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
Department of Pediatrics, Program in Immunology, Stanford University, Stanford, CA, USA.
Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.
Clin Immunol. 2016 Feb;163:66-74. doi: 10.1016/j.clim.2015.12.011. Epub 2015 Dec 31.
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.
全身型幼年特发性关节炎(sJIA)的特征是全身炎症和关节炎。单核细胞与sJIA的发病机制有关,但其在疾病中的作用尚不清楚。sJIA单核细胞对干扰素的反应可能失调。我们在2个患者组中研究了sJIA活动期和静止期单核细胞对I型干扰素(IFNα)和II型干扰素(IFNγ)的细胞内信号传导。与疾病活动无关,第1组(2002年至2009年收集)的单核细胞在干扰素下游显示STAT1磷酸化缺陷,并表达更高水平的IFN信号抑制剂SOCS1转录本。在第2组(2011年至2014年收集)中,近期发病患者的单核细胞对IFNγ反应低下,但在接受治疗的静止期患者中,单核细胞对IFNγ反应过度。sJIA中近期用药的变化可能会改变IFN反应低下的情况。IFN/pSTAT1信号受损与sJIA单核细胞偏离M1表型一致,可能导致疾病病理改变。