Pregled bibliografske jedinice broj: 784277
RAE-1γ ligand expression by MCMV vector promotes induction and maintenance of protective immune memory
RAE-1γ ligand expression by MCMV vector promotes induction and maintenance of protective immune memory // NK2013 14th Meeting of the Society for Natural Immunity
Heidelberg, Njemačka, 2013. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 784277 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
RAE-1γ ligand expression by MCMV vector promotes induction and maintenance of protective immune memory
Autori
Tršan, T., Busche, A., Abram, M., Wensveen, F., Lemmermann, N.A., Arapović, M., Babić, M., Tomić, A., Golemac, M., Brinkmann, M.M., Jäger, W., Oxenius, A., Polić, B., Krmpotić, A., Messerle, M., Jonjić, S.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
NK2013 14th Meeting of the Society for Natural Immunity
/ - , 2013
Skup
NK2013 14th Meeting of the Society for Natural Immunity
Mjesto i datum
Heidelberg, Njemačka, 18.09.2013. - 22.09.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
MCMV; CD8 T cell vaccine vector; NKG2D
Sažetak
NKG2D is lymphocyte-expressed receptor whose ligands are stress-induced proteins structurally related to MHC class I molecules. Engagement of NKG2D on natural killer (NK) cells potentiate NK cell-mediated killing of stressed cells. In addition, its engagement on NK cells leads to NK cells cytokine production, which modulates the intensity of immune response. On CD8 T cells NKG2D has a co- stimulatory role, increasing the magnitude of specific immune response. Here we demonstrate the exceptional capacity of mouse CMV (MCMV) expressing NKG2D ligand RAE-1γ to serve as highly protective vaccine-vector. We show that co-expression of RAE-1γ and foreign CD8 T cell epitope in the context of MCMV augmented epitope-specific CD8 T cell response and promoted induction of memory precursor CD8 T cells. Immunization with RAE-1γ expressing MCMV and foreign CD8 T cell epitope resulted in long-term protection against respective pathogen by means of CD8 T cells specific to vectored epitope. Moreover, MCMV expressing RAE-1γ preserved splenic dendritic cells (DCs) and hence rescued their co- stimulatory capacity. Improved antigen presentation was retained also in mice unable to cross-present antigens. Surprisingly, we found that RAE-1γ expressing MCMV vector was highly attenuated and equally protective even in NKG2D deficient mice, suggesting additional, NKG2D independent immune function of RAE1γ.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
062-0621261-1263 - Molekularni mehanizmi citomegalovirusnog izmicanja imunološkom nadzoru (Jonjić, Stipan, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Adriana Tomić
(autor)
Astrid Krmpotić
(autor)
Maja Arapović
(autor)
Stipan Jonjić
(autor)
Bojan Polić
(autor)
Tihana Tršan
(autor)
Felix Martinus Wensveen
(autor)