Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2011-9-1
pubmed:abstractText
One of the problems possibly related to the use of biological agents targeting tumor necrosis factor (TNF)-alpha is the increased risk of infections, including the activation of hepatitis B virus (HBV). HBV activation can occur in carriers of hepatitis B surface antigen (HBsAg), but the risk may also involve the HBsAg-negative (anti-HBc ± anti-HBs) occult carriers. Precise data on the safety of anti-TNF and/or other immunosuppressive drugs in HBV occult carriers are not available. We performed a retrospective analysis of 62 psoriatic patients with occult HBV infection treated with anti-TNF biological agents over a period of approximately 4 years: 44 subjects were treated with etanercept, 8 with infliximab and 10 with adalimumab. During the observational treatment period, no signs of HBV activation were observed. Only in one patient the reappearance of HBsAg, without detectable HBV-DNA, was noted before retreatment with etanercept and after 10 months from discontinuation of the previous course. In this patient etanercept was re-administered in association with lamivudine without any adverse event. Our results suggest the overall safety of treatment with anti-TNF drugs in HBV occult carriers, although a careful and constant monitoring of virological markers is required in such patients during treatment with anti-TNF drugs in order to have an early recognition of viral reactivation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Inflammatory Agents, http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, Humanized, http://linkedlifedata.com/resource/pubmed/chemical/Drug Combinations, http://linkedlifedata.com/resource/pubmed/chemical/Hepatitis B Surface Antigens, http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G, http://linkedlifedata.com/resource/pubmed/chemical/Lamivudine, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor, http://linkedlifedata.com/resource/pubmed/chemical/Reverse Transcriptase Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/TNFR-Fc fusion protein, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha, http://linkedlifedata.com/resource/pubmed/chemical/adalimumab, http://linkedlifedata.com/resource/pubmed/chemical/infliximab
pubmed:status
MEDLINE
pubmed:issn
0393-974X
pubmed:author
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
285-9
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:21880218-Adult, pubmed-meshheading:21880218-Aged, pubmed-meshheading:21880218-Anti-Inflammatory Agents, pubmed-meshheading:21880218-Antibodies, pubmed-meshheading:21880218-Antibodies, Monoclonal, pubmed-meshheading:21880218-Antibodies, Monoclonal, Humanized, pubmed-meshheading:21880218-Carrier State, pubmed-meshheading:21880218-Drug Combinations, pubmed-meshheading:21880218-Female, pubmed-meshheading:21880218-Hepatitis B, pubmed-meshheading:21880218-Hepatitis B Surface Antigens, pubmed-meshheading:21880218-Hepatitis B virus, pubmed-meshheading:21880218-Humans, pubmed-meshheading:21880218-Immunoglobulin G, pubmed-meshheading:21880218-Lamivudine, pubmed-meshheading:21880218-Male, pubmed-meshheading:21880218-Middle Aged, pubmed-meshheading:21880218-Psoriasis, pubmed-meshheading:21880218-Receptors, Tumor Necrosis Factor, pubmed-meshheading:21880218-Retrospective Studies, pubmed-meshheading:21880218-Reverse Transcriptase Inhibitors, pubmed-meshheading:21880218-Tumor Necrosis Factor-alpha, pubmed-meshheading:21880218-Virus Latency
pubmed:articleTitle
Anti-tumor necrosis factor treatment in occult hepatitis B virus infection: a retrospective analysis of 62 patients with psoriatic disease.
pubmed:publicationType
Letter