Le Pennec P Y, Rouger P, Klein M T, Robert N, Salmon C
Vox Sang. 1987;52(3):246-9. doi: 10.1111/j.1423-0410.1987.tb03037.x.
Fya antibodies were detected in 5 Fy(a-b-) black patients during a 5-year period. The Duffy phenotype was confirmed using anti-Fya, anti-Fyb, and anti-Fy3 by an adsorption-elution technique. These 5 patients had sickle cell disease and had received multiple blood transfusions. The antibodies were all found during the investigation of a hemolytic transfusion reaction or failure to achieve the desired red cell increments after transfusion.
在5年期间,在5名Fy(a-b-)黑人患者中检测到了Fya抗体。采用吸附洗脱技术,使用抗Fya、抗Fyb和抗Fy3确认了达菲血型。这5名患者患有镰状细胞病,且接受过多次输血。所有抗体均在溶血性输血反应调查期间或输血后未能实现预期的红细胞增加量时发现。