Fredrick J, Hunter J, Greenwell P, Winter K, Gottschall J L
Transfusion. 1985 Jan-Feb;25(1):30-3. doi: 10.1046/j.1537-2995.1985.25185116498.x.
Two paternity cases involving black persons are reported in which possible paternal exclusions existed if the A2B red cell phenotype represented the genotype A2B. ABH transferase assays were performed to determine if the A2B phenotypes arose from the genotype A1B or A2B. These assays confirmed that all group A members carried the A1 gene and not the A2 gene. Therefore, the alleged father was not excluded in either case. The B transferase showed increased activity in both AB individuals, possibly accounting for the observed A2B red cell phenotypes. Therefore, in the presence of a B gene, accurate assignment of A subtypes using standard serological methods may not be possible.
报告了两起涉及黑人的亲子鉴定案例,如果A2B红细胞表型代表基因型A2B,则存在可能排除父系的情况。进行了ABH转移酶检测,以确定A2B表型是由基因型A1B还是A2B产生的。这些检测证实,所有A血型个体携带的是A1基因而非A2基因。因此,在这两起案例中所谓的父亲均未被排除。B转移酶在两名AB血型个体中均显示出活性增加,这可能解释了所观察到的A2B红细胞表型。因此,在存在B基因的情况下,使用标准血清学方法可能无法准确鉴定A亚型。