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多发性硬化症严重复发实验大鼠模型中单核细胞 M1/M2 激活模式的改变。M2 激活的单核细胞给药改善临床状况。

Altered M1/M2 activation patterns of monocytes in severe relapsing experimental rat model of multiple sclerosis. Amelioration of clinical status by M2 activated monocyte administration.

机构信息

University Victor Segalen, France.

出版信息

Mult Scler. 2011 Jan;17(1):2-15. doi: 10.1177/1352458510379243. Epub 2010 Sep 2.

DOI:10.1177/1352458510379243
PMID:20813772
Abstract

OBJECTIVES

We investigated proinflammatory M1 and immunomodulatory M2 activation profiles of circulating monocytes in relapsing experimental autoimmune encephalomyelitis (EAE) model of multiple sclerosis, and tested whether altered M1/M2 equilibrium promotes CNS inflammation.

RESULTS

Approaches of MRI macrophage tracking with USPIO nanoparticles and expression patterns of M1/M2 macrophages and microglia in brain and M1/M2 monocytes in blood samples at various disease stages revealed that M1/M2 equilibrium in blood and CNS favors mild EAE, while imbalance towards M1 promotes relapsing EAE. We consequently investigated whether M2 activated monocyte restoration in peripheral blood could cure acute clinical EAE disease. Administration of ex vivo activated M2 monocytes both suppressed ongoing severe EAE and increased immunomodulatory expression pattern in lesions, confirming their role in the induction of recovery.

CONCLUSION

We conclude that imbalance of monocyte activation profiles and impaired M2 expression, are key factors in development of relapses. Our study opens new perspectives for therapeutic applications in MS.

摘要

目的

我们研究了多发性硬化症复发型实验性自身免疫性脑脊髓炎(EAE)模型中循环单核细胞的促炎 M1 和免疫调节 M2 激活谱,并检验了 M1/M2 平衡的改变是否会促进中枢神经系统炎症。

结果

采用 USPIO 纳米颗粒进行 MRI 巨噬细胞追踪,以及在不同疾病阶段检测大脑中的 M1/M2 巨噬细胞和小胶质细胞以及血液中的 M1/M2 单核细胞的表达模式,揭示了血液和中枢神经系统中 M1/M2 的平衡有利于轻度 EAE,而向 M1 失衡则会促进复发型 EAE。因此,我们研究了外周血中 M2 激活单核细胞的恢复是否可以治愈急性临床 EAE 疾病。体外激活的 M2 单核细胞的给药不仅抑制了正在进行的严重 EAE,而且增加了病变中的免疫调节表达模式,证实了它们在诱导恢复中的作用。

结论

我们得出结论,单核细胞激活谱的失衡和 M2 表达的受损是复发发展的关键因素。我们的研究为 MS 的治疗应用开辟了新的前景。

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