Saas Philippe, Bonnefoy Francis, Toussirot Eric, Perruche Sylvain
INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, Fédération Hospitalo-Universitaire INCREASE, LabEx LipSTIC, Université Bourgogne Franche-Comté, Besançon, France.
INSERM CIC-1431, University Hospital of Besançon, Clinical Investigation Center in Biotherapy, Fédération Hospitalo-Universitaire INCREASE, LabEx LipSTIC, Besançon, France.
Front Immunol. 2017 Oct 9;8:1191. doi: 10.3389/fimmu.2017.01191. eCollection 2017.
Early-stage apoptotic cells possess immunomodulatory properties. Proper apoptotic cell clearance during homeostasis has been shown to limit subsequent immune responses. Based on these observations, early-stage apoptotic cell infusion has been used to prevent unwanted inflammatory responses in different experimental models of autoimmune diseases or transplantation. Moreover, this approach has been shown to be feasible without any toxicity in patients undergoing allogeneic hematopoietic cell transplantation to prevent graft--host disease. However, whether early-stage apoptotic cell infusion can be used to treat ongoing inflammatory disorders has not been reported extensively. Recently, we have provided evidence that early-stage apoptotic cell infusion is able to control, at least transiently, ongoing collagen-induced arthritis. This beneficial therapeutic effect is associated with the modulation of antigen-presenting cell functions mainly of macrophages and plasmacytoid dendritic cells, as well as the induction of collagen-specific regulatory CD4 T cells (Treg). Furthermore, the efficacy of this approach is not altered by the association with two standard treatments of rheumatoid arthritis (RA), methotrexate and tumor necrosis factor (TNF) inhibition. Here, in the light of these observations and recent data of the literature, we discuss the mechanisms of early-stage apoptotic cell infusion and how this therapeutic approach can be transposed to patients with RA.
早期凋亡细胞具有免疫调节特性。研究表明,稳态过程中适当清除凋亡细胞可限制后续免疫反应。基于这些观察结果,在自身免疫性疾病或移植的不同实验模型中,已采用输注早期凋亡细胞来预防不必要的炎症反应。此外,在接受异基因造血细胞移植以预防移植物抗宿主病的患者中,该方法已被证明可行且无任何毒性。然而,早期凋亡细胞输注是否可用于治疗正在发生的炎症性疾病尚未有广泛报道。最近,我们提供了证据表明早期凋亡细胞输注能够至少短暂地控制正在发生的胶原诱导性关节炎。这种有益的治疗效果与主要针对巨噬细胞和浆细胞样树突状细胞的抗原呈递细胞功能的调节以及胶原特异性调节性CD4 T细胞(Treg)的诱导有关。此外,该方法的疗效不会因与类风湿关节炎(RA)的两种标准治疗方法甲氨蝶呤和肿瘤坏死因子(TNF)抑制联合使用而改变。在此,鉴于这些观察结果和文献中的最新数据,我们讨论早期凋亡细胞输注的机制以及这种治疗方法如何应用于RA患者。