{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,10]],"date-time":"2025-10-10T01:56:54Z","timestamp":1760061414274},"reference-count":31,"publisher":"Oxford University Press (OUP)","issue":"2","license":[{"start":{"date-parts":[[2006,11,29]],"date-time":"2006-11-29T00:00:00Z","timestamp":1164758400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2007,1,5]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>Alcoholic liver disease and hepatitis C are associated with the production of autoantibodies such as rheumatoid factors (RF), which bind to IgG and can aid in host defence, but are also associated with pathological conditions such as rheumatoid arthritis. Because little is known about the role of RF in liver disease, we characterized the RF production that either occurred spontaneously in response to alcohol consumption or was induced by injection of an Escherichia coli glycolipoprotein in C57Bl\/6 mice. Whereas severe liver damage was induced by carbon tetrachloride (CCl4), minimal damage was caused by chronic alcohol consumption. Liver damage was monitored by measurements of serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST). Circulating RF was induced in response to chronic alcohol consumption; the latter probably involved Toll-like receptor ligation. In contrast, CCl4-induced damage was not associated with RF induction. However, concurrent treatment with an E. coli glycolipoprotein macromolecule that induced RF, protected against CCL4-induced liver damage as measured by a highly significant decrease (P\u2003=\u20030\u00b7008) at 4 weeks in AST and ALT. RF induced by E. coli glycolipoprotein correlated with \u2018protection\u2019 from liver damage, indicating that the RF autoimmune response does not necessarily exacerbate liver disease.<\/jats:p>","DOI":"10.1111\/j.1365-2249.2006.03277.x","type":"journal-article","created":{"date-parts":[[2006,11,29]],"date-time":"2006-11-29T15:58:10Z","timestamp":1164815890000},"page":"324-329","source":"Crossref","is-referenced-by-count":7,"title":["Rheumatoid factor induction in murine models of liver injury"],"prefix":"10.1093","volume":"147","author":[{"given":"U","family":"Nowak","sequence":"first","affiliation":[{"name":"Research Institute of the McGill University Health Centre, Department of Medicine, Microbiology and Immunology"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K","family":"Gill","sequence":"additional","affiliation":[{"name":"Research Institute of the McGill University Health Centre, Department of Medicine, Microbiology and Immunology"},{"name":"Departments of 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