Acute induction of cell death-related IFN stimulated genes (ISG) differentiates highly from moderately virulent CSFV strains
Vet. Res., 41 1 (2010) 07
Published online: 2009-10-01
Articles citing this article
The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).
Cited article:
This article has been cited by the following article(s):
Strategies of Classical Swine Fever Immune Evasion
Yuanji Zhang, Fangtao Li and Yebing LiuInternational Journal of Molecular Sciences 26 (16) 7838 (2025)
https://doi.org/10.3390/ijms26167838
Genome-wide CRISPR screen reveals specific role of type I interferon signaling pathway in Newcastle disease virus establishment of persistent infection
Hao Li, Yuqing Li, Tiejun Zhang, Song Liu, Cailiang Song, Kailu Wang, Wenjun Yan, Zheng Wang, Qingcheng Yang, Xin Yang and Hongning WangVeterinary Microbiology 300 110288 (2025)
https://doi.org/10.1016/j.vetmic.2024.110288
699 (2025)
https://doi.org/10.1002/9781394179466.ch35
A IFI27 gene contributes to ER-stress mediated apoptosis and benefits for white spot syndrome virus infection in Litopenaeus vannamei
Jin-Quan Fan, Yu-Tao Miao, Ke-Cheng Lu, Guo-liang Chen, Bin-Bin Li, Qian-Ming Hong, Xin-Jun Yang, Ze-Yu Yan and Yi-Hong ChenFish & Shellfish Immunology 120 180 (2022)
https://doi.org/10.1016/j.fsi.2021.11.032
Classical Swine Fever Virus NproAntagonizes IRF3 To Prevent Interferon-Independent TLR3- and RIG-I-Mediated Apoptosis
Samuel Hardy, Ben Jackson, Stephen Goodbourn, Julian Seago and Bryan R. G. WilliamsJournal of Virology 95 (5) (2021)
https://doi.org/10.1128/JVI.01136-20
Immunogene expression analysis in betanodavirus infected-Senegalese sole using an OpenArray® platform
Juan Gémez-Mata, Alejandro M. Labella, Isabel Bandín, Juan J. Borrego and Esther García-RosadoGene 774 145430 (2021)
https://doi.org/10.1016/j.gene.2021.145430
HERC5 and the ISGylation Pathway: Critical Modulators of the Antiviral Immune Response
Nicholas A. Mathieu, Ermela Paparisto, Stephen D. Barr and Donald E. SprattViruses 13 (6) 1102 (2021)
https://doi.org/10.3390/v13061102
Plasmacytoid dendritic cells have divergent effects on HIV infection of initial target cells and induce a pro-retention phenotype
Orion Tong, Gabriel Duette, Thomas R. O’Neil, et al.PLOS Pathogens 17 (4) e1009522 (2021)
https://doi.org/10.1371/journal.ppat.1009522
High-Resolution Profiling of Innate Immune Responses by Porcine Dendritic Cell Subsets in vitro and in vivo
Gaël Auray, Stephanie C. Talker, Irene Keller, et al.Frontiers in Immunology 11 (2020)
https://doi.org/10.3389/fimmu.2020.01429
Classical swine fever virus: the past, present and future
Llilianne Ganges, Helen R. Crooke, Jose Alejandro Bohórquez, Alexander Postel, Yoshihiro Sakoda, Paul Becher and Nicolas RuggliVirus Research 289 198151 (2020)
https://doi.org/10.1016/j.virusres.2020.198151
MERTK is a host factor that promotes classical swine fever virus entry and antagonizes innate immune response in PK-15 cells
Guanglai Zheng, Lian-Feng Li, Yuexiu Zhang, Liang Qu, Wenjing Wang, Miao Li, Shaoxiong Yu, Mo Zhou, Yuzi Luo, Yuan Sun, Muhammad Munir, Su Li and Hua-Ji QiuEmerging Microbes & Infections 9 (1) 571 (2020)
https://doi.org/10.1080/22221751.2020.1738278
A cloned classical swine fever virus derived from the vaccine strain GPE− causes cytopathic effect in CPK-NS cells via type-I interferon-dependent necroptosis
