Molecular fingerprinting reveals non-overlapping T cell oligoclonality between an inflamed site and peripheral blood

We have demonstrated a stable expansion of CD8(+) T cells in the peripheral blood of a child with chronic arthritis. The expanded TCRBV family (TCRBV14) was enriched for CD57(hi)CD28(-) T cells. Sequencing of the TCRBV14 amplification products showed a TCR sequence which contributed 32% of the total TCR in the CD8(+)TCRBV14 population. Using the modified heteroduplex technique, the CD8(+)TCRBV14 cells showed a clonal pattern and these bands were restricted to the CD28(-) population. This method also detected multiple other clones within the CD8(+) population but few in the CD4(+) cells. The dominant TCRBV14(+) done was not detectable in synovial fluid T cells from two inflamed joints by CDR3 length analysis or heteroduplex probing, suggesting that this long-lived clone is excluded from inflammatory sites. Synovial fluid T cells showed an unexpected discordance of the CD28 and CD57 phenotype compared to peripheral blood mononuclear cells. T cells from both inflamed joints both showed marked oligoclonality in all TCR families and had almost identical heteroduplex patterns. Taken together these data suggest that some clones are actively excluded from inflamed sites in juvenile chronic arthritis, yet the pattern of restricted T cell expansion is shared between sites of inflammation.