Ghasemi, A.* ; Mohammad, N.* ; Mautner, J. ; Taghipour Karsabet, M.* ; Amani, J.* ; Ardjmand, A.* ; Vakili, Z.*
     
    
        
Immunization with a recombinant fusion protein protects mice against Helicobacter pylori infection.
    
    
        
    
    
        
        Vaccine 36, 5124-5132 (2018)
    
    
 	
    
	
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			Open Access Green as soon as Postprint is submitted to ZB.
		
     
    
      
      
	
	    More than 50% of the world's population is infected with the bacterium Helicobacter pylori. If left untreated, infection with H. pylori can cause chronic gastritis and peptic ulcer disease, which may progress into gastric cancer. Owing to the limited efficacy of anti-H. pylori antibiotic therapy in clinical practice, the development of a protective vaccine to combat this pathogen has been a tempting goal for several years. In this study, a chimeric gene coding for the antigenic parts of H. pylori FIiD, UreB, VacA, and CagL was generated and expressed in bacteria and the potential of the resulting fusion protein (rFUVL) to induce humoral and cellular immune responses and to provide protection against H. pylori infection was evaluated in mice. Three different immunization adjuvants were tested along with rFUVL: CpG oligodeoxynucleotides (CpG ODN), Addavax, and Cholera toxin subunit B. Compared to the control group that had received PBS, vaccinated mice showed significantly higher cellular recall responses and antigen-specific IgG2a, IgG1, and gastric IgA antibody titers. Importantly, rFUVL immunized mice exhibited a reduction of about three orders of magnitude in their stomach bacterial loads. Thus, adjuvanted rFUVL might be considered as a promising vaccine candidate for the control of H. pylori infection.
	
	
	    
	
       
      
	
	    
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        Publication type
        Article: Journal article
    
 
    
        Document type
        Scientific Article
    
 
    
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        Keywords
        Helicobacter Pylori ; Immunization ; Chimeric ; Adjuvant ; Fusion Protection; Brucella-melitensis Infection; Vaccine Ctb-ue; Confers Protection; Therapeutic-efficacy; Provides Protection; Oral Immunization; Mucosal Immunity; Gastric-cancer; Mouse Model; Nod Mice
    
 
    
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        Publication Year
        2018
    
 
    
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        2018
    
 
    
    
        ISSN (print) / ISBN
        0264-410X
    
 
    
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        1358-8745
    
 
    
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	    Volume: 36,  
	    Issue: 34,  
	    Pages: 5124-5132 
	    Article Number: ,  
	    Supplement: ,  
	
    
 
    
        
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            Elsevier
        
 
        
            Publishing Place
            The Boulevard, Langford Lane, Kidlington, Oxford Ox5 1gb, Oxon, England
        
 
	
        
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        Reviewing status
        Peer reviewed
    
 
     
    
        POF-Topic(s)
        30203 - Molecular Targets and Therapies
    
 
    
        Research field(s)
        Immune Response and Infection
    
 
    
        PSP Element(s)
        G-501500-001
    
 
    
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        Erfassungsdatum
        2018-07-27