Does maternal autoantibody that transfer to newborn cause disease?

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 deliv...

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Main Authors: Toshio Ichiwata, Manabu Ishida, Yuko Itoh, Nobutaka Kitamura, Koh Nakata
Format: Article
Language:English
Published: Wiley 2019-12-01
Series:Respirology Case Reports
Subjects:
Online Access:https://doi.org/10.1002/rcr2.494
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spelling doaj-bd8e213140f54ebb9e40d3ed9aba87152020-11-25T01:17:18ZengWileyRespirology Case Reports2051-33802019-12-0179n/an/a10.1002/rcr2.494Does maternal autoantibody that transfer to newborn cause disease?Toshio Ichiwata0Manabu Ishida1Yuko Itoh2Nobutaka Kitamura3Koh Nakata4Hachioji Medical Center Tokyo Medical University Tokyo JapanHachioji Medical Center Tokyo Medical University Tokyo JapanBioscience Medical Research Center Niigata University Medical and Dental Hospital Niigata JapanBioscience Medical Research Center Niigata University Medical and Dental Hospital Niigata JapanBioscience Medical Research Center Niigata University Medical and Dental Hospital Niigata JapanAutoimmune 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.https://doi.org/10.1002/rcr2.494Autoimmune pulmonary alveolar proteinosisgranulocyte‐macrophage colony‐stimulating factor autoantibodypregnancychildbirth
collection DOAJ
language English
format Article
sources DOAJ
author Toshio Ichiwata
Manabu Ishida
Yuko Itoh
Nobutaka Kitamura
Koh Nakata
spellingShingle Toshio Ichiwata
Manabu Ishida
Yuko Itoh
Nobutaka Kitamura
Koh Nakata
Does maternal autoantibody that transfer to newborn cause disease?
Respirology Case Reports
Autoimmune pulmonary alveolar proteinosis
granulocyte‐macrophage colony‐stimulating factor autoantibody
pregnancy
childbirth
author_facet Toshio Ichiwata
Manabu Ishida
Yuko Itoh
Nobutaka Kitamura
Koh Nakata
author_sort Toshio Ichiwata
title Does maternal autoantibody that transfer to newborn cause disease?
title_short Does maternal autoantibody that transfer to newborn cause disease?
title_full Does maternal autoantibody that transfer to newborn cause disease?
title_fullStr Does maternal autoantibody that transfer to newborn cause disease?
title_full_unstemmed Does maternal autoantibody that transfer to newborn cause disease?
title_sort does maternal autoantibody that transfer to newborn cause disease?
publisher Wiley
series Respirology Case Reports
issn 2051-3380
publishDate 2019-12-01
description 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.
topic Autoimmune pulmonary alveolar proteinosis
granulocyte‐macrophage colony‐stimulating factor autoantibody
pregnancy
childbirth
url https://doi.org/10.1002/rcr2.494
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