CD8型                        
                
                                
                        
                            CD3型                        
                
                                
                        
                            发病机制                        
                
                                
                        
                            T淋巴细胞                        
                
                                
                        
                            甲状腺                        
                
                                
                        
                            细胞因子                        
                
                                
                        
                            渗透(HVAC)                        
                
                                
                        
                            表型                        
                
                                
                        
                            分子生物学                        
                
                                
                        
                            生物                        
                
                                
                        
                            病理                        
                
                                
                        
                            医学                        
                
                                
                        
                            免疫学                        
                
                                
                        
                            内分泌学                        
                
                                
                        
                            免疫系统                        
                
                                
                        
                            基因                        
                
                                
                        
                            遗传学                        
                
                                
                        
                            物理                        
                
                                
                        
                            热力学                        
                
                        
                    
            作者
            
                Damu Yang,Yuji Hiromatsu,Tomoaki Hoshino,Yoichi Inoue,Kyogo Itoh,Kyohei Nonaka            
         
                    
            出处
            
                                    期刊:Thyroid
                                                         [Mary Ann Liebert, Inc.]
                                                        日期:1999-03-01
                                                        卷期号:9 (3): 305-310
                                                        被引量:67
                                 
         
        
    
            
            标识
            
                                    DOI:10.1089/thy.1999.9.305
                                    
                                
                                 
         
        
                
            摘要
            
            Lymphocyte infiltration in the retrobulbar space is a prominent histological feature of thyroid-associated ophthalmopathy (TAO). We have characterized phenotypic and functional features of T cells derived from retrobulbar infiltrates of 3 TAO patients to better understand their roles in the disease. One hundred four T-cell clones (TCC) were directly established from cells of retrobulbar tissues using a highly efficient cloning procedure. Phenotypic analysis of TCC showed approximately 70% to 80% were CD3+ CD4+ CD8- T cells, and approximately 20% to 30% were CD3+ CD8+ CD4- T cells. None of the TCC were CD3+ CD4- CD8- T cells. Analysis of the cytokine profile of TCC, as documented by the ability to express interferon-γ, interleukin (IL)-2, IL-4, and IL-10 demonstrated that the majority of TCC expressed T helper (TH)l-like profile in both the mRNA and protein levels. A few TCC showed TH0-like profile, but no TCC showed Tn2-like profile. These results suggest that THl-type CD4+ T cells play important roles in the pathogenesis of TAO.
         
            
 
                 
                
                    
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