Effects of doxorubicin on IL-2 release and LAK activity of human fetal thymocytes
	    		
		   		
	    	
    	
    	
   		
        
        	
        		- VernacularTitle:阿霉素对人胚胸腺细胞IL-2产生及LAK活性的影响
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Tihui FU
			        		
			        		;
		        		
		        		
		        		
			        		Zhirong XIE
			        		
			        		;
		        		
		        		
		        		
			        		Bifang DENG
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		doxorubicin;
			        		
			        		
			        		
				        		human fetal thy-mocyte;
			        		
			        		
			        		
				        		IL-2;
			        		
			        		
			        		
				        		LAK activity
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Pharmacological Bulletin
	            		
	            		 1987;0(02):-
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	The immunoregulatory effects of some anti-cancer drugs have important role in their anti-tumor mechanisms. Our results showed that doxorubicin (DXR) of 0.04 mg ?L-1 could enhance the interleukin 2 (IL-2) release and induction of lymphokine-activated killer (LAK) activity of human fetal thymocytes(HFT). Higher concentration of this drug (4 mg ?L-1) exhibited inhibition on IL-2 release but no effect on LAK activity. These data suggest that lower concentration of DXR have some immunopotentiation effects on HFT.