They propose that the immune enhancement observed is explained by the cross-presentation of tumor Ag by the Ab and subsequent activation of FcR. Our data would suggest that the human IgG1 DNA vaccine exploits both pathways of direct presentation

and cross-presentation through FcγR1 to induce high-frequency and high-avidity CD8+ T-cell responses, a phenomenon Protease Inhibitor Library ic50 that is not possible with a similar protein vaccine. The CD4 T-cell responses appears to be unaffected by the absence of the Fc region. Recently the literature describes a variety of intracellular autophagic routes by which Ag can gain access to MHC class II 41. It is possible that the CD4 epitope is processed via one of these routes upon direct transfection of APC. We also observe no difference in the CD4 responses generated when secretion is of HuIgG1 construct is prevented (data not shown). Further studies into the precise mechanism of Ag presentation CHIR-99021 research buy will be necessary to clarify this. In conclusion, a DNA vaccine incorporating CTL epitopes within an Ab molecule

results in high-frequency and high-avidity T-cell responses that result in effective tumor immunity. The vaccine appears to work by presenting low doses of CTL epitopes within an inert carrier for both direct and Fc-mediated cross-presentation. Further studies will determine if the avidity to other viral and self Ag can also be enhanced by this method of immunization. B16F10 and RMAS mouse cell lines were obtained from the ATCC and were maintained in RPMI (Cambrex, Wokingham, UK) with 10% FBS (Sigma, Poole, UK). To knockdown expression of H-2Kb in the cell line B16F10, RNA interference was utilized. The complimentary oligonucleotides siKB forward and reverse targeting H-2Kb (Table 1) were annealed www.selleck.co.jp/products/erlotinib.html cloned into the vector psiRNA-h7SKGFPzeo (Invivogen, Calne, UK). The stable cell line B16F10 siKb was generated by transfection using genejuice (Novagen, Nottingham, UK) and selection in the presence of 200 μg/mL of zeocin.

B16F10 cells were transfected with the plasmid pORF-IFN-α (Invivogen, Calne, UK) and selected by growth in the presence of 500 μg/mL of G418. To confirm the expression of IFN-α and psiKb-h7SKGFPzeo, the levels of MHC class I on the cell surface was analyzed by flow cytometry. Media used for splenocyte culture was RPMI-1640 with 10% FBS (Sigma), 2 mM glutamine, 20 mM HEPES buffer, 100 units/mL penicillin, 100 μg/mL streptomycin and 10−5 M 2-mercaptoethanol. CDRs within ImmunoBody™ single heavy and light chain vectors had been replaced with unique restriction sites enabling rapid insertion of epitope sequences 26. In brief, to generate the human IgG1 TRP2 and OVA constructs, oligos encoding the TRP2 epitope SVYDFFVWL 42 and OVA epitope SIINFEKL 43 were incorporated into CDRH2 or in direct replacement of CDRH3 (Table 1). Into the same plasmids the I-Ab restricted helper CD4 epitope from the HepB nucleoprotein TPPAYRPPNAPIL 44 was inserted in replacement of CDRL1 of the kappa chain.