Department of Medical Biology, UiT The Arctic University of Norway, Tromsø, Norway.
Department of Hematological and Transfusion Immunology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
J Reprod Immunol. 2023 Dec;160:104168. doi: 10.1016/j.jri.2023.104168. Epub 2023 Nov 7.
Fetomaternal incompatibility in human platelet antigens (HPAs) can cause maternal alloimmunization, which in turn may lead to thrombocytopenia with or without intracranial hemorrhage (ICH) in the fetus or newborn. Retrospective studies suggest that boys from alloimmunized mothers may have higher risk of ICH and lower birth weight than girls. The objective of this study was to assess how maternal HPA-1a alloimmunization, sex of the neonate and birth weight relates in a large prospective cohort. Through a national screening study in Poland (PREVFNAIT) involving HPA-1 typing of 24,259 pregnant women during 2013-2017, 606 HPA-1a negative pregnant women and their offspring were identified and included. Various multivariate models were used to assess if and how maternal HPA-1a alloimmunization status was associated with birth weight and risk of having a small for gestational age (SGA) neonate, and if and how sex of the neonate mattered. Most immunized pregnancies had male fetuses (69 %). Women carrying a male fetus had increased likelihood of having an SGA newborn if they were HPA-1a alloimmunized compared to non-immunized mothers. Increasing maternal anti-HPA-1a antibody levels were significantly associated with reduced birth weight and SGA risk among male-fetus pregnancies, but not if the fetus was female. In conclusion, anti-HPA-1a antibodies in a male fetus pregnancy is associated with increased risk of SGA and lower birth weight, especially if the antibody level is high. Sex of the fetus may therefore be considered as a new clinical predictor of more severe FNAIT neonatal outcome.
人类血小板抗原(HPAs)的母婴不相容可导致母体同种免疫,进而可能导致胎儿或新生儿出现血小板减少症,伴或不伴颅内出血(ICH)。回顾性研究表明,来自同种免疫母亲的男孩发生 ICH 的风险高于女孩,且出生体重较低。本研究的目的是评估母体 HPA-1a 同种免疫、新生儿性别和出生体重在一个大型前瞻性队列中的关系。通过在波兰进行的一项全国性筛查研究(PREVFNAIT),在 2013 年至 2017 年间对 24259 名孕妇进行了 HPA-1 分型,鉴定并纳入了 606 名 HPA-1a 阴性孕妇及其后代。使用各种多变量模型来评估母体 HPA-1a 同种免疫状态是否以及如何与出生体重和发生小于胎龄儿(SGA)的风险相关,以及新生儿性别是否以及如何影响。大多数免疫妊娠的胎儿为男性(69%)。与非免疫母亲相比,如果携带男性胎儿的女性存在 HPA-1a 同种免疫,则她们更有可能出现 SGA 新生儿。母体抗-HPA-1a 抗体水平升高与男性胎儿妊娠的出生体重降低和 SGA 风险增加显著相关,但如果胎儿为女性则无此关联。总之,男性胎儿妊娠中的抗-HPA-1a 抗体与 SGA 和出生体重降低的风险增加相关,尤其是当抗体水平较高时。因此,胎儿性别可被视为预测更严重的新生儿同种免疫不良结局的新临床指标。