Rui Ke, Shen Ziwei, Peng Na, Zhao Futao, Tang Yuan, Liu Shiyi, Xu Xinyi, Liu Chang, Wu Ling, Tian Jie, Lu Liwei
Institute of Medical Immunology, Affiliated Hospital of Jiangsu University, Zhenjiang 212003, Jiangsu Province, China.
Department of Laboratory Medicine, Affiliated Hospital of Jiangsu University, Zhenjiang 212003, Jiangsu Province, China.
Rheumatol Immunol Res. 2022 Dec 31;3(4):198-207. doi: 10.2478/rir-2022-0035. eCollection 2022 Dec.
To investigate the effect of olfactory ecto-mesenchymal stem cell-derived exosomes (OE-MSC-Exos) on T follicular helper (Tfh) cell response and their implication in treating experimental Sjögrens syndrome (ESS).
C57BL/6 mice were immunized with salivary glands (SG) proteins to induce ESS mouse model. OE-MSC-Exos were added to the Tfh cell polarization condition, and the proportion of Tfh cells was detected by FCM. The PD-L1 of OE-MSCs was silenced with small interfering RNA to extract siPD-L1-OE-MSC-Exos.
We found that transfer of OE-MSC-Exos markedly attenuated disease progression and reduced Tfh cell response in mice with ESS. In culture, OE-MSC-Exos potently inhibited the differentiation of Tfh cells from naïve T cells. Moreover, OE-MSC-Exos expressed high level of the ligand for the programmed cell death protein 1 (PD-L1), knocking down PD-L1 expression in OE-MSC-Exos significantly decreased their capacity to suppress Tfh cell differentiation in vitro. Consistently, transfer of OE-MSC-Exos with PD-L1 knockdown exhibited profoundly diminished therapeutic effect in ESS mice, accompanied with sustained Tfh cell response and high levels of autoantibody production.
Our results suggest that OE-MSC-Exos may exert their therapeutic effect in ameliorating ESS progression via suppressing Tfh cell response in a PD-L1-dependent manner.
研究嗅外胚层间充质干细胞来源的外泌体(OE-MSC-Exos)对滤泡辅助性T细胞(Tfh)反应的影响及其在治疗实验性干燥综合征(ESS)中的作用。
用唾液腺(SG)蛋白免疫C57BL/6小鼠以诱导ESS小鼠模型。将OE-MSC-Exos添加到Tfh细胞极化条件中,通过流式细胞术检测Tfh细胞的比例。用小干扰RNA沉默OE-MSCs的PD-L1以提取siPD-L1-OE-MSC-Exos。
我们发现,在ESS小鼠中,转移OE-MSC-Exos可显著减轻疾病进展并降低Tfh细胞反应。在培养中,OE-MSC-Exos强烈抑制幼稚T细胞向Tfh细胞的分化。此外,OE-MSC-Exos表达高水平的程序性细胞死亡蛋白1(PD-L1)的配体,敲低OE-MSC-Exos中的PD-L1表达显著降低了它们在体外抑制Tfh细胞分化的能力。一致地,转移敲低PD-L1的OE-MSC-Exos在ESS小鼠中表现出明显减弱的治疗效果,伴有持续的Tfh细胞反应和高水平的自身抗体产生。
我们的结果表明,OE-MSC-Exos可能通过以PD-L1依赖的方式抑制Tfh细胞反应,在改善ESS进展中发挥治疗作用。