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. 2014 Jan 22;4(1):36–44. doi: 10.5005/jp-journals-10018-1094

Table 1: Identification of the specificity and phenotype of IFNγ- secreting T cells by intracellular staining. Splenocytes were collected 1 week after the last immunization. Individual peptides (2 |jg/ml final) derived from pools were used to stimulate splenocytes ex vivo for 1 hour prior to an overnight incubation with brefeldin A (2 jg/ml final). Cells were then stained with anti-CD3, -CD4 and -CD8 labeled antibodies. After fixation and permeabilization, intracellular IFNγ- detection was performed. ND: Not determined due to the lack of cells

      NASVAC         DNAs    
Pools   A2-DR1     HBs-A2-DR1     A2-DR1     HBs-A2-DR1    
  Peptide   ICS   Peptide   ICS   Peptide   ICS   Peptide   ICS  
C1-55   21-35   CD4   21-35   ND   ND   CD4 CD8   16-30   CD8  
C46-95   56-70   CD4   56-70   ND   ND   CD4 CD8   ND   ND  
  61-75   CD4   61-75            
C86-140   111-125   CD4   111-125   CD4   ND   CD4 CD8      
  115-130   CD4   115-130   CD4          
PreS2           164-128   CD4      
S164-218   200-214 ad   CD4   200-214 ad   CD4   164-178   CD8   164-178   ND  
          170-181   CD8   200-214 ad   CD8  
          200-214 ad   CD8   204-212 ad   CD8  
          204-212 ad   CD8      
S338-389       348-357   CD8