Li Wenchao, Chen Weiwei, Huang Saisai, Tang Xiaojun, Yao Genhong, Sun Lingyun
Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, Jiangsu 210008, China.
Stem Cells Int. 2020 Mar 28;2020:3169469. doi: 10.1155/2020/3169469. eCollection 2020.
Immunosuppressants such as cyclophosphamide (CTX) have been employed to treat a wide array of autoimmune diseases. The most unfavourable side effects of these drugs are their suppression on the antimicrobial immunity and increasing the risk of infection. As a promising substitution/adjunct, mesenchymal stem cells (MSCs) are currently being tested in several clinical trials. However, their influence on the recipients' antimicrobial immunity remains unclear.
In this study, C57BL/6 mice were treated with either CTX or MSCs, and then both the innate and adaptive immunity of the lung were determined. To investigate the influence of CTX and MSCs on the immune defence against infection, the treated mice were intranasally infected with opportunistic pathogen (Hi). Bacterial clearance and antibacterial immune responses were analysed.
Our data showed that CTX strongly inhibited the proliferation of lung immune cells, including alveolar macrophages (AMs) and T cells, whereas MSCs increased the numbers of these cells. CTX suppressed the phagocytic activity of AMs; on the contrary, MSCs enhanced it. Notably, infusion of MSCs led to a remarkable increase of regulatory T cells and Th1 cells in the lung. When infected by Hi, CTX did not significantly impair the elimination of invaded bacteria. However, MSC-treated mice exhibited accelerated bacterial clearance and moderate inflammation and tissue damage.
Our study reported that unlike traditional immunosuppressants, modulation of MSCs on the recipient's immune response is more elegant. It could preserve and even enhance the antimicrobial defence, suggesting that MSCs are better choice for patients with high risk of infection or those who need long-term immunosuppressive regimen.
免疫抑制剂如环磷酰胺(CTX)已被用于治疗多种自身免疫性疾病。这些药物最不利的副作用是抑制抗菌免疫并增加感染风险。作为一种有前景的替代/辅助药物,间充质干细胞(MSCs)目前正在多项临床试验中进行测试。然而,它们对受体抗菌免疫的影响仍不清楚。
在本研究中,对C57BL/6小鼠进行CTX或MSCs治疗,然后测定肺的固有免疫和适应性免疫。为了研究CTX和MSCs对感染免疫防御的影响,将治疗后的小鼠经鼻感染机会性病原体(Hi)。分析细菌清除和抗菌免疫反应。
我们的数据表明,CTX强烈抑制肺免疫细胞的增殖,包括肺泡巨噬细胞(AMs)和T细胞,而MSCs增加了这些细胞的数量。CTX抑制AMs的吞噬活性;相反,MSCs增强了它。值得注意的是,输注MSCs导致肺中调节性T细胞和Th1细胞显著增加。当被Hi感染时,CTX并没有显著损害入侵细菌的清除。然而,经MSCs治疗的小鼠表现出加速的细菌清除以及适度的炎症和组织损伤。
我们的研究报告称,与传统免疫抑制剂不同,MSCs对受体免疫反应的调节更为精妙。它可以保留甚至增强抗菌防御能力,这表明MSCs对于感染风险高的患者或需要长期免疫抑制方案的患者是更好的选择。