Department of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois.
Department of Veterinary & Animal Sciences, University of Massachusetts, Amherst, Massachusetts.
Transplant Cell Ther. 2024 Jan;30(1):79.e1-79.e10. doi: 10.1016/j.jtct.2023.10.023. Epub 2023 Nov 2.
Graft-versus-host disease (GVHD) is a primary and often lethal complication of allogenic hematopoietic stem cell transplantation (HSCT). Prophylactic regimens for GVHD are given as standard pretransplantation therapy; however, up to 50% of these patients develop acute GVHD (aGVHD) and require additional immunosuppressive intervention. Using a mouse GVHD model, we previously showed that injecting mice with exopolysaccharide (EPS) from Bacillus subtilis prior to GVHD induction significantly increased 80-day survival after transplantation of complete allogeneic major histocompatibility complex-mismatched cells. To ask whether EPS might also inhibit GVHD in humans, we used humanized NSG-HLA-A2 mice and induced GVHD by i.v. injection of A2 human peripheral blood mononuclear cells (PBMCs). Because we could not inject human donors with EPS, we transferred EPS-pretreated dendritic cells (DCs) to inhibit aGVHD. We derived these DCs from CD34 human cord blood cells, treated them with EPS, and then injected them together with PBMCs into the NSG-HLA-A2 mice. We found that all mice that received untreated DCs were dead by day 35, whereas 25% of mice receiving EPS-treated DCs (EPS-DCs) survived. This DC cell therapy could be readily translatable to humans, because we can generate large numbers of human EPS-DCs and use them as an "off the shelf" treatment for patients undergoing HSCT.
移植物抗宿主病 (GVHD) 是异基因造血干细胞移植 (HSCT) 的主要且常致命的并发症。GVHD 的预防方案作为标准的移植前治疗给予;然而,多达 50%的这些患者发生急性 GVHD (aGVHD),需要额外的免疫抑制干预。在使用小鼠 GVHD 模型的研究中,我们之前表明,在 GVHD 诱导前给小鼠注射枯草芽孢杆菌的胞外多糖 (EPS),可显著提高完全同种异体主要组织相容性复合物错配细胞移植后的 80 天存活率。为了研究 EPS 是否也能抑制人类的 GVHD,我们使用了人源化 NSG-HLA-A2 小鼠,并通过静脉注射 A2 人类外周血单核细胞 (PBMCs) 诱导 GVHD。由于我们不能给人类供体注射 EPS,我们转输了经过 EPS 预处理的树突状细胞 (DCs) 来抑制 aGVHD。我们从 CD34 人脐血细胞中获得这些 DCs,用 EPS 处理,然后将其与 PBMCs 一起注入 NSG-HLA-A2 小鼠。我们发现,所有接受未处理 DC 的小鼠在第 35 天前均死亡,而接受 EPS 处理的 DC (EPS-DCs) 的 25%的小鼠存活。这种 DC 细胞疗法很容易转化为人类,因为我们可以生成大量的人源 EPS-DCs,并将其作为接受 HSCT 的患者的“现成”治疗方法。