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Basal Activation of Type I Interferons (Alpha2 and Beta) and25OAS Genes: Insights into Differential Expression Profiles of Interferon System Components in Systemic Sclerosis
Author(s) -
Danilo Bretas de Oliveira,
Gabriel Magno de Freitas Almeida,
Antônio Carlos Martins Guedes,
Flávia Patrícia Sena Teixeira Santos,
Cláudio Antônio Bonjardim,
Paulo César Peregrino Ferreira,
Erna Geessien Kroon
Publication year - 2011
Publication title -
international journal of rheumatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.8
H-Index - 33
eISSN - 1687-9279
pISSN - 1687-9260
DOI - 10.1155/2011/275617
Subject(s) - basal (medicine) , beta (programming language) , computer science , algorithm , medicine , programming language , insulin
Objective . Systemic sclerosis (SSc) is a complex autoimmune disease in which interferons (IFNs) may play an essential role. We hypothesized that type I and III IFNs may be found in increased levels in patients and be responsible for SSc autoimmune status. Methods . Type I and III IFN and ISG basal expression profiles were measured by qPCR using RNA from PBMCs of patients and controls . Results . Type I IFNs are increased in SSc patients, while no induction of type III IFNs was detected. This induction cannot be related to IRF7, since no upregulation of this gene was seen on patients. Of the ISGs tested, 2′5′OAS levels were increased in patients, while 6–16 and MxA levels were not. Conclusions . While there is no indication of type III IFN induction, increased levels of type I IFNs may lead to abnormal regulation of ISGs that can be responsible for immune system alterations described for SSc.

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