Andersson B, Skoglund A C, Rosen A
J Immunol. 1979 Nov;123(5):1936-9.
The function of mouse T lymphocytes with receptors for IgM-Fc was analyzed by using immunofluorescence and a column separation method. The cellular uptake of FITC-IgM was inhibited with unlabeled Fc5 mu. IgM-FcR+ cells were active in ADCC against IgM-sensitized target cells, but not against IgG-coated target cells. The cells mediating ADCC with IgM antibody were shown to be distinct and physically separable from those mediating ADCC with IgG antibody. Helper T lymphocytes for humoral antibody formation in a hapten-carrier system were shown to be IgM-FcR+ and Fc-IgG-.
通过免疫荧光和柱分离法分析了带有IgM-Fc受体的小鼠T淋巴细胞的功能。未标记的Fc5μ可抑制FITC-IgM的细胞摄取。IgM-FcR +细胞对IgM致敏的靶细胞具有ADCC活性,但对IgG包被的靶细胞无活性。结果表明,介导IgM抗体ADCC的细胞与介导IgG抗体ADCC的细胞不同且在物理上可分离。在半抗原-载体系统中,体液抗体形成的辅助性T淋巴细胞显示为IgM-FcR +和Fc-IgG-。