Nizar N. Zein, Jorge Rakela, John J. Poterucha, Jeffery L. Steers, Russell H. Wiesner, David H. Persing – 1 November 1995 – Chronic hepatitis C infection (CH‐C) accounts for a significant number of patients undergoing orthotopic liver transplantation (OLT). Recently, hepatitis C virus (HCV) genotype‐dependent differences in disease outcome and therapeutic responses have been suggested.
Steven H. Belle, Katherine M. Detre, Kimberly C. Beringer – 1 November 1995 – For several medical interventions, increasing experience results in improved outcome. This finding may result from better patient selection or increased skill levels. This report examines whether there is a relationship between center experience and patient outcome for liver transplantation, and if so, whether the relationship is explained by patient or donor selection or level of experience required to obtain optimal results.
Dietmar Wurbs, Reinhild Klein, Luigi‐Maria Terracciano, Peter A. Berg, Leonardo Bianchi – 1 November 1995
Marja A. Boermeester, Irene H. Straatsburg, Alexander P. J. Houdijk, Catharina Meyer, Wilma M. Frederiks, Robert I. C. Wesdorp, Cornelis J. F. van Noorden, Paul A. M. van Leeuwen – 1 November 1995 – Impairment of various functions of the liver and concomitantly increased levels of parameters of liver damage, a clinical entity termed liver failure, is commonly seen after partial hepatectomy. We investigated in a rat model whether damage of the remnant liver was due to local inflammatory responses, and related to endotoxin or interleukin‐1 (IL‐1).
You‐Chen Chao, Tong‐Ho Young, Wei‐Kuo Chang, Hung‐Shang Tang, Chung‐Te Hsu – 1 November 1995 – The human cytochrome P4502E1 gene (P4502E1), coding for an ethanol‐inducible nitrosamine‐metabolizing P‐450, is involved in the metabolism of ethanol and many known carcinogens. Recently, restriction fragment length polymorphisms (RFLps) within the P4502E1 have been suggested as genetic markers of susceptibility to alcohol‐induced liver disease but the previous studies disagree whether alcoholics with c1 or c2 allele are more susceptible to alcohol‐induced liver disease.
Daniela Simon, Brian I. Carr – 1 November 1995 – We have studied the genetic profile of the host genome and hepatitis B virus (HBV) in HBV‐associated primary hepatocellular carcinoma (HCC). Comparative analyses of HCC cell line Hep 40 and the original biopsy specimens showed the episomal and replicating form of HBV only in the biopsy specimen from nontumor (NT) cirrhotic liver tissue, where a molecular change in the 1p36 region was detected (NT tissue showed a normal 46XY karyotype). In contrast, only integrated HBV was detected in HCC tumor (T) tissue and Hep 40 cells.
Bernard Campillo, Pierre‐Etienne Chabrier, Gabriel Pelle, Said Sediame, Guy Atlan, Paul Fouet, Serge Adnot – 1 November 1995 – Increased vascular production of nitric oxide (NO) may contribute to the peripheral vasodilation and hyperdynamic state complicating advanced liver cirrhosis.
Yun‐Fan Liaw, Ching‐Song Lee, Sun‐Lung Tsai, Bo‐Wen Liaw, Tse‐Ching Chen, I‐Shyan Sheen, Chia‐Ming Chu – 1 November 1995 – Virus‐specific cytotoxic T lymphocytes (CTLs) have been suggested to be responsible for the liver injuries in patients with hepatitis C virus (HCV) infection. However, there has been no report of direct evidence to substantiate this hypothesis. In this study, we performed in vitro autologous hepatocytotoxicity assay in 45 patients to examine a possible role of CTLs to HCV‐in‐fected liver cells.
Gotaro Yamada, Masahiro Takatani, Fumitoshi Kishi, Michiko Takahashi, Toshihiko Doi, Takao Tsuji, Sadahito Shin, Masashi Tanno, Mickey S. Urdea, Janice A. Kolberg – 1 November 1995 – To clarify the viral factors that may predict the therapeutic effect of interferon (IFN) in chronic hepatitis C (CHC) patients, we investigated the quantitative serum hepatitis C virus (HCV) RNA level, genotype, and liver biopsy histological features in 60 patients who were treated with 360 × 106 U of natural IFN‐α for 36 to 48 weeks and for more than 12 months after therapy.
Marijke van Oosten, Erika van de Bilt, Helga E. de Vries, Theo J. C. van Berkel, Johan Kuiper – 1 November 1995 – During sepsis the infiltration of leukocytes plays a pivotal role in tissue damage. Induction of septic shock results in an early accumulation of polymorphonuclear leukocytes in the liver (after 3 hours), which is followed by an infiltration of mononuclear phagocytes (after 30 hours). Expression of adhesion molecules may contribute to the migration of leukocytes to the site of inflammation.