Silva Francisco, Specks Ulrich, Sethi Sanjeev, Irazabal Maria Valentina, Fervenza Fernando C
Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Am J Kidney Dis. 2009 Sep;54(3):542-5. doi: 10.1053/j.ajkd.2009.02.016. Epub 2009 Apr 23.
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.
髓过氧化物酶(MPO)特异性抗中性粒细胞胞浆抗体被认为是显微镜下多血管炎的致病因素。支持这一假说的是,一份关于经胎盘抗MPO抗体转移可能导致新生儿出现血管炎样综合征的病例报告经常被引用。在此,我们报告一例经胎盘高水平抗MPO抗体转移但未导致新生儿临床损害的病例。母亲在怀孕前5年患显微镜下多血管炎。诱导治疗后,尽管抗MPO抗体水平较高(>100 U/mL),但低剂量泼尼松和硫唑嘌呤维持缓解4.5年。患者选择怀孕,孕期维持免疫抑制,足月分娩一名新生儿。新生儿静脉血抗MPO抗体水平从出生时大于100 U/mL逐渐下降至120天时检测不到。新生儿未出现血管炎临床表现。该病例支持在没有其他辅助因素的情况下,单独的抗MPO抗体不具有致病性。