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成年慢性免疫性血小板减少症患者的抗血小板自身抗体对体外巨核细胞生成的抑制作用

Suppression of in vitro megakaryocyte production by antiplatelet autoantibodies from adult patients with chronic ITP.

作者信息

McMillan Robert, Wang Lei, Tomer Aaron, Nichol Janet, Pistillo Jeanne

机构信息

The Scripps Research Institute, MEM 215, 10550 N Torrey Pines Rd, La Jolla, CA 92037, USA.

出版信息

Blood. 2004 Feb 15;103(4):1364-9. doi: 10.1182/blood-2003-08-2672. Epub 2003 Oct 23.

Abstract

Chronic immune thrombocytopenic purpura (ITP) is manifested by autoantibody-induced platelet destruction. Platelet turnover studies suggest that autoantibody may also affect platelet production. To evaluate this, we studied the effect of plasma from adult patients with chronic ITP on in vitro megakaryocyte production. CD34(+) cells, obtained from healthy donors, were cultured in medium containing PEG-rHuMGDF and 10% plasma from either ITP patients or healthy subjects. Cultures containing plasma from 12 of 18 ITP patients showed a significant decrease (26%-95%) in megakaryocyte production when compared with control cultures. Positive ITP plasmas not only reduced the total number of megakaryocytes produced during the culture period but also inhibited megakaryocyte maturation, resulting in fewer 4N, 8N, and 16N cells. The role of antibody in this suppression is supported by 2 factors: (1) immunoglobulin G (IgG) from ITP patients inhibited megakaryocyte production when compared with control IgG; and (2) adsorption of autoantibody, using immobilized antigen, resulted in significantly less inhibition of megakaryocyte production when compared with unadsorbed plasma. These results show that plasma autoantibody from some adult patients with ITP inhibits in vitro megakaryocyte production, suggesting that a similar effect may occur in vivo.

摘要

慢性免疫性血小板减少性紫癜(ITP)表现为自身抗体诱导的血小板破坏。血小板周转率研究表明,自身抗体也可能影响血小板生成。为评估这一点,我们研究了成年慢性ITP患者的血浆对体外巨核细胞生成的影响。从健康供体获取的CD34(+)细胞,在含有聚乙二醇化重组人巨核细胞生长发育因子(PEG-rHuMGDF)和来自ITP患者或健康受试者的10%血浆的培养基中培养。与对照培养物相比,18例ITP患者中有12例患者的血浆培养物显示巨核细胞生成显著减少(26%-95%)。阳性ITP血浆不仅减少了培养期间产生的巨核细胞总数,还抑制了巨核细胞成熟,导致4N、8N和16N细胞数量减少。抗体在这种抑制作用中的作用得到两个因素的支持:(1)与对照IgG相比,ITP患者的免疫球蛋白G(IgG)抑制了巨核细胞生成;(2)使用固定化抗原吸附自身抗体后与未吸附血浆相比,巨核细胞生成的抑制作用明显减弱。这些结果表明,一些成年ITP患者的血浆自身抗体抑制体外巨核细胞生成,提示体内可能发生类似作用。

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