Hepatitis B and D Protocols | Volume 2: Immunology, Model Systems, and Clinical Studies | ISBN 9781617373633

Hepatitis B and D Protocols

Volume 2: Immunology, Model Systems, and Clinical Studies

herausgegeben von Robert K. Hamatake und Johnson Y. N. Lau
Mitwirkende
Herausgegeben vonRobert K. Hamatake
Herausgegeben vonJohnson Y. N. Lau
Buchcover Hepatitis B and D Protocols  | EAN 9781617373633 | ISBN 1-61737-363-X | ISBN 978-1-61737-363-3

„Both volumes provide an excellent reference for background information and detailed experimental investigations for both Hepatitis B and Hepatitis D. A major attribute of the volumes is that as they cover a wide range of subjects, the reader has the opportunity to access information they would not normally encounter. Volumes 1 and 2 are an excellent reference source and the methodologies described present the opportunity for both new and experienced researchers to study the molecular aspects of HBV and HDV infection.“-SGM Quarterly

„... an excellent reference for background information and detailed experimental investigations for both Hepatitis B and Hepatitis D...“ - Microbiology Today

Hepatitis B and D Protocols

Volume 2: Immunology, Model Systems, and Clinical Studies

herausgegeben von Robert K. Hamatake und Johnson Y. N. Lau
Mitwirkende
Herausgegeben vonRobert K. Hamatake
Herausgegeben vonJohnson Y. N. Lau
Despite the availability of an effective vaccine, there are still 400 million people, worldwide who are chronically infected with hepatitis B virus (HBV). For them, the vaccine, as currently applied, has no value. Given the possible consequences of HBV infection, the number of those chronically infected with HBV presents an enormous public health challenge. For example, the major etiology of hepatocellular carcinoma (HCC) is chronic infection with HBV. Although fifth in cancer incidence, worldwide, HCC/liver cancer is the third leading cause of cancer death. The high mortality as- ciated with HCC arises because the disease is often detected late and is unresponsive to treatment. The number of deaths caused by PHCC is expected to rise over the next 20 years. Those chronically infected with HBV have a life risk of death to HCC of between 10 and 25%. Even the limited efficacy of drugs for the treatment of chronic HBV helps underscore the point that this disease is responsive to therapy. Drugs that target the polymerase (e. g. , hepsera and lamivudine) and interferon alpha represent two distinct strategies and show that both conventional antiviral and immunothe- peutic approaches can be used in management. However, the current inventory of therapeutics is inadequate. Interferon alpha is of limited value, only parenterally ava- able, and fraught with adverse reactions.