Interferon‐α and zidovudine combination therapy for chronic hepatitis B: Results of a randomized, placebo‐controlled trial

Harry L. A. Janssen, Luuk Berk, Rudolf A. Heijtink, Fiebo J. W. Ten Kate, Solko W. Schalm – 1 March 1993 – Interferon‐α therapy leads to HBeAg seroconversion in only one third of patients with chronic hepatitis B. In an attempt to increase the seroconversion rate, we investigated the combination of interferon‐α and zidovudine in a subset of patients with presumably low response rates for interferon‐α monotherapy.

A scanning electron microscopic study of liver microcirculation disarrangement in experimental rat cirrhosis

Eugenio Gaudio, Luigi Pannarale, Paolo Onori, Oliviero Riggio – 1 March 1993 – Hepatic microcirculation has been related to liver function in several studies. The principle of this relationship lies in the sequential distribution of blood from the feeding vessels of the hepatic acinus to the central vein. This study was undertaken to investigate the progressive changes at different sites of the liver microvascular bed in the developing cirrhosis, both by light microscopy and scanning electron microscopy of corrosion casts.

Mitochondrial dysfunction in alcoholic patients as assessed by breath analysis

Bernhard H. Lauterburg, Dana Liang, Felix A. Schwarzenbach, Kerry J. Breen – 1 March 1993 – Mitochondria of patients with alcoholic liver disease are morphologically abnormal, and mitochondria isolated from animals exposed to ethanol exhibit functional deficiencies in vitro. Because the functional consequences of the morphological alterations and the relevance of in vitro observations to mitochondrial function in alcoholic subjects are not clear, we assessed mitochondrial function noninvasively with a breath test.

Non‐A, non‐B posttransfusion hepatitis: Comparing C and non‐C hepatitis

Ronald L. Koretz, Maria Brezina, Alan J. Polito, Stella Quan, Judith Wilber, Robert Dinello, Gary Gitnick – 1 March 1993 – Using assays to detect antibodies against antigens (C‐100, 5‐1‐1, C‐22 and C‐33) of the hepatitis C virus, we tested stored sera from 40 patients prospectively identified as having non‐A, non‐B posttransfusion hepatitis. The 28 patients who demonstrated seroconversion (“documented hepatitis C”) had more severe initial disease; all 20 cases of chronic hepatitis occurred in this subgroup.

Peroxisomes in cirrhosis of the human liver: A cytochemical, ultrastructural and quantitative study

Dirk De Craemer, Marina Pauwels, Frank Roels – 1 March 1993 – Hepatocellular peroxisomes in 32 patients with cirrhosis were studied by means of catalase cytochemical and morphometric analysis. Seven normal human livers were used as controls. The severity of the cirrhosis was determined with the Child‐Turcotte criteria. Under the light microscope, a decrease in catalase staining was observed in 12 livers. Staining showed a weak inverse correlation with severity of the cirrhotic process. Peroxisomes revealed a perinuclear configuration in 24 patients.

Recombinant interferon‐α in inoperable hepatocellular carcinoma: A randomized controlled trial

Ching‐Lung Lai, Johnson Y. N. Lau, Pui‐Chee Wu, Henry Ngan, Hau‐Tim Chung, Stuart J. Mitchell, Timothy J. Corbett, Anthony W. C. Chow, Hsiang‐Ju Lin – 1 March 1993 – To evaluate the clinical efficacy of interferon‐α in hepatocellular carcinoma, 71 adult Chinese patients with histologically proven inoperable hepatocellular carcinoma were randomized to receive recombinant interferon‐α2a (50 × 106 IU/m2) intramuscularly three times a week (n = 35) or no antitumor therapy (n = 36).

Push me–pull you: The challenge of endocytic sorting

James J. Crawford – 1 February 1993 – The vectorial nature of hepatocyte receptor‐mediated endocytosis (RME) and its susceptibility to cytoskeletal disruptors has suggested that a polarized network of microtubules plays a vital role in directed movement during sorting. Using as markers a wellknown ligand, asialoorosomucoid, and its receptor, we have isolated endocytic vesicles that bind directly to and interact with stabilized endogenous hepatocyte microtubules at specific times during a synchronous, experimentally initiated, single wave of RME.

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