Immune-inflammatory Processes and Gene Therapeutics Group, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Internal Medicine Service, Bellvitge University Hospital, University of Barcelona and Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Front Immunol. 2022 Apr 25;13:883743. doi: 10.3389/fimmu.2022.883743. eCollection 2022.
C4b-binding protein (C4BP) is a well-known regulator of the complement system that holds additional and important activities unrelated to complement inhibition. Recently, we have described a novel immunomodulatory activity in the minor C4BP(β-) isoform directly acting over inflammatory phagocytes. Here we show that incorporation of the β-chain to the C4BP α-chain oligomer interferes with this immunomodulatory activity of C4BP. Moreover, an oligomeric form including only the complement control protein 6 (CCP6) domain of the C4BP α-chain (PRP6-HO7) is sufficient to "reprogram" monocyte-derived DCs (Mo-DCs) from a pro-inflammatory and immunogenic phenotype to an anti-inflammatory and tolerogenic state. PRP6-HO7 lacks complement regulatory activity but retains full immunomodulatory activity over inflammatory Mo-DCs induced by TLRs, characterized by downregulation of relevant surface markers such as CD83, HLA-DR, co-stimulatory molecules such as CD86, CD80 and CD40, and pro-inflammatory cytokines such as IL-12 and TNF-α. Furthermore, PRP6-HO7-treated Mo-DCs shows increased endocytosis, significantly reduced CCR7 expression and CCL21-mediated chemotaxis, and prevents T cell alloproliferation. Finally, PRP6-HO7 shows also full immunomodulatory activity over Mo-DCs isolated from lupus nephritis patients with active disease, even without further pro-inflammatory stimulation. Therefore PRP6-HO7, retaining the immunomodulatory activity of C4BP(β-) and lacking its complement regulatory activity, might represent a promising and novel alternative to treat autoimmune diseases.
C4 结合蛋白 (C4BP) 是补体系统的一种熟知的调节剂,具有与补体抑制无关的额外且重要的活性。最近,我们描述了 C4BP 小分子β-异构体在炎症吞噬细胞上的一种新的免疫调节活性。在此,我们发现 C4BP 小分子β-异构体与 C4BPα链寡聚体的结合会干扰 C4BP 的这种免疫调节活性。此外,包含 C4BPα 链的补体控制蛋白 6(CCP6)结构域的寡聚形式(PRP6-HO7)足以“重新编程”单核细胞衍生的树突状细胞(Mo-DC),使其从促炎和免疫原性表型转变为抗炎和耐受状态。PRP6-HO7 缺乏补体调节活性,但保留了对 TLR 诱导的炎症 Mo-DC 的完整免疫调节活性,其特征是下调相关表面标志物,如 CD83、HLA-DR、共刺激分子如 CD86、CD80 和 CD40,以及促炎细胞因子如 IL-12 和 TNF-α。此外,PRP6-HO7 处理的 Mo-DC 显示出增加的内吞作用,显著降低 CCR7 表达和 CCL21 介导的趋化作用,并防止 T 细胞同种增殖。最后,PRP6-HO7 对狼疮肾炎患者活动期的 Mo-DC 也具有完整的免疫调节活性,甚至无需进一步的促炎刺激。因此,PRP6-HO7 保留了 C4BP(β-)的免疫调节活性,且缺乏其补体调节活性,可能是治疗自身免疫性疾病的一种很有前途和新颖的选择。