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淋巴增生性疾病患者的间接血小板放射性抗球蛋白试验

Indirect platelet radioactive antiglobulin test in patients with lymphoproliferative disease.

作者信息

Garvey M B, Freedman J

出版信息

J Lab Clin Med. 1986 Feb;107(2):123-8.

PMID:3944493
Abstract

An indirect platelet radioactive antiglobulin test (PRAT) was used to evaluate serum antiplatelet antibody and complement activation in 114 patients with lymphoproliferative disease. Overall, 60% of serum samples gave a positive indirect PRAT. Positive PRAT was observed in 85% of patients with chronic lymphocytic leukemia (CLL) and megakaryocytic thrombocytopenia, as well as in about half the patients with CLL and a normal platelet count or amegakaryocytic thrombocytopenia. In contrast to findings in patients with idiopathic autoimmune thrombocytopenic purpura or in those with leukemia who were alloimmunized, positive PRAT in patients with lymphoproliferative disease was predominantly caused by C3-only sensitization of platelets. Results were analyzed in relation to other clinical and laboratory findings. There was no significant difference in antiglobulin sensitization pattern between CLL and other lymphomas, different cell type, stage of disease, presence or absence of splenomegaly, recent or distant chemotherapy, sex, or history of pregnancy. Previous transfusion did affect antiglobulin sensitization patterns, as did presence of autoimmune hemolytic anemia. A high frequency of low serum complements (CH50, C3, C4, and factor B) and increased circulating immune complexes was observed; these did not correlate with frequency or sensitization pattern of positive PRAT. Amounts of bound anti-C3 and anti-IgG were significantly higher in patients with lymphoproliferative disease and positive antiglobulin test than in normal individuals; there was, however, no correlation between amount of antiglobulin serum bound and platelet counts. There was an 87% correlation in direct and indirect PRAT in 24 patients tested.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用间接血小板放射性抗球蛋白试验(PRAT)对114例淋巴增生性疾病患者的血清抗血小板抗体及补体激活情况进行评估。总体而言,60%的血清样本间接PRAT呈阳性。85%的慢性淋巴细胞白血病(CLL)合并巨核细胞性血小板减少症患者间接PRAT呈阳性,约半数CLL合并血小板计数正常或无巨核细胞性血小板减少症的患者间接PRAT也呈阳性。与特发性自身免疫性血小板减少性紫癜患者或allo免疫的白血病患者的结果不同,淋巴增生性疾病患者间接PRAT阳性主要是由仅C3致敏血小板所致。结合其他临床和实验室检查结果进行分析。CLL与其他淋巴瘤、不同细胞类型、疾病分期、有无脾肿大、近期或远期化疗、性别或妊娠史之间在抗球蛋白致敏模式上无显著差异。既往输血及自身免疫性溶血性贫血的存在确实会影响抗球蛋白致敏模式。观察到低血清补体(CH50、C3、C4和B因子)频率较高且循环免疫复合物增加;这些与间接PRAT阳性频率或致敏模式无关。淋巴增生性疾病且抗球蛋白试验阳性的患者结合的抗C3和抗IgG量显著高于正常个体;然而,抗球蛋白血清结合量与血小板计数之间无相关性。在24例接受检测的患者中,直接和间接PRAT的相关性为87%。(摘要截选至250字)

相似文献

1
Indirect platelet radioactive antiglobulin test in patients with lymphoproliferative disease.淋巴增生性疾病患者的间接血小板放射性抗球蛋白试验
J Lab Clin Med. 1986 Feb;107(2):123-8.
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Unexplained periparturient thrombocytopenia.不明原因的围产期血小板减少症。
Am J Hematol. 1986 Apr;21(4):397-407. doi: 10.1002/ajh.2830210408.
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Immunologic thrombocytopenic purpura in human immunodeficiency virus--seropositive patients with hemophilia. Comparison with patients with classic autoimmune thrombocytopenic purpura, homosexuals with thrombocytopenia, and narcotic addicts with thrombocytopenia.人类免疫缺陷病毒血清阳性血友病患者的免疫性血小板减少性紫癜。与经典自身免疫性血小板减少性紫癜患者、血小板减少的同性恋者以及血小板减少的麻醉品成瘾者的比较。
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Immune thrombocytopenia. Use of a Coombs antiglobulin test to detect IgG and C3 on platelets.免疫性血小板减少症。使用抗人球蛋白试验检测血小板上的IgG和C3。
N Engl J Med. 1979 Jan 18;300(3):106-11. doi: 10.1056/NEJM197901183000302.
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Use of the indirect platelet radioactive antiglobulin test with anti-IgG and anti-C3 in immune and nonimmune thrombocytopenias.间接血小板放射性抗球蛋白试验联合抗IgG和抗C3在免疫性和非免疫性血小板减少症中的应用
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Reactions of immunoglobulin G-binding ligands with platelets and platelet-associated immunoglobulin G.免疫球蛋白G结合配体与血小板及血小板相关免疫球蛋白G的反应
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[Detection of platelet antibodies in idiopathic thrombocytopenic purpura (author's transl)].特发性血小板减少性紫癜中血小板抗体的检测(作者译)
Nouv Rev Fr Hematol (1978). 1979;21(1):47-56.
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On the mechanism of thrombocytopenic purpura in sexually active homosexual men.关于性活跃同性恋男性血小板减少性紫癜的发病机制
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Immune thrombocytopenia in lymphoproliferative diseases.淋巴增殖性疾病中的免疫性血小板减少症
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Incidence and prognostic significance of autoantibodies against erythrocytes and platelets in chronic lymphocytic leukemia (CLL).慢性淋巴细胞白血病(CLL)中抗红细胞和血小板自身抗体的发生率及预后意义。
Nouv Rev Fr Hematol (1978). 1988;30(5-6):403-6.

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