Increase of CD57+ T cells in knee joints and adjacent bone marrow of rheumatoid arthritis (RA) patients: implication for an anti-inflammatory role
Article first published online: 25 DEC 2001
DOI: 10.1046/j.1365-2249.1998.00511.x
Blackwell Science Ltd, Oxford
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How to Cite
Arai, Yamamura, Seki, Hanyu, Takahashi and Abo (1998), Increase of CD57+ T cells in knee joints and adjacent bone marrow of rheumatoid arthritis (RA) patients: implication for an anti-inflammatory role. Clinical & Experimental Immunology, 111: 345–352. doi: 10.1046/j.1365-2249.1998.00511.x
Publication History
- Issue published online: 25 DEC 2001
- Article first published online: 25 DEC 2001
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Keywords:
- rheumatoid arthritis;
- CD3+ CD57+ T cells;
- joint fluid;
- joint-adjacent bone marrow;
- erythrocyte sedimentation rate
The distribution of CD57+ T and CD56+ T cells in patients with RA was examined. In control osteoarthritis patients, these cells exist as a minor population in the peripheral blood. Our data show that in patients with RA, CD57+ T cell levels are elevated in peripheral blood, knee joint fluid, knee synovial membrane and bone marrow (BM), compared with peripheral blood of controls. CD57+ T cells are especially high in knee joint fluid and joint-adjacent BM, while CD56+ T cells show no such increase. CD57+ T cells contain a major population of CD8+ cells and higher proportions of CD4−8− cells and γδ T cells than do CD57−T cells. CD57+T cells in peripheral blood and joint fluid increase with the duration of disease. Erythrocyte sedimentation rate (ESR) is inversely correlated with the proportion of CD57+T cells in the joint fluid. Although RA frequently occurrs in patients with CD3+57+ cell leukaemia, and some CD57+T cells are likely to be involved in the onset of RA, we suggest that CD57+T cells may rather suppress inflammation of RA, and other cellular components (e. g. granulocytes) may govern the severity of the inflammation of RA. These CD57+ T cells are probably generated extrathymically in the adjacent BM or joint space.

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