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Recognition of single-stranded RNA viruses by Toll-like receptor 7
Open accessAbstract
Viral infection of mammalian host results in the activation of innate immune responses. Toll-like receptors (TLRs) have been shown to mediate the recognition of many types of pathogens, including viruses. The genomes of viruses possess unique characteristics that are not found in mammalian genomes, such as high CpG content and double-stranded RNA. These genomic nucleic acids serve as molecular signatures associated with viral infections. Here we show that TLR7 recognizes the single-stranded RNA viruses, vesicular stomatitis virus and influenza virus. The recognition of these viruses by plasmacytoid dendritic cells and B cells through TLR7 results in their activation of costimulatory molecules and production of cytokines. Moreover, this recognition required intact endocytic pathways. Mice deficient in either the TLR7 or the TLR adaptor protein MyD88 demonstrated reduced responses to in vivo infection with vesicular stomatitis virus. These results demonstrate microbial ligand recognition by TLR7 and provide insights into the pathways used by the innate immune cells in the recognition of viral pathogens.
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Cites
A Toll-like receptor recognizes bacterial DNA
Hemmi, H., Takeuchi, O., Kawai, T., Kaisho, T., Sato, S., Sanjo, H., Matsumoto, M., Hoshino, K., Wagner, H., Takeda, K., et al. (2000) · Nature · doi:10.1038/35047123 · Cited by 6,491
Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3
Alexopoulou, L., Holt, A. C., Medzhitov, R., & Flavell, R. A. (2001) · Nature · doi:10.1038/35099560 · Cited by 6,129
Viruses and interferon: a fight for supremacy
Katze, M. G., He, Y., & Gale, M. (2002) · Nature Reviews Immunology · doi:10.1038/nri888 · Cited by 1,419
Research works printed but not linked: 33
- 10.1016/S0065-2776(01)78001-7 · DOI · Paper page
- 10.1034/j.1600-065X.2000.917309.x · DOI · Paper page
- 10.1016/S0952-7915(02)00349-7 · DOI
- 10.1182/blood-2003-08-2674 · DOI · Paper page
- 10.1084/jem.20030162 · DOI · Paper page
- 10.1016/S1286-4579(02)01583-6 · DOI
- Cella, M., Facchetti, F., Lanzavecchia, A. & Colonna, M. (2000) Nat. Immunol. 4, 305–310.
- 10.1084/jem.194.8.1171 · DOI · Paper page
- 10.1038/ni736 · DOI · Paper page
- 10.1038/nature01783 · DOI · Paper page
- 10.1006/viro.2000.0736 · DOI
- 10.1006/viro.1998.9535 · DOI
- 10.1038/nbt822 · DOI · Paper page
- Schlaeger, T. M., Qin, Y., Fujiwara, Y., Magram, J. & Sato, T. N. (1995) Development (Cambridge, U.K.) 121, 1089–1098.
- 10.1016/S1074-7613(00)80596-8 · DOI · Paper page
- 10.4049/jimmunol.171.12.6466 · DOI · Paper page
- 10.1126/science.278.5343.1612 · DOI · Paper page
- 10.1002/eji.200323797 · DOI · Paper page
- 10.1084/jem.20021908 · DOI · Paper page
- 10.1016/0022-2836(82)90269-8 · DOI · Paper page
- 10.1002/1521-4141(200207)32:7<1958::AID-IMMU1958>3.0.CO;2-U · DOI
- 10.1002/eji.200324238 · DOI · Paper page
- 10.1038/ni758 · DOI · Paper page
- 10.1002/1521-4141(200111)31:11<3388::AID-IMMU3388>3.0.CO;2-Q · DOI · Paper page
- 10.1073/pnas.0631696100 · DOI · Paper page
- 10.1083/jcb.89.3.674 · DOI · Paper page
- 10.1128/jvi.47.1.171-177.1983 · DOI · Paper page
- 10.1084/jem.20011666 · DOI
- 10.1038/nature01889 · DOI · Paper page
- 10.1126/science.1087262 · DOI · Paper page
- 10.1128/jvi.43.1.361-364.1982 · DOI
- Perussia, B., Fanning, V. & Trinchieri, G. (1985) Nat. Immun. Cell Growth Regul. 4, 120–137.2995798
- 10.1002/cyto.10118 · DOI
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O'Neill, L. A. J., Golenbock, D., & Bowie, A. G. (2013) · Nature reviews. Immunology · doi:10.1038/nri3446 · Cited by 1,765
