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血小板减少的人类免疫缺陷病毒感染患者中血小板生成无效。

Ineffective platelet production in thrombocytopenic human immunodeficiency virus-infected patients.

作者信息

Cole J L, Marzec U M, Gunthel C J, Karpatkin S, Worford L, Sundell I B, Lennox J L, Nichol J L, Harker L A

机构信息

Department of Medicine, Emory University School of Medicine, Ponce de Leon Center, Atlanta, GA, USA.

出版信息

Blood. 1998 May 1;91(9):3239-46.

PMID:9558379
Abstract

Thrombocytopenia has been characterized in six patients infected with human immunodeficiency virus (HIV) with respect to the delivery of viable platelets into the peripheral circulation (peripheral platelet mass turnover), marrow megakaryocyte mass (product of megakaryocyte number and volume), megakaryocyte progenitor cells, circulating levels of endogenous thrombopoietin (TPO) and platelet TPO receptor number, and serum antiplatelet glycoprotein (GP) IIIa49-66 antibody (GPIIIa49-66Ab), an antibody associated with thrombocytopenia in HIV-infected patients. Peripheral platelet counts in these patients averaged 46 +/- 43 x 10(3)/microL (P = . 0001 compared to normal controls of 250 +/- 40x 10(3)/microL), and the mean platelet volume (MPV) was 10.5 +/- 2.0 fL (P > 0.3 compared with normal control of 9.5 +/- 1.7 fL). The mean life span of autologous 111In-platelets was 87 +/- 39 hours (P = .0001 compared with 232 +/- 38 hours in 20 normal controls), and immediate mean recovery of 111In-platelets injected into the systemic circulation was 33% +/- 16% (P = .0001 compared with 65% +/- 5% in 20 normal controls). The resultant mean peripheral platelet mass turnover was 3.8 +/- 1.5 x 10(5) fL/microL/d versus 3.8 +/- 0.4 x 10(5) fL/microL/d in 20 normal controls (P > .5). The mean endogenous TPO level was 596 +/- 471 pg/mL (P = .0001 compared with 95 +/- 6 pg/mL in 98 normal control subjects), and mean platelet TPO receptor number was 461 +/- 259 receptors/platelet (P = .05 compared with 207 +/- 99 receptors/platelet in nine normal controls). Antiplatelet GPIIIa49-66Ab levels in sera were uniformly increased in HIV thrombocytopenic patients (P < .001). In this cohort of thrombocytopenic HIV patients, marrow megakaryocyte number was increased to 30 +/- 15 x 10(6)/kg (P = .02 compared with 11 +/- 2.1 x 10(6)/kg in 20 normal controls), and marrow megakaryocyte volume was 32 +/- 0.9 x 10(3) fL (P = .05 compared with 28 +/- 4.5 x 10(3) fL in normal controls). Marrow megakaryocyte mass was expanded to 93 +/- 47 x 10(10) fL/kg (P = .007 compared with normal control of 31 +/- 5.3 x 10(10) fL/kg). Marrow megakaryocyte progenitor cells averaged 3.3 (range, 0.4 to 7.3) CFU-Meg/1,000 CD34(+) cells compared with 27 (range, 0.1 to 84) CFU-Meg/1,000 CD34(+) cells in seven normal subjects (P = .02). Thus, thrombocytopenia in these HIV patients was caused by a combination of shortening of platelet life span by two thirds and doubling of splenic platelet sequestration, coupled with ineffective delivery of viable platelets to the peripheral blood, despite a threefold TPO-driven expansion in marrow megakaryocyte mass. We postulate that this disparity between circulating platelet product and marrow platelet substrate results from direct impairment in platelet formation by HIV-infected marrow megakaryocytes.

摘要

对6例感染人类免疫缺陷病毒(HIV)的患者的血小板减少症进行了如下特征分析:外周循环中存活血小板的输送(外周血小板质量周转率)、骨髓巨核细胞质量(巨核细胞数量与体积的乘积)、巨核细胞祖细胞、内源性血小板生成素(TPO)的循环水平、血小板TPO受体数量,以及血清抗血小板糖蛋白(GP)IIIa49 - 66抗体(GPIIIa49 - 66Ab),该抗体与HIV感染患者的血小板减少症相关。这些患者的外周血小板计数平均为46±43×10³/μL(与正常对照组250±40×10³/μL相比,P = 0.0001),平均血小板体积(MPV)为10.5±2.0 fL(与正常对照组9.5±1.7 fL相比,P > 0.3)。自体¹¹¹In标记血小板的平均寿命为87±39小时(与20例正常对照的232±38小时相比,P = 0.0001),注入体循环的¹¹¹In标记血小板的即时平均回收率为33%±16%(与20例正常对照的65%±5%相比,P = 0.0001)。由此得出的平均外周血小板质量周转率为3.8±1.5×10⁵ fL/μL/d,而20例正常对照为3.8±0.4×10⁵ fL/μL/d(P > 0.5)。内源性TPO的平均水平为596±471 pg/mL(与98例正常对照受试者的95±6 pg/mL相比,P = 0.0001),平均血小板TPO受体数量为461±259个受体/血小板(与9例正常对照的207±99个受体/血小板相比,P = 0.05)。HIV血小板减少症患者血清中的抗血小板GPIIIa49 - 66Ab水平均升高(P < 0.001)。在这组血小板减少的HIV患者中,骨髓巨核细胞数量增加至30±15×10⁶/kg(与20例正常对照的11±2.1×10⁶/kg相比,P = 0.02),骨髓巨核细胞体积为32±0.9×10³ fL(与正常对照的28±4.5×10³ fL相比,P = 0.05)。骨髓巨核细胞质量扩大至93±47×10¹⁰ fL/kg(与正常对照的31±5.3×10¹⁰ fL/kg相比,P = 0.007)。骨髓巨核细胞祖细胞平均为3.3(范围为0.4至7.3)个CFU - Meg/1000个CD34⁺细胞,而7例正常受试者为27(范围为0.1至84)个CFU - Meg/1000个CD34⁺细胞(P = 0.02)。因此,这些HIV患者的血小板减少症是由血小板寿命缩短三分之二和脾脏血小板扣押增加一倍共同导致的,同时尽管TPO驱动骨髓巨核细胞质量增加了三倍,但存活血小板向外周血的输送效率低下。我们推测,循环血小板产物与骨髓血小板底物之间的这种差异是由HIV感染的骨髓巨核细胞对血小板形成的直接损害所致。

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