| Project/Area Number |
13670872
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Dermatology
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| Research Institution | Kanazawa university |
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Principal Investigator |
INAOKI Makoto Kanazawa University Hospital, Assistant professor, 医学部附属病院, 講師 (40242549)
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| Co-Investigator(Kenkyū-buntansha) |
TAKEHARA Kazuhiko Kanazawa University Graduate School of Medical Science, Professor., 大学院・医学系研究科, 教授 (50142253)
SATO Shinichi Kanazawa University Graduate School of Medical Science, Associate Professor., 大学院・医学系研究科, 助教授 (20215792)
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| Project Period (FY) |
2001 – 2002
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| Project Status |
Completed (Fiscal Year 2002)
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| Budget Amount *help |
¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 2002: ¥1,400,000 (Direct Cost: ¥1,400,000)
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| Keywords | Psoriasis vulgaris / Lymphocytes / CCR4 / CXCR3 / Interferon-γ / Interleukin-4 / 乾癬 / T細胞 / インターロイキン4 |
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| Research Abstract |
Studies have suggested that psoriasis vulgaris is mediated by type 1 T cells. In this study, we examined both chemokine receptor expression and intracellular cytokine production by circulating T cells to check the type 1 / type 2 balance in psoriasis. CCR4^+ and CXCR3^+ T cells predominantly produced interleukin-4 and interferon-γ, respectively. The frequency of interferon-γ-producing cells and that of CXCR3^+ cells in circulating CD4^+ T cells were similar for psoriatic patients and healthy control subjects. By contrast, the frequency of CCR4^+ CD8^+ T cells and CCR4/CXCR3 ratio in circulating CD8^+ T cells were significantly higher in psoriatic patients than in healthy control subjects. Analysis of intracellular cytokine production also indicated relative increase of type 2 CD8^+ T (Tc2) cells in peripheral blood from psoriatic patients. The frequency of circulating Tc2 cells directly correlated with Psoriasis Area and Severity Index. Immunohistochemical analysis showed that not only CXCR3^+ CD8^+ T cells, but also a similar number of CCR4^+ CD8^+ T cells infiltrated the psoriatic epidermis and dermis. Our findings suggest an increase in Tc2 cell number in blood from psoriatic patients, and the association of Tc2 cells with inflammation in psoriasis.
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