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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
The IRF Family Transcription Factors in Immunity and Oncogenesis
Tamura, T., Yanai, H., Savitsky, D., & Taniguchi, T. (2008) · Annual Review of Immunology · doi:10.1146/annurev.immunol.26.021607.090400 · Cited by 1,259
Plasmacytoid dendritic cells: sensing nucleic acids in viral infection and autoimmune diseases
Gilliet, M., Cao, W., & Liu, Y.-J. (2008) · Nature Reviews Immunology · doi:10.1038/nri2358 · Cited by 1,190
Hayden, M. S., West, A. P., & Ghosh, S. (2006) · Oncogene · doi:10.1038/sj.onc.1209943 · Cited by 1,178
Toll-like receptors in systemic autoimmune disease
Marshak-Rothstein, A. (2006) · Nature Reviews Immunology · doi:10.1038/nri1957 · Cited by 1,116
Karikó, K., Muramatsu, H., Ludwig, J., & Weissman, D. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr695 · Cited by 898
Beutler, B. A. (2009) · Blood · doi:10.1182/blood-2008-07-019307 · Cited by 840
Insights into the Interaction between Influenza Virus and Pneumococcus
McCullers, J. A. (2006) · Clinical Microbiology Reviews · doi:10.1128/cmr.00058-05 · Cited by 846
Toll‐like receptors control autophagy
Delgado, M. A., Elmaoued, R. A., Davis, A. S., Kyei, G., & Deretic, V. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.31 · Cited by 744
Toll‐like receptors and adaptor molecules in liver disease: Update†
Seki, E., & Brenner, D. A. (2008) · Hepatology · doi:10.1002/hep.22306 · Cited by 722
Guillot, L., Le Goffic, R., Bloch, S., Escriou, N., Akira, S., Chignard, M., & Si-Tahar, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m410592200 · Cited by 689
The airway epithelium: soldier in the fight against respiratory viruses
Vareille, M., Kieninger, E., Edwards, M. R., & Regamey, N. (2011) · Clinical Microbiology Reviews · doi:10.1128/cmr.00014-10 · Cited by 655
Jensen, S., & Thomsen, A. R. (2012) · Journal of Virology · doi:10.1128/jvi.05738-11 · Cited by 604
Tabeta, K., Hoebe, K., Janssen, E. M., Du, X., Georgel, P., Crozat, K., Mudd, S., Mann, N., Sovath, S., Goode, J., et al. (2006) · Nature Immunology · doi:10.1038/ni1297 · Cited by 600
Opposing Effects of Fasting Metabolism on Tissue Tolerance in Bacterial and Viral Inflammation
Wang, A., Huen, S. C., Luan, H. H., Yu, S., Zhang, C., Gallezot, J.-D., Booth, C. J., & Medzhitov, R. (2016) · Cell · doi:10.1016/j.cell.2016.07.026 · Cited by 579
Nucleic acid recognition by the innate immune system
Barbalat, R., Ewald, S. E., Mouchess, M. L., & Barton, G. M. (2011) · Annual Review of Immunology · doi:10.1146/annurev-immunol-031210-101340 · Cited by 577
GDF15 Is an Inflammation-Induced Central Mediator of Tissue Tolerance
Luan, H. H., Wang, A., Hilliard, B. K., Carvalho, F., Rosen, C. E., Ahasic, A. M., Herzog, E. L., Kang, I., Pisani, M. A., Yu, S., et al. (2019) · Cell · doi:10.1016/j.cell.2019.07.033 · Cited by 527
The interferon regulatory factor, IRF5, is a central mediator of toll-like receptor 7 signaling
Schoenemeyer, A., Barnes, B. J., Mancl, M. E., Latz, E., Goutagny, N., Pitha, P. M., Fitzgerald, K. A., & Golenbock, D. T. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m412584200 · Cited by 411
Toll-like receptor 8 senses degradation products of single-stranded RNA
Tanji, H., Ohto, U., Shibata, T., Taoka, M., Yamauchi, Y., Isobe, T., Miyake, K., & Shimizu, T. (2015) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2943 · Cited by 404
Swiecki, M., & Colonna, M. (2010) · Immunological Reviews · doi:10.1111/j.0105-2896.2009.00881.x · Cited by 397
Cell-to-cell communication: microRNAs as hormones.
