Literature DB >> 1374762

Protein composition of the hepatitis B virus e antigen in the natural course of disease and following interferon therapy.

M L Campillo1, J A Quiroga, J Bartolomé, G Moraleda, I Castillo, V Carreño.   

Abstract

The protein composition of hepatitis B virus (HBV) e antigen (HBeAg) in serum was analyzed for 63 viremic patients with chronic HBV and found to consist of polypeptides with molecular masses of 16, 18, and 20 kDa (P16e, P18e, and P20e, respectively). Several experiments demonstrated their viral nature and HBeAg specificity and that P16e occurs either in free soluble form or as aggregates or immunocomplexes, while P18e and P20e occur essentially as immunocomplexes. Of 63 patients, 45 (71%) had P16e, P18e, and P20e, and the remaining 18 (29%) had only P16e. During the natural history of the disease, spontaneous clearance of HBV DNA and HBeAg took place only in six of nine (67%) patients with the three HBe polypeptides but in none of the five patients having P16e alone (P less than 0.05). Similarly, 22 of 23 (96%) patients responding to interferon therapy had P16e, P18e, and P20e, but these polypeptides occurred in only 14 of 26 (54%) nonresponder patients (P less than 0.001). Following the loss of HBV DNA and HBeAg, before the development of anti-HBe, the only HBe species detected were P18e and P20e, but these became no longer detectable after complete normalization of liver function tests. Therefore, persistence of P16e represents a failure to recover from HBV, and the appearance of HBe polypeptides P18e and P20e is associated with virus clearance and a favorable outcome of the disease.

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Year:  1992        PMID: 1374762      PMCID: PMC265260          DOI: 10.1128/jcm.30.5.1256-1261.1992

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  26 in total

1.  Hepatitis B virus suppresses expression of human beta-interferon.

Authors:  J S Twu; C H Lee; P M Lin; R H Schloemer
Journal:  Proc Natl Acad Sci U S A       Date:  1988-01       Impact factor: 11.205

2.  Expression of hepatitis B virus surface and core antigens: influences of pre-S and precore sequences.

Authors:  A McLachlan; D R Milich; A K Raney; M G Riggs; J L Hughes; J Sorge; F V Chisari
Journal:  J Virol       Date:  1987-03       Impact factor: 5.103

3.  Formation of transmembraneous hepatitis B e-antigen by cotranslational in vitro processing of the viral precore protein.

Authors:  V Bruss; W H Gerlich
Journal:  Virology       Date:  1988-04       Impact factor: 3.616

4.  Randomized, controlled trial of recombinant human alpha-interferon in patients with chronic hepatitis B.

Authors:  J H Hoofnagle; M Peters; K D Mullen; D B Jones; V Rustgi; A Di Bisceglie; C Hallahan; Y Park; C Meschievitz; E A Jones
Journal:  Gastroenterology       Date:  1988-11       Impact factor: 22.682

5.  Hepatitis B virus gene function: the precore region targets the core antigen to cellular membranes and causes the secretion of the e antigen.

Authors:  J H Ou; O Laub; W J Rutter
Journal:  Proc Natl Acad Sci U S A       Date:  1986-03       Impact factor: 11.205

6.  Precore sequence of hepatitis B virus inducing e antigen and membrane association of the viral core protein.

Authors:  A Uy; V Bruss; W H Gerlich; H G Köchel; R Thomssen
Journal:  Virology       Date:  1986-11       Impact factor: 3.616

7.  Cytotoxic T-cell responses to the nucleocapsid proteins of HBV in chronic hepatitis. Evidence that antibody modulation may cause protracted infection.

Authors:  M Pignatelli; J Waters; A Lever; S Iwarson; R Gerety; H C Thomas
Journal:  J Hepatol       Date:  1987-02       Impact factor: 25.083

8.  Prolonged (6 months) treatment of chronic hepatitis B virus infection with recombinant leukocyte A interferon.

Authors:  V Carreño; J C Porres; I Mora; J Bartolomé; C Bas; J Gutiez; J Cortés; C Hernández Guio
Journal:  Liver       Date:  1987-12

9.  Changes of hepatitis B virus (HBV) markers during prolonged recombinant interferon alpha-2A treatment of chronic HBV infection.

Authors:  I Mora; J C Porres; J Bartolomé; J A Quiroga; J Gutiez; C Hernández Guio; C Bas; V Carreño
Journal:  J Hepatol       Date:  1987-02       Impact factor: 25.083

10.  Targeting of the hepatitis B virus precore protein to the endoplasmic reticulum membrane: after signal peptide cleavage translocation can be aborted and the product released into the cytoplasm.

Authors:  P D Garcia; J H Ou; W J Rutter; P Walter
Journal:  J Cell Biol       Date:  1988-04       Impact factor: 10.539

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  1 in total

Review 1.  Interferon-alpha-2a. A review of its pharmacological properties and therapeutic use in the management of viral hepatitis.

Authors:  M Haria; P Benfield
Journal:  Drugs       Date:  1995-11       Impact factor: 9.546

  1 in total

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