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    Modulating the natural history of type 1 diabetes in children at high genetic risk by mucosal insulin immunization.
        
        Curr. Diab. Rep. 8, 87-93 (2008)
    
    
    
				Mucosal administration of insulin represents an attractive antigen-specific therapeutic approach to preventing type 1 diabetes. It can prevent autoimmune diabetes in animal models, but although it has been shown to be safe, it has not yet been proven effective in human studies. Efficacy may depend on the dose and route at which insulin is administered, the stage in type 1 diabetes pathogenesis at which treatment is initiated, and the study cohort that is treated. We have proposed Pre-POINT (Primary Oral/intranasal INsulin Trial), a dose-finding safety and immune efficacy pilot study for primary mucosal insulin therapy in islet autoantibody-negative children at high genetic risk for type 1 diabetes who naturally first develop autoimmunity to insulin. Pre-POINT aims to identify an optimal insulin dose and route of application (orally or intranasally) that is well tolerated and can induce an immune response to insulin for additional use in a phase II/III primary prevention trial in children at risk.
			
			
		Impact Factor
					Scopus SNIP
					Web of Science
Times Cited
					Times Cited
Scopus
Cited By
					
					Cited By
Altmetric
					
				0.000
					0.590
					63
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
     
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2008
    
 
     
    
        HGF-Berichtsjahr
        0
    
 
    
    
        ISSN (print) / ISBN
        1534-4827
    
 
    
        e-ISSN
        1539-0829
    
 
     
     
     
	     
	 
	 
    
        Zeitschrift
        Current Diabetes Reports
    
 
		
    
        Quellenangaben
        
	    Band: 8,  
	    Heft: 2,  
	    Seiten: 87-93 
	    
	    
	
    
 
  
         
        
            Verlag
            Springer
        
 
        
            Verlagsort
            Heidelberg [u.a.]
        
 
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Institute of Diabetes Research (IDF)
Institute of Diabetes and Obesity (IDO)
Institute of Pancreatic Islet Research (IPI)
 
    Institute of Diabetes and Obesity (IDO)
Institute of Pancreatic Islet Research (IPI)
        POF Topic(s)
        30201 - Metabolic Health
30502 - Diabetes: Pathophysiology, Prevention and Therapy
    
 
    30502 - Diabetes: Pathophysiology, Prevention and Therapy
        Forschungsfeld(er)
        Helmholtz Diabetes Center
    
 
    
        PSP-Element(e)
        G-502100-001
G-502290-001
 
     
     	
    G-502290-001
        PubMed ID
        18445349
    
    
    
        WOS ID
        000261100300002
    
    
        Erfassungsdatum
        2008-04-30