Yukari Itakura, Keita Matsuno, Asako Ito, Markus Gerber, Matthias Liniger, Yuri Fujimoto, Tomokazu Tamura, Ken-ichiro Kameyama, Masatoshi Okamatsu, Nicolas Ruggli, Hiroshi Kida and Yoshihiro SakodaVirus Research 276 197809 (2020)
https://doi.org/10.1016/j.virusres.2019.197809
Differential immunogene expression profile of European sea bass (Dicentrarchus labrax, L.) in response to highly and low virulent NNV
Patricia Moreno, Juan Gemez-Mata, Esther Garcia-Rosado, Julia Bejar, Alejandro M. Labella, Sandra Souto and M. Carmen AlonsoFish & Shellfish Immunology 106 56 (2020)
https://doi.org/10.1016/j.fsi.2020.06.052
Porcine Dendritic Cells and Viruses: An Update
Giulia Franzoni, Simon P. Graham, Silvia Dei Giudici and Annalisa OggianoViruses 11 (5) 445 (2019)
https://doi.org/10.3390/v11050445
Diseases of Swine
Peter D. Kirkland, Marie‐Frédérique Le Potier and Deborah FinlaisonDiseases of Swine 622 (2019)
https://doi.org/10.1002/9781119350927.ch39
Antiviral Role of IFITM Proteins in Classical Swine Fever Virus Infection
Cheng Li, Hongqing Zheng, Yifan Wang, Wang Dong, Yaru Liu, Liang Zhang and Yanming ZhangViruses 11 (2) 126 (2019)
https://doi.org/10.3390/v11020126
Head Start Immunity: Characterizing the Early Protection of C Strain Vaccine Against Subsequent Classical Swine Fever Virus Infection
Ronan R. McCarthy, Helen E. Everett, Simon P. Graham, Falko Steinbach and Helen R. CrookeFrontiers in Immunology 10 (2019)
https://doi.org/10.3389/fimmu.2019.01584
Comprehensive evaluation of the host responses to infection with differentially virulent classical swine fever virus strains in pigs
Jinghan Wang, Yuan Sun, Xing-Yu Meng, et al.Virus Research 255 68 (2018)
https://doi.org/10.1016/j.virusres.2018.06.012
Regulators of Salmonella-host interaction identified by peripheral blood transcriptome profiling: roles of TGFB1 and TRP53 in intracellular Salmonella replication in pigs
Tinghua Huang, Xiali Huang, Bomei Shi, et al.Veterinary Research 49 (1) (2018)
https://doi.org/10.1186/s13567-018-0616-9
Role of innate immunity in pathophysiology of classical swine fever virus infection
Mohsan Ullah Goraya, Fozia Ziaghum, Shilong Chen, et al.Microbial Pathogenesis 119 248 (2018)
https://doi.org/10.1016/j.micpath.2018.04.020
Autophagy induces apoptosis and death of T lymphocytes in the spleen of pigs infected with CSFV
Hongchao Gou, Mingqiu Zhao, Shuangqi Fan, et al.Scientific Reports 7 (1) (2017)
https://doi.org/10.1038/s41598-017-14082-9
Expression profiling of immune genes in classical swine fever vaccinated indigenous and crossbred piglets
SHALU KUMARI PATHAK, VAISHALI SAH, LALRENGPUII SAILO, et al.The Indian Journal of Animal Sciences 87 (10) (2017)
https://doi.org/10.56093/ijans.v87i10.75238
Classical Swine Fever—An Updated Review
Sandra Blome, Christoph Staubach, Julia Henke, Jolene Carlson and Martin BeerViruses 9 (4) 86 (2017)
https://doi.org/10.3390/v9040086
Veterinary Medicine
Veterinary Medicine 2002 (2017)https://doi.org/10.1016/B978-0-7020-5246-0.00021-8
Absence of autophagy promotes apoptosis by modulating the ROS-dependent RLR signaling pathway in classical swine fever virus-infected cells
Jingjing Pei, Jieru Deng, Zuodong Ye, et al.Autophagy 12 (10) 1738 (2016)
