White C A, Stedman C M, Frank S
Am J Obstet Gynecol. 1983 Apr 15;145(8):1069-75. doi: 10.1016/0002-9378(83)90868-2.
Regardless of the decrease in Rh sensitization as a cause of hemolytic disease of the newborn, antenatal antibody screening must be performed in all patients to detect not only anti-D sensitization, but other less common antibodies capable of provoking hemolytic disease of the newborn. The relative incidence of hemolytic disease of the newborn due to sensitization to such irregular antibodies as Kell, Kidd, and Duffy is increasing. We report here five patients who had D- or Du-positive blood with antenatal anti-D sensitization, and whose neonates had hemolytic disease of the newborn of varying severity. Blood that is D- and Du-positive with anti-D has been classified by Tippett; such blood types lack part of the D mosaic and are considered to be "D variants" yet are typed routinely as Rh positive. Anti-D antibody produced by D- and Du-positive blood is indistinguishable from the ordinary variety of anti-D.
尽管作为新生儿溶血病病因的Rh致敏发生率有所下降,但仍必须对所有患者进行产前抗体筛查,以不仅检测抗-D致敏,还要检测其他能够引发新生儿溶血病的较罕见抗体。因对凯尔(Kell)、基德(Kidd)和达菲(Duffy)等不规则抗体致敏而导致的新生儿溶血病的相对发生率正在上升。我们在此报告5例产前抗-D致敏的D型或Du型阳性血患者,其新生儿患有不同严重程度的新生儿溶血病。蒂皮特(Tippett)已对具有抗-D的D型和Du型阳性血进行了分类;此类血型缺少部分D镶嵌结构,被视为“D变异型”,但常规分型为Rh阳性。D型和Du型阳性血产生的抗-D抗体与普通抗-D无法区分。