胶原性关节炎
表位
II型胶原
胶原蛋白,I型,α1
关节炎
化学
Ⅰ型胶原
细胞生物学
分子生物学
免疫学
医学
生物
抗体
病理
生物化学
细胞外基质
作者
Linda K. Myers,Jerome M. Seyer,J M Stuart,Kuniaki Terato,Chella S. David,Andrew H. Kang
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:1993-07-01
卷期号:151 (1): 500-505
被引量:58
标识
DOI:10.4049/jimmunol.151.1.500
摘要
Chick type II collagen (CII), a protein commonly found in joint cartilage, induces an autoimmune arthritis when administered to susceptible strains of mice. A cyanogen bromide fragment of CII, CB11, contains the requisite epitopes critical for inducing collagen-induced arthritis. If administered as a tolerogen, however, before immunization, CB11 prevents the onset of disease. Therefore, delineation of structural elements of CB11 that can regulate autoreactive T cells became the goal of this study. To delineate the structural elements of CB11 antigenic to T cells, 14 peptides containing overlapping sequences of CB11 were generated. Mononuclear cells from CII-immunized DBA/1 mice were cultured with these peptides and the resulting supernatants examined for the production of IFN-gamma. Two peptides, CII 181-209 and CII 245-270, generated the greatest responses. The ability of these two peptides to regulate arthritis was tested by administering them to neonatal DBA/1 mice as tolerogens before immunization with CII. Both peptides suppressed the incidence of arthritis whereas no other peptide used as a tolerogen significantly altered the course of the disease. T cells from four arthritis-resistant murine strains did not recognize either peptide when immunized with CII, whereas cells from the disease-susceptible B10.Q mice responded well to both. Thus, the coincidence of T cell responses to CII 181-209 and CII 245-270 in CIA-susceptible mice and the lack of response in disease-resistant strains or CII-tolerized mice identify these two peptides as containing important T cell epitopes that regulate CIA.
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