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Hepatiit C virus 1. 2. 3. 4. HCV virion Virion on sfääriline Diameetr ca 50 nm V iiruspartiklid on kaetud ümbrisega (valgud E1 ja E2) Nukleokapsiidi sees on +ss RNA http://www.stanford.edu/group/virus/flavi/2005/intro.htm 5. HCV genoom ja valgud HCV genoom u 9,4-9,6 kb Struktuursed valgud: kapsiidivalk (C),ümbrise valgud (E1, E2), p7 Mittestruktuursed valgud NS2, NS3, NS4A, NS4B, NS5A, NS5B moodustavad replikatsioonikompleksi http://www.ibcp.fr/rhaser/creze/viro/G9_2005_Flavi_Introd_Viro.html 6. 7. 8. 9. TÖÖ EESMÄRK Kirjanduse alusel analüüsida HCV immuundominantseid epitoope, mis on võimelised esile kutsuma tugevat rakulist immuunvastust 10. HLA I ja II Viiruse antigeen töödeldakse peptiidideks ja eksponeeritakse raku pinnal suure koesobivuskompleksi (MHC, inimestel-HLA) valkude abil: HLA- Ι esitlevad viiruse peptiide ( epitoope ) CD8+ T-rakkudele (CTL) HLA- II esitlevad epitoope CD4+ T-rakkudele (abistaja T-rakud) www.mcld.co.uk/hiv/?q=CD8 11. HLA- ΙΙ poolt esitatavad epitoobid (CD4+ epitoobid) 12. HLA- Ι poolt esitatavad epitoobid (CD8+ epitoobid) 13. 14. 15. Kokkuvõte Kroonilise HCV infektsiooni puhul T-rakuline immuunvastus (CD4+ ja CD8+) mängib kõige olulisemat rolli viirusest vabanemises T-rakulised epitoobid kutsuvad esile tugeva HCV-vastase immuunvastuse ja neid peetakse potentsiaalseteks kandidaatideks efektiivse terapeutilise vaktsiini loomisel HCV-vastase vaktsiini edasises arenemises on oluline pidev ja põhjalik uute immuundominantsete epitoopide avastamine ja kirjeldamine 16.