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异基因干细胞移植后血浆凝溶胶蛋白水平下降的预后意义

Prognostic implications of declining plasma gelsolin levels after allogeneic stem cell transplantation.

作者信息

DiNubile Mark J, Stossel Thomas P, Ljunghusen Olof C, Ferrara James L M, Antin Joseph H

机构信息

Division of Infectious Diseases, Department of Medicine, University of Medicine and Dentistry of New Jersey/Robert Wood Johnson Medical School, Camden, NJ, USA.

出版信息

Blood. 2002 Dec 15;100(13):4367-71. doi: 10.1182/blood-2002-06-1672. Epub 2002 Aug 1.

Abstract

The idiopathic pneumonia syndrome (IPS) represents a common and often fatal complication of hematopoietic stem cell transplantation (HSCT). Gelsolin is a highly conserved actin-binding protein normally present in plasma that may serve a basic physiological role in limiting acute lung injury of diverse etiologies. We hypothesized that depletion of circulating gelsolin following HSCT might play a permissive role in the pathogenesis of IPS. Plasma gelsolin levels were measured by immunoblotting in frozen samples obtained weekly from 24 patients undergoing allogeneic HSCT. Patients with and without IPS were similar with respect to age, diagnosis, histocompatibility differences between donor and recipient, and conditioning regimen. Mean gelsolin levels in the 9 patients with rapidly fatal IPS were significantly lower than those in patients without this complication by week 3 after HSCT (101 +/- 61 mg/L versus 221 +/- 54 mg/L; P =.0002). Seven (88%) of the 8 patients with gelsolin levels of less than 100 mg/L in the first month after HSCT died from IPS within 3 months; conversely, gelsolin levels fell to less than 100 mg/L in 7 (78%) of the 9 patients who died from IPS within 3 months of HSCT (P =.0007). These findings suggest that gelsolin levels shortly after allogeneic HSCT can predict the later development of fatal IPS. Gelsolin replacement in selected transplant patients may offer a novel strategy to prevent or reverse IPS.

摘要

特发性肺炎综合征(IPS)是造血干细胞移植(HSCT)常见且往往致命的并发症。凝溶胶蛋白是一种高度保守的肌动蛋白结合蛋白,通常存在于血浆中,可能在限制各种病因引起的急性肺损伤中发挥基本生理作用。我们推测,HSCT后循环凝溶胶蛋白的消耗可能在IPS的发病机制中起促进作用。通过免疫印迹法测量了从24例接受异基因HSCT的患者每周获取的冷冻样本中的血浆凝溶胶蛋白水平。有或没有IPS的患者在年龄、诊断、供体与受体之间的组织相容性差异以及预处理方案方面相似。在HSCT后第3周,9例迅速致命的IPS患者的平均凝溶胶蛋白水平显著低于无此并发症的患者(101±61mg/L对221±54mg/L;P=0.0002)。HSCT后第一个月凝溶胶蛋白水平低于100mg/L的8例患者中有7例(88%)在3个月内死于IPS;相反,在HSCT后3个月内死于IPS的9例患者中有7例(78%)凝溶胶蛋白水平降至低于100mg/L(P=0.0007)。这些发现表明,异基因HSCT后不久的凝溶胶蛋白水平可以预测致命IPS的后期发展。在选定的移植患者中补充凝溶胶蛋白可能提供一种预防或逆转IPS的新策略。

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