期刊
TRANSFUSION
卷 63, 期 6, 页码 1141-1149出版社
WILEY
DOI: 10.1111/trf.17342
关键词
antibodies; FNAIT; HLA; neonatal; pregnancy; thrombocytopenia
类别
This study examined whether suspected cases of fetal and neonatal alloimmune thrombocytopenia (FNAIT) without maternal human platelet antigens (HPA) antibodies had different human leukocyte antigen (HLA) antibody strength and specificity compared to controls. The results showed that FNAIT cases had significantly higher HLA antibody strength and broader HLA antibody specificity compared to matched controls.
BackgroundFetal and neonatal alloimmune thrombocytopenia (FNAIT) is caused by antibodies against human platelet antigens (HPA). However, in many cases that meet clinical criteria for the condition, maternal sera do not have HPA antibodies. In studies examining whether human leukocyte antigen (HLA) antibodies cause FNAIT, the results are limited and inconclusive. This study sought to examine whether clinically suspected FNAIT cases with absent maternal HPA antibodies had different HLA antibody strength and specificity compared to controls. Study Design and MethodsA retrospective case-control study assessed class I HLA antibody strength and specificity in cases submitted for testing to Versiti, Wisconsin. There were 813 cases that met initial screening criteria, but written consent could only be obtained for 50. After review of medical records and expert panel review, 31 cases with clinical criteria of FNAIT and maternal HLA but not HPA antibodies were included. Each case was matched for maternal age, gestational age at delivery, parity, and race/ethnicity to two controls from unaffected pregnancies that had maternal serum HLA antibodies. ResultsFNAIT cases were found to have both significantly higher HLA antibody strength, measured by mean fluorescence index (MFI), and broader HLA antibody specificity at antigen epitope level, compared to matched controls (p < .001). p-values remained significant after controlling for parity and gestational age at delivery. DiscussionAdditional studies are needed to further examine whether the strong HLA antibodies identified in HPA-antibody-negative cases directly cause neonatal thrombocytopenia and whether prenatal treatment may be warranted in select cases to prevent recurrence.
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