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包涵体肌炎和多发性肌炎中的髓样树突状细胞

Myeloid dendritic cells in inclusion-body myositis and polymyositis.

作者信息

Greenberg Steven A, Pinkus Geraldine S, Amato Anthony A, Pinkus Jack L

机构信息

Department of Neurology, Division of Neuromuscular Disease, Brigham and Women's Hospital, 75 Francis Street, and Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Muscle Nerve. 2007 Jan;35(1):17-23. doi: 10.1002/mus.20649.

Abstract

Dendritic cells (DCs), immune system cells central to the development of immunity, have not previously been reported in muscle in inclusion-body myositis (IBM). We performed immunohistochemical studies on muscle biopsy specimens from 50 patients using monoclonal antibodies that distinguish two classes of DCs, myeloid DC and plasmacytoid DC. In 17 of 20 IBM and 9 of 10 polymyositis (PM) specimens, myeloid DCs were present in substantial numbers, frequently surrounded and sometimes invading otherwise intact myofibers, and were part of dense collections of cells that included T cells. Dermatomyositis muscle had more plasmacytoid DCs than myeloid DCs, whereas IBM and PM had greater numbers of myeloid DCs. The stellate morphology of myeloid DCs in dense collections of cells that included T cells suggests local intramuscular antigen presentation in IBM and PM.

摘要

树突状细胞(DCs)是免疫系统中对免疫发育至关重要的细胞,此前在包涵体肌炎(IBM)的肌肉中尚未有报道。我们使用可区分两类DCs(髓样DC和浆细胞样DC)的单克隆抗体,对50例患者的肌肉活检标本进行了免疫组织化学研究。在20例IBM标本中的17例以及10例多发性肌炎(PM)标本中的9例中,存在大量髓样DC,它们常常围绕并有时侵入原本完整的肌纤维,并且是包括T细胞在内的密集细胞群的一部分。皮肌炎肌肉中的浆细胞样DC比髓样DC更多,而IBM和PM中的髓样DC数量更多。在包括T细胞在内的密集细胞群中,髓样DC的星状形态提示IBM和PM中存在局部肌肉内抗原呈递。

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