10.1016/j.immuni.2011.05.006 · Cited by 3,658 · see citing works
Into the Eye of the Cytokine Storm
Tisoncik, J. R., Korth, M. J., Simmons, C. P., Farrar, J., Martin, T. R., & Katze, M. G. (2012) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.05015-11 · Cited by 1,940 · see citing works
Damage-associated molecular patterns in inflammatory diseases
Roh, J. S., & Sohn, D. H. (2018) · Immune Network · doi:10.4110/in.2018.18.e27 · Cited by 1,261 · see citing works
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Collaborative Association Study of Psoriasis (CASP), Tsoi, L. C., Genetic Analysis of Psoriasis Consortium, Psoriasis Association Genetics Extension, Wellcome Trust Case Control Consortium 2, Spain, S. L., Knight, J., Ellinghaus, E., Stuart, P. E., Capon, F., et al. (2012) · Nature Genetics · doi:10.1038/ng.2467 · Cited by 1,024 · see citing works
Apoptotic Caspases Prevent the Induction of Type I Interferons by Mitochondrial DNA
Rongvaux, A., Jackson, R., Harman, C. C. D., Li, T., West, A. P., de Zoete, M. R., Wu, Y., Yordy, B., Lakhani, S. A., Kuan, C.-Y., et al. (2014) · Cell · doi:10.1016/j.cell.2014.11.037 · Cited by 847 · see citing works
Tools for translation: non-viral materials for therapeutic mRNA delivery
Hajj, K. A., & Whitehead, K. A. (2017) · Nature Reviews Materials · doi:10.1038/natrevmats.2017.56 · Cited by 799 · see citing works
COVID-19 and the human innate immune system
Schultze, J. L., & Aschenbrenner, A. C. (2021) · Cell · doi:10.1016/j.cell.2021.02.029 · Cited by 714 · see citing works
Alameh, M.-G., Tombácz, I., Bettini, E., Lederer, K., Ndeupen, S., Sittplangkoon, C., Wilmore, J. R., Gaudette, B. T., Soliman, O. Y., Pine, M., et al. (2021) · Immunity · doi:10.1016/j.immuni.2021.11.001 · Cited by 775 · see citing works
Lee (2019) · doi:10.1038/s12276-019-0299-y · Cited by 635 · see citing works
Neutrophil cell surface receptors and their intracellular signal transduction pathways
Futosi, K., Fodor, S., & Mócsai, A. (2013) · International Immunopharmacology · doi:10.1016/j.intimp.2013.06.034 · Cited by 642 · see citing works
RNA Circularization Diminishes Immunogenicity and Can Extend Translation Duration In Vivo
Wesselhoeft, R. A., Kowalski, P. S., Parker-Hale, F. C., Huang, Y., Bisaria, N., & Anderson, D. G. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.02.015 · Cited by 482 · see citing works
Interplay between SARS-CoV-2 and the type I interferon response
Sa Ribero, M., Jouvenet, N., Dreux, M., & Nisole, S. (2020) · PLOS Pathogens · doi:10.1371/journal.ppat.1008737 · Cited by 443 · see citing works
The challenge and prospect of mRNA therapeutics landscape
Weng, Y., Li, C., Yang, T., Hu, B., Zhang, M., Guo, S., Xiao, H., Liang, X.-J., & Huang, Y. (2020) · Biotechnology Advances · doi:10.1016/j.biotechadv.2020.107534 · Cited by 417 · see citing works
Dealing with danger in the CNS: the response of the immune system to injury
Gadani, S. P., Walsh, J. T., Lukens, J. R., & Kipnis, J. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.019 · Cited by 342 · see citing works
Regulation of hepatic innate immunity by hepatitis C virus
Horner, S. M., & Gale, M. (2013) · Nature Medicine · doi:10.1038/nm.3253 · Cited by 278 · see citing works
Self-citationSweeten 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 · see citing works
Human TBK1: A Gatekeeper of Neuroinflammation
Ahmad, L., Zhang, S.-Y., Casanova, J.-L., & Sancho-Shimizu, V. (2016) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2016.04.006 · Cited by 208 · see citing works
Hoang, T. N., Pino, M., Boddapati, A. K., Viox, E. G., Starke, C. E., Upadhyay, A. A., Gumber, S., Nekorchuk, M., Busman-Sahay, K., Strongin, Z., et al. (2021) · Cell · doi:10.1016/j.cell.2020.11.007 · Cited by 212 · see citing works
Autophagy and ALS: mechanistic insights and therapeutic implications
Chua, J. P., De Calbiac, H., Kabashi, E., & Barmada, S. J. (2022) · Autophagy · doi:10.1080/15548627.2021.1926656 · Cited by 189 · see citing works
