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European Journal of Clinical Microbiology & Infectious Diseases
Erschienen in: European Journal of Clinical Microbiology & Infectious Diseases 6/2015

01.06.2015 | Review

Prevention of hepatitis B virus infection: from the past to the future

verfasst von: R. Orlando, M. Foggia, A. E. Maraolo, S. Mascolo, G. Palmiero, O. Tambaro, G. Tosone

Erschienen in: European Journal of Clinical Microbiology & Infectious Diseases | Ausgabe 6/2015

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Abstract

About 3–5 % of the world’s population is chronically infected by hepatitis B virus (HBV) and is at risk of developing liver cirrhosis or hepatocellular carcinoma. The risk of dying prematurely because of chronic HBV infection is higher in younger people. The current strategies to prevent HBV infection involve immunization (active and/or passive) and antiviral chemoprophylaxis. The vaccines available for active immunization, containing hepatitis B surface antigen, are safe and confer long-term immunity in most healthy subjects. Since the vaccination is unsatisfactory in some patients, e.g., those with chronic kidney disease, human immunodeficiency virus infection, type I diabetes mellitus, and celiac disease, new strategies of vaccination are required. The neonatal, infant, and adolescent routine program vaccination in about 180 countries has greatly decreased the disease burden. Passive immunization with specific HBV immunoglobulins is recommended after single acute exposure, in infants born to infected mothers, and in HBV-infected patients undergoing liver transplantation combined with nucleoside/nucleotide analogues (chemoprophylaxis). Chemoprophylaxis is also indicated in HBV carrier candidates for immunosuppressive treatment and in patients with occult B infection undergoing immunosuppressive therapy or hematopoietic stem cell transplantation. Since HBV is not eradicable by an immune response or by antiviral drugs developed so far, the only preventive strategy remains global neonatal vaccination in all countries, firstly in HBV-endemic countries.
Fußnoten
1
The plasmid DNA vaccines rely on a small part of circular DNA capable of reproducing itself in bacteria; the desired gene can be inserted into plasmid and, so, injected in the host’s tissue; they can bypass the several problems linked to the other systems of gene transfer, in which DNA is packaged into recombinant viral vectors or attached to cationically charged molecules, such as the immune responses against the delivery vector [92].
 
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Metadaten
Titel
Prevention of hepatitis B virus infection: from the past to the future
verfasst von
R. Orlando
M. Foggia
A. E. Maraolo
S. Mascolo
G. Palmiero
O. Tambaro
G. Tosone
Publikationsdatum
01.06.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
European Journal of Clinical Microbiology & Infectious Diseases / Ausgabe 6/2015
Print ISSN: 0934-9723
Elektronische ISSN: 1435-4373
DOI
https://doi.org/10.1007/s10096-015-2341-x

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