BCL-2 rearranged B cell clones in chronic HCV infection: a possibile factor negatively influencing the virological response to treatment

2002 ◽  
Vol 36 ◽  
pp. 17
Author(s):  
Francesca Giannelli ◽  
Monica Monti ◽  
Patrizio Caini ◽  
Stefania Moscarella ◽  
Roberto Romanelli ◽  
...  
2001 ◽  
Vol 34 ◽  
pp. 120-121
Author(s):  
F. Giannelli ◽  
S. Moscarella ◽  
R.G. Romanelli ◽  
M.E. Marrocchi ◽  
M. Monti ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Masahiko Ito ◽  
Hideki Kusunoki ◽  
Keiko Mochida ◽  
Kazunari Yamaguchi ◽  
Toshiaki Mizuochi

Hepatitis C virus (HCV) has been recognized as a major cause of chronic liver diseases worldwide. It has been suggested that HCV infects not only hepatocytes but also mononuclear lymphocytes including B cells that express the CD81 molecule, a putative HCV receptor. HCV infection of B cells is the likely cause of B-cell dysregulation disorders such as mixed cryoglobulinemia, rheumatoid factor production, and B-cell lymphoproliferative disorders that may evolve into non-Hodgkin's lymphoma (NHL). Epidemiological data indicate an association between HCV chronic infection and the occurrence of B-cell NHL, suggesting that chronic HCV infection is associated at least in part with B-cell lymphomagenesis. In this paper, we aim to provide an overview of recent literature, including our own, to elucidate a possible role of HCV chronic infection in B-cell lymphomagenesis.


2015 ◽  
Vol 62 (2) ◽  
pp. 303-310 ◽  
Author(s):  
Michelle Spaan ◽  
Kim Kreefft ◽  
Gretchen N. de Graav ◽  
Willem P. Brouwer ◽  
Robert J. de Knegt ◽  
...  

2017 ◽  
Vol 65 (4) ◽  
pp. 765-771 ◽  
Author(s):  
Prashant Pandya ◽  
Chaitanya Pant ◽  
Ryan Taylor ◽  
Olurinde Oni

The high cost associated with antiviral treatment for chronic hepatitis C virus (HCV) infection mandates further investigation in the context of preventing complications such as type 2 diabetes mellitus (DM2). We determined the cumulative incidence of DM2 in subjects with chronic HCV infection who received concomitant pegylated interferon (Peg-IFN) and ribavirin. We conducted a retrospective analysis of data obtained from Veterans Administrations Informatics and Computing Infrastructure (VINCI) to identify an adult cohort of patients without diabetes with chronic HCV infection who received Peg-IFN-based therapy between October 2001 and December 2011. Patients with history of HIV, hepatitis B infection, hepatocellular cancer (HCC), non-HCC cancers, and history of transplantation were excluded. Sustained virological response (SVR) was defined as negative HCV RNA 3 months after completion of therapy. Using Cox proportional hazards regression for multivariable analysis, we determined that patients who achieved SVR were at a significantly less risk of developing DM2. Adjusted survival rates showed that the responders' group was significantly less likely to develop DM2 over time (HR 0.60, CI 0.48 to 0.74, p<0.001). Peg-IFN-based therapy in chronic HCV patients that resulted in SVR significantly decreased the risk of developing DM2 and independently predicts the development of new onset disease after controlling for correlates of metabolic syndrome.


2014 ◽  
Vol 13 (3) ◽  
pp. 319-326 ◽  
Author(s):  
Benjamin Terrier ◽  
Wahiba Chaara ◽  
Laurent Dufat ◽  
Guillaume Geri ◽  
Michelle Rosenzwajg ◽  
...  

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