Xiao Chongjun, Lu Di, Chen Jinshuo, Chen Xiaoyan, Lin Huizhu, Huang Mudan, Cheng Shimei, Wang Yuge, Liu Qiuli, Zheng Haiqing
Department of Rehabilitation Medicine, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
The Biotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Front Pharmacol. 2021 Dec 10;12:770884. doi: 10.3389/fphar.2021.770884. eCollection 2021.
Human olfactory mesenchymal stem cells (OMSC) have become a novel therapeutic option for immune disorder or demyelinating disease due to their immunomodulatory and regenerative potentials. However, the immunomodulatory effects of OMSC still need to be elucidated, and comparisons of the effects of different MSCs are also required in order to select an optimal cell source for further applications. In animal experiments, we found neural functional recovery and delayed EAE attack in the OMSC treatment group. Compared with umbilical cord-derived mesenchymal stem cells (UMSC) treatment group and the control group, the OMSC treatment group had a better neurological improvement, lower serum levels of IFN-γ, and a lower proportion of CD4+IFN-γ+ T splenic lymphocyte. We also observed OMSC effectively suppressed CD4+IFN-γ+ T cell proportion when co-cultured with human peripheral blood-derived lymphocytes. The OMSC-mediated immunosuppressive effect on human CD4+IFN-γ+ T cells was attenuated by blocking cyclooxygenase activity. Our results suggest that OMSC treatment delayed the onset and promoted the neural functional recovery in the EAE mouse model possibly by suppressing CD4+IFN-γ+ T cells. OMSC transplantation might become an alternative therapeutic option for neurological autoimmune disease.
人嗅间充质干细胞(OMSC)因其免疫调节和再生潜能,已成为免疫紊乱或脱髓鞘疾病的一种新型治疗选择。然而,OMSC的免疫调节作用仍有待阐明,为进一步应用选择最佳细胞来源还需要比较不同间充质干细胞的作用。在动物实验中,我们发现OMSC治疗组神经功能得到恢复,实验性自身免疫性脑脊髓炎(EAE)发作延迟。与脐带间充质干细胞(UMSC)治疗组和对照组相比,OMSC治疗组神经功能改善更好,血清干扰素-γ(IFN-γ)水平更低,脾脏CD4+IFN-γ+ T淋巴细胞比例更低。我们还观察到,OMSC与人外周血淋巴细胞共培养时可有效抑制CD4+IFN-γ+ T细胞比例。通过阻断环氧化酶活性,OMSC对人CD4+IFN-γ+ T细胞的免疫抑制作用减弱。我们的结果表明,OMSC治疗可能通过抑制CD4+IFN-γ+ T细胞,延缓EAE小鼠模型发病并促进神经功能恢复。OMSC移植可能成为神经自身免疫性疾病的一种替代治疗选择。