1998
DOI: 10.1006/clin.1998.4521
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Intranasal Administration of Denatured Type II Collagen and Its Fragments Can Delay the Onset of Collagen-Induced Arthritis

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Cited by 18 publications
(7 citation statements)
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“…16). This suggests a dominant Th1 response in Fc␥RIIa-transgenic mice following induction of CIA and is consistent with previous data obtained from DBA/1 mice (25). Thus, expression of Fc␥RIIa, which binds mouse IgG2a avidly, may cause effector cells in the Fc␥RIIa-transgenic mice to be sensitive to low levels of autoantibody/immune complex activation, possibly triggering the early release of inflammatory mediators.…”
Section: Expression Of Transgenic and Endogenous Fcrsupporting
confidence: 91%
“…16). This suggests a dominant Th1 response in Fc␥RIIa-transgenic mice following induction of CIA and is consistent with previous data obtained from DBA/1 mice (25). Thus, expression of Fc␥RIIa, which binds mouse IgG2a avidly, may cause effector cells in the Fc␥RIIa-transgenic mice to be sensitive to low levels of autoantibody/immune complex activation, possibly triggering the early release of inflammatory mediators.…”
Section: Expression Of Transgenic and Endogenous Fcrsupporting
confidence: 91%
“…Twenty-one days after primary immunization, they were immunized by an intradermal injection of 400 µ g of type II collagen emulsified in FIA (Freund incomplete adjuvant) at 4 mg/ml. Arthritic severity was classifi ed into three levels based on [20].…”
Section: Methodsmentioning
confidence: 99%
“…The mice in the arthritic group were immunized from 60 to 81 days after birth. Type II collagen was solubilized from fetal bovine articular cartilage by limited proteolysis with pepsin [20]. Type II collagen was dissolved in 0.01 M acetic acid at 4 ° C prior to use.…”
mentioning
confidence: 99%
“…Since the first demonstration that inducing mucosal tolerance, by giving type II collagen (CII) orally, could prevent the development of collageninduced arthritis (CIA) in rats (1) and mice (2), other studies have illustrated the general principle that different experimental arthropathies can be prevented or ameliorated by giving CII or other appropriate antigens or their peptides orally or nasally (3)(4)(5)(6)(7)(8)(9)(10)(11). The effectiveness of induced oral or nasal tolerance in controlling arthritis extends to many other experimental autoimmune conditions (for review, see refs.…”
mentioning
confidence: 99%