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输血后紫癜:一项血清学和免疫化学研究。

Post-transfusion purpura: a serological and immunochemical study.

作者信息

Pegels J G, Bruynes E C, Engelfriet C P, von dem Borne A E

出版信息

Br J Haematol. 1981 Dec;49(4):521-30. doi: 10.1111/j.1365-2141.1981.tb07260.x.

DOI:10.1111/j.1365-2141.1981.tb07260.x
PMID:7198482
Abstract

By applying the platelet suspension immunofluorescence test (PSIFT), platelet-specific alloantibodies responsible for post-transfusion purpura were detected in eight patients within a period of 2 years. All patients were female and had previously received blood or had been pregnant. The platelet-specific alloantibodies had the specificity anti-Zwa in all the patients, who were all Aw(a-). In two patients the platelets were tested in the acute phase of the disease and found to be coated with IgG. In one patient an ether eluate was prepared from the platelets that reacted strongly with Zw(a+) platelets, but weakly with platelets from Zwb-homozygous individuals. The sera of these two patients, and of two others whose platelets were not directly tested, taken in the acute phase of the purpura, reacted strongly with Zwa-positive platelets. The four sera also reacted, however weakly, with Zwa-negative platelets, with autologous platelets taken during remission and with platelets from patients with Glanzmann's disease. It is postulated that Zwa-anti-Zwa complexes, present in the eluate and the sera, caused the reaction with Zwa-negative platelets and the patients' own platelets. Immunochemical characterization of the post-transfusion purpura antibodies showed that in all patients these were IgG, in two combined with IgM antibodies. Antibodies of the sub-class IgG1 were found in all patients, sometimes together with IgG3. In the indirect immunofluorescence test with anti-complement serum, the PTP antibodies in only four sera were able to fix complement. In only two of these sera were these complement-binding antibodies detectable in the 51 Cr-lysis technique and then in a much lower titre than in the immunofluorescence technique.

摘要

通过应用血小板悬液免疫荧光试验(PSIFT),在2年时间内检测到8例患者体内存在导致输血后紫癜的血小板特异性同种抗体。所有患者均为女性,既往有输血史或妊娠史。所有患者体内的血小板特异性同种抗体均具有抗-Zwa特异性,且均为Aw(a-)型。2例患者在疾病急性期检测血小板,发现其表面包被有IgG。1例患者从血小板制备了乙醚洗脱液,该洗脱液与Zw(a+)血小板反应强烈,但与Zwb纯合个体的血小板反应较弱。这2例患者以及另外2例未直接检测血小板的患者在紫癜急性期采集的血清,与Zwa阳性血小板反应强烈。然而,这4份血清与Zwa阴性血小板、缓解期采集的自身血小板以及血小板无力症患者的血小板反应较弱。据推测,洗脱液和血清中存在的Zwa-抗-Zwa复合物导致了与Zwa阴性血小板和患者自身血小板的反应。输血后紫癜抗体的免疫化学特征表明,所有患者的这些抗体均为IgG,其中2例还伴有IgM抗体。所有患者均检测到IgG1亚类抗体,有时还伴有IgG3。在使用抗补体血清的间接免疫荧光试验中,仅4份血清中的PTP抗体能够固定补体。在这4份血清中,只有2份血清在51Cr溶解技术中可检测到这些补体结合抗体,且其滴度远低于免疫荧光技术中的滴度。

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Post-transfusion purpura: a serological and immunochemical study.输血后紫癜:一项血清学和免疫化学研究。
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引用本文的文献

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Post-Transfusion Purpura: Current Perspectives.输血后紫癜:当前观点
J Blood Med. 2019 Dec 9;10:405-415. doi: 10.2147/JBM.S189176. eCollection 2019.
2
An unexpected development after surgery-post-transfusion purpura!术后输血后紫癜——一个意外的术后情况!
Am J Hematol. 2016 Aug;91(8):848-51. doi: 10.1002/ajh.24414. Epub 2016 Jun 3.
3
Posttransfusion purpura. A survey of 13 cases.输血后紫癜。13例病例调查。
Klin Wochenschr. 1986 Nov 17;64(22):1198-203. doi: 10.1007/BF01728461.
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Antigenic polymorphism of human very late activation protein-2 (platelet glycoprotein Ia-IIa). Platelet alloantigen Hca.人极晚期活化蛋白-2(血小板糖蛋白Ia-IIa)的抗原多态性。血小板同种抗原Hca。
J Clin Invest. 1989 Mar;83(3):978-85. doi: 10.1172/JCI113984.