Ramasamy R
Immunology. 1976 Apr;30(4):559-64.
It is shown that the binding of bivalent anti-immunoglobulin preparations to the surface immunoglobulin of murine B lymphocytes as well as the binding of aggregates of IgG or immune complexes does not lead to detectable increase in cell division in microcultures. Treating lymphocytes with immune complexes and aggregated IgG does not abolish the subsequent mitogenic response induced by LPS. The background mitosis observed in culture is inhibited with anti-immunoglobulin antibodies.
结果表明,二价抗免疫球蛋白制剂与鼠B淋巴细胞表面免疫球蛋白的结合以及IgG聚集体或免疫复合物的结合,在微量培养中不会导致可检测到的细胞分裂增加。用免疫复合物和聚集的IgG处理淋巴细胞不会消除随后由LPS诱导的促有丝分裂反应。培养中观察到的背景有丝分裂被抗免疫球蛋白抗体抑制。