Vaughan J I, Warwick R, Letsky E, Nicolini U, Rodeck C H, Fisk N M
Royal Postgraduate Medical School, Institute of Obstetrics and Gynaecology, Queen Charlotte's and Chelsea Hospital, London, United Kingdom.
Am J Obstet Gynecol. 1994 Jul;171(1):247-52. doi: 10.1016/0002-9378(94)90477-4.
Our purpose was to test the hypothesis that maternal anti-Kell alloimmunization produces fetal anemia by erythroid suppression.
Erythropoiesis in 11 anemic fetuses from maternal anti-Kell alloimmunization was compared with that in 11 fetuses where the mother was alloimmunized to RhD; each was matched for hematocrit, gestational age, hydrops, and perinatal outcome. Comparisons of the difference were performed by either paired t or Wilcoxon tests.
The anti-Kell group had reduced reticulocytosis (p = 0.007) and erythroblastosis (p = 0.045) and lower amniotic fluid bilirubin concentrations (p = 0.02) in comparison with the anti-D group. No correlation was found between hematocrit and reticulocytosis in the anti-Kell group, whereas the anti-D group had a significant linear relationship (r = 0.63, p < 0.05), indicating a progressive reticulocytosis in response to the degree of anemia.
These findings suggest that erythroid suppression, rather than hemolysis, is the predominant mechanism in producing fetal anemia related to maternal Kell alloimmunization. Fetal blood sampling is the investigation of choice in the evaluation of anemia related to maternal Kell alloimmunization, because reduced hemolysis means amniotic fluid bilirubin concentrations correlate poorly with anemia.
我们旨在验证以下假设,即母体抗凯尔同种免疫通过红系抑制导致胎儿贫血。
将11例因母体抗凯尔同种免疫而贫血的胎儿的红细胞生成情况与11例母亲为RhD同种免疫的胎儿进行比较;每组在血细胞比容、胎龄、水肿和围产期结局方面进行匹配。差异比较采用配对t检验或威尔科克森检验。
与抗D组相比,抗凯尔组的网织红细胞增多症(p = 0.007)、成红细胞增多症(p = 0.045)减少,羊水胆红素浓度降低(p = 0.02)。抗凯尔组血细胞比容与网织红细胞增多症之间未发现相关性,而抗D组存在显著的线性关系(r = 0.63,p < 0.05),表明网织红细胞增多症随贫血程度加重。
这些发现表明,红系抑制而非溶血是与母体凯尔同种免疫相关的胎儿贫血的主要机制。胎儿血样采集是评估与母体凯尔同种免疫相关贫血的首选检查方法,因为溶血减少意味着羊水胆红素浓度与贫血的相关性较差。