Maniecki Maciej Bogdan, Hasle Henrik, Friis-Hansen Lennart, Lausen Birgitte, Nielsen Ove Juul, Bendix Knud, Moestrup Søren Kragh, Møller Holger Jon
Department of Clinical Biochemistry, Arhus Sygehus, Aarhus University Hospital, Aarhus, Denmark.
Blood. 2008 Aug 15;112(4):1510-4. doi: 10.1182/blood-2007-09-114165. Epub 2008 Jun 11.
We describe a novel syndrome of severe toxic symptoms during intravascular hemolysis due to impaired hemoglobin scavenging in 2 children with acute myeloid leukemia undergoing CD33-directed therapy with the immunotoxin gemtuzumab ozogamicin (GO). A simultaneous high plasma hemoglobin, haptoglobin, and low bilirubin after septicemia-induced intravascular hemolysis indicated abrogated clearance of haptoglobin-hemoglobin complexes. This was further supported by low levels of plasma soluble CD163 and a concordant low number of CD163-expressing monocytes. We show that CD163 positive monocytes and macrophages from liver, spleen, and bone marrow coexpress CD33, thus suggesting that the GO-induced cellular cytotoxicity of CD33 positive cells eradicates a significant part of the CD163 positive monocytes and macrophages. The risk of severe toxic symptoms from plasma hemoglobin should be considered after CD33-targeted chemotherapy when the disease is complicated by a pathologic intravascular hemolysis. Furthermore, the cases provide further circumstantial evidence of a key role of (CD163-expressing) monocytes/macrophages in plasma hemoglobin clearance in vivo.
我们描述了一种新型综合征,在2例接受免疫毒素吉妥单抗奥唑米星(GO)进行CD33靶向治疗的急性髓系白血病儿童中,由于血红蛋白清除受损,在血管内溶血期间出现严重毒性症状。败血症诱导的血管内溶血后,同时出现高血浆血红蛋白、触珠蛋白和低胆红素,表明触珠蛋白-血红蛋白复合物清除受损。血浆可溶性CD163水平低以及表达CD163的单核细胞数量相应减少进一步支持了这一点。我们发现,来自肝脏、脾脏和骨髓的CD163阳性单核细胞和巨噬细胞共表达CD33,因此表明GO诱导的CD33阳性细胞的细胞毒性消除了很大一部分CD163阳性单核细胞和巨噬细胞。当疾病并发病理性血管内溶血时,在CD33靶向化疗后应考虑血浆血红蛋白引起严重毒性症状的风险。此外,这些病例进一步间接证明了(表达CD163的)单核细胞/巨噬细胞在体内血浆血红蛋白清除中的关键作用。