Malkovský M, Bubeník J, Holán V, Hasek M
Folia Biol (Praha). 1979;25(3):179-87.
Transplantation immunity against a product of the D-region of mouse H-2 gene complex was examined by the macrophage electrophoretic mobility assay. The results obtained with the MEM assay depended upon selection of the guinea pig peritoneal exudate macrophages used for measurements. The macrophages 16--20 micrometers in diameter and containing liquid paraffin droplets were best suited for electrophoretic mobility measurements. The cells, containing liquid paraffin droplets but smaller than 16 micrometers in diameter, were affected by lymphocyte-antigen interaction product(s) much less. The increasing antigen concentration resulted in a sharp rise of macrophage percentage slowing from zero but reached a plateau value. The critical number of lymph node cells for a significant response was not less than 10(5) cells and there was a direct relationship between the number of lymphocytes and the magnitude of the response.
通过巨噬细胞电泳迁移率测定法检测了针对小鼠H-2基因复合体D区产物的移植免疫。用MEM测定法获得的结果取决于用于测量的豚鼠腹腔渗出巨噬细胞的选择。直径为16 - 20微米且含有液体石蜡滴的巨噬细胞最适合进行电泳迁移率测量。含有液体石蜡滴但直径小于16微米的细胞受淋巴细胞 - 抗原相互作用产物的影响要小得多。抗原浓度的增加导致巨噬细胞百分比从零急剧上升,但达到一个稳定值。产生显著反应的淋巴结细胞的临界数量不少于10⁵个细胞,并且淋巴细胞数量与反应强度之间存在直接关系。