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活化的树突状细胞亚群可表征包涵体肌炎患者的肌肉,并与KLRG1+和TBX21+ CD8+ T细胞相关。

Activated Dendritic Cell Subsets Characterize Muscle of Inclusion Body Myositis Patients and Correlate with KLRG1+ and TBX21+ CD8+ T cells.

作者信息

Kirou Raphael A, Pinal-Fernandez Iago, Casal-Dominguez Maria, Pak Katherine, Ikenaga Chiseko, Nelke Christopher, Wischnewski Sven, Del Orso Stefania, Naz Faiza, Islam Shamima, Gutierrez-Cruz Gustavo, Lloyd Thomas E, Schirmer Lucas, Ruck Tobias, Stenzel Werner, Selva-O'Callaghan Albert, Milisenda Jose C, Mammen Andrew L

机构信息

Muscle Disease Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, USA.

College of Medicine, State University of New York Downstate Health Sciences University, Brooklyn, NY, USA.

出版信息

medRxiv. 2025 Jun 5:2025.06.04.25328910. doi: 10.1101/2025.06.04.25328910.

Abstract

Inclusion body myositis (IBM) is an idiopathic inflammatory myopathy characterized by muscle-infiltrating KLRG1+ and TBX21+ cytotoxic T cells and type 1 inflammation. Myeloid dendritic cells (mDCs), including type 1 conventional dendritic (cDC1) cells, type 2 conventional dendritic (cDC2) cells, and mature immunoregulatory dendritic (mregDC) cells, have previously been reported in skeletal muscle of IBM patients and may activate these cytotoxic T cells. Here, we analyzed single-nucleus RNA-sequencing (snRNA-seq) and bulk RNA-sequencing (RNA-seq) data from skeletal muscle of IBM, other myositis, and control patients to identify and quantify these mDC subsets and characterize their contribution to IBM inflammation. Our findings reveal that all three mDC subsets are relatively increased and activated in muscle of IBM patients and correlate with IBM-specific inflammatory markers. Our data specifically implicates cDC1 cells in CD8+ T cell activation via specific expression of both KLRG1 ligands, and , as well as in IBM muscle.

摘要

包涵体肌炎(IBM)是一种特发性炎性肌病,其特征为肌肉浸润的KLRG1+和TBX21+细胞毒性T细胞以及1型炎症。此前有报道称,在IBM患者的骨骼肌中存在髓样树突状细胞(mDC),包括1型传统树突状(cDC1)细胞、2型传统树突状(cDC2)细胞和成熟免疫调节树突状(mregDC)细胞,这些细胞可能激活这些细胞毒性T细胞。在此,我们分析了来自IBM患者、其他肌炎患者和对照患者骨骼肌的单核RNA测序(snRNA-seq)和批量RNA测序(RNA-seq)数据,以识别和量化这些mDC亚群,并描述它们对IBM炎症的作用。我们的研究结果表明,在IBM患者的肌肉中,所有三种mDC亚群均相对增加且被激活,并与IBM特异性炎症标志物相关。我们的数据特别表明,cDC1细胞通过KLRG1配体 和 以及IBM肌肉中的 的特异性表达,参与CD8+T细胞的激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0552/12155022/a69847e219c8/nihpp-2025.06.04.25328910v1-f0001.jpg

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