Naslov
CMV expressing NKG2D ligand RAE-1γ employed as a highly immunogenic CD8 T cell vaccine-vector

Autori
Tršan, T., Abram, M., Lemmermann, N.A., Del Val, M., Krmpotić, A., Messerle, M., Jonjić, S.

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
2014 Annual Meeting of the Croatian Immunological Society / - , 2014

Skup
2014 Annual Meeting of the Croatian Immunological Society

Mjesto i datum
Krk, Hrvatska, 17.10.2014. - 18.10.2014

Vrsta sudjelovanja
Predavanje

Vrsta recenzije
Nije recenziran

Ključne riječi
MCMV; CD8 T cell vaccine vector; NKG2D

Sažetak
Antigen-specific CD8 T cells provide long-term protection against intracellular pathogens and some tumors. This makes CD8 T cell-based vaccines especially attractive option for vaccine design. Cytomegalovirus (CMV) represents the most suitable candidate for CD8 T cell vaccine-vector since it establishes life-long infection which ensures continuous supply of virus specific effector-memory CD8 T cells. Having these facts in mind, we have constructed highly attenuated murine CMV (MCMV) expressing NKG2D ligand RAE-1γ and foreign CD8 T cell epitope. Such a recombinant vaccine- vector provided outstanding CD8 T cell- dependent protective capacity against respective pathogens and maintained this specific response long-term (Trsan et al., PNAS 2013). Although it is generally accepted that the ligation of NKG2D receptor augments CD8 T cell response by providing co-stimulatory signals to CD8 T cells, we showed that the enhanced CD8 T cell response induced by MCMV vector expressing RAE-1γ existed even in mice lacking NKG2D receptor, pointing to an additional, NKG2D-independent immune function of RAE-1γ. Our results indicated that RAE-1γ expression in the context of MCMV vector induced improved antigen presentation via DCs to CD8 T cells. Moreover, RAE-1γMCMV vector was efficient even in N-ras deficient mice, otherwise defective in generating memory CD8 T cells, suggesting that RAE-1γ can circumvent this immune deficit. Altogether, RAE-1γ expressing MCMV demonstrated a powerful capacity to serve as a vaccine-vector. We believe that similar vaccine vectors can be employed to combat various intracellular pathogens and tumors. Since RAE-1γ represents a homologue of human NKG2D ligand ULBP2, one can expect that the results obtained with RAE- 1γMCMV vector can be translated to the HCMV vaccine-vector model.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti

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