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首页> 外文期刊>Journal of dermatological science >Nadifloxacin, an antiacne quinolone antimicrobial, inhibits the production of proinflammatory cytokines by human peripheral blood mononuclear cells and normal human keratinocytes.
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Nadifloxacin, an antiacne quinolone antimicrobial, inhibits the production of proinflammatory cytokines by human peripheral blood mononuclear cells and normal human keratinocytes.

机译:纳地沙星,一种抗痤疮喹诺酮类抗菌药,可抑制人外周血单核细胞和正常人角质形成细胞促炎细胞因子的产生。

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摘要

BACKGROUND: Acne vulgaris is a chronic inflammatory disease involving colonization of Propionibacterium acnes (P. acnes), activation of neutrophils and lymphocytes. Circumstantial evidence suggests that antigen-independent and -dependent immune responses against P. acnes are involved in the pathogenesis of inflammatory acne. Epidermal keratinocytes are also suggested to be involved in initiation and progression of cutaneous inflammation. Nadifloxacin, a fluorinated quinolone, has potent antimicrobial activities against Gram-negative and -positive microbes and is used to treat multiple inflamed acne lesions. However, its effect on immune conferring cells such as mononuclear cells and keratinocytes has not been examined. OBJECTIVE: To evaluate the possible involvement of potential anti-inflammatory activity of nadifloxacin in its therapeutic effect on inflammatory acne, we examined the effects of nadifloxacin, in comparison with other antibiotics used to treat acne vulgaris, on cytokine production by human peripheral blood mononuclear cells (PBMC) and keratinocytes. METHODS: Cytokine production by PBMC was determined after treatment with heat-killed P. acnes in the presence or absence of antimicrobials using a real-time PCR and ELISA. Cultured human epidermal keratinocytes were stimulated by IFN-gamma plus IL-1beta and the effects of antimicrobials were examined by using ELISA. RESULTS: Nadifloxacin as well as macrolide antibiotics and clindamycin inhibited IL-12 and IFN-gamma production by PBMC stimulated by heat-killed P. acnes. The drug also inhibited the IL-1alpha, Il-6, IL-8 and GM-CMS production by keratinocytes treated with IFN-gamma plus IL-1beta. CONCLUSIONS: Inhibitory effects of nadifloxacin to activate T cells and keratinocytes may be involved at least in part in the mechanism of its therapeutic effect against inflammatory acne.
机译:背景:寻常痤疮是一种慢性炎症性疾病,涉及痤疮丙酸杆菌(痤疮丙酸杆菌)的定植,嗜中性粒细胞和淋巴细胞的激活。间接证据表明,针对痤疮丙酸杆菌的抗原非依赖性和依赖性免疫反应与炎性痤疮的发病机理有关。还建议表皮角质形成细胞参与皮肤炎症的发生和发展。纳迪沙星是一种氟喹诺酮,对革兰氏阴性和阳性微生物具有有效的抗菌活性,可用于治疗多发性痤疮炎症。然而,尚未检查其对免疫赋予细胞如单核细胞和角质形成细胞的作用。目的:为了评估纳迪沙星潜在的抗炎活性可能参与其对炎性痤疮的治疗作用,我们与其他用于治疗寻常性痤疮的抗生素相比,研究了纳迪沙星对人外周血单核细胞产生细胞因子的影响(PBMC)和角质形成细胞。方法:在存在或不存在抗微生物剂的情况下,使用实时PCR和ELISA在热灭活的痤疮丙酸杆菌治疗后测定PBMC的细胞因子产生。 IFN-γ加IL-1β刺激培养的人表皮角质形成细胞,并通过ELISA检测抗菌剂的作用。结果:纳迪沙星,大环内酯类抗生素和克林霉素可抑制热杀死的痤疮丙酸杆菌刺激的PBMC产生IL-12和IFN-γ。该药物还抑制了用IFN-γ加IL-1beta处理的角质形成细胞产生的IL-1alpha,II-6,IL-8和GM-CMS。结论:纳迪沙星激活T细胞和角质形成细胞的抑制作用可能至少部分参与了其对炎性痤疮的治疗作用机理。

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