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Eur Cytokine Netw ; 17(4): 290-3, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17353164

ABSTRACT

BACKGROUND: Chronic hepatitis C infection is frequently associated with a mixed cryoglobulinaemia and circulating auto-antibodies, especially anti-smooth muscle cells (SMA) and anti-liver/kidney/microsome type 1 (LKM-1) anti-tissue antibodies. Treatments with TNF antagonists favour the emergence of auto-antibodies, and particularly anti-dsDNA antibodies. OBJECTIVE: To determine the impact of TNF antagonists on hepatitis C-related immune abnormalities. METHODS: We prospectively monitored for 14 weeks, six patients with actively replicating chronic hepatitis C, initiating an anti-TNF treatment for an associated rheumatoid arthritis. RESULTS: Anti-nuclear and anti-dsDNA antibodies were induced in two and three patients, respectively. Treatment had no impact on the production of antibodies against extractable nuclear antigens, and it did not induce anti-tissues antibodies in any patient. Cryoglobulinaemia appeared in 2/6 patients, and it persisted in 2 others. No patient developed any news signs of autoimmunity. HCV viraemia remained unchanged. CONCLUSIONS: Induction of auto-antibodies by TNF antagonist treatments does not involve anti-tissues antibodies, even in patients with actively replicating chronic hepatitis C prone to produce anti-SMA and anti-LKM-1 antibodies. In contrast, TNF antagonists may favour emergence of cryoglobulinaemia in such patients.


Subject(s)
Antibodies, Monoclonal/therapeutic use , Autoantibodies/blood , Hepatitis C, Chronic/drug therapy , Tumor Necrosis Factors/immunology , Adult , Antibodies, Antinuclear/blood , Antibodies, Monoclonal/adverse effects , Antirheumatic Agents/adverse effects , Antirheumatic Agents/therapeutic use , Cryoglobulinemia/etiology , Etanercept , Female , Hepacivirus/genetics , Hepatitis C, Chronic/blood , Hepatitis C, Chronic/immunology , Humans , Immunoglobulin G/adverse effects , Immunoglobulin G/therapeutic use , Infliximab , Male , Middle Aged , Polymerase Chain Reaction , Prospective Studies , Receptors, Tumor Necrosis Factor/therapeutic use , Time Factors , Treatment Outcome , Tumor Necrosis Factor Inhibitors , Viral Load , Viremia/drug therapy
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