Developmental and Molecular Immunology, Department of Biomedicine, University of Basel, Basel, Switzerland.
Front Immunol. 2018 Apr 4;9:656. doi: 10.3389/fimmu.2018.00656. eCollection 2018.
Murine chronic graft-versus-host-disease (cGvHD) induced by injection of parental lymphocytes into F1 hybrids results in a disease similar to systemic lupus erythematosus. Here, we have used DBA/2 T cell injection into (C57BL/6 × DBA/2)F1 (BDF1) mice as a model system to test the prophylactic and therapeutic effects of interleukin-2 (IL-2)/anti-IL-2 immune complexes on the course of cGvHD. Our findings demonstrate that pretreatment with Treg inducing JES6/IL-2 complexes render BDF1 mice largely resistant to induction of cGvHD, whereas pretreatment with CD8 T cell/NK cell inducing S4B6/IL-2 complexes results in a more severe cGvHD. In contrast, treatment with JES6/IL-2 complexes 4 weeks after induction had no beneficial effect on disease symptoms. However, similar treatment with S4B6/IL-2 complexes led to a significant amelioration of the disease. This therapeutic effect seems to be mediated by donor CD8 T cells. The fact that a much stronger cGvHD is induced in BDF1 mice depleted of donor CD8 T cells strongly supports this conclusion. The contrasting effects of the two different IL-2 complexes are likely due to different mechanisms.
鼠慢性移植物抗宿主病(cGvHD)由注射亲代淋巴细胞到 F1 杂种中诱导,导致类似于系统性红斑狼疮的疾病。在这里,我们使用 DBA/2 T 细胞注射到(C57BL/6×DBA/2)F1(BDF1)小鼠中作为模型系统,以测试白细胞介素 2(IL-2)/抗 IL-2 免疫复合物对 cGvHD 病程的预防和治疗作用。我们的研究结果表明,用诱导 Treg 的 JES6/IL-2 复合物预处理使 BDF1 小鼠对 cGvHD 的诱导具有很大的抗性,而用诱导 CD8 T 细胞/NK 细胞的 S4B6/IL-2 复合物预处理导致更严重的 cGvHD。相比之下,在诱导后 4 周用 JES6/IL-2 复合物治疗对疾病症状没有有益的影响。然而,用 S4B6/IL-2 复合物进行类似的治疗导致疾病显著改善。这种治疗效果似乎是由供体 CD8 T 细胞介导的。在耗尽供体 CD8 T 细胞的 BDF1 小鼠中诱导出更强的 cGvHD 的事实强烈支持了这一结论。两种不同的 IL-2 复合物的对比效果可能是由于不同的机制所致。