Macrophage subpopulations in the thymic hyperplasia of patients with myasthenia gravis.

Jian Zhang, S. Cohen-Kaminsky, Sonia Berrih-Aknin
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引用次数: 3

Abstract

Macrophages were studied in sections of the thymus from patients with Myasthenia Gravis, using a panel of monoclonal antibodies against the monocyte/macrophage lineage. In normal areas, CD14 and CD35 were preferentially expressed in the medulla while RM3/1 and 25F9 markers stained essentially cortical macrophages. CD11c-labelled cells were densely located throughout the thymus. The antibody 27E10 recognized clusters of cells located around or in the perivascular areas, that could be migrating monocytes. In the germinal centers, cells were stained with CD14, CD35, CD11c and 25F9 but not with RM3/1 and 27E10 markers. The numbers of CD14- and CD35-positive cells were significantly increased in Myasthenia Gravis thymic hyperplasia compared to control thymus (p < 0.025 and p < 0.01, respectively). This increase was clearly due to the higher number of positive cells in the germinal centers and in the areas surrounding the lymphoid follicles. The potential role of these cells in accessory cell function and antigen presentation could be relevant in terms of intrathymic sensitization and autoantibody production that have been demonstrated in thymic hyperplasia from Myasthenia Gravis patients.
巨噬细胞亚群在重症肌无力患者胸腺增生中的作用。
巨噬细胞在重症肌无力患者胸腺切片中进行了研究,使用了一组针对单核细胞/巨噬细胞谱系的单克隆抗体。在正常区域,CD14和CD35优先在髓质中表达,而RM3/1和25F9标记物主要染色皮质巨噬细胞。cd11c标记细胞密集分布于整个胸腺。抗体27E10识别位于血管周围或血管周围区域的细胞簇,可能是迁移的单核细胞。在生发中心,细胞被CD14、CD35、CD11c和25F9染色,但不被RM3/1和27E10标记染色。与对照组相比,重症肌无力胸腺增生组CD14-和cd35阳性细胞数量显著增加(p < 0.025和p < 0.01)。这种增加显然是由于生发中心和淋巴滤泡周围区域的阳性细胞数量较多。这些细胞在辅助细胞功能和抗原呈递中的潜在作用可能与重症肌无力患者胸腺增生引起的胸腺内致敏和自身抗体产生有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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