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자료유형
학술저널
저자정보
Han, Shin-Ha (Department of Pharmacy, Sahmyook University) Kim, Kwang-Hee (Department of Pharmacy, Sahmyook University) Song, Young-Cheon (Department of Pharmacy, Sahmyook University) Kim, Hyun-Yul (Department of Pharmacy, Sahmyook University) Kwon, Jeung-Hak (Department of Pharmacy, Sahmyook University) Lee, Young-Hee (College of Pharmacy, Chungbuk National University) Lee, Chong-Kil (College of Pharmacy, Chungbuk National University) Lee, Sang-Jin (Department of Pharmacy, Sahmyook University) Ha, Nam-Joo (Department of Pharmacy, Sahmyook University) Kim, Kyung-Jae (Department of Pharmacy, Sahmyook University)
저널정보
대한약학회 Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea 제31권 제3호
발행연도
2008.1
수록면
370 - 376 (7page)

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Auranofin (AF), an orally administered, gold-based, anti-arthritic agent, has emerged as a clinically useful therapeutic drug for the treatment of rheumatoid arthritis. In the present study, we examined the effects of AF on major histocompatibility complex (MHC)-restricted antigen presentation in dendritic cells (DCs), which are the most important accessory cells for the induction of T cell responses. A mouse dendritic cell line, DC2.4 cells, and DCs that were generated from mouse bone marrow cells by culturing with granulocyte macrophage-colony stimulating factor (GM-CSF) and interleukin (IL)-4 were each pretreated with AF for 2 hr, and then incubated with ovalbumin (OVA). After the 2-hr incubation, the DCs were fixed, and the amounts of OVA $peptide-H-2K^b$ complexes were assessed using OVA-specific $CD8_+$ T cells. AF inhibited MHC class I-restricted presentation of exogenous OVA. This inhibitory activity of AF appeared to be due not only to the inhibition of the phagocytic activity of DCs, but also to the suppression of MHC molecule expression on DCs. AF also inhibited MHC class II-restricted presentation of exogenous OVA. These results show that AF exerts immunosuppressive activity at least in part by inhibiting MHC-restricted antigen presentation in professional antigen-presenting cells.

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