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Hepatitis A Virus

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Viral Infections of Humans

Abstract

Hepatitis A virus (HAV) infection is a preventable, self-limiting necro-inflammatory disease of the liver which has been infecting humans for millennia. Major progress has been made in the past six decades in understanding the pathogenesis, epidemiology, clinical presentation, and prevention of hepatitis A. The HAV is a non-cytopathic, hepatotropic RNA virus which replicates in hepatocytes and generates immune-mediated liver injury. Infection is mainly transmitted through fecal–oral route, close person-to-person contact, and intake of contaminated water or food. The epidemiology of HAV infection is driven by the level of sanitary and socioeconomic conditions in defined geographic regions and, recently, by the introduction of hepatitis A vaccines. According to the World Health Organization, endemicity of HAV infection is assessed through the age-dependant prevalence of anti-HAV (IgG) antibodies which is used for calculation of the incidence. Thus, endemicity can be defined as high, intermediate, low, and very low. In countries with low or very low endemicity of HAV, almost all children and adults below the age of 40 years have not been exposed to HAV and remain susceptible, i.e., when traveling to areas endemic for HAV. In contrast, in endemic countries in Africa and Asia, almost 100 % of children have been infected by the age of 10 years. However, progressive improvement in sanitary and socioeconomic conditions in countries with high and intermediate endemicity is leading to a shift in the age of infection which becomes more symptomatic >5 years of age and especially in adolescents and adults, in whom infection causes significant morbidity and incapacitation, albeit for a limited period. Thus, the improving socioeconomic conditions and level of hygienic standards in many countries with intermediate endemicity in transition have led to a shift in susceptibility to infection in adolescents and young adults. Several attenuated HAV strains have been used for over 20 years in the United States, Europe, and China for manufacturing of formalin-inactivated vaccines. All these vaccines given at two doses, separated by a flexible interval of 6–12 months, have had an excellent record of safety and tolerability and have been shown to be highly immunogenic. Mass and universal vaccination programs in the United States, Israel, several European countries, and Australia have led to an unprecedented decline in the incidence of HAV infection in these regions.

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Abbreviations

ACIP:

Advisory Committee on Immunization Practices

ALF:

Acute liver failure

ALT:

Alanine aminotransferase

Anti-HAV:

Antibodies to hepatitis A virus

BMI:

Body mass index

CDC:

Centers for Disease Control (USA)

cDNA:

Complementary DNA

EIA:

Enzyme-linked immunoassay

ELISA:

Enzyme-linked immunosorbent assay

EPI:

Expanded Program on Immunization

GBD:

Global burden of disease

GID:

Global incidence of disease

GMC:

Geometric mean concentration

HAV:

Hepatitis A virus

HBsAg:

Hepatitis B surface antigen

HBV:

Hepatitis B virus

HCV:

Hepatitis C virus

HIV:

Human immunodeficiency virus

HLA:

Histocompatibility leukocyte antigen

IDU:

Intravenous drug use

IEM:

Immune electron microscopy

IG:

Immunoglobulin

IV:

Intravenous

LAK:

Lymphokine-activated killer cells

MSM:

Men who have sex with men

NHANES:

National Health and Nutrition Examination Survey

NK:

Cells natural killer cells

PBMC:

Peripheral blood mononuclear cells

RIFIT:

Radioimmunofocus inhibition assay

RNA:

Ribonucleic acid

WHO:

World Health Organization

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Acknowledgments

This chapter is an extensively revised and updated version of the chapter printed in the 4th edition of this book authored by HS Margolis, MJ Alter, and SC Hadler.

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Shouval, D. (2014). Hepatitis A Virus. In: Kaslow, R., Stanberry, L., Le Duc, J. (eds) Viral Infections of Humans. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-7448-8_17

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