Figure 4.

Cytokine responses to A12-tetramer+ cells. DR1 mice were immunized with Ova (open bars), CII (solid bars), or A12 (hashed and striped bars), and the draining inguinal lymph node cells were selected to obtain the CD4+ populations. The A12-immunized lymph node cells were further fractionated into tetramer+ (left hashed bars) and tetramer- (striped bars) populations. The cells were cultured (5 × 105 CD4+ T cells/ml) with wild-type APC (DR1-positive splenocytes; 1:2 ratio) prepulsed in vitro with the immunodominant collagen peptide. Supernatants were collected and tested for the presence of each cytokine by using a multiplexed ELISA. The supernatants were collected from Ova-specific CD4+ T cells (open bars), CII-specific T cells (solid bars), DR1-A12 tetramer+ T cells (left hashed bars), or tetramer- T cells (striped bars). Results shown represent the mean ± SD of three separate experiments and are expressed in picograms per milliliter of culture supernatants. The Th1/Th2 ratio was 13:1 in T cells responding to CII, whereas the Th1/Th2 ration was 0.5:1 in the DR1-A12 tetramer+ T cells.

Kimata et al. Arthritis Research & Therapy 2012 14:R107   doi:10.1186/ar3832
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