The Current Status and Issues Concerning Monoclonal Antibody Therapy
        The bulletin of the Yamaguchi Medical School Volume 51 Issue 3-4
        Page 41-50
        
    published_at 2004-12
            Title
        
        The Current Status and Issues Concerning Monoclonal Antibody Therapy
        
        
    
        
            Source Identifiers
        
    
    
            Creator Keywords
        
            monoclonal antibody
            HER2
            epidermal growth factor receptor
            vascular endothelial growth factor
            VEGF receptor
            human anti-mouse antibody
            epithelial cell adhesion molecule
            cytotoxic T lymphocyte-associated antigen 4
            dendritic cells
    Monoclomal antibodies (mAbs) against growth factor or its receptor have raised the second wave of antibody therapy for solid tumors. Transtuzumab (humanized anti-HER2mAb) is the first mAb approved for the treatment of a solid tumor, metastatic breast cancer. Large-scale phase Ⅲ clinical trials are now ongoing to further evaluate the additive effects on chemotherapy and the efficacy as a maintenance  monotherapy. Overexpression of HER2 is found only a small percentage of patients with solid tumor, whereas epidermal growth factor receptor is expressed in a variety of solid tumors with high frequency. More broadly applicable for solid tumors is anti-angiogenesis therapy because it is targeting not tumor cells but tumor vasculature. Cetuximab (chimeric anti-EGFR mAb) and bevacizumab (humanized anti-VEGF mAb)have recently been shown to be clinically of remarkable effect for metastatic colorectal cancer. The points at issue are thrombotic events of bevacizumab. In contrast to the mAbs as signal inhibitors, no apparent objective responses were seen in most clinical studies of mAbs against cell surface glycoproteins or adhesion molecules. However, several groups reported the survival benefit of those mAbs, in which anti-idiotypic antibody response may play an important role. In addition, some of their anti-idiotype mAbs showed the survival benefit in patients with solid tumor. Altered self-antigens have recently been attempted to intensify active immunotherapy including dendritic cell therapy. Considering that dendritic cells efficientry cross-present tumor antigens after  ingesting them as immune complex those ”modest″ mAbs may be of use for dendritic cell therapy as immune complex with altered  self-antigens.
        
        
            Languages
        
            eng
    
    
        
            Resource Type
        
        departmental bulletin paper
    
    
        
            Publishers
        
            Yamaguchi University Graduate School of Medicine
    
    
        
            Date Issued
        
        2004-12
    
    
        
            File Version
        
        Version of Record
    
    
        
            Access Rights
        
        open access
    
    
            Relations
        
            
                
                
                [ISSN]0513-1812
            
            
                
                
                [NCID]AA00594272
            
    
        
            Schools
        
            医学部
    
                
