SITI, CHU Rennes, Etablissement Français du Sang Bretagne, Rennes, France.
INSERM UMR 1236, Université Rennes, INSERM, Etablissement Français du Sang Bretagne, Rennes, France.
Stem Cells Transl Med. 2023 Apr 17;12(4):194-206. doi: 10.1093/stcltm/szad010.
Mesenchymal stromal cells (MSCs) have recently emerged as an interesting therapeutic approach for patients with progressive systemic sclerosis (SSc), a rare and life-threatening orphan autoimmune disease. Whereas MSC immunomodulatory potential is considered as a central mechanism for their clinical benefit, very few data are available on the impact of MSCs on immune cell subsets in vivo. In the current extended study of a phase I/II clinical trial exploring the injection of a single dose of allogeneic bone marrow-MSCs (alloBM-MSCs) in patients with severe SSc (NCT02213705), we performed a longitudinal in-depth characterization of circulating immune cells in 19 MSC-treated patients, including 14 responders and 5 non-responders. By a combination of flow cytometry and transcriptomic analyses, we highlighted an increase in circulating CD24hiCD27posCD38lo/neg memory B cells, the main IL-10-producing regulatory B cell (Breg) subset, and an upregulation of IL10 expression in ex-vivo purified B cells, specifically in responder patients, early after the alloBM-MSC infusion. In addition, a deeper alteration of the B-cell compartment before alloBM-MSC treatment, including a higher expression of profibrotic cytokines IL6 and TGFβ by sorted B cells was associated with a non-responder clinical status. Finally, BM-MSCs were able to directly upregulate IL-10 production in activated B cells in vitro. These data suggest that cytokine-producing B cells, in particular Breg, are pivotal effectors of BM-MSC therapeutic activity in SSc. Their quantification as activity biomarkers in MSC potency assays and patient selection criteria may be considered to reach optimal clinical benefit when designing MSC-based clinical trials.
间充质基质细胞(MSCs)最近成为治疗进行性系统性硬化症(SSc)患者的一种有前途的方法,SSc 是一种罕见且危及生命的孤儿自身免疫性疾病。虽然 MSCs 的免疫调节潜力被认为是其临床获益的核心机制,但关于 MSCs 对体内免疫细胞亚群的影响的数据非常有限。在一项探索单次输注同种异体骨髓间充质基质细胞(alloBM-MSCs)治疗严重 SSc 患者的 I/II 期临床试验的扩展研究中(NCT02213705),我们对 19 名接受 MSC 治疗的患者的循环免疫细胞进行了纵向深入的特征描述,包括 14 名应答者和 5 名无应答者。通过流式细胞术和转录组分析的组合,我们发现循环 CD24hiCD27posCD38lo/neg 记忆 B 细胞、主要的 IL-10 产生调节性 B 细胞(Breg)亚群增加,以及体外纯化 B 细胞中 IL10 表达上调,特别是在应答者患者中,在 alloBM-MSC 输注后早期。此外,在 alloBM-MSC 治疗前 B 细胞区室的更深层次改变,包括分选 B 细胞中纤维化细胞因子 IL6 和 TGFβ的更高表达与无应答者的临床状态相关。最后,BM-MSCs 能够在体外直接上调激活的 B 细胞中 IL-10 的产生。这些数据表明,产生细胞因子的 B 细胞,特别是 Breg,是 BM-MSC 在 SSc 中治疗活性的关键效应物。在设计基于 MSC 的临床试验时,将它们作为 MSC 效力测定和患者选择标准中的活性生物标志物进行定量,可能有助于获得最佳的临床获益。