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[霍顿病中颞动脉炎病变的免疫组织化学研究]

[Immunohistochemical study of lesions of temporal arteritis in Horton's disease].

作者信息

Liozon F, Lavignac C, Emilie D, Liozon E, Crevon M C, Vidal E, Bordessoule D, Catanzano G, Galanaud P

机构信息

Service de Médecine Interne A, CHRU de Limoges.

出版信息

Ann Med Interne (Paris). 1993;144(2):85-91.

PMID:8333665
Abstract

Fourteen monoclonal antibodies were used to immunohistochemically label 22 temporal artery biopsy specimens taken from patients with temporal arteritis before treatment (n = 10), after 1.3 days of corticotherapy (n = 6) and after 12-30 days of steroids (n = 6). Histological sections from untreated patients revealed an inflammatory infiltrate comprised of approximately equal proportions of macrophages and T lymphocytes; the majority of the latter belonged to the CD4+ subset (the CD4+/CD8+ ratio varied from 2/1 to 4/1, depending upon the biopsy). These cells expressed high levels of HLA DR and low levels of interleukin-2 (IL2) receptors. A few B lymphocytes and plasmocytes were seen, mainly in the adventitia. Antigen-presenting cells (APC) were always found in the damaged media and natural killer cells (few in number) were sometimes present. Some macrophages were positively immunolabeled for IL6. A short, 1-to-3-day course of corticosteroids did not appreciably modify the lesions: cells remained highly activated, APC were seen in half the biopsies and IL6 immunolabeling persisted. The findings were essentially the same in treated but poorly controlled patients. Biopsies from 2 patients in clinical and biological remission revealed the persistence of an active immunological process. These observations indicate that the immunological process is poorly controlled by corticosteroid therapy.

摘要

使用14种单克隆抗体对22份颞动脉活检标本进行免疫组织化学标记,这些标本取自颞动脉炎患者治疗前(n = 10)、皮质激素治疗1.3天后(n = 6)以及使用类固醇12 - 30天后(n = 6)。未经治疗患者的组织学切片显示炎症浸润,巨噬细胞和T淋巴细胞比例大致相等;后者大多数属于CD4 + 亚群(CD4 + /CD8 + 比值根据活检情况在2/1至4/1之间变化)。这些细胞表达高水平的HLA DR和低水平的白细胞介素 - 2(IL2)受体。可见少量B淋巴细胞和浆细胞,主要在外膜。抗原呈递细胞(APC)总是出现在受损的中膜,自然杀伤细胞(数量很少)有时也会出现。一些巨噬细胞对IL6呈阳性免疫标记。短期(1至3天)的皮质类固醇治疗并未明显改变病变:细胞仍高度活化,一半的活检标本中可见APC,IL6免疫标记持续存在。在治疗但控制不佳的患者中,结果基本相同。2例临床和生物学缓解患者的活检显示活跃的免疫过程持续存在。这些观察结果表明,皮质类固醇治疗对免疫过程控制不佳。

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