Bayraktar, R., Van Roosbroeck, K., & Calin, G. A. (2017) · Molecular Oncology · doi:10.1002/1878-0261.12144 · Cited by 361
Zhu, J., Huang, X., & Yang, Y. (2009) · Journal of Clinical Investigation · doi:10.1172/jci37607 · Cited by 330
A diet-sensitive commensal Lactobacillus strain Mediates TLR7-dependent systemic autoimmunity
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Type I interferons directly regulate lymphocyte recirculation and cause transient blood lymphopenia
Kamphuis, E., Junt, T., Waibler, Z., Forster, R., & Kalinke, U. (2006) · Blood · doi:10.1182/blood-2006-06-027599 · Cited by 306
The function and clinical application of extracellular vesicles in innate immune regulation
Zhou, X., Xie, F., Wang, L., Zhang, L., Zhang, S., Fang, M., & Zhou, F. (2020) · Cellular & Molecular Immunology · doi:10.1038/s41423-020-0391-1 · Cited by 294
Identification of RNA Sequence Motifs Stimulating Sequence-Specific TLR8-Dependent Immune Responses
Forsbach, A., Nemorin, J.-G., Montino, C., Müller, C., Samulowitz, U., Vicari, A. P., Jurk, M., Mutwiri, G. K., Krieg, A. M., Lipford, G. B., et al. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.6.3729 · Cited by 281
Mx1 reveals innate pathways to antiviral resistance and lethal influenza disease
Pillai, P. S., Molony, R. D., Martinod, K., Dong, H., Pang, I. K., Tal, M. C., Solis, A. G., Bielecki, P., Mohanty, S., Trentalange, M., et al. (2016) · Science · doi:10.1126/science.aaf3926 · Cited by 229
Self-citationDysregulation of human Toll-like receptor function in aging
Shaw, A. C., Panda, A., Joshi, S. R., Qian, F., Allore, H. G., & Montgomery, R. R. (2011) · Ageing Research Reviews · doi:10.1016/j.arr.2010.10.007 · Cited by 215
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Moller-Larsen, S., Nyegaard, M., Haagerup, A., Vestbo, J., Kruse, T. A., & Borglum, A. D. (2008) · Thorax · doi:10.1136/thx.2007.094128 · Cited by 154
Pang, I. K., Ichinohe, T., & Iwasaki, A. (2013) · Nature Immunology · doi:10.1038/ni.2514 · Cited by 145
Self-citationThe role of type I interferons in TLR responses
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Jounai, K., Ikado, K., Sugimura, T., Ano, Y., Braun, J., & Fujiwara, D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032588 · Cited by 133
The Interleukin‐1 Receptor Family
Boraschi, D., & Tagliabue, A. (2006) · Vitamins & Hormones · doi:10.1016/s0083-6729(06)74009-2 · Cited by 133
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The role of alternative polyadenylation in the antiviral innate immune response
Jia, X., Yuan, S., Wang, Y., Fu, Y., Ge, Y., Ge, Y., Lan, X., Feng, Y., Qiu, F., Li, P., et al. (2017) · Nature Communications · doi:10.1038/ncomms14605 · Cited by 122
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Wu, S., Jiang, Z.-Y., Sun, Y.-F., Yu, B., Chen, J., Dai, C.-Q., Wu, X.-L., Tang, X.-L., & Chen, X.-Y. (2013) · Current Microbiology · doi:10.1007/s00284-013-0380-z · Cited by 116
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Hildebrand, J. M., Yi, Z., Buchta, C. M., Poovassery, J., Stunz, L. L., & Bishop, G. A. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01055.x · Cited by 110
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Hung, Y.-F., Chen, C.-Y., Shih, Y.-C., Liu, H.-Y., Huang, C.-M., & Hsueh, Y.-P. (2018) · Journal of Cell Biology · doi:10.1083/jcb.201712113 · Cited by 86
Bode, C., Fox, M., Tewary, P., Steinhagen, A., Ellerkmann, R. K., Klinman, D., Baumgarten, G., Hornung, V., & Steinhagen, F. (2016) · European Journal of Immunology · doi:10.1002/eji.201546113 · Cited by 79
