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CD34 选择的干细胞增强剂可改善儿童异基因干细胞移植后不良的移植物功能。

CD34 selected stem cell boosts can improve poor graft function after paediatric allogeneic stem cell transplantation.

作者信息

Mainardi Chiara, Ebinger Martin, Enkel Sigrid, Feuchtinger Tobias, Teltschik Heiko-Manuel, Eyrich Matthias, Schumm Michael, Rabsteyn Armin, Schlegel Patrick, Seitz Christian, Schwarze Carl-Phillip, Müller Ingo, Greil Johann, Bader Peter, Schlegel Paul-Gerhardt, Martin David, Holzer Ursula, Döring Michaela, Handgretinger Rupert, Lang Peter

机构信息

Department of Paediatric Oncology, Children's University Hospital, University of Padova, Padova, Italy.

Department of Paediatric Haematology/Oncology, Children's University Hospital, Tübingen, Germany.

出版信息

Br J Haematol. 2018 Jan;180(1):90-99. doi: 10.1111/bjh.15012. Epub 2017 Dec 3.

Abstract

Poor graft function (PGF) is a severe complication of haematopoietic stem cell transplantation (HSCT) and administration of donor stem cell boosts (SCBs) represents a therapeutic option. We report 50 paediatric patients with PGF who received 61 boosts with CD34 selected peripheral blood stem cells (PBSC) after transplantation from matched unrelated (n = 25) or mismatched related (n = 25) donors. Within 8 weeks, a significant increase in median neutrophil counts (0·6 vs. 1·516 × 10 /l, P < 0·05) and a decrease in red blood cell and platelet transfusion requirement (median frequencies 1 and 7 vs. 0, P < 0·0001 and <0·001), were observed, and 78·8% of patients resolved one or two of their cytopenias. 36·5% had a complete haematological response. Median lymphocyte counts for CD3 , CD3 CD4 , CD19 and CD56 increased 8·3-, 14·2-, 22.- and 1·6-fold. The rate of de novo acute graft-versus-host disease (GvHD) grade I-III was only 6% and resolved completely. No GvHD grade IV or chronic GvHD occurred. Patients who responded to SCB displayed a trend toward better overall survival (OS) (P = 0·07). Thus, administration of CD34 selected SCBs from alternative donors is safe and effective. Further studies are warranted to clarify the impact on immune reconstitution and survival.

摘要

移植功能不良(PGF)是造血干细胞移植(HSCT)的一种严重并发症,给予供体干细胞增强治疗(SCBs)是一种治疗选择。我们报告了50例PGF儿科患者,他们在接受来自匹配无关供体(n = 25)或不匹配相关供体(n = 25)的移植后,接受了61次CD34选择的外周血干细胞(PBSC)增强治疗。在8周内,观察到中性粒细胞计数中位数显著增加(0·6对1·516×10⁹/l,P < 0·05),红细胞和血小板输注需求减少(中位数频率分别为1和7对0,P < 0·0001和<0·001),78·8%的患者一种或两种血细胞减少症得到缓解。36·5%的患者有完全血液学反应。CD3、CD3⁺CD4⁺、CD19和CD56的淋巴细胞计数中位数分别增加了8·3倍、14·2倍、22倍和1·6倍。新发急性移植物抗宿主病(GvHD)I - III级的发生率仅为6%且完全缓解。未发生IV级GvHD或慢性GvHD。对SCB有反应的患者总体生存率(OS)有改善趋势(P = 0·07)。因此,给予来自替代供体的CD34选择的SCBs是安全有效的。有必要进一步研究以阐明其对免疫重建和生存的影响。

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