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Does maternal autoantibody that transfer to newborn cause disease?

机译:转移至新生儿的母体自身抗体会引起疾病吗?

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摘要

Autoimmune pulmonary alveolar proteinosis (aPAP) is associated with excess amount of granulocyte‐macrophage colony‐stimulating factor (GM‐CSF) autoantibody (GMAb) in the lung and blood. We experienced a female case with severe aPAP who could continue her pregnancy under home oxygen therapy and delivered a newborn by caesarean section. Maternal serum GMAb remained high level for up to one year after the delivery, although aPAP entered remission by whole lung lavage. While the newborn oxygen saturation as well as serum Krebs von den Lungen‐6 and surfactant protein‐D levels had been normal until one year. As GMAb likely transfer to the newborn and might cause the same disease, we carefully monitored both maternal and the newborn serum GMAb levels after the birth for up to one year. We confirmed that GMAb passively transferred to the newborn circulation but rapidly decreased exponentially to the cut‐off level. It is suggested that this rapid decrease might prevent the newborn from developing aPAP.
机译:自身免疫性肺泡蛋白沉着症(aPAP)与肺和血液中过量的粒细胞-巨噬细胞集落刺激因子(GM-CSF)自身抗体(GMAb)相关。我们遇到了一位患有严重aPAP的女性病例,她可以在家庭氧气治疗下继续怀孕,并通过剖腹产分娩了新生儿。尽管aPAP通过全肺灌洗进入缓解期,但分娩后母体血清GMAb仍保持高水平长达一年。直到一年之前,新生儿的血氧饱和度以及血清Krebs von den Lungen-6和表面活性剂蛋白D的水平都正常。由于GMAb可能会转移至新生儿并可能引起相同的疾病,因此我们对出生后长达一年的孕妇和新生儿血清GMAb水平进行了仔细监测。我们证实GMAb被动转移至新生儿循环,但迅速下降至临界水平。提示这种快速下降可能会阻止新生儿发展aPAP。

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