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10.1053/j.gastro.2017.02.009

http://scihub22266oqcxt.onion/10.1053/j.gastro.2017.02.009
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suck abstract from ncbi


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pmid28219691      Gastroenterology 2017 ; 152 (6): 1297-309
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  • Hepatitis B reactivation associated with immune suppressive and biological modifier therapies: current concepts, management strategies and future directions #MMPMID28219691
  • Loomba R; Liang TJ
  • Gastroenterology 2017[May]; 152 (6): 1297-309 PMID28219691show ga
  • Hepatitis B reactivation associated with immune suppressive and biological therapies is emerging to be an important cause of morbidity and mortality in patients with current or prior exposure to hepatitis B virus infection. The population at risk for HBV reactivation includes those who are either currently infected with HBV or have past exposure to HBV. Since curative and eradicative therapy for HBV is not currently available, there is a large reservoir of individuals at risk for HBV reactivation in the general population. HBV reactivation with its potential consequences is particularly a concern when these people are exposed to either cancer chemotherapy, immunosuppressive or biologic therapies for the management of rheumatologic conditions, malignancies, inflammatory bowel disease, dermatologic conditions, or solid organ or bone marrow transplantation. With the advent of newer and emerging forms of targeted biologic therapies, it has become important to understand the mechanisms whereby certain therapies are more prone to HBV reactivation. The aim of this review is to provide a comprehensive update on the current concepts, risk factors, molecular mechanisms, prevention and management of hepatitis B reactivation. In addition, we provide recommendations for future research in this area.
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