Source:http://linkedlifedata.com/resource/pubmed/id/17594944
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2007-8-1
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pubmed:abstractText |
Through the activation of Toll-like receptors (TLRs) or cytosolic RNA helicases, a large number of pathogenic or synthetic components can induce the transcription of genes coding for type I interferons (IFNs). This family of related cytokines includes notably, a single IFN-beta protein and 13 different IFN-alpha subtypes, whose biological activities are probably not the same. The aim of this study was to characterize the type I IFN subtypes produced in vitro by human peripheral blood mononuclear cells (PBMCs) in response to specific inducers. Thus, PBMCs obtained from a single donor, were exposed to various agents including Sendai virus, Herpes simplex virus-1 (HSV-1), poliovirus-IgG complexes and serum from a patient with systemic lupus erythematosus (SLE). Six hours later, mRNA was extracted and amplified by RT-PCR using primers which recognize IFN-B mRNA and the different IFN-A mRNA subtypes. IFN-A subtypes were identified by cloning and sequencing the amplification product. Antiviral activity was assayed in supernatant at 18 hours. Human PBMCs were found to express constitutively type I IFNs mRNA. Antiviral activity and expression of IFN-A and IFN-B mRNA increased with each inducing agent. Although almost all the IFN-A subtypes were detected, their relative abundance appeared to be dependent upon the inducing agent. Incubation of PBMCs with a neutralizing monoclonal antibody directed against the type I IFN receptor (IFNAR) did not affect the level of antiviral activity in the supernatant of induced PBMCs. Our results suggest that the level of IFN-alpha expressed by PBMCs cells is independent of IFNAR feedback signalling and that the nature of the inducing agent modifies the pattern of IFN-A subtypes preferentially expressed by these cells.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antiviral Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon Type I,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/RNA Helicases,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Interferon alpha-beta
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1148-5493
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
108-14
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pubmed:meshHeading |
pubmed-meshheading:17594944-Antiviral Agents,
pubmed-meshheading:17594944-Cells, Cultured,
pubmed-meshheading:17594944-Cloning, Molecular,
pubmed-meshheading:17594944-Cytosol,
pubmed-meshheading:17594944-Herpesvirus 1, Human,
pubmed-meshheading:17594944-Humans,
pubmed-meshheading:17594944-Immunoglobulin G,
pubmed-meshheading:17594944-Interferon Type I,
pubmed-meshheading:17594944-Interferon-alpha,
pubmed-meshheading:17594944-Leukocytes, Mononuclear,
pubmed-meshheading:17594944-Lupus Erythematosus, Systemic,
pubmed-meshheading:17594944-Poliovirus,
pubmed-meshheading:17594944-RNA Helicases,
pubmed-meshheading:17594944-Receptor, Interferon alpha-beta,
pubmed-meshheading:17594944-Sendai virus
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pubmed:year |
2007
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pubmed:articleTitle |
Type I interferon subtypes produced by human peripheral mononuclear cells from one normal donor stimulated by viral and non-viral inducing factors.
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pubmed:affiliation |
Université Paris Descartes - Faculté de Médecine - Laboratory of Virology, Cochin-Saint-Vincent-de-Paul Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), 82, avenue Denfert-Rochereau, 75674 Paris Cedex 14, France.
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pubmed:publicationType |
Journal Article
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