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输血后紫癜中的自身反应性血小板抗体。

Autoreactive platelet antibody in post transfusion purpura.

作者信息

Minchinton R M, Cunningham I, Cole-Sinclair M, Van der Weyden M, Vaughan S, McGrath K M

机构信息

Red Cross Blood Transfusion Service, Brisbane, Qld, Australia.

出版信息

Aust N Z J Med. 1990 Apr;20(2):111-5. doi: 10.1111/j.1445-5994.1990.tb01284.x.

Abstract

Post transfusion purpura in a DR3, DRw52 positive, PlA1 negative woman rapidly responded to high-dose intravenous gammaglobulin therapy. Using the platelet immunofluorescence test (PIFT) high titre IgG and IgM alloantibodies were detected in the patient's acute serum. These alloantibodies had PlA1 specificity and the patient's serum produced a broad, 100 kDa band on Western Blot with PlA1 positive platelets. Acute phase serum also contained an IgG antibody which reacted in the PIFT with the patient's own platelets, and PlA1 negative platelets. When tested by Western Blot with PlA1 negative and Glanzmann's Thrombasthenia platelets, the acute serum produced bands at 180 and 200 kDa. The autoreactive antibody was not detected once the platelet count returned to normal. These findings provide evidence for the hypothesis that the mechanism of autologous platelet destruction in PTP is autoimmune.

摘要

一名DR3、DRw52阳性、PlA1阴性的女性发生输血后紫癜,对大剂量静脉注射丙种球蛋白治疗迅速产生反应。通过血小板免疫荧光试验(PIFT)在患者急性血清中检测到高滴度的IgG和IgM同种抗体。这些同种抗体具有PlA1特异性,并且患者血清在蛋白质印迹法中与PlA1阳性血小板产生一条宽的100 kDa条带。急性期血清还含有一种IgG抗体,该抗体在PIFT中与患者自身血小板以及PlA1阴性血小板发生反应。当用PlA1阴性和Glanzmann血小板无力症血小板进行蛋白质印迹法检测时,急性血清在180和200 kDa处产生条带。血小板计数恢复正常后未检测到自身反应性抗体。这些发现为输血后紫癜中自体血小板破坏机制是自身免疫性的这一假说提供了证据。

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