Roblot P, Morel F, Lelièvre E, Biais-Sauvètre M H, de Groote D, Preud'homme J L, Lecron J C
Service de Medicine Interne, Chu la Miletrie, Poitiers, France.
Immunol Lett. 1996 Oct;53(1):41-4. doi: 10.1016/0165-2478(96)02612-0.
Lymphocytes and monocytes express various levels of membrane-bound CD23, the low affinity receptor for IgE (Fc epsilon RII), and in some cases release it as a soluble form. Soluble CD23 (sCD23) has been implicated in the regulation of many immunological functions of T and B lymphocytes, macrophages and myeloid cells in humans. To study serum sCD23 levels in inflammatory conditions, we selected a systemic disease sensitive to corticotherapy, the giant cell arteritis, which is characterized by an inflammation of the temporal artery. Serum sCD23 levels, as measured by a radioimmunoassay, were increased in these patients, and returned to normal values within the 24 h following initiation of corticotherapy. The data suggest that the increase in sCD23 levels in giant cell arteritis results from an overproduction.
淋巴细胞和单核细胞表达不同水平的膜结合型CD23,即IgE的低亲和力受体(FcεRII),在某些情况下还会以可溶性形式释放它。可溶性CD23(sCD23)参与了人类T和B淋巴细胞、巨噬细胞及髓样细胞的多种免疫功能调节。为研究炎症状态下的血清sCD23水平,我们选择了一种对皮质激素治疗敏感的全身性疾病——巨细胞动脉炎,其特征为颞动脉炎症。通过放射免疫测定法测得,这些患者的血清sCD23水平升高,且在开始皮质激素治疗后的24小时内恢复至正常水平。数据表明,巨细胞动脉炎患者sCD23水平升高是由过度产生所致。