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角质细胞生长因子增强了鼠同种异体脐血造血细胞移植中的免疫重建。

Keratinocyte growth factor enhanced immune reconstitution in murine allogeneic umbilical cord blood cell transplant.

机构信息

Jiangsu Institute of Hematology, Key Laboratory of Thrombosis and Hemostasis, Ministry of Health, the First Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Leuk Lymphoma. 2011 Aug;52(8):1556-66. doi: 10.3109/10428194.2011.573037. Epub 2011 Jun 8.

DOI:10.3109/10428194.2011.573037
PMID:21649545
Abstract

Umbilical cord blood (UCB) is used increasingly as a source of hematopoietic cells because of a lower risk of graft-versus-host disease (GVHD). Myeloablative conditioning before allogeneic umbilical cord blood transplant (allo-UCBT) results in thymic epithelial cell injury and T-cell immune deficiency. Full-term fetal blood cells were used as hematopoietic cells in a previous murine allo-UCBT model with a limited number of mice surviving the myeloablative conditioning. We designed a viable murine allo-UCBT protocol with platelet concentrate support. Keratinocyte growth factor (KGF) is a mitogen of thymic epithelial cells that promotes recovery of thymic epithelium when given before total body irradiation (TBI)-containing conditioning in experimental murine models. We hypothesized that KGF pre-administration would improve post-allo-UCBT thymopoiesis. To test this hypothesis, allo-UCBT recipient mice were given KGF or control saline prior to UCBT. Platelet concentrate support significantly improved the survival rate of murine allo-UCBT recipients. KGF administration significantly increased donor-derived T and natural killer T (NKT) cells at day +35 in spleens of allo-UCBT recipients. KGF administration also improved thymic function after allo-UCBT, resulting in higher copies of signal joint T-cell receptor rearrangement excision circles (sjTRECs) in splenocytes. Finally, we found that KGF pre-administration could enhance the graft-versus-leukemia effect. In conclusion, KGF can be administered safely to recipients of allo-UCBT to enhance T-cell immune reconstitution.

摘要

脐带血 (UCB) 因其移植物抗宿主病 (GVHD) 的风险较低而越来越多地被用作造血细胞的来源。异基因脐带血移植 (allo-UCBT) 前的清髓性预处理会导致胸腺上皮细胞损伤和 T 细胞免疫缺陷。在之前的小鼠 allo-UCBT 模型中,使用足月胎儿血细胞作为造血细胞,只有少数小鼠能在清髓性预处理后存活。我们设计了一种可行的小鼠 allo-UCBT 方案,并用血小板浓缩物支持。角质细胞生长因子 (KGF) 是一种胸腺上皮细胞的有丝分裂原,在实验性小鼠模型中,在包含全身照射 (TBI) 的预处理前给予 KGF 可促进胸腺上皮细胞的恢复。我们假设 KGF 预先给药会改善 allo-UCBT 后的胸腺生成。为了验证这一假设,allo-UCBT 受者在 UCBT 前给予 KGF 或对照生理盐水。血小板浓缩物支持显著提高了小鼠 allo-UCBT 受者的存活率。KGF 给药显著增加了 allo-UCBT 受者脾脏中供体衍生的 T 和自然杀伤 T (NKT) 细胞在第 +35 天的数量。KGF 给药还改善了 allo-UCBT 后的胸腺功能,导致脾细胞中信号接头 T 细胞受体重排切除环 (sjTRECs) 的拷贝数增加。最后,我们发现 KGF 预先给药可以增强移植物抗白血病效应。总之,KGF 可以安全地给予 allo-UCBT 受者,以增强 T 细胞免疫重建。

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