23. Hepatitis A and E

  1. Eugene R. Schiff MD, MACP, FRCP2,
  2. Willis C. Maddrey MD, MACP, FRCP3,
  3. Michael F. Sorrell MD, FACP4
  1. Joshua Watson MD,
  2. Maria H. Sjogren MD, MPH

Published Online: 31 OCT 2011

DOI: 10.1002/9781119950509.ch23

Schiff's Diseases of the Liver, Eleventh Edition

Schiff's Diseases of the Liver, Eleventh Edition

How to Cite

Watson, J. and Sjogren, M. H. (2011) Hepatitis A and E, in Schiff's Diseases of the Liver, Eleventh Edition (eds E. R. Schiff, W. C. Maddrey and M. F. Sorrell), Wiley-Blackwell, Oxford, UK. doi: 10.1002/9781119950509.ch23

Editor Information

  1. 2

    Center for Liver Diseases and Schiff Liver Institute, University of Miami Miller School of Medicine, Miami, FL, USA

  2. 3

    Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA

  3. 4

    University of Nebraska College of Medicine, Omaha, NE, USA

Author Information

  1. Gastroenterology Service, Department of Medicine, Walter Reed Army Medical Center, Washington, DC, USA

Publication History

  1. Published Online: 31 OCT 2011
  2. Published Print: 9 DEC 2011

ISBN Information

Print ISBN: 9780470654682

Online ISBN: 9781119950509

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Keywords:

  • Hepatitis A;
  • hepatitis E;
  • viral hepatitis;
  • hepatitis A vaccine;
  • hepatitis E vaccine;
  • acute viral hepatitis;
  • infectious hepatitis;
  • human hepatitis;
  • acute hepatitis A;
  • acute hepatitis E

Summary

Experimental work in humans led to the clinical recognition that viruses were etiologic agents of hepatitis A (infectious hepatitis) and hepatitis B (serum hepatitis). Later, the existence of two distinct hepatitis viruses was demonstrated: hepatitis A virus (HAV) and hepatitis B virus (HBV). HAV was first characterized in 1973 when scientists detected the virus in stools from human volunteers who were infected with HAV. The ensuing development of sensitive and specific serologic assays for the diagnosis of HAV infection and the isolation of HAV in cell culture were important advances that permitted the understanding of the epidemiology of HAV infection and, ultimately, control of the disease. With the accurate diagnosis of hepatitis A and hepatitis B, it became apparent that at least two non-A, non-B infectious agents existed. One was similar to hepatitis B, mainly transmitted parenterally, and another was similar to hepatitis A, transmitted by the fecal–oral route. In the 1980s, two seminal discoveries correctly identified the first one as hepatitis C and the second one became known as hepatitis E. Since then, hepatitis E virus (HEV) has been recognized as the agent responsible for enterically transmitted non-A, non-B hepatitis. Research to understand the epidemiology, viral characteristics, and immunity against this viral agent was propelled by the work of Balayan et al. and subsequently by cloning the virus, which allowed the development of diagnostic assays, better understanding of its epidemiology, and the development of vaccine candidates.