Pregled bibliografske jedinice broj: 580542
''Genetic manipulation of viral genome as a tool to generate more efficient virus vaccine and vaccine vectors''
''Genetic manipulation of viral genome as a tool to generate more efficient virus vaccine and vaccine vectors'' // Book of abstracts / Jasna Franekić, Verica Garaj-Vrhovac (ur.).
Zagreb: Hrvatsko genetičko društvo, 2012. str. 16-16 (pozvano predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 580542 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
''Genetic manipulation of viral genome as a tool to generate more efficient virus vaccine and vaccine vectors''
Autori
Jonjić, Stipan
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of abstracts
/ Jasna Franekić, Verica Garaj-Vrhovac - Zagreb : Hrvatsko genetičko društvo, 2012, 16-16
ISBN
978-953-57128-0-0
Skup
3rd Congress of Croatian Geneticists
Mjesto i datum
Krk, Hrvatska, 13.05.2012. - 16.05.2012
Vrsta sudjelovanja
Pozvano predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
NKG2D; cytomegalovirus; immune evasion; CMV proteins
Sažetak
NKG2D is a potent activating receptor expressed by cells of innate and adaptive immunity that recognizes cell surface molecules structurally related to MHC-I proteins induced by infection or other type of cellular stress. Engagement of NKG2D leads to cytotoxicity and cytokine secretion by NK cells, or to costimulation of CD8+ T cells. Both human cytomegalovirus (CMV) and mouse CMV deployed evasive mechanisms to prevent expression of NKG2D ligands. So far we have characterized four mouse CMV proteins involved in the down-modulation of NKG2D ligands in infected cells. Deletion of any of these viral immunoevasive genes involved in regulation of NKG2D ligands resulted in virus attenuation in vivo. Based on the attenuation of viruses lacking NKG2D immunoevasins we proposed that the insertion of genes encoding NKG2D ligands in place of genes encoding their viral inhibitors, could be an appropriate approach for immunological attenuation of live vaccine. We have recently shown that despite the strong NK cell-mediated attenuation, mouse CMV engineered to express NKG2D ligand RAE-1gamma elicits a strong and long-lasting antiviral CD8 response, providing protection against lethal virus challenge (Slavuljica et al, JCI 2010). In this talk I will overview the current knowledge on CMV downregulation of NKG2D signaling and our recent results using CMV expressing NKG2D ligand as a live attenuated vaccine and vaccine vector.
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:
Stipan Jonjić
(autor)