Dikiniene N P, Miliukiene V V, Tamosiũnas V J
Vet Immunol Immunopathol. 1986 Sep;13(1-2):111-20. doi: 10.1016/0165-2427(86)90053-x.
Receptors for IgG1 and IgG2 (FcR) on peripheral blood lymphocytes from cows with chronic lymphocytic leukemia (CLL) were detected by their ability to bind homologous IgG1 and IgG2 in fluorometric binding assay. Scatchard plots at 4 degrees C demonstrated that IgG1 bound the same number of FcR per cell (3.12 +/- 0.69 X 10(5)) as IgG2 (2.89 +/- 0.69 X 10(5)). The receptors bound IgG2 with an affinity of 4.09 +/- 1.08 X 10(5) 1/M and IgG1 with an affinity of 2.73 +/- 0.55 X 10(5) 1/M, although the difference was not of statistical significance (0.1 greater than P greater than 0.05). Inhibition studies demonstrated that the two ligands could inhibit each other. It might be assumed that FcR for the two subclasses were identical.
通过荧光结合试验中同源IgG1和IgG2的结合能力,检测慢性淋巴细胞白血病(CLL)奶牛外周血淋巴细胞上IgG1和IgG2的受体(FcR)。4℃下的Scatchard图显示,IgG1与IgG2结合的每个细胞的FcR数量相同(IgG1为3.12±0.69×10⁵,IgG2为2.89±0.69×10⁵)。受体与IgG2的亲和力为4.09±1.08×10⁵ 1/M,与IgG1的亲和力为2.73±0.55×10⁵ 1/M,尽管差异无统计学意义(0.1>P>0.05)。抑制研究表明,两种配体可相互抑制。可以推测,这两个亚类的FcR是相同的。