- Author:
	        		
		        		
		        		
			        		Ami WOO
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Jin Hee KIM
			        		
			        		;
		        		
		        		
		        		
			        		Young Joo JEONG
			        		
			        		;
		        		
		        		
		        		
			        		Hyung Gun MAENG
			        		
			        		;
		        		
		        		
		        		
			        		Yong Taek LEE
			        		
			        		;
		        		
		        		
		        		
			        		Jae Seung KANG
			        		
			        		;
		        		
		        		
		        		
			        		Wang Jae LEE
			        		
			        		;
		        		
		        		
		        		
			        		Young il HWANG
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:In Vitro ; Original Article
 - Keywords: Vitamin C; antioxidant; reactive oxygen species; mouse B cell; isotype switching
 - MeSH: Animals; Apoptosis; Ascorbic Acid; B-Lymphocytes; Dendritic Cells; Immunity, Humoral; Immunoglobulin Class Switching; Immunoglobulin G; Injections, Intraperitoneal; Mammals; Mice; Micronutrients; Reactive Oxygen Species; Vitamins
 - From:Anatomy & Cell Biology 2010;43(1):25-35
 - CountryRepublic of Korea
 - Language:English
 - Abstract: Vitamin C, one of essential micronutrients, has been reported to modulate the humoral immune responses in some mammals. We investigated whether vitamin C might modulate this response in mice by directly affecting B cells. Splenic B cells were isolated and activated by CD40- and B cell receptor-ligation in vitro. The cells were cultured with a pretreatment of vitamin C from 0 to 1 mM of concentrations. Vitamin C slightly increased apoptosis of B cells dose-dependently and behaved as an antioxidant. We found that in vivo administration of vitamin C by intraperitoneal injection affected isotype switching as previously reported: the titer of antigen-specific IgG1 antibody was decreased, while that of IgG2a was unaffected. Somewhat different from those observed in vivo, in vitro exposure to vitamin C slightly decreased isotype switching to IgG1 and increased isotype switching to IgG2a. Pretreatment with vitamin C in the safe range did not affect either proliferation of cultured B cells or the expression of CD80 and CD86 in those cells. Taken together, in vivo results suggest that vitamin C acts to modulate isotype switching in the mouse. However, because of our in vitro results, we suggest that the modulation exerted by vitamin C in vivo is by indirectly affecting B cells, perhaps by directly influencing other immune cells such as dendritic cells.
 
            
