Oxenhandler R, Hart M N
Hum Pathol. 1983 Apr;14(4):326-37. doi: 10.1016/s0046-8177(83)80118-x.
The inflammatory myopathies are a heterogeneous group of diseases currently categorized by clinical findings, laboratory data, and routine histopathologic features. In the ten years since the direct immunofluorescent (DIF) findings in idiopathic inflammatory myopathy were described, there have been a variety of series reporting DIF findings in various rheumatic and non-rheumatic diseases. This paper reviews this experience and attempts to relate the observations to immunologic mechanisms applicable to skeletal muscle. The potential contributions of direct immunohistochemical methodologies have yet to be realized, because 1) there is a paucity of data actually correlating these findings to clinicopathologic data in patients and experimental models and 2) these techniques have been limited to probing for the humoral response. The future expanded use of this technique should include histochemically tagged antisera to T-lymphocyte antigens, macrophages, biologic modifiers, and suspected etiologic agents.
炎症性肌病是一组异质性疾病,目前根据临床表现、实验室数据和常规组织病理学特征进行分类。自从描述了特发性炎症性肌病的直接免疫荧光(DIF)结果以来的十年里,有各种各样的系列报道了各种风湿性和非风湿性疾病中的DIF结果。本文回顾了这一经验,并试图将这些观察结果与适用于骨骼肌的免疫机制联系起来。直接免疫组织化学方法的潜在贡献尚未实现,原因如下:1)实际将这些结果与患者和实验模型中的临床病理数据相关联的数据很少;2)这些技术仅限于检测体液反应。该技术未来的扩展应用应包括对T淋巴细胞抗原、巨噬细胞、生物修饰剂和可疑病原体进行组织化学标记的抗血清。