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输血后紫癜中的全反应性血小板抗体

Pan-reactive platelet antibodies in post-transfusion purpura.

作者信息

Taaning E, Tønnesen F

机构信息

Department of Clinical Immunology, Glostrup Hospital, Denmark.

出版信息

Vox Sang. 1999;76(2):120-3.

Abstract

BACKGROUND AND OBJECTIVES

The mechanism for the destruction of a patient's own platelets in post-transfusion purpura (PTP) is unknown. In order to test the hypothesis that the destruction of autologous platelets in PTP is related to the presence of platelet antibodies with pan-reactivity, we investigated sera from patients with PTP.

MATERIALS AND METHODS

Sera from 12 patients with PTP were investigated for platelet antibodies by platelet-ELISA and monoclonal antibody-specific immobilization of platelet antigen assay.

RESULTS

During the thrombocytopenic phase, antibodies of IgG and IgM classes with pan-specificity against platelet GPIIb-IIIa, GPIb-IX and GPIa-IIa were found together with HPA alloantibodies. After recovery, the pan-specific antibodies disappeared or the extent of reactivity diminished, whereas the IgG HPA alloantibodies persisted.

CONCLUSION

These findings provide evidence that transient panreactive antibodies may be responsible for the autologous platelet destruction in PTP.

摘要

背景与目的

输血后紫癜(PTP)中患者自身血小板被破坏的机制尚不清楚。为了验证PTP中自体血小板破坏与具有泛反应性的血小板抗体的存在有关这一假说,我们对PTP患者的血清进行了研究。

材料与方法

采用血小板酶联免疫吸附测定法(platelet-ELISA)和血小板抗原单克隆抗体特异性固定分析法,对12例PTP患者的血清进行血小板抗体检测。

结果

在血小板减少期,发现了针对血小板糖蛋白IIb-IIIa、GPIb-IX和GPIa-IIa具有泛特异性的IgG和IgM类抗体,同时还存在血小板同种异体抗体(HPA alloantibodies)。恢复后,泛特异性抗体消失或反应程度降低,而IgG HPA同种异体抗体持续存在。

结论

这些发现提供了证据,表明短暂的泛反应性抗体可能是PTP中自体血小板破坏的原因。

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