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特发性炎性肌病中肌浸润 T 细胞的单细胞分析。

Single-cell profiling of muscle-infiltrating T cells in idiopathic inflammatory myopathies.

机构信息

Division of Rheumatology, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden.

Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.

出版信息

EMBO Mol Med. 2023 Oct 11;15(10):e17240. doi: 10.15252/emmm.202217240. Epub 2023 Jul 31.

Abstract

Idiopathic inflammatory myopathies (IIM) are rare autoimmune systemic diseases characterized by muscle weakness and the presence of muscle-infiltrating T cells. IIM represent a clinical challenge due to heterogeneity of symptoms and variability of response to immunosuppressive treatment. Here, we performed in-depth single-cell sequencing on muscle-infiltrating T cells and peripheral blood memory T cells in six patients with recently diagnosed IIM. We identified tissue resident memory T-cell (T ) signatures including the expression of HOBIT, XCL1 and CXCR6 in the muscle biopsies of all patients with IIM. Clonally expanded T-cell clones were mainly found among cytotoxic and T implying their role in the disease pathogenesis. Finally, identical expanded T-cell clones persisting at follow-up in the muscle tissue of two patients suggest their involvement in disease chronicity. Our study reveals a muscle tissue resident memory T-cell signature in patients with IIM and a transcriptomic map to identify novel therapeutic targets in IIM.

摘要

特发性炎性肌病(IIM)是一种罕见的自身免疫性系统性疾病,其特征为肌肉无力和肌肉浸润 T 细胞的存在。由于症状的异质性和对免疫抑制治疗的反应变异性,IIM 构成了临床挑战。在这里,我们对六名新诊断为 IIM 的患者的肌肉浸润 T 细胞和外周血记忆 T 细胞进行了深入的单细胞测序。我们在所有 IIM 患者的肌肉活检中鉴定了组织驻留记忆 T 细胞(T 细胞)特征,包括 HOBIT、XCL1 和 CXCR6 的表达。克隆扩增的 T 细胞克隆主要存在于细胞毒性 T 细胞和 T 细胞中,表明它们在疾病发病机制中的作用。最后,两名患者的肌肉组织中在随访时持续存在相同的扩增 T 细胞克隆提示它们与疾病慢性化有关。我们的研究在 IIM 患者中揭示了一种肌肉组织驻留记忆 T 细胞特征,并绘制了转录组图谱以鉴定 IIM 的新治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818e/10565639/fa931d419038/EMMM-15-e17240-g006.jpg

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