Department of Surgery, Comprehensive Transplant Center, and the College of Medicine, The Ohio State University, Columbus, OH.
Biomedical Sciences Graduate Program, The Ohio State University College of Medicine, Columbus, OH.
J Immunol. 2024 May 1;212(9):1504-1518. doi: 10.4049/jimmunol.2300289.
Adoptive cell therapy (ACT), especially with CD4+ regulatory T cells (CD4+ Tregs), is an emerging therapeutic strategy to minimize immunosuppression and promote long-term allograft acceptance, although much research remains to realize its potential. In this study, we investigated the potency of novel Ab-suppressor CXCR5+CD8+ T cells (CD8+ TAb-supp) in comparison with conventional CD25highFoxp3+CD4+ Tregs for suppression of humoral alloimmunity in a murine kidney transplant (KTx) model of Ab-mediated rejection (AMR). We examined quantity of peripheral blood, splenic and graft-infiltrating CD8+ TAb-supp, and CD4+ Tregs in KTx recipients and found that high alloantibody-producing CCR5 knockout KTx recipients have significantly fewer post-transplant peripheral blood and splenic CD8+ TAb-supp, as well as fewer splenic and graft-infiltrating CD4+ Tregs compared with wild-type KTx recipients. ACT with alloprimed CXCR5+CD8+ T cells reduced alloantibody titer, splenic alloprimed germinal center (GC) B cell quantity, and improved AMR histology in CCR5 knockout KTx recipients. ACT with alloprimed CD4+ Treg cells improved AMR histology without significantly inhibiting alloantibody production or the quantity of splenic alloprimed GC B cells. Studies with TCR transgenic mice confirmed Ag specificity of CD8+ TAb-supp-mediated effector function. In wild-type recipients, CD8 depletion significantly increased alloantibody titer, GC B cells, and severity of AMR pathology compared with isotype-treated controls. Anti-CD25 mAb treatment also resulted in increased but less pronounced effect on alloantibody titer, quantity of GC B cells, and AMR pathology than CD8 depletion. To our knowledge, this is the first report that CD8+ TAb-supp cells are more potent regulators of humoral alloimmunity than CD4+ Treg cells.
过继细胞疗法(ACT),特别是使用 CD4+ 调节性 T 细胞(CD4+Tregs),是一种新兴的治疗策略,可以最大限度地减少免疫抑制并促进长期同种异体移植物接受,尽管仍有许多研究工作要实现其潜力。在这项研究中,我们研究了新型 Ab 抑制性 CXCR5+CD8+T 细胞(CD8+TAb-supp)与传统 CD25highFoxp3+CD4+Tregs 相比在 Ab 介导的排斥(AMR)的小鼠肾移植(KTx)模型中抑制体液同种免疫的效力。我们检查了 KTx 受者外周血、脾和移植物浸润 CD8+TAb-supp 和 CD4+Tregs 的数量,发现高同种抗体产生的 CCR5 敲除 KTx 受者在移植后外周血和脾 CD8+TAb-supp 以及脾和移植物浸润的 CD4+Tregs 明显少于野生型 KTx 受者。用同种预刺激的 CXCR5+CD8+T 细胞进行 ACT 可降低同种抗体滴度、脾同种预刺激生发中心(GC)B 细胞数量,并改善 CCR5 敲除 KTx 受者的 AMR 组织学。用同种预刺激的 CD4+Treg 细胞进行 ACT 可改善 AMR 组织学,而不会显著抑制同种抗体产生或脾同种预刺激 GC B 细胞的数量。用 TCR 转基因小鼠进行的研究证实了 CD8+TAb-supp 介导的效应功能的 Ag 特异性。在野生型受者中,与同种型处理的对照组相比,CD8 耗竭显着增加了同种抗体滴度、GC B 细胞和 AMR 病理的严重程度。抗 CD25 mAb 治疗也导致同种抗体滴度、GC B 细胞数量和 AMR 病理的增加,但比 CD8 耗竭的效果更不明显。据我们所知,这是第一项报道 CD8+TAb-supp 细胞比 CD4+Treg 细胞更有效地调节体液同种免疫的研究。