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靶向治疗幼年特发性关节炎和幼年皮肌炎——来自其他疾病的启示。

Targeting Tregs in Juvenile Idiopathic Arthritis and Juvenile Dermatomyositis-Insights From Other Diseases.

机构信息

Department of Surgery, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, BC, Canada.

Division of Infection and Immunity, Institute of Immunity and Transplantation, University College London, London, United Kingdom.

出版信息

Front Immunol. 2019 Jan 25;10:46. doi: 10.3389/fimmu.2019.00046. eCollection 2019.

Abstract

Regulatory T cells (Tregs) are believed to be dysfunctional in autoimmunity. Juvenile idiopathic arthritis (JIA) and juvenile dermatomyositis (JDM) result from a loss of normal immune regulation in specific tissues such as joints or muscle and skin, respectively. Here, we discuss recent findings in regard to Treg biology in oligo-/polyarticular JIA and JDM, as well as what we can learn about Treg-related disease mechanism, treatment and biomarkers in JIA/JDM from studies of other diseases. We explore the potential use of Treg immunoregulatory markers and gene signatures as biomarkers for disease course and/or treatment success. Further, we discuss how Tregs are affected by several treatment strategies already employed in the therapy of JIA and JDM and by alternative immunotherapies such as anti-cytokine or co-receptor targeting. Finally, we review recent successes in using Tregs as a treatment target with low-dose IL-2 or cellular immunotherapy. Thus, this mini review will highlight our current understanding and identify open questions in regard to Treg biology, and how recent findings may advance biomarkers and new therapies for JIA and JDM.

摘要

调节性 T 细胞(Tregs)被认为在自身免疫中功能失调。幼年特发性关节炎(JIA)和幼年皮肌炎(JDM)分别是由于关节或肌肉和皮肤等特定组织中正常免疫调节的丧失而导致的。在这里,我们讨论了关于寡关节/多关节 JIA 和 JDM 中 Treg 生物学的最新发现,以及我们可以从其他疾病的研究中了解到关于 JIA/JDM 中与 Treg 相关的疾病机制、治疗和生物标志物的信息。我们探讨了 Treg 免疫调节标志物和基因特征作为疾病进程和/或治疗成功的生物标志物的潜在用途。此外,我们还讨论了 Tregs 如何受到 JIA 和 JDM 治疗中已经采用的几种治疗策略以及替代免疫疗法(如抗细胞因子或共受体靶向)的影响。最后,我们回顾了使用低剂量 IL-2 或细胞免疫疗法作为治疗靶点的最新成功案例。因此,这篇小型综述将强调我们目前对 Treg 生物学的理解,并确定与 Treg 生物学相关的开放性问题,以及最近的发现如何为 JIA 和 JDM 推进生物标志物和新疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/106f/6355674/3f3b74a9b6fe/fimmu-10-00046-g0001.jpg

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