Rossman M D, Chien P, Cassizzi A, Elias J A, Schreiber A D
Ann N Y Acad Sci. 1986;465:260-7. doi: 10.1111/j.1749-6632.1986.tb18502.x.
Since the macrophage Fc(IgG) receptor appears to be modulated by inflammatory stimuli, we measured the binding of monomeric IgG to monocytes and alveolar macrophages from patients with pulmonary sarcoidosis. Equilibrium binding studies were performed, and the number and affinity of Fc(IgG) receptors were calculated from Scatchard plots of the data. Monocytes from patients with sarcoidosis had nearly twice the number of binding sites for monomeric IgG as did the monocytes from normals. In contrast to the findings with monocytes, alveolar macrophages from patients with sarcoidosis did not have a greater number of monomeric IgG binding sites than did normal alveolar macrophages. These findings are consistent with those on the activation of circulating monocytes in sarcoidosis. That the number of Fc(IgG) receptors on sarcoid alveolar macrophages was not greater than that on normal alveolar macrophages suggests that Fc(IgG) receptor activity on alveolar macrophages does not reflect the activated state of sarcoidosis.
由于巨噬细胞Fc(IgG)受体似乎受炎症刺激的调节,我们检测了肺结节病患者的单核细胞和肺泡巨噬细胞对单体IgG的结合情况。进行了平衡结合研究,并根据数据的Scatchard图计算Fc(IgG)受体的数量和亲和力。结节病患者的单核细胞对单体IgG的结合位点数几乎是正常人单核细胞的两倍。与单核细胞的研究结果相反,结节病患者的肺泡巨噬细胞的单体IgG结合位点数并不比正常肺泡巨噬细胞多。这些发现与结节病中循环单核细胞激活的研究结果一致。结节病肺泡巨噬细胞上Fc(IgG)受体的数量不大于正常肺泡巨噬细胞,这表明肺泡巨噬细胞上Fc(IgG)受体的活性并不反映结节病的激活状态。