Department of Hematology, Erasmus Medical Center, Rotterdam, the Netherlands.
Biol Blood Marrow Transplant. 2012 Jan;18(1):55-65. doi: 10.1016/j.bbmt.2011.09.010. Epub 2011 Oct 1.
Deficient thymopoiesis and retarded recovery of naive CD4(+) T cells are important determinants of insufficient immune-competence following hematopoietic stem cell transplantation (HSCT). Although keratinocyte growth factor (KGF) may protect the thymic epithelium, stem cell factor (SCF) is involved in early thymopoiesis. We evaluated whether KGF alone or combined with SCF would affect thymopoiesis and hematologic recovery following myeloablative autologous HSCT into rhesus macaques. Purpose-bred adult rhesus macaques received 10(6) autologous CD34(+)-selected mononuclear bone marrow cells (BMC)/kg after 9 Gy myeloablative conditioning. Animals were treated with phosphate-buffered saline (PBS) (n = 2), KGF alone (n = 2), or KGF combined with SCF (n = 2). KGF-treated animals showed accelerated hematologic recovery, improved thymopoiesis, and enhanced naive T-cell recovery following transplantation. Improved T cell recovery was not associated with protection against cytomegalovirus reactivation nor with improved antibody response to tetanus toxoid vaccination. Animals treated with KGF and SCF experienced severe adverse events that precluded evaluation of thymopoiesis and T cell recovery. Collectively, our data confirm that KGF may enhance thymopoiesis.
造血干细胞移植(HSCT)后免疫能力不足的重要决定因素是胸腺生成不足和幼稚 CD4(+) T 细胞恢复缓慢。角质细胞生长因子(KGF)可能保护胸腺上皮细胞,而干细胞因子(SCF)则参与早期胸腺生成。我们评估了 KGF 单独或与 SCF 联合应用是否会影响猕猴自体骨髓 CD34(+) 选择的单个核细胞(BMC)/kg 经 9 Gy 清髓性预处理后进行自体 HSCT 后的胸腺生成和血液学恢复。目的饲养的成年猕猴接受 10(6) 自体 CD34(+) 选择的单核骨髓细胞(BMC)/kg,接受 9 Gy 清髓性预处理。动物接受磷酸盐缓冲盐水(PBS)(n = 2)、KGF 单独(n = 2)或 KGF 联合 SCF(n = 2)治疗。KGF 治疗的动物在移植后表现出血液学恢复加速、胸腺生成改善和幼稚 T 细胞恢复增强。T 细胞恢复改善与巨细胞病毒再激活的保护无关,也与破伤风类毒素疫苗接种的抗体反应改善无关。接受 KGF 和 SCF 治疗的动物出现严重不良事件,无法评估胸腺生成和 T 细胞恢复。总之,我们的数据证实 KGF 可能增强胸腺生成。