C57BL/6 mice need MHC class II Aq to develop collagen-induced arthritis dependent on autoreactive T cells

被引:43
作者
Backlund, Johan [1 ]
Li, Cuiqin [1 ,2 ]
Jansson, Erik [1 ]
Carlsen, Stefan [1 ]
Merky, Patrick [1 ]
Nandakumar, Kutty-Selva [1 ]
Haag, Sabrina [1 ]
Ytterberg, Jimmy [3 ]
Zubarev, Roman A. [4 ]
Holmdahl, Rikard [1 ]
机构
[1] Karolinska Inst, Dept Biochem & Biophys, S-17177 Stockholm, Sweden
[2] Shaanxi Normal Univ, Coll Life Sci, Minist Educ Med Resources & Nat Pharmaceut Chem, Key Lab, Xian, Peoples R China
[3] Karolinska Univ Hosp, Dept Med, Rheumatol Unit, Stockholm, Sweden
[4] Karolinska Inst, Dept Med Biochem & Biophys, Chem Div 1, S-17177 Stockholm, Sweden
基金
英国医学研究理事会;
关键词
RHEUMATOID-ARTHRITIS; AUTOIMMUNE ARTHRITIS; TRANSGENIC MICE; H-2(B) MICE; CONFERS SUSCEPTIBILITY; BALB/C MICE; CARTILAGE; INDUCTION; EPITOPE; MOUSE;
D O I
10.1136/annrheumdis-2012-202055
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Introduction Collagen-induced arthritis (CIA) has traditionally been performed in MHC class II A(q)-expressing mice, whereas most genetically modified mice are on the C57BL/6 background (expressing the b haplotype of the major histocompatibility complex (MHC) class II region). However, C57BL/6 mice develop arthritis after immunisation with chicken-derived collagen type II (CII), but arthritis susceptibility has been variable, and the immune specificity has not been clarified. Objective To establish a CIA model on the C57BL/6 background with a more predictable and defined immune response to CII. Results Both chicken and rat CII were arthritogenic in C57BL/6 mice provided they were introduced with high doses of Mycobacterium tuberculosis adjuvant. However, contaminating pepsin was strongly immunogenic and was essential for arthritis development. H-2(b)-restricted T cell epitopes on chicken or rat CII could not be identified, but expression of A(q) on the C57BL/6 background induced T cell response to the CII260-270 epitope, and also prolonged the arthritis to be more chronic. Conclusions The putative (auto) antigen and its arthritogenic determinants in C57BL/6 mice remains undisclosed, questioning the value of the model for addressing T cell-driven pathological pathways in arthritis. To circumvent this impediment, we recommend MHC class II congenic C57BL/6N.Q mice, expressing A(q), with which T cell determinants have been thoroughly characterised.
引用
收藏
页码:1225 / 1232
页数:8
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