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 Vaccine Detail
                        
                          
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                              ChAd63 -PvTRAP  (chimpanzee adenovirus vaccine vector)                               | 
                           
                          
                            | Vaccine Information | 
                           
                          
                            
							
							  - Vaccine Name: ChAd63 -PvTRAP  (chimpanzee adenovirus vaccine vector)
 
					- Target Pathogen: malaria
 
                              - Type: Recombinant vector vaccine
 
                              - Status: Licensed
 
                              - Host Species for Licensed Use: Baboon
 
	
                          - Vector: simian adenovirus ChAd63 vaccine vector
                            
						
 
              
 					
	     	 	                      
                                   - Preparation: Recombinant ChAd63 and MVA vectors expressing P. vivax TRAP (PvTRAP) (Bauza et al., 2014).
 
                              - Immunization Route: Intramuscular injection (i.m.)
 
							 
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                            | Host Response | 
                           
                          
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                           Mouse Response  
                            
                              - Vaccination Protocol: Mice were primed with simian adenoviral vector 63 (ChAd63) encoding PvTRAP at a dose of 1 × 108 infectious units (IU) and 8 weeks later boosted with modified vaccinia virus strain Ankara (MVA) carrying the same transgene at a concentration of 1 × 107 PFU per ml, unless otherwise stated. All viral vector vaccines were administered intramuscularly in endotoxin-free PBS (Bauza et al., 2014).
 
						  - Vaccine Immune Response Type: VO_0003057
 
                              - Challenge Protocol: Wild-type and transgenic parasites used to challenge mice were fed on infected TO mice, and then were released on to the vaccinated mice (Bauza et al., 2014).
 
                              - Efficacy: Using this model, we found that both CD8+ T cells and antibodies mediated protection against malaria using virus-vectored vaccines (Bauza et al., 2014).
 
				
					
                             
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