Nordhagen R, Heier Larsen A M, Beckers D
Vox Sang. 1979;37(3):170-8. doi: 10.1111/j.1423-0410.1979.tb02287.x.
C4 sucrose/low ionic strength (LIS)-coated red blood cells (RBC) are excellent for the detection of the previously 'nebulous' antibodies, anti-Chido and anti-Rodgers, as well as for serum/plasma typing of these antigens by an inhibition technique. By enzyme treatment of such cells, it is confirmed that the Ch and Rg antigens reside on the C4d part of the C4 molecule. Freshly taken RBC from normal individuals were examined with a sensitive Auto-Analyzer technique with anti-Chido, anti-C4 and anti-C3 sera. All normal RBC were shown to have C4d and C3d components on their surface. The technique was also very sensitive for the detection of the Ch antigen, which was detected on the RBC of all Chido-positive individuals, and which did not show great variation in strength by this method. The mode of in vivo C4 fixation on normal RBC seems to be different from the fixation in LIS or by RBC antibody-mediated activation.
C4蔗糖/低离子强度(LIS)包被的红细胞(RBC)对于检测先前“模糊不清”的抗体、抗奇多和抗罗杰斯抗体非常出色,同时也适用于通过抑制技术对这些抗原进行血清/血浆分型。通过对这类细胞进行酶处理,证实了Ch和Rg抗原位于C4分子的C4d部分。采用灵敏的自动分析仪技术,用抗奇多、抗C4和抗C3血清对正常个体新鲜采集的红细胞进行检测。结果显示,所有正常红细胞表面均有C4d和C3d成分。该技术对Ch抗原的检测也非常灵敏,在所有奇多阳性个体的红细胞上均能检测到Ch抗原,且通过该方法检测到的强度变化不大。正常红细胞体内C4固定的模式似乎与LIS中或红细胞抗体介导激活时的固定模式不同。