Walker P S, Reid M E
Immunohematology. 2010;26(2):60-5.
Antigens in the Gebrich blood group system are expressed on glycophorin C (GPC) and glycophorin D (GPD), which are both encoded by a single gene, GYPC. The GYPC gene is located on the long arm of chromosome 2, and Gebrich antigens are inherited as autosomal dominant traits. There are 11 antigens in the Gebrich blood group system, six of high prevalence (Ge2, Ge3, Ge4, GEPL [Ge10*], GEAT [Ge11*], GETI [Ge12*]) and five of low prevalence (Wb [Ge5], Ls(a) [Ge6], An(a) [Ge7], Dh(a) [Ge8], GEIS [Ge9]). GPC and GPD interact with protein 4.1R, contributing stability to RBC membrane. Reduced levels of GPC and GPD are associated with hereditary elliptocytosis, and Gebrich antigens act as receptors for the malarial parasite Plasmodium falciparum. Anti-Ge2 and anti-Ge3 have caused hemolytic transfusion reactions, and anti-Ge3 has produced hemolytic disease of the fetus and newborn (HDFN).
吉布赖希血型系统中的抗原在血型糖蛋白C(GPC)和血型糖蛋白D(GPD)上表达,这两种蛋白均由单个基因GYPC编码。GYPC基因位于2号染色体长臂上,吉布赖希抗原作为常染色体显性性状遗传。吉布赖希血型系统中有11种抗原,6种高频率抗原(Ge2、Ge3、Ge4、GEPL [Ge10*]、GEAT [Ge11*]、GETI [Ge12*])和5种低频率抗原(Wb [Ge5]、Ls(a) [Ge6]、An(a) [Ge7]、Dh(a) [Ge8]、GEIS [Ge9])。GPC和GPD与蛋白4.1R相互作用,为红细胞膜提供稳定性。GPC和GPD水平降低与遗传性椭圆形红细胞增多症有关,并且吉布赖希抗原可作为恶性疟原虫的受体。抗Ge2和抗Ge3已引发溶血性输血反应,抗Ge3已导致胎儿和新生儿溶血病(HDFN)。