The peptide resin was washed with N,N-dimethylformamide after treatment with hydrazine. After completion of the synthesis the peptide was removed from the resin and all side chain protection groups were eliminated by treatment having a cleavage cocktail containing 5% phenol, 2% 1,2-ethanedithiol, 5% methyl phenyl sulfide, 5% water and 84% trifluoroacetic acid. therapy with disease-modifying medicines such as antibodies against tumor necrosis element- or methotrexate reduce disease manifestations, and treatment with anti-CD20 antibodies depleting B cells gives promising results [1]. The autoimmune focuses on in RA are not known but autoantibodies against numerous joint-related epitopes are recognized in BMS-962212 sera. BMS-962212 Antibodies against epitopes altered by citrullination display the highest specificity for RA and may be detected very early in the disease program [2-4]. Antibodies against type II collagen (CII) happen in a subset of RA, and CII-specific B and T-cells have been recognized in rheumatoid synovium and synovial fluid [5-10]. Immunization of mice with CII leads to the development of arthritis, the collagen-induced arthritis (CIA) model for RA. CII-specific activation of both T and B cells is critical for the development of arthritis, and the transfer of both rodent [11] and human being [12] serum with CII-specific antibodies induces arthritis in mice. Monoclonal CII-specific autoantibodies bind cartilage in vivo and induce arthritis [13]; the injection of large BMS-962212 amounts of several of such mAbs in cocktails induces severe arthritis [14,15]. Collagen-antibody-induced arthritis (CAIA) is an inflammation that is dependent on Fc receptor and match, involving the infiltration of both neutrophils and macrophages [15-18]. The antibody response to CII is definitely mainly directed towards conformational triple-helical constructions. Immunization with CII -chains (denatured CII) induces only a poor antibody response and is not arthritogenic [19]. Consequently identification of the relevant B cell epitopes required the building of recombinant triple-helical proteins and synthetic triple-helical peptides [10,20]. The major epitopes were recognized with the use of series of mAbs from both mice and rats [13,20-22]. Interestingly, antibodies against some of the major epitopes (C1 and J1) are arthritogenic, whereas antibodies against others (F4) are not [10]. The immunodominance of these epitopes seems to be shared between both CIA in mice and rats and in humans with RA [10,20,22,23]. Until now, CIA offers primarily been analyzed as an acute disease. Because RA is definitely chronic progressive and shows relapsing inflammatory damage of cartilage, we wished to investigate the antibody response and B cell epitope specificity in chronic CIA models; that is, with an active joint swelling later on than 6 weeks after the onset. The advantages of following a antibody response over a longer period are that we can find possible associations between epitope specificities and the different phases of the disease and may also find epitope shifts during the course of the disease. We have observed previously that mice with C57Bl/10 backgrounds tend to get more chronic arthritis although they are initially relatively more resistant than DBA/1 mice, for example [24]. We therefore immunized B10.Q mice, which have an arthritis-susceptible Aq class II congenic fragment within the C57B1/10 background, with rat CII, and found that they develop a chronic relapsing disease. We have also recently defined another strain combination, an Rabbit polyclonal to HYAL2 F2 mix between B10.Q BMS-962212 and BALB/c, that give an even more pronounced development of chronic arthritis. It could be demonstrated the changes in epitope specificity happen during the course of the disease. Interestingly, the C1, U1 and J1 epitope-specific antibodies were associated with the development of severe and chronic arthritis. Single injections of antibodies of each of these epitopes induced a relapse in chronic arthritic mice. Materials and methods Mice All animals were bred and kept inside a climate-controlled environment (heat and BMS-962212 moisture) with cycles of 12 hours light/12 hours dark at the animal facility of Medical Swelling Research, Lund University or college..