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PGIA and RA. METHODS.: Recombinant G1 \ndomain (rhG1) of human cartilage PG containing \"arthritogenic\" \nT-cell epitopes was generated in a mammalian expression system \nand used for immunization of BALB/c mice. The development and \nprogression of arthritis in rhG1-immunized mice (designated \nrhG1-induced arthritis, GIA) was monitored, and disease \nparameters were compared to those in the parent PGIA model. \nRESULTS.: GIA highly resembles PGIA, though the clinical \nsymptoms and immune responses in mice with GIA are more uniform \nthan in those with PGIA. Mice with GIA showed evidence of \nstronger T-helper 1 (Th1) and 17 (Th17) polarization than those \nwith PGIA, and anti-mouse PG autoantibodies were produced in \ndifferent isotype ratios in the two models. RF and anti-cyclic \ncitrullinated peptide (anti-CCP) antibodies were detected in \nboth models; however, serum levels of IgG-RF and anti-CCP \nantibodies were different in GIA and PGIA, and both parameters \ncorrelated better with disease severity in GIA than in PGIA. \nCONCLUSION.: GIA is a novel seropositive model of RA, exhibiting \nall of the characteristics of PGIA. 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