Hohlfeld R, Engel A G
Department of Neurology, University of Munich, FRG.
Chem Immunol. 1992;53:75-85.
During the course of a systematic study of T cell lines derived from muscle of patients with various inflammatory myopathies, we identified a new form of polymyositis that is mediated by gamma-delta T cells. In the affected patient's muscle CD3+CD4-CD8- gamma-delta T cells surrounded and invaded nonnecrotic muscle fibers in the same way as CD3+CD8+ alpha-beta T cells surround and invade nonnecrotic muscle fibers in inclusion body myositis and other forms of polymyositis. Gamma-delta T cells were extremely rare or absent in muscles and muscle-derived T cell lines in other patients with polymyositis, inclusion-body myositis, dermatomyositis or granulomatous myopathy. This new form of polymyositis has provided us with a unique opportunity to study cytotoxic gamma-delta T cells and their muscle-fiber targets in situ. All muscle fibers expressed HLA-class I antigen and the 65-kD heat-shock protein. The autoaggressive behavior of the gamma-delta T cells is consistent with the hypothesis that in some inflammatory myopathies autoinvasive T cells recognize muscle fiber associated antigen(s). Further studies are needed to define the type of gamma-delta T cell receptor used and the antigen(s) recognized by gamma-delta T cells in this rare type of autoimmune muscle disease.
在对源自各种炎性肌病患者肌肉的T细胞系进行系统研究的过程中,我们发现了一种由γδ T细胞介导的新型多发性肌炎。在受影响患者的肌肉中,CD3⁺CD4⁻CD8⁻γδ T细胞以与包涵体肌炎和其他形式的多发性肌炎中CD3⁺CD8⁺αβ T细胞包围并侵入非坏死性肌纤维相同的方式包围并侵入非坏死性肌纤维。在其他患有多发性肌炎、包涵体肌炎、皮肌炎或肉芽肿性肌病的患者的肌肉和肌肉来源的T细胞系中,γδ T细胞极其罕见或不存在。这种新型的多发性肌炎为我们提供了一个独特的机会,来原位研究细胞毒性γδ T细胞及其肌纤维靶标。所有肌纤维均表达HLA-I类抗原和65-kD热休克蛋白。γδ T细胞的自身攻击行为与以下假设一致:在某些炎性肌病中,自身侵入性T细胞识别与肌纤维相关的抗原。需要进一步研究来确定在这种罕见的自身免疫性肌肉疾病中使用的γδ T细胞受体类型以及γδ T细胞识别的抗原。