- Author:
	        		
		        		
		        		
			        		Akiko TOMOKUNI
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Takemi OTSUKI
			        		
			        		;
		        		
		        		
		        		
			        		Haruko SAKAGUCHI
			        		
			        		;
		        		
		        		
		        		
			        		Yumika ISOZAKI
			        		
			        		;
		        		
		        		
		        		
			        		Fuminori HYODOH
			        		
			        		;
		        		
		        		
		        		
			        		Masayasu KUSAKA
			        		
			        		;
		        		
		        		
		        		
			        		Ayako UEKI
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Journal Article
 - Keywords: apoptosis; autoantibody; autoimmunity; silicosis; topoisomerase I
 - From:Environmental Health and Preventive Medicine 2002;7(1):7-10
 - CountryJapan
 - Language:English
 - 
		        	Abstract:
			       	
			       		
				        
				        	
OBJECTIVESThe aim of this study was to detect anti-topoisomerase I (anti-topo I) autoantibodies, which are known to be limited in systemic sclerosis patients, in silicosis patients with no clinical symptoms of autoimmune disease.
METHODSSerum anti-topo I autoantibodies were detected using ELISA. Differences in clinical parameters between patients with and without anti-topo I autoantibodies were analyzed.
RESULTSSeven of 69 patients had anti-topo I autoantibodies. These 7 patients showed elevated PaCO(2) values (P=0.0212), and inverse correlations between serum soluble Fas levels and PaCO(2) values were found.
CONCLUSIONAnti-topo I autoantibodies were detected in 10.1% of silicosis patients without any clinical symptoms of autoimmune disease. The findings here suggest that the genesis of anti-topo I autoantibodies might be related to pulmonary involvement or lung fibrosis associated with progression of silicosis.
 
            
