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Altered signaling in systemic juvenile idiopathic arthritis monocytes.
Macaubas, Claudia; Wong, Elizabeth; Zhang, Yujuan; Nguyen, Khoa D; Lee, Justin; Milojevic, Diana; Shenoi, Susan; Stevens, Anne M; Ilowite, Norman; Saper, Vivian; Lee, Tzielan; Mellins, Elizabeth D.
Afiliação
  • Macaubas C; Department of Pediatrics, Program in Immunology, Stanford University, Stanford, CA, USA.
  • Wong E; Department of Pediatrics, Program in Immunology, Stanford University, Stanford, CA, USA.
  • Zhang Y; Department of Pediatrics, Program in Immunology, Stanford University, Stanford, CA, USA.
  • Nguyen KD; Department of Pediatrics, Program in Immunology, Stanford University, Stanford, CA, USA.
  • Lee J; Department of Pediatrics, Program in Immunology, Stanford University, Stanford, CA, USA.
  • Milojevic D; Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.
  • Shenoi S; Department of Pediatrics, Seattle Children's Hospital & University of Washington School of Medicine, Seattle, WA, USA.
  • Stevens AM; Department of Pediatrics, Seattle Children's Hospital & University of Washington School of Medicine, Seattle, WA, USA.
  • Ilowite N; Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Saper V; Department of Pediatrics, Program in Immunology, Stanford University, Stanford, CA, USA.
  • Lee T; Department of Pediatrics, Program in Immunology, Stanford University, Stanford, CA, USA.
  • Mellins ED; Department of Pediatrics, Program in Immunology, Stanford University, Stanford, CA, USA. Electronic address: mellins@stanford.edu.
Clin Immunol ; 163: 66-74, 2016 Feb.
Article em En | MEDLINE | ID: mdl-26747737
Systemic juvenile idiopathic arthritis (sJIA) is characterized by systemic inflammation and arthritis. Monocytes are implicated in sJIA pathogenesis, but their role in disease is unclear. The response of sJIA monocytes to IFN may be dysregulated. We examined intracellular signaling in response to IFN type I (IFNα) and type II (IFNγ) in monocytes during sJIA activity and quiescence, in 2 patient groups. Independent of disease activity, monocytes from Group 1 (collected between 2002 and 2009) showed defective STAT1 phosphorylation downstream of IFNs, and expressed higher transcript levels of SOCS1, an inhibitor of IFN signaling. In the Group 2 (collected between 2011 and 2014), monocytes of patients with recent disease onset were IFNγ hyporesponsive, but in treated, quiescent subjects, monocytes were hyperresponsive to IFNγ. Recent changes in medication in sJIA may alter the IFN hyporesponsiveness. Impaired IFN/pSTAT1 signaling is consistent with skewing of sJIA monocytes away from an M1 phenotype and may contribute to disease pathology.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Juvenil / Monócitos / Interferons / Fator de Transcrição STAT1 / Proteínas Supressoras da Sinalização de Citocina Tipo de estudo: Observational_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Juvenil / Monócitos / Interferons / Fator de Transcrição STAT1 / Proteínas Supressoras da Sinalização de Citocina Tipo de estudo: Observational_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos