High Rates of Anti-αIIbβ3 Antibodies Produced by a Glanzmann Thrombasthenia Patient after First and Unique Red Blood Cells Administration.

IF 1.7 4区 医学 Q3 HEMATOLOGY Acta Haematologica Pub Date : 2023-01-01 DOI:10.1159/000526224
Yoann Huguenin, Laure Levoir, Muriel Bouton, Mathieu Fiore
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Abstract

Immunization against the platelet αIIbβ3 glycoprotein due to blood transfusion represents one of the most severe complications in Glanzmann thrombasthenia (GT) disease. Anti-αIIbβ3 isoantibodies development may lead to ineffective platelet transfusion and can, in case of pregnancy, cross the placenta leading to fetal thrombocytopenia. We describe here the case of a girl with type I GT who developed high rates of anti-αIIbβ3 isoantibodies after first and unique blood transfusion. Surprisingly, this patient had only received red blood cell concentrates and immunization was presumably stimulated by the residual presence of platelets in concentrates. This study emphasizes the need for regular anti-αIIbβ3 antibodies screening in GT, even though patients have never been previously transfused with platelet concentrates.

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格兰兹曼血栓患者第一次和独特的红细胞治疗后产生的抗α iib β3抗体率高
输血引起的血小板α ib β3糖蛋白免疫是Glanzmann血栓减少症(GT)最严重的并发症之一。抗α ib β3同工抗体的产生可能导致血小板输注无效,并且在怀孕的情况下,可能穿过胎盘导致胎儿血小板减少。我们在这里描述了一个1型GT的女孩,她在第一次输血后出现了高比例的抗α iib β3同工抗体。令人惊讶的是,该患者只接受了红细胞浓缩物,免疫可能是由浓缩物中残留的血小板刺激的。本研究强调了在GT患者中定期筛查抗α iib β3抗体的必要性,即使患者以前从未输注过血小板浓缩物。
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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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