Abstract
Myeloperoxidase (MPO)-specific antineutrophil cytoplasmic antibodies have been proposed as pathogenic for microscopic polyangiitis. Supporting this hypothesis, a case report of transplacental anti-MPO antibody transfer presumably causing a vasculitis-like syndrome in the newborn is cited frequently. Here, we report a case of transplacental transfer of high levels of anti-MPO antibodies not resulting in clinical compromise in the newborn. The mother developed microscopic polyangiitis 5 years before the pregnancy. After induction therapy, remission was maintained with low-dose prednisone and azathioprine for 4.5 years despite high levels of anti-MPO antibodies (>100 U/mL). The patient elected to become pregnant, immunosuppression was maintained during pregnancy, and a normal-term neonate was delivered. The newborn's venous blood anti-MPO antibody levels decreased gradually from greater than 100 U/mL at birth to undetectable by day 120. No clinical manifestation of vasculitis developed in the newborn. This case supports that anti-MPO antibodies alone are not pathogenic without additional cofactors.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 542-545 |
| Number of pages | 4 |
| Journal | American Journal of Kidney Diseases |
| Volume | 54 |
| Issue number | 3 |
| DOIs | |
| State | Published - Sep 2009 |
Keywords
- Vasculitis
- antineutrophil cytoplasmic antibodies (ANCAs)
- microscopic polyangiitis (MPA)
- myeloperoxidase (MPO)
ASJC Scopus subject areas
- Nephrology
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