Hippen Keli L, Harker-Murray Paul, Porter Stephen B, Merkel Sarah C, Londer Aryel, Taylor Dawn K, Bina Megan, Panoskaltsis-Mortari Angela, Rubinstein Pablo, Van Rooijen Nico, Golovina Tatiana N, Suhoski Megan M, Miller Jeffrey S, Wagner John E, June Carl H, Riley James L, Blazar Bruce R
University of Minnesota Cancer Center and Department of Pediatrics, Division of Bone, Blood and Marrow Transplantation, Minneapolis, USA.
Blood. 2008 Oct 1;112(7):2847-57. doi: 10.1182/blood-2008-01-132951. Epub 2008 Jul 21.
Previously, we showed that human umbilical cord blood (UCB) regulatory T cells (Tregs) could be expanded approximately 100-fold using anti-CD3/28 monoclonal antibody (mAb)-coated beads to provide T-cell receptor and costimulatory signals. Because Treg numbers from a single UCB unit are limited, we explored the use of cell-based artificial antigen-presenting cells (aAPCs) preloaded with anti-CD3/28 mAbs to achieve higher levels of Treg expansion. Compared with beads, aAPCs had similar expansion properties while significantly increasing transforming growth factor beta (TGF-beta) secretion and the potency of Treg suppressor function. aAPCs modified to coexpress OX40L or 4-1BBL expanded UCB Tregs to a significantly greater extent than bead- or nonmodified aAPC cultures, reaching mean expansion levels exceeding 1250-fold. Despite the high expansion and in contrast to studies using other Treg sources, neither OX40 nor 4-1BB signaling of UCB Tregs reduced in vitro suppression. UCB Tregs expanded with 4-1BBL expressing aAPCs had decreased levels of proapoptotic bim. UCB Tregs expanded with nonmodified or modified aAPCs versus beads resulted in higher survival associated with increased Treg persistence in a xeno-geneic graft-versus-host disease lethality model. These data offer a novel approach for UCB Treg expansion using aAPCs, including those coexpressing OX40L or 4-1BBL.
此前,我们发现使用包被抗CD3/28单克隆抗体(mAb)的磁珠可使人类脐带血(UCB)调节性T细胞(Tregs)扩增约100倍,从而提供T细胞受体和共刺激信号。由于单个UCB单位中的Treg数量有限,我们探索了使用预先装载抗CD3/28 mAb的基于细胞的人工抗原呈递细胞(aAPCs)来实现更高水平的Treg扩增。与磁珠相比,aAPCs具有相似的扩增特性,同时显著增加了转化生长因子β(TGF-β)的分泌以及Treg抑制功能的效力。经修饰共表达OX40L或4-1BBL的aAPCs比磁珠或未修饰的aAPC培养物能更大程度地扩增UCB Tregs,平均扩增水平超过1250倍。尽管扩增倍数高,且与使用其他Treg来源的研究不同,但UCB Tregs的OX40或4-1BB信号传导均未降低体外抑制作用。用表达4-1BBL的aAPCs扩增的UCB Tregs中促凋亡蛋白bim的水平降低。与磁珠相比,用未修饰或修饰的aAPCs扩增UCB Tregs可提高存活率,并与异种移植物抗宿主病致死模型中Treg持久性增加相关。这些数据为使用aAPCs(包括共表达OX40L或4-1BBL的aAPCs)扩增UCB Tregs提供了一种新方法。