Immunological properties of inulin-type fructans
Vogt, L., Meyer, D., Pullens, G., Faas, M., Smelt, M., Venema, K., Ramasamy, U., Schols, H. A., & De Vos, P. (2015) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2012.656772 · Cited by 195 · see citing works
The inflammatory function of human IgA
Hansen, I. S., Baeten, D. L. P., & den Dunnen, J. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2976-8 · Cited by 170 · see citing works
Sikorski, P. J., Warminski, M., Kubacka, D., Ratajczak, T., Nowis, D., Kowalska, J., & Jemielity, J. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa032 · Cited by 142 · see citing works
Mitochondria as a centrally positioned hub in the innate immune response
Sandhir, R., Halder, A., & Sunkaria, A. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2016.10.020 · Cited by 135 · see citing works
Chen, X., Wang, K., Xing, Y., Tu, J., Yang, X., Zhao, Q., Li, K., & Chen, Z. (2014) · Protein & Cell · doi:10.1007/s13238-014-0104-6 · Cited by 130 · see citing works
Progresses on three pattern recognition receptor families (TLRs, RLRs and NLRs) in teleost
Liao, Z., & Su, J. (2021) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2021.104131 · Cited by 118 · see citing works
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 · see citing works
Zou, J., Kawai, T., Tsuchida, T., Kozaki, T., Tanaka, H., Shin, K.-S., Kumar, H., & Akira, S. (2013) · Immunity · doi:10.1016/j.immuni.2012.12.007 · Cited by 103 · see citing works
Biologically informed deep learning to query gene programs in single-cell atlases
Lotfollahi, M., Rybakov, S., Hrovatin, K., Hediyeh-zadeh, S., Talavera-López, C., Misharin, A. V., & Theis, F. J. (2023) · Nature Cell Biology · doi:10.1038/s41556-022-01072-x · Cited by 100 · see citing works
Extracellular RNA sensing by pattern recognition receptors
Tatematsu, M., Funami, K., Seya, T., & Matsumoto, M. (2018) · Journal of Innate Immunity · doi:10.1159/000494034 · Cited by 90 · see citing works
The many ways tissue phagocytes respond to dying cells
Blander, J. M. (2017) · Immunological Reviews · doi:10.1111/imr.12537 · Cited by 84 · see citing works
Pattern recognition receptor‐mediated inflammation in diabetic vascular complications
Wang, X., Antony, V., Wang, Y., Wu, G., & Liang, G. (2020) · Medicinal Research Reviews · doi:10.1002/med.21711 · Cited by 73 · see citing works
Innate immune sensing of adeno-associated virus vectors
Cao, D., Byrne, B. J., de Jong, Y. P., Terhorst, C., Duan, D., Herzog, R. W., & Kumar, S. R. P. (2024) · Human Gene Therapy · doi:10.1089/hum.2024.040 · Cited by 50 · see citing works
- Authors
- Loo, Y.-M., & Gale, M.
- Affiliations
- University of Washington (US)
- Corresponding author
- Gale, Michael
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2011-05
- Volume
- 34
- Issue
- 5
- Pages
- 680-692
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC3177755
- OpenAlex
- W1973646620
- Cited by
- 1,875
- References
- 174
- Citations by year
- 2026: 69 · 2025: 88 · 2024: 137 · 2023: 136 · 2022: 145 · 2021: 192 · 2020: 158 · 2019: 125 · 2018: 128 · 2017: 115 · 2016: 102 · 2015: 105 · 2014: 125 · 2013: 122 · 2012: 97
- FWCI
- 10.70
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 808 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Drug Abuse (R01DA024563)
- National Institute of Allergy and Infectious Diseases (R01AI060389, U19AI083019, R21AI057568, U19AI088778)
- 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 › Molecular Biology › RNA regulation and disease
- Keywords
- RIG-I-like receptors, RIG-I, MDA5, LGP2, antiviral innate immunity, RNA virus sensing, cytoplasmic RNA, post-translational modification, autoimmune disease
- MeSH terms
- Animals, Enzyme Activation, Humans, Immunity, Innate, Signal Transduction, DEAD-box RNA Helicases, Ubiquitination, Adaptive Immunity
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