Impaired CD163-mediated hemoglobin-scavenging and severe toxic symptoms in patients treated with gemtuzumab ozogamicin

被引:27
作者
Maniecki, Maciej Bogdan [1 ]
Hasle, Henrik [2 ]
Friis-Hansen, Lennart [3 ]
Lausen, Birgitte [4 ]
Nielsen, Ove Juul [5 ]
Bendix, Knud [6 ]
Moestrup, Soren Kragh [1 ,7 ]
Moller, Holger Jon [1 ]
机构
[1] Aarhus Univ Hosp, Dept Clin Biochem, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp Skejby, Dept Pediat, Aarhus, Denmark
[3] Copenhagen Univ Hosp, Dept Clin Biochem, Rigshosp, Copenhagen, Denmark
[4] Copenhagen Univ Hosp, Pediat Clin 2, Rigshosp, Juliane Marie Ctr, Copenhagen, Denmark
[5] Copenhagen Univ Hosp, Dept Hematol, Rigshosp, Copenhagen, Denmark
[6] Aarhus Univ Hosp, Inst Pathol, DK-8000 Aarhus C, Denmark
[7] Univ Aarhus, Inst Med Biochem, Aarhus, Denmark
关键词
D O I
10.1182/blood-2007-09-114165
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 cytotoxcity 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.
引用
收藏
页码:1510 / 1514
页数:5
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