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患有血小板减少症的男同性恋者网状内皮系统Fc受体特异性清除功能受损。

Homosexual men with thrombocytopenia have impaired reticuloendothelial system Fc receptor-specific clearance.

作者信息

Bender B S, Quinn T C, Spivak J L

出版信息

Blood. 1987 Aug;70(2):392-5.

PMID:3607278
Abstract

Classic immune thrombocytopenia purpura (ITP) occurs predominantly in women and is associated with either normal or impaired Fc receptor-mediated clearance of antibody-coated cells. Recently, an increasing incidence of thrombocytopenia has been observed in homosexual men, but whether Fc receptor-mediated clearance of antibody-coated cells is normal or impaired in these men is unknown. To study this question, we measured the in vivo clearance of anti-Rho(D) IgG antibody-sensitized 51Cr-labeled autologous red cells in five homosexual men with thrombocytopenia without an evident cause. All five had antibodies to human immunodeficiency virus, and four had circulating immune complexes as determined by a Clq-binding assay. Two of the men tested also had an increase in platelet-associated IgG. In the four homosexual men with platelet counts of 20,000/microL or less, the clearance half-time of IgG-sensitized red cells was prolonged (mean, 106 minutes; range, 72 to 140 minutes) as compared with the clearance of such cells in five hematologically normal men (mean, 39 minutes; range 30 to 50 minutes; P less than .005). One homosexual man with a platelet count of 81,000/microL had a normal clearance half-time (30 minutes). Three patients whose platelet counts increased after corticosteroid therapy were restudied. In all three, the clearance of antibody-coated cells was shortened and returned to normal in the one patient who had achieved a complete remission. No correlation was observed between the presence of platelet-associated IgG or circulating immune complexes and the clearance half-time. These data indicate that severe thrombocytopenia occurring in homosexual men as in some patients with classic ITP is associated with defective in vivo Fc receptor-mediated clearance of antibody-coated cells.

摘要

经典免疫性血小板减少性紫癜(ITP)主要发生于女性,与Fc受体介导的抗体包被细胞清除正常或受损有关。最近,在男同性恋者中观察到血小板减少症的发病率不断上升,但这些男性中Fc受体介导的抗体包被细胞清除是正常还是受损尚不清楚。为研究此问题,我们测量了5名原因不明的血小板减少症男同性恋者体内抗Rho(D)IgG抗体致敏的51Cr标记自体红细胞的清除情况。所有5人均有抗人类免疫缺陷病毒抗体,4人通过Clq结合试验检测到循环免疫复合物。其中2名接受检测的男性血小板相关IgG也升高。在4名血小板计数为20,000/μL或更低的男同性恋者中,IgG致敏红细胞的清除半衰期延长(平均106分钟;范围72至140分钟),而5名血液学正常男性中此类细胞的清除半衰期平均为39分钟(范围30至50分钟;P<0.005)。1名血小板计数为81,000/μL的男同性恋者清除半衰期正常(30分钟)。对3名接受皮质类固醇治疗后血小板计数升高的患者进行了再次研究。在所有3名患者中,抗体包被细胞的清除均缩短,在1名实现完全缓解的患者中恢复正常。未观察到血小板相关IgG或循环免疫复合物的存在与清除半衰期之间的相关性。这些数据表明,男同性恋者中出现的严重血小板减少症与经典ITP的一些患者一样,与体内Fc受体介导的抗体包被细胞清除缺陷有关。

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