Immunophenotyping of eighty six children with acute lymphoblastic leukemia by three-color flow cytometry.
- Author:
	        		
		        		
		        		
			        		Suigui WAN
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Wenyu GONG
			        		
			        		;
		        		
		        		
		        		
			        		Xuejing SUN
			        		
			        		;
		        		
		        		
		        		
			        		Juan XU
			        		
			        		;
		        		
		        		
		        		
			        		Ding TIAN
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Journal Article
 - MeSH: Antigens, CD; analysis; Child; Flow Cytometry; methods; Humans; Immunophenotyping; Precursor Cell Lymphoblastic Leukemia-Lymphoma; immunology
 - From: Chinese Journal of Hematology 2002;23(2):83-86
 - CountryChina
 - Language:Chinese
 - 
		        	Abstract:
			       	
			       		
				        
				        	
OBJECTIVESTo evaluate the specificity of three-color flow cytometry in childhood acute lymphoblastic leukemia (ALL) immunophenotyping.
METHODSImmunophenotyping was performed by three-color flow cytometry analysis using CD(45)/SSC gating.
RESULTSThe percentage of blasts was correlated better with leukemic cell count compared with that of FSC/SSC, and the false positive results were low. Among eighty six cases of ALL, 95.3% was B-ALL, in which common-ALL and Pro-B-ALL were 76.8% and 6.1%, respectively, and 2.3% was T-ALL. CD(34)(+) and myeloid-associated antigen expression were observed in 57.0% and 34.9% of the cases, respectively, among which Pro-B-ALL was the commonest. CD(33) was more commonly expressed than CD(13) in Pro-B-ALL cases, but no difference in the expression between these two antigens in other subtypes.
CONCLUSIONGating of CD(45)/SSC eliminated effection of normal cells to blasts in bone marrow, with which the immunophenotyping results were more reliable.
 
            