Hughes-Jones N C, Gorick B D, Brown D
Department of Immunology, Institute of Animal Physiology and Genetic Research, AFRC Babraham, Cambridge, U.K.
Immunol Lett. 1991 Feb;27(2):101-3. doi: 10.1016/0165-2478(91)90135-w.
The D polypeptide of the human Rh blood group system has a number of different epitopes on its surface. It is also known that there is considerable variation in the number of D antigen sites available to different human monoclonal anti-D antibodies. For instance, certain monoclonal antibodies recognise only a small number of sites on the red cell surface (about 9,000 sites/red cell on R1R2 cells) whereas other antibodies recognise a high number (about 20,000-30,000 sites/red cell). It has been found that cholesterol enrichment of the red cell membrane increases the number of sites available to those antibodies which recognize only a few sites but has no effect on those recognising many sites. The results are consistent with the view that access to some of the D epitopes is partially hindered by neighbouring molecules in the membrane and that alteration of the lipid content of the membrane changes it in such a way as to allow increased access to these obstructed epitopes.
人类Rh血型系统的D多肽在其表面有许多不同的表位。还已知不同的人源单克隆抗-D抗体可识别的D抗原位点数量存在相当大的差异。例如,某些单克隆抗体仅识别红细胞表面的少数位点(R1R2细胞上约9000个位点/红细胞),而其他抗体识别的位点数量较多(约20000 - 30000个位点/红细胞)。已发现红细胞膜的胆固醇富集增加了仅识别少数位点的抗体可识别的位点数量,但对识别多个位点的抗体没有影响。这些结果与以下观点一致,即膜中相邻分子会部分阻碍对某些D表位的识别,并且膜脂质含量的改变会以某种方式改变膜,从而增加对这些受阻表位的识别机会。