Greenbaum, B. D., Rabadan, R., & Levine, A. J. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005969 · Cited by 76
Functions of double‐negative B cells in autoimmune diseases, infections, and cancers
Chung, M. K. Y., Gong, L., Kwong, D. L., Lee, V. H., Lee, A. W., Guan, X., Kam, N., & Dai, W. (2023) · EMBO Molecular Medicine · doi:10.15252/emmm.202217341 · Cited by 73
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Liu, H.-Y., Hong, Y.-F., Huang, C.-M., Chen, C.-Y., Huang, T.-N., & Hsueh, Y.-P. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5566-12.2013 · Cited by 71
Extracellularly Delivered Single-Stranded Viral RNA Causes Neurodegeneration Dependent on TLR7
Lehmann, S. M., Rosenberger, K., Krüger, C., Habbel, P., Derkow, K., Kaul, D., Rybak, A., Brandt, C., Schott, E., Wulczyn, F. G., et al. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1201078 · Cited by 64
Liu, H.-Y., Huang, C.-M., Hung, Y.-F., & Hsueh, Y.-P. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.04.011 · Cited by 59
TLR8 escapes X chromosome inactivation in human monocytes and CD4+ T cells
Youness, A., Cenac, C., Faz-López, B., Grunenwald, S., Barrat, F. J., Chaumeil, J., Mejía, J. E., & Guéry, J.-C. (2023) · Biology of Sex Differences · doi:10.1186/s13293-023-00544-5 · Cited by 58
Regulation and functions of the RhoA regulatory guanine nucleotide exchange factor GEF-H1
Joo, E., & Olson, M. F. (2021) · Small GTPases · doi:10.1080/21541248.2020.1840889 · Cited by 56
Chandler, L., Yusuf, I., McClements, M., Barnard, A., MacLaren, R., & Xue, K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144972 · Cited by 49
Wallach, T., Mossmann, Z. J., Szczepek, M., Wetzel, M., Machado, R., Raden, M., Miladi, M., Kleinau, G., Krüger, C., Dembny, P., et al. (2021) · Molecular Neurodegeneration · doi:10.1186/s13024-021-00498-5 · Cited by 48
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Byrnes, A. E., Dominguez, S. L., Yen, C.-W., Laufer, B. I., Foreman, O., Reichelt, M., Lin, H., Sagolla, M., Hötzel, K., Ngu, H., et al. (2023) · Molecular Therapy - Nucleic Acids · doi:10.1016/j.omtn.2023.05.005 · Cited by 38
Wallach, T., Wetzel, M., Dembny, P., Staszewski, O., Krüger, C., Buonfiglioli, A., Prinz, M., & Lehnardt, S. (2020) · Cells · doi:10.3390/cells9010186 · Cited by 26
Structure-aware machine learning identifies microRNAs operating as Toll-like receptor 7/8 ligands
Raden, M., Wallach, T., Miladi, M., Zhai, Y., Krüger, C., Mossmann, Z. J., Dembny, P., Backofen, R., & Lehnardt, S. (2021) · RNA Biology · doi:10.1080/15476286.2021.1940697 · Cited by 14
Piccoli, L., Park, Y.-J., Tortorici, M. A., Czudnochowski, N., Walls, A. C., Beltramello, M., Silacci-Fregni, C., Pinto, D., Rosen, L. E., Bowen, J. E., et al. (2020) · Cell · doi:10.1016/j.cell.2020.09.037 · Cited by 1,395
Innovative Vaccine Strategy: Self-Adjuvanting Conjugate Vaccines
Manabe, Y., & Fukase, K. (2023) · Methods in Molecular Biology · doi:10.1007/978-1-0716-2910-9_5 · Cited by 5
Metadata
- Authors
- Lund, J. M., Alexopoulou, L., Sato, A., Karow, M., Adams, N. C., Gale, N. W., Iwasaki, A., & Flavell, R. A.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2004-03-19
- Volume
- 101
- Issue
- 15
- Pages
- 5598-5603
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2161208630
- Cited by
- 1,861
- References
- 3
- FWCI
- 47.38
- Type
- journal article
- Language
- en
- Open access
- green
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