Cleveland Clinic Foundation, Cleveland, Ohio; Platelet & Neutrophil Immunology Laboratory, Blood Research Institute, BloodCenter of Wisconsin, Milwaukee, Wisconsin; Division of Hematology, Duke University Medical Center, Durham, North Carolina; Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Transfusion. 2013 Oct;53(10):2158-63. doi: 10.1111/trf.12112. Epub 2013 Feb 5.
Protamine is widely used to reverse the anticoagulant effects of heparin. Although mild thrombocytopenia is common in patients given protamine after cardiac procedures, acute severe thrombocytopenia has not been described. We encountered a patient who experienced profound thrombocytopenia and bleeding shortly after administration of protamine and performed studies to characterize the responsible mechanism.
Patient serum was studied for antibodies that recognize protamine, heparin-protamine complexes, and platelets (PLTs) treated with protamine using flow cytometry, enzyme-linked immunosorbent assay, and serotonin release from labeled PLTs.
A high-titer immunoglobulin G antibody was detected in patient serum that recognizes protamine in a complex with heparin or PLT surface glycosaminoglycans (GAGs) and activates PLTs treated with protamine at concentrations achieved in vivo after protamine infusion. The antibody is distinctly different from those found in patients with heparin-induced thrombocytopenia on the basis of its failure to recognize heparin in a complex with PLT factor 4 (PF4) and to release serotonin from labeled PLTs in the absence of protamine.
Findings made suggest that the patient's antibody is specific for conformational changes induced in protamine when it reacts with heparin or a PLT surface GAG. Development of severe thrombocytopenia after treatment of this patient with protamine defines a previously undescribed mechanism of drug-induced immune thrombocytopenia. Patients given protamine who produce this type of antibody may be at risk of experiencing thrombocytopenia if given the drug a second time while antibody is still present.
鱼精蛋白被广泛用于逆转肝素的抗凝作用。尽管心脏手术后给予鱼精蛋白的患者常发生轻度血小板减少症,但尚未描述急性严重血小板减少症。我们遇到了一位患者,在给予鱼精蛋白后不久即发生严重的血小板减少症和出血,并进行了相关研究以确定其发病机制。
使用流式细胞术、酶联免疫吸附试验和标记血小板(PLT)释放 5-羟色胺,研究患者血清中识别鱼精蛋白、肝素-鱼精蛋白复合物和用鱼精蛋白处理的血小板(PLT)的抗体。
患者血清中检测到一种高滴度的免疫球蛋白 G 抗体,该抗体识别与肝素或 PLT 表面糖胺聚糖(GAG)结合的鱼精蛋白,并在鱼精蛋白输注后体内达到的浓度下激活用鱼精蛋白处理的 PLT。该抗体与肝素诱导的血小板减少症患者中发现的抗体明显不同,因为它不能识别与 PLT 因子 4(PF4)结合的肝素,并且在没有鱼精蛋白的情况下不能从标记的 PLT 释放 5-羟色胺。
研究结果表明,患者的抗体是针对鱼精蛋白与肝素或 PLT 表面 GAG 反应时诱导的构象变化特异性的。该患者在接受鱼精蛋白治疗后发生严重血小板减少症,定义了一种以前未描述的药物诱导免疫性血小板减少症的发病机制。如果此类抗体仍存在而再次给予鱼精蛋白,那么给予该药物的患者可能会有发生血小板减少症的风险。