Pregled bibliografske jedinice broj: 549760
HUMAN LIVER CELLS CAN BE PROTECTED FROM HCV INFECTION BY CONTINUOUS INTRACELLULAR EXPRESSION OF HCV RNA ANALOGS
HUMAN LIVER CELLS CAN BE PROTECTED FROM HCV INFECTION BY CONTINUOUS INTRACELLULAR EXPRESSION OF HCV RNA ANALOGS // 7th ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine
Zagreb: International Society for Applied Biological Sciences (ISABS), 2011. str. 213-213 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 549760 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
HUMAN LIVER CELLS CAN BE PROTECTED FROM HCV INFECTION BY CONTINUOUS INTRACELLULAR EXPRESSION OF HCV RNA ANALOGS
Autori
Smolić R, Smolić M, Smith RM, Wu CH, Včev A, Wu GY
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
7th ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine
/ - Zagreb : International Society for Applied Biological Sciences (ISABS), 2011, 213-213
Skup
7th ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine June 20-24, 2011, Bol, Island of Brač, Croatia
Mjesto i datum
Bol, Hrvatska, 20.06.2011. - 24.06.2011
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
hepatitis C virus (HCV) infection; liver transplantation; graft failure; HCV RNA structural analogs; Japanese fulminant hepatitis-1 (JFH-1) HCV
Sažetak
Hepatitis C virus infection frequently results chronic liver disease and liver failure. It is the most common indication for liver transplantation. The incidence of re-infection is virtually 100% for new livers transplanted into HCV (+) recipients. That infection results in a rapidly progressive liver damage which can result in failure of the graft. Currently, such infection and subsequent progressive liver disease cannot be prevented. We have shown that HCV RNA structural analogs can inhibit HCV RNA replication in infectious HCV systems. To determine whether human liver cells continuously expressing HCV structural analogs would be resistant to HCV infection. HCV RNA structural analogs were constructed and tested in a HCV genotype 1b BB7 replicon, and a Japanese fulminant hepatitis-1 (JFH-1) HCV genotype 2a infection model. An Huh7.5 cell line continuously expressing HCV structural analogs were prepared by stable transfection by a retroviral vector. The efficacy in preventing HCV replication in JFH-1 infection model was determined by real-time PCR quantification of HCV RNA. In stable transfected Huh7.5 cells with HCV structural analogs after exposure to JFH-1 HCV, cellular HCV RNA levels were significantly lower than in controls, indicating that the JFH-1 HCV genome replicated with lower efficiency in cells stable transfected with HCV structural analogs than in control cells. HCV infection is inhibited in human liver cells that continuously produce HCV structural analogs. If such cells were introduced into HCV-infected patients, these cells would be predicted to decrease HCV re-infection, and therefore, increase long-term success rates.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
219-2192190-2182 - Osobitosti koštane pregradnje u bolesnika s urolitijazom (Milas-Ahić, Jasminka, MZOS ) ( CroRIS)
219-2192190-2186 - Prevencija stvaranja i recidiva mokraćnih kamenca (Tucak, Antun, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Osijek