Raja Karthick Raja Muthu, Plasil Martin, Rihova Lucie, Pelcova Jana, Adam Zdenek, Hajek Roman
Babak Myeloma Group, Department of Pathological Physiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic; Department of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech Republic.
Cytometry B Clin Cytom. 2013 Jul 3. doi: 10.1002/cytob.21109.
Multiple myeloma (MM) is a malignancy of plasma cells frequently associated with immune abnormalities. Several studies have confirmed that in MM immune deregulation can be mediated by increased numbers of CD4 T regulatory (Treg) cells, and these cells were also associated with poor outcome. In the present study, we aimed to study CD8 Treg cells before and after lenalidomide plus dexamethasone (len-dex) treatment in MM patients.
Using flow cytometry, we enumerated and assessed suppressive function of CD8 Treg cells in 16 MM patients before and after len-dex treatment.
Numbers of CD8 Treg cells (CD8+CD25hi+FoxP3+) (P<0.01) were significantly increased in MM patients (before treatment) compared to healthy donors. However, no significant changes were observed in CD4 and CD8 T cells. A significant increase in CD8 Treg cells was observed after len-dex treatment compared to pre-treatment but no significant difference was observed in CD4 and CD8 T cells. Proliferation assay data showed that CD8 Treg cells inhibited proliferation of CD4 T cells and IFN-γ secretion in a concentration dependent manner. Suppressive activity of CD8 Treg cells did not differ significantly between healthy donors, untreated and len-dex treated MM patients. A significant abnormal level of IL-10 was observed from proliferation assays of untreated and len-dex treated MM patients compared to healthy donors (P≤0.03).
Using flow cytometry, we have shown that suppressive CD8 Treg cells are increased in MM patients and len-dex treatment is unable to control these suppressive CD8 Treg cells. © 2013 Clinical Cytometry Society.
多发性骨髓瘤(MM)是一种浆细胞恶性肿瘤,常伴有免疫异常。多项研究证实,在MM中,免疫失调可由CD4调节性T(Treg)细胞数量增加介导,且这些细胞也与不良预后相关。在本研究中,我们旨在研究来那度胺联合地塞米松(来那度胺 - 地塞米松)治疗前后MM患者体内的CD8 Treg细胞。
我们运用流式细胞术,对16例MM患者在来那度胺 - 地塞米松治疗前后的CD8 Treg细胞数量进行计数,并评估其抑制功能。
与健康供体相比,MM患者(治疗前)的CD8 Treg细胞(CD8 + CD25hi + FoxP3 +)数量显著增加(P < 0.01)。然而,CD4和CD8 T细胞未观察到显著变化。与治疗前相比,来那度胺 - 地塞米松治疗后CD8 Treg细胞显著增加,但CD4和CD8 T细胞未观察到显著差异。增殖试验数据显示,CD8 Treg细胞以浓度依赖性方式抑制CD4 T细胞增殖和IFN - γ分泌。健康供体、未经治疗和来那度胺 - 地塞米松治疗的MM患者之间,CD8 Treg细胞的抑制活性无显著差异。与健康供体相比,未经治疗和来那度胺 - 地塞米松治疗的MM患者增殖试验中观察到IL - 10水平显著异常(P≤0.03)。
通过流式细胞术,我们发现MM患者体内具有抑制作用的CD8 Treg细胞增加,而来那度胺 - 地塞米松治疗无法控制这些具有抑制作用的CD8 Treg细胞。© 2013临床细胞计量学会。