Umbilical cord mesenchymal stem cell transplantation modulated Th17/Treg balance and delayed lupus progression in MRL/lpr mice
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3760/cma.j.issn.1007-7480.2015.03.003
   		
        
        	
        		- VernacularTitle:脐带间充质干细胞移植调节Th17/调节性T细胞平衡延缓MRL/lpr鼠狼疮进展
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Zhuoya ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Wei KONG
			        		
			        		;
		        		
		        		
		        		
			        		Weiwei CHEN
			        		
			        		;
		        		
		        		
		        		
			        		Genhong YAO
			        		
			        		;
		        		
		        		
		        		
			        		Xuebing FENG
			        		
			        		;
		        		
		        		
		        		
			        		Lingyun SUN
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Mesenchymal stem cell;
			        		
			        		
			        		
				        		Lupus erythematosus,systemic;
			        		
			        		
			        		
				        		Mice;
			        		
			        		
			        		
				        		Th17 cells;
			        		
			        		
			        		
				        		T-Lymphocytes,regulatory
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Rheumatology
	            		
	            		 2015;19(3):152-155
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Objective To explore the preventive effect of early umbilical cord mesenchymal stem cells (UC-MSCs) transplantation on MRL/lpr mice and the underly mechanisms.Methods Fourteen 10-week-old MRL/lpr mice were labeled and numbered.They were randomly divided into 2 groups by using random number table and injected with 1 ×106 UC-MSCs or PBS via tail vein respectively.Proteinuria was measured with Bradford method every 4 weeks.All mice were sacrificed at the age of 28 weeks, with the level of serum antidsDNA antibody and IL-17 detected by enzyme linked immunosorbent assay (ELISA).Splenic Th17 cells, as well as regulatory T cells (Treg) were examined by flow cytometry.Data were analyzed with t test and Pearson's correlation test.Results The onset of proteinuria was delayed for 4 weeks in UC-MSC-treated group compared with that in the control group.At the age of 28 weeks, the 24 hour proteinuria [(1.78±0.17) mg vs (4.77±0.98)mg, t=2.99, P<0.05] and the spleen weight [(0.149±0.009) g vs (0.273±0.052) g, t=2.33, P<0.05] in UC-MSCtreated group were significantly lower than those in the control group.There was also a trend of the decline of serum anti-dsDNA antibody and IL-17 level after UC-MSCs transplantation.Compared with those in the control group, both the percentage and the absolute number of Th17 cells were significantly decreased in UC-MSC-treated group [(0.90±0.19)% vs (2.81±0.50)%, t=3.54, P<0.01 and (3.7±0.8)×105 vs (19.3±3.7)×105, t=4.12,P<0.01].Meanwhile, the percentage of Treg elevated after UC-MSCs treatment.The ratio of Th17/Treg was significantly lower in UC-MSC-treated group than that in the control group (0.11±0.03 vs 0.50±0.09, t=4.23,P<0.01).Both the ratio of Th17/Treg (r=0.73, P<0.01;r=0.59, P<0.05) and serum IL-17 level (r=0.78, P<0.01;r=0.56, P<0.05) was positively correlated with the level of 24 hour proteinuria and anti-dsDNA antibody respectively in MRL/lpr mice.Conclusion Early UC-MSCs transplantation helps to delay disease onset and ameliorate disease progression in MRL/lpr mice, which may act through the modulation of Th17/Treg balance.