Abstract |
NKB1 inhibits cytoxic activity of T lymphocytes mediated by superantigens, which is one of the contributing factors in the pathogenesis of rheumatoid arthritis (RA). In this study, we determined the expression of NKB1 on peripheral blood T cells in patients with RA. Our findings revealed that among patients with RA, NKB1(+) CD8(+ )T cells decreased significantly in comparison to controls (ratio: P < 0.05; absolute number: P < 0.005), and this decrease was not related to or influenced by HLA-Bw4 as a ligand of NKB1. This result may suggest that decreased expression of NKB1(+) CD8(+ )T cells contributes to the pathogenesis of RA mediated by the activation of CD8(+) T cells.
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Authors | Y Nakiri, H Kaneko, S Morimoto, J Suzuki, Y Tokano, H Hashimoto |
Journal | Clinical rheumatology
(Clin Rheumatol)
Vol. 22
Issue 4-5
Pg. 305-8
(Oct 2003)
ISSN: 0770-3198 [Print] Germany |
PMID | 14579161
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Biomarkers
- CD4 Antigens
- HLA-B Antigens
- Receptors, Immunologic
- Receptors, KIR
- Receptors, KIR3DL1
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Arthritis, Rheumatoid
(immunology, physiopathology)
- Biomarkers
(analysis)
- CD4 Antigens
(immunology)
- Case-Control Studies
- Cohort Studies
- Female
- HLA-B Antigens
(immunology)
- Humans
- Lupus Erythematosus, Systemic
(immunology, physiopathology)
- Male
- Middle Aged
- Probability
- Prognosis
- Receptors, Immunologic
(immunology)
- Receptors, KIR
- Receptors, KIR3DL1
- Reference Values
- Sensitivity and Specificity
- Severity of Illness Index
- Statistics, Nonparametric
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