https://doi.org/10.1080/15548627.2016.1196318
Guanylate-Binding Protein 1, an Interferon-Induced GTPase, Exerts an Antiviral Activity against Classical Swine Fever Virus Depending on Its GTPase Activity
Lian-Feng Li, Jiahui Yu, Yongfeng Li, et al.Journal of Virology 90 (9) 4412 (2016)
https://doi.org/10.1128/JVI.02718-15
Classical Swine Fever Virus vs. Classical Swine Fever Virus: The Superinfection Exclusion Phenomenon in Experimentally Infected Wild Boar
Sara Muñoz-González, Marta Pérez-Simó, Andreu Colom-Cadena, et al.PLOS ONE 11 (2) e0149469 (2016)
https://doi.org/10.1371/journal.pone.0149469
Treatment with interferon-alpha delays disease in swine infected with a highly virulent CSFV strain
I. Fernandez-Sainz, P. Ramanathan, V. O’Donnell, F. Diaz-San Segundo, L. Velazquez-Salinas, D.F. Sturza, J. Zhu, T. de los Santos and M.V. BorcaVirology 483 284 (2015)
https://doi.org/10.1016/j.virol.2015.04.024
Immune Responses Against Classical Swine Fever Virus: Between Ignorance and Lunacy
Artur Summerfield and Nicolas RuggliFrontiers in Veterinary Science 2 (2015)
https://doi.org/10.3389/fvets.2015.00010
Partial Activation of Natural Killer and γδ T Cells by Classical Swine Fever Viruses Is Associated with Type I Interferon Elicited from Plasmacytoid Dendritic Cells
Giulia Franzoni, Jane C. Edwards, Nitin V. Kurkure, et al.Clinical and Vaccine Immunology 21 (10) 1410 (2014)
https://doi.org/10.1128/CVI.00382-14
The impact of CSFV on the immune response to control infection
Joan Tarradas, Maria Eugenia de la Torre, Rosa Rosell, et al.Virus Research 185 82 (2014)
https://doi.org/10.1016/j.virusres.2014.03.004
The Untranslated Regions of Classic Swine Fever Virus RNA Trigger Apoptosis
Wei-Li Hsu, Chung-Lun Chen, Shi-Wei Huang, et al.PLoS ONE 9 (2) e88863 (2014)
https://doi.org/10.1371/journal.pone.0088863
Differential cellular gene expression in duck trachea infected with a highly or low pathogenic H5N1 avian influenza virus
Pascale Massin, Claire Deleage, Aurélie Oger, et al.Virology Journal 10 (1) (2013)
https://doi.org/10.1186/1743-422X-10-279
CP7_E2alf oral vaccination confers partial protection against early classical swine fever virus challenge and interferes with pathogeny-related cytokine responses
Patricia Renson, Mireille Le Dimna, André Keranflech, et al.Veterinary Research 44 (1) (2013)
https://doi.org/10.1186/1297-9716-44-9
Pathway analysis in blood cells of pigs infected with classical swine fever virus: comparison of pigs that develop a chronic form of infection or recover
Marcel Hulst, Willie Loeffen and Eefke WeesendorpArchives of Virology 158 (2) 325 (2013)
https://doi.org/10.1007/s00705-012-1491-8
Veterinary Hematology
John W. HarveyVeterinary Hematology 122 (2012)
https://doi.org/10.1016/B978-1-4377-0173-9.00005-1
Viewpoint: Factors involved in type I interferon responses during porcine virus infections
Artur SummerfieldVeterinary Immunology and Immunopathology 148 (1-2) 168 (2012)
https://doi.org/10.1016/j.vetimm.2011.03.011
Distinct Peripheral Blood RNA Responses to Salmonella in Pigs Differing in Salmonella Shedding Levels: Intersection of IFNG, TLR and miRNA Pathways
Ting-Hua Huang, Jolita J. Uthe, Shawn M. D. Bearson, et al.PLoS ONE 6 (12) e28768 (2011)
https://doi.org/10.1371/journal.pone.0028768