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本文引用的文献

1
Cord-blood engraftment with ex vivo mesenchymal-cell coculture.体外间充质细胞共培养促进脐血植入。
N Engl J Med. 2012 Dec 13;367(24):2305-15. doi: 10.1056/NEJMoa1207285.
2
CXCR4 expression in CD34+ cells and unit predominance after double umbilical cord blood transplantation.双份脐带血移植后CD34+细胞中CXCR4的表达及单位优势
Leukemia. 2013 Apr;27(5):1181-3. doi: 10.1038/leu.2012.261. Epub 2012 Sep 7.
3
Correlation of infused CD3+CD8+ cells with single-donor dominance after double-unit cord blood transplantation.输注的 CD3+CD8+ 细胞与双份脐血移植后单供体优势的相关性。
Biol Blood Marrow Transplant. 2013 Jan;19(1):156-60. doi: 10.1016/j.bbmt.2012.09.004. Epub 2012 Sep 16.
4
Prostaglandin E2 receptor subtypes in human blood and vascular cells.人血和血管细胞中的前列腺素 E2 受体亚型。
Eur J Pharmacol. 2012 Nov 15;695(1-3):1-6. doi: 10.1016/j.ejphar.2012.08.009. Epub 2012 Sep 3.
5
Reduced-intensity conditioning with combined haploidentical and cord blood transplantation results in rapid engraftment, low GVHD, and durable remissions.采用亲缘单倍体相合联合脐带血移植的减低强度预处理方案可实现快速植入、低移植物抗宿主病发生率和持久缓解。
Blood. 2011 Dec 8;118(24):6438-45. doi: 10.1182/blood-2011-08-372508. Epub 2011 Oct 5.
6
Factors predicting single-unit predominance after double umbilical cord blood transplantation.双份脐血移植后单倍体优势的预测因素。
Bone Marrow Transplant. 2012 Jun;47(6):799-803. doi: 10.1038/bmt.2011.184. Epub 2011 Sep 26.
7
Donor-specific anti-HLA antibodies predict outcome in double umbilical cord blood transplantation.供者特异性抗 HLA 抗体可预测双脐血造血干细胞移植的结局。
Blood. 2011 Dec 15;118(25):6691-7. doi: 10.1182/blood-2011-05-355263. Epub 2011 Sep 22.
8
Pulse exposure of haematopoietic grafts to prostaglandin E2 in vitro facilitates engraftment and recovery.体外给予造血移植物前列腺素 E2 脉冲暴露可促进植入和恢复。
Cell Prolif. 2011 Apr;44 Suppl 1(Suppl 1):22-9. doi: 10.1111/j.1365-2184.2010.00726.x.
9
Prostaglandin E2 enhances human cord blood stem cell xenotransplants and shows long-term safety in preclinical nonhuman primate transplant models.前列腺素 E2 增强了人脐血干细胞异种移植,并在临床前非人类灵长类动物移植模型中显示出长期安全性。
Cell Stem Cell. 2011 Apr 8;8(4):445-58. doi: 10.1016/j.stem.2011.02.003.
10
Influence of infused cell dose and HLA match on engraftment after double-unit cord blood allografts.输注细胞剂量和 HLA 配型对双份脐血移植后植入的影响。
Blood. 2011 Mar 24;117(12):3277-85; quiz 3478. doi: 10.1182/blood-2010-08-300491. Epub 2010 Dec 13.

前列腺素调节的脐带血造血干细胞移植。

Prostaglandin-modulated umbilical cord blood hematopoietic stem cell transplantation.

机构信息

Dana-Farber Cancer Institute, Boston, MA;

出版信息

Blood. 2013 Oct 24;122(17):3074-81. doi: 10.1182/blood-2013-05-503177. Epub 2013 Aug 30.

DOI:10.1182/blood-2013-05-503177
PMID:23996087
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3811179/
Abstract

Umbilical cord blood (UCB) is a valuable source of hematopoietic stem cells (HSCs) for use in allogeneic transplantation. Key advantages of UCB are rapid availability and less stringent requirements for HLA matching. However, UCB contains an inherently limited HSC count, which is associated with delayed time to engraftment, high graft failure rates, and early mortality. 16,16-Dimethyl prostaglandin E2 (dmPGE2) was previously identified to be a critical regulator of HSC homeostasis, and we hypothesized that brief ex vivo modulation with dmPGE2 could improve patient outcomes by increasing the "effective dose" of HSCs. Molecular profiling approaches were used to determine the optimal ex vivo modulation conditions (temperature, time, concentration, and media) for use in the clinical setting. A phase 1 trial was performed to evaluate the safety and therapeutic potential of ex vivo modulation of a single UCB unit using dmPGE2 before reduced-intensity, double UCB transplantation. Results from this study demonstrated clear safety with durable, multilineage engraftment of dmPGE2-treated UCB units. We observed encouraging trends in efficacy, with accelerated neutrophil recovery (17.5 vs 21 days, P = .045), coupled with preferential, long-term engraftment of the dmPGE2-treated UCB unit in 10 of 12 treated participants.

摘要

脐带血 (UCB) 是异体移植中造血干细胞 (HSCs) 的宝贵来源。UCB 的主要优势在于其快速可用性和对 HLA 匹配要求较低。然而,UCB 中 HSC 的固有数量有限,这与植入延迟、高移植物失败率和早期死亡率有关。16,16-二甲基前列腺素 E2 (dmPGE2) 先前被确定为 HSC 动态平衡的关键调节因子,我们假设通过增加 HSCs 的“有效剂量”,短暂的体外 dmPGE2 调节可以改善患者的预后。采用分子谱分析方法确定了用于临床的最佳体外调节条件(温度、时间、浓度和培养基)。进行了一项 I 期试验,以评估在减少强度、双脐带血移植前使用 dmPGE2 体外调节单个脐带血单位的安全性和治疗潜力。这项研究的结果表明,dmPGE2 处理的脐带血单位具有明显的安全性,可实现持久的多谱系植入。我们观察到在疗效方面有令人鼓舞的趋势,中性粒细胞恢复加速(17.5 天 vs 21 天,P =.045),同时 dmPGE2 处理的脐带血单位在 12 名接受治疗的参与者中有 10 名优先、长期植入。