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血小板减少症患者的血小板抗体。

Platelet antibodies in thrombocytopenic patients.

作者信息

Hegde U M, Gordon-Smith E C, Worlledge S

出版信息

Br J Haematol. 1977 Jan;35(1):113-22. doi: 10.1111/j.1365-2141.1977.tb00567.x.

Abstract

Platelet antibodies either bound to the surface of platelets or free in the serum were sought in patients who had low platelet counts for a variety of reasons. They were detected by finding excess IgG on the surface of washed platelets either directly or after incubation of the serum with normal platelets. The technique used was a modification of that described recently (Dixon et al, 1975) in which the greater the amount of anti-IgG consumed by the reaction with platelets the less the subsequent lysis of sheep red cells coated with IgG. This test could be calibrated by adding known quantities of IgG to the antisera and thus the amount of bound IgG could be measured. Platelets from normal donors and those with thrombocytopenia due to non-immunological causes such as aplastic anaemia or acute leukaemia were found to have 15-70 ng IgG/10(7) platelets (mean 53 ng). 37 out of 38 thrombocytopenic patients in whom immune destruction of platelets was suspected were found to have excess IgG on their platelets ranging from 70 to 720 ng/10(7) (mean 297 ng, P less than 0.001) and there was a significant inverse correlation between this amount and the platelet count (r = 0.85, P less than 0.001). Antibody in the serum was found in 14 of 22 patients with 'idiopathic' thrombocytopenic purpura (ITP), three of four patients with underlying lymphoma and in all five cases of systemic lupus erythematosus (SLE). Four non-thrombocytopenic patients with autoimmune haemolytic anaemia (AIHA) due to IgG on the red cells were also studied and were shown to have no increase in platelet-bound IgG. Our results confirm the work of Dixon et al (1975) that platelet antibody as excess IgG can be readily detected on the surface of platelets in patients with immune thrombocytopenia. The clinical implications of these findings are discussed.

摘要

在因各种原因导致血小板计数低的患者中,寻找结合在血小板表面或游离于血清中的血小板抗体。通过直接检测洗涤过的血小板表面的过量IgG,或在血清与正常血小板孵育后检测,来发现这些抗体。所采用的技术是对最近描述的方法(Dixon等人,1975年)的改进,即与血小板反应消耗的抗IgG量越大,随后被IgG包被的绵羊红细胞的裂解就越少。通过向抗血清中加入已知量的IgG,可以对该试验进行校准,从而能够测量结合的IgG量。发现正常供者的血小板以及因再生障碍性贫血或急性白血病等非免疫性原因导致血小板减少的患者的血小板,每10⁷个血小板含有15 - 70 ng IgG(平均53 ng)。在38例怀疑血小板免疫破坏的血小板减少患者中,有37例其血小板上有过量的IgG,范围为70至720 ng/10⁷(平均297 ng,P < 0.001),并且该量与血小板计数之间存在显著的负相关(r = 0.85,P < 0.001)。在22例“特发性”血小板减少性紫癜(ITP)患者中的14例、4例潜在淋巴瘤患者中的3例以及所有5例系统性红斑狼疮(SLE)患者的血清中均发现了抗体。还对4例因红细胞上存在IgG导致自身免疫性溶血性贫血(AIHA)的非血小板减少患者进行了研究,结果显示其血小板结合的IgG没有增加。我们的结果证实了Dixon等人(1975年)的研究成果,即在免疫性血小板减少患者的血小板表面能够轻易检测到作为过量IgG的血小板抗体。讨论了这些发现的临床意义。

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