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pubmed-article:7542004pubmed:abstractTextToxic oil syndrome (TOS) was caused by the consumption of rapeseed oil contaminated with derivatives of aniline. Many persons who survived the acute phase developed a puzzling, multi-year chronic disease considered to be inflammatory or autoimmune in nature. In attempting to characterize their autoantibodies, we found that 74% of TOS patients with chronic disease had IgG antibodies to C-reactive protein (CRP). This activity was detectable only when CRP was chemically or physically denatured and behaved like a previously described antibody produced by immunization with the CRP monomer. Significant antibody reactivities to other acute phase proteins, especially alpha 1-antitrypsin and fibrinogen (P < 0.025) and ceruloplasmin (P < 0.05) were also observed. IgG antibodies to cryptic epitopes in CRP and other major serum proteins that increase during the acute phase response may reflect an earlier toxin-mediated insult to the liver that included abnormal biosynthesis of and/or damage to acute phase proteins.lld:pubmed
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pubmed-article:7542004pubmed:articleTitleAutoantibodies to cryptic epitopes of C-reactive protein and other acute phase proteins in the toxic oil syndrome.lld:pubmed
pubmed-article:7542004pubmed:affiliationW.M. Keck Autoimmune Disease Center, Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, California 92037, USA.lld:pubmed
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pubmed-article:7542004pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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