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2.
Infection ; 34(2): 62-5, 2006 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16703294

RESUMO

BACKGROUND: Hepatitis C virus (HCV) circulates as a mixture of different but closely related genomes: this quasispecies nature could be essential for virus persistence and could induce resistance to interferon therapy. Since little is known on the behavior of HCV quasispecies in children and adolescents with chronic hepatitis C, we analyzed the virus population in six untreated children during a 5-year follow-up. METHODS: Six children aged 1-8 years, infected early in life with HCV, were included in the study. From each of them, 2 or 3 sequential serum samples obtained over a 5-year follow-up period were examined. The HCV quasispecies heterogeneity and diversity in the E2 hypervariable region-1 (HVR-1) were analyzed among samples by the heteroduplex mobility assay, and the distance between variants was estimated by the heteroduplex mobility ratio (HMR). RESULTS: The HCV population was initially highly homogeneous in all six children. During follow-up, diversification of HVR-1 leading to a more complex viral population occurred in all cases, and was particularly evident in the three older children (HMR: 0.82-0.54). Changes in the HVR-1 sequence occurred without relation to the profile of ALT and HCV-RNA levels. CONCLUSIONS: HCV quasispecies diversification is a common event during chronic hepatitis C in childhood. Host and environmental pressure could be major determinants. The increasing viral heterogeneity could impair the response to antiviral therapy, thus indicating a rationale for early antiviral treatment in children with chronic hepatitis C.


Assuntos
Evolução Molecular , Hepacivirus/classificação , Hepacivirus/genética , Hepatite C Crônica/virologia , Criança , Pré-Escolar , Feminino , Variação Genética , Análise Heteroduplex , Humanos , Lactente , Masculino , Reação em Cadeia da Polimerase/métodos , RNA Viral/sangue , Proteínas Virais/genética
3.
J Hepatol ; 34(5): 723-9, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11434619

RESUMO

BACKGROUND: Chronic hepatitis C virus (HCV) infection is associated with a variety of extrahepatic disorders that may relate to direct or indirect effects of virus infection. Increased levels of soluble forms of tumor necrosis factor (TNF) receptors I and II, found in lymphoproliferative and infectious diseases, can interfere with TNF induced apoptotic cell death. The aim of the present study was to evaluate soluble TNF family receptors levels in lymphoproliferative disorders associated with HCV infection. METHODS: One hundred and forty-nine subjects were studied, including 120 anti-HCV positive patients (60 without lymphoproliferative manifestations, 47 with type II cryoglobulinemia and 13 with low-grade B-cell non-Hodgkin's lymphoma (B-NHL)) and 29 anti-HCV negative subjects (19 with low-grade B-NHLs and ten normal controls). RESULTS: Soluble forms of TNF receptor I, TNF receptor II and Fas were significantly higher in HCV positive patients compared with normal controls. The highest levels were found in patients affected by type II cryoglobulinemia or HCV positive lymphoplasmacytoid lymphomas (LP-NHLs), while HCV positive patients without type II cryoglobulinemia or with other B-NHLs had lower values (P < 0.01). CONCLUSIONS: Among HCV infected individuals, very high levels of soluble TNF receptors are significantly associated with type II cryoglobulinemia and LP-NHLs, suggesting that they may be involved in these proliferative disorders.


Assuntos
Hepatite C/sangue , Hepatite C/complicações , Transtornos Linfoproliferativos/sangue , Transtornos Linfoproliferativos/virologia , Receptores do Fator de Necrose Tumoral/sangue , Adulto , Idoso , Crioglobulinemia/sangue , Crioglobulinemia/virologia , Feminino , Genótipo , Hepacivirus/genética , Humanos , Leucemia Linfocítica Crônica de Células B/sangue , Leucemia Linfocítica Crônica de Células B/virologia , Linfoma de Células B/sangue , Linfoma de Células B/virologia , Linfoma não Hodgkin/sangue , Linfoma não Hodgkin/virologia , Masculino , Pessoa de Meia-Idade , Solubilidade , Fator de Necrose Tumoral alfa/metabolismo , Receptor fas/sangue
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