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淋巴细胞和单核细胞上Fc受体对豚鼠IgG1和IgG2的特异性:红细胞的吞噬作用。

Specificity of Fc-receptors on lymphocytes and monocytes for guinea-pig IgG1 and IgG2: phagocytosis of erythrocytes.

作者信息

Ohlander C, Larsson A, Perlmann P

出版信息

Scand J Immunol. 1978 Apr;7(4):285-96. doi: 10.1111/j.1365-3083.1978.tb00456.x.

Abstract

The capacity of guinea-pig IgG1 and IgG2 antibodies to induce lymphocyte (K-cell) mediated lysis or monocyte/macrophage mediated phagocytosis of erythrocytes was studied with both human and guinea-pig effector cells. For both species, induction of K-cell mediated lysis was restricted to IgG2 whereas both IgG1 and IgG2 could induce monocyte/macrophage mediated phagocytosis. In competitive inhibition experiments, only complexed IgG2 inhibited lysis mediated by K-cells. The results suggest that the fc-receptors on K-cells only recognize IgG2. In contrast, complexes of both subclasses inhibited phagocytosis by human monocytes, regardless of the subclass of the inducing antibodies. Inhibition of guinea-pig macrophage mediated phagocytosis by IgG2 complexes was also independent of the inducing antibody. Hence, Fc-receptors common for IgG1 and IgG2 seem to be involved in themonocyte/macrophage mediated effector reaction. Free IgG1 was significantly less ingibitory than free IgG2 for human monocytes and hardly at all for guinea-pig macrophages. However, free IgG2, which was cytophilic for these cells, was more aggregated than IgG1. Thus, both molecular structure and state of aggregation determine interaction of IgG with cellular Fc-receptors.

摘要

利用人和豚鼠效应细胞,研究了豚鼠IgG1和IgG2抗体诱导淋巴细胞(K细胞)介导的红细胞裂解或单核细胞/巨噬细胞介导的红细胞吞噬作用的能力。对于这两个物种,K细胞介导的裂解诱导仅限于IgG2,而IgG1和IgG2均可诱导单核细胞/巨噬细胞介导的吞噬作用。在竞争性抑制实验中,只有复合的IgG2抑制K细胞介导的裂解。结果表明,K细胞上的Fc受体仅识别IgG2。相反,无论诱导抗体的亚类如何,两个亚类的复合物均抑制人单核细胞的吞噬作用。IgG2复合物对豚鼠巨噬细胞介导的吞噬作用的抑制也与诱导抗体无关。因此,IgG1和IgG2共有的Fc受体似乎参与了单核细胞/巨噬细胞介导的效应反应。游离IgG1对人单核细胞的抑制作用明显小于游离IgG2,对豚鼠巨噬细胞几乎没有抑制作用。然而,对这些细胞具有亲细胞性的游离IgG2比IgG1更易聚集。因此,分子结构和聚集状态均决定IgG与细胞Fc受体的相互作用。

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