{"title":"新的抗炎化合物FR167653下调人单核细胞和骨髓CD34+细胞向树突状细胞的分化和成熟","authors":"Naoki Nishimura, Yasuhiko Nishioka, Tsutomu Shinohara, Kenji Tani, Saburo Sone","doi":"10.1016/S0192-0561(00)00014-X","DOIUrl":null,"url":null,"abstract":"<div><p>FR167653 (1-[7-(4-fluorophenyl)-1,2,3,4-tetrahydro-8 (4-pyridyl) pyrazoro [5-1-c] <span>[1]</span>, <span>[2]</span>, <span>[4]</span> triazin-2-<em>yl</em><span><span><span>]-2-phenylethanedion sulfate monohydrate), one of the pyridinyl imidazoles, is an </span>immunosuppressive agent<span><span> which was developed to inhibit proinflammatory cytokine production<span>. We examined the effect of FR167653 on the differentiation and maturation phases of both human bone marrow-derived dendritic cells (BM-DC) and blood monocyte-derived DC (Mo-DC). DC induced from either BM-DC or Mo-DC progenitors in the presence of FR167653 had lower expression of CD1a, CD83<span> and CD86 (B7.2). FR167653 also significantly suppressed the ability of Mo-DC to produce both TNF-α and IL-1β in response to LPS stimulation. </span></span></span>Mixed lymphocyte reaction (MLR) stimulation was significantly lower in FR167653-treated Mo-DC than in control Mo-DC, although the suppressive effect of FR167653 was much less on BM-DC. These results indicate novel immunosuppressive properties of FR167653, which may be therapeutically useful in controlling chronic immune and/or </span></span>inflammatory diseases through down-regulation of DC differentiation and maturation.</span></p></div>","PeriodicalId":14002,"journal":{"name":"International journal of immunopharmacology","volume":"22 7","pages":"Pages 501-514"},"PeriodicalIF":0.0000,"publicationDate":"2000-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0192-0561(00)00014-X","citationCount":"3","resultStr":"{\"title\":\"Down-regulation by a new anti-inflammatory compound, FR167653, of differentiation and maturation of human monocytes and bone marrow CD34+ cells to dendritic cells\",\"authors\":\"Naoki Nishimura, Yasuhiko Nishioka, Tsutomu Shinohara, Kenji Tani, Saburo Sone\",\"doi\":\"10.1016/S0192-0561(00)00014-X\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>FR167653 (1-[7-(4-fluorophenyl)-1,2,3,4-tetrahydro-8 (4-pyridyl) pyrazoro [5-1-c] <span>[1]</span>, <span>[2]</span>, <span>[4]</span> triazin-2-<em>yl</em><span><span><span>]-2-phenylethanedion sulfate monohydrate), one of the pyridinyl imidazoles, is an </span>immunosuppressive agent<span><span> which was developed to inhibit proinflammatory cytokine production<span>. We examined the effect of FR167653 on the differentiation and maturation phases of both human bone marrow-derived dendritic cells (BM-DC) and blood monocyte-derived DC (Mo-DC). DC induced from either BM-DC or Mo-DC progenitors in the presence of FR167653 had lower expression of CD1a, CD83<span> and CD86 (B7.2). FR167653 also significantly suppressed the ability of Mo-DC to produce both TNF-α and IL-1β in response to LPS stimulation. </span></span></span>Mixed lymphocyte reaction (MLR) stimulation was significantly lower in FR167653-treated Mo-DC than in control Mo-DC, although the suppressive effect of FR167653 was much less on BM-DC. These results indicate novel immunosuppressive properties of FR167653, which may be therapeutically useful in controlling chronic immune and/or </span></span>inflammatory diseases through down-regulation of DC differentiation and maturation.</span></p></div>\",\"PeriodicalId\":14002,\"journal\":{\"name\":\"International journal of immunopharmacology\",\"volume\":\"22 7\",\"pages\":\"Pages 501-514\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0192-0561(00)00014-X\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal of immunopharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S019205610000014X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of immunopharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S019205610000014X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Down-regulation by a new anti-inflammatory compound, FR167653, of differentiation and maturation of human monocytes and bone marrow CD34+ cells to dendritic cells
FR167653 (1-[7-(4-fluorophenyl)-1,2,3,4-tetrahydro-8 (4-pyridyl) pyrazoro [5-1-c] [1], [2], [4] triazin-2-yl]-2-phenylethanedion sulfate monohydrate), one of the pyridinyl imidazoles, is an immunosuppressive agent which was developed to inhibit proinflammatory cytokine production. We examined the effect of FR167653 on the differentiation and maturation phases of both human bone marrow-derived dendritic cells (BM-DC) and blood monocyte-derived DC (Mo-DC). DC induced from either BM-DC or Mo-DC progenitors in the presence of FR167653 had lower expression of CD1a, CD83 and CD86 (B7.2). FR167653 also significantly suppressed the ability of Mo-DC to produce both TNF-α and IL-1β in response to LPS stimulation. Mixed lymphocyte reaction (MLR) stimulation was significantly lower in FR167653-treated Mo-DC than in control Mo-DC, although the suppressive effect of FR167653 was much less on BM-DC. These results indicate novel immunosuppressive properties of FR167653, which may be therapeutically useful in controlling chronic immune and/or inflammatory diseases through down-regulation of DC differentiation and maturation.