Zwiers Carolien, Koelewijn Joke M, Vermij Lisa, van Sambeeck Joost, Oepkes Dick, de Haas Masja, van der Schoot C Ellen
Department of Obstetrics, Leiden University Medical Center, Leiden, the Netherlands.
Department of Experimental Immunohematology, Sanquin Research and Landsteiner Laboratory, Academic Medical Center, University of Amsterdam, Amsterdam.
Transfusion. 2018 Jul;58(7):1611-1617. doi: 10.1111/trf.14606. Epub 2018 Apr 6.
Hemolytic disease of the fetus and newborn (HDFN) is caused by maternal antibodies against fetal red blood cell antigens, most often anti-D, -K, or -c. ABO incompatibility between mother and child and anti-D immunoprophylaxis (RhIG) are known to reduce the risk of D immunization and subsequent HDFN. However, no immunoprophylaxis has been developed to prevent non-D immunizations.
We evaluated whether ABO incompatibility has a preventive effect on formation of non-D alloantibodies, by performing a case-control study including pregnant women with newly detected non-D antibodies, identified within a nationwide data set, immunized during their first pregnancy and/or delivery. Subsequently, we assessed a possible protective effect of RhIG in a subgroup with non-Rh antibodies only. The proportions of previous ABO incompatibility and of RhIG administrations of these women were compared to the known rate of 19.4% ABO incompatibility and 9.9% RhIG administrations (D- women carrying a D+ child) in the general population of pregnant women.
A total of 11.9% of the 232 included immunized women had a possible ABO incompatibility in their first pregnancy (vs. expected 19.4%; 95% confidence interval [CI], 7.3-18.8; p = 0.036). Furthermore, 1.0% women with non-Rh antibodies were D-, delivered a D+ child, and had therefore received RhIG, whereas 9.9% was expected (95% CI, 0.18-5.50; p = 0.003).
We found that ABO incompatibility and RhIG reduce the risks not only for D, but also for non-Rh immunizations, suggesting that antibody-mediated immune suppression in this condition is not antigen specific.
胎儿和新生儿溶血病(HDFN)由母体针对胎儿红细胞抗原的抗体引起,最常见的是抗-D、-K或-c。已知母婴ABO血型不合和抗-D免疫预防(Rh免疫球蛋白)可降低D免疫和随后发生HDFN的风险。然而,尚未开发出预防非D免疫的免疫预防措施。
我们通过开展一项病例对照研究来评估ABO血型不合对非D同种抗体形成是否具有预防作用,该研究纳入了在全国范围内的数据集中识别出的、在首次妊娠和/或分娩期间免疫的、新检测到非D抗体的孕妇。随后,我们在仅具有非Rh抗体的亚组中评估了Rh免疫球蛋白的可能保护作用。将这些女性既往ABO血型不合和Rh免疫球蛋白给药的比例与孕妇总体人群中已知的19.4%的ABO血型不合率和9.9%的Rh免疫球蛋白给药率(D阴性女性怀有D阳性胎儿)进行比较。
在纳入研究的232名免疫女性中,共有11.9%在首次妊娠时可能存在ABO血型不合(与预期的19.4%相比;95%置信区间[CI],7.3-18.8;p = 0.036)。此外,具有非Rh抗体的女性中有1.0%为D阴性,分娩了D阳性胎儿,因此接受了Rh免疫球蛋白,而预期比例为9.9%(95% CI,0.18-5.50;p = 0.003)。
我们发现ABO血型不合和Rh免疫球蛋白不仅降低了D免疫的风险,也降低了非Rh免疫的风险,这表明在这种情况下抗体介导的免疫抑制并非抗原特异性的。