首页> 外文期刊>Journal of dermatological science >Alterations of serum Th1 and Th2 chemokines by combination therapy of interferon-gamma and narrowband UVB in patients with mycosis fungoides.
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Alterations of serum Th1 and Th2 chemokines by combination therapy of interferon-gamma and narrowband UVB in patients with mycosis fungoides.

机译:真菌病真菌病患者联合应用干扰素-γ和窄带UVB可以改变血清Th1和Th2趋化因子。

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BACKGROUND: Mycosis fungoides (MF) is a T cell neoplasm with elevation of serum Th2 chemokines. Although interferon-gamma (IFN-gamma) administration and narrowband-UVB (NB-UVB) phototherapy are used for the treatment of MF, a combination therapy of these two modalities is not fully established. OBJECTIVES: To define whether the combination of IFN-gamma and NB-UVB affects the balance of serum levels of Th1 and Th2 chemokines in patients with MF. METHODS: Twelve patients with MF received intravenous or intramuscular injections of recombinant IFN-gamma (rIFN-gamma) or natural IFN-gamma (nIFN-gamma) in combination with NB-UVB phototherapy. As control, three MF patients were treated with NB-UVB monotherapy. At the beginning and cessation of therapy, the concentrations of serum Th2 chemokines, TARC/CCL17 and MDC/CCL22, and Th1 chemokines, IP-10/CXCL10 and MIG/CXCL9 were measured by ELISA. RESULTS: Before treatment, not only Th2 chemokines but also Th1 chemokines were elevated in the patients. Whereas no significant changes were observed in the levels of TARC and MDC, IP-10 and MIG were further elevated by the combination of IFN-gamma and NB-UVB. On the other hand, NB-UVB monotherapy did not change the level of either Th1 or Th2 chemokine. CONCLUSIONS: The combination of IFN-gamma and NB-UVB elevated serum Th1 chemokines but unaffected Th2 chemokines. Since NB-UVB monotherapy could not affect the chemokine levels, the effect of the combination therapy is attributable to IFN-gamma. Given the role of Th1 chemokines for tumor-attacking T cell recruitment at the early stage of MF, the therapy may exert a beneficial effect for early MF.
机译:背景:蕈样真菌病(MF)是一种T细胞肿瘤,其血清Th2趋化因子升高。尽管使用干扰素-γ(IFN-γ)和窄带-UVB(NB-UVB)光疗来治疗MF,但这两种方式的联合治疗尚未完全确立。目的:确定IFN-γ和NB-UVB的组合是否影响MF患者血清Th1和Th2趋化因子的平衡。方法:12例MF患者接受了重组IFN-γ(rIFN-γ)或天然IFN-γ(nIFN-γ)联合NB-UVB光疗的静脉内或肌内注射。作为对照,三名MF患者接受了NB-UVB单药治疗。在治疗开始和停止时,通过ELISA测量血清Th2趋化因子,TARC / CCL17和MDC / CCL22以及Th1趋化因子,IP-10 / CXCL10和MIG / CXCL9的浓度。结果:治疗前,患者不仅Th2趋化因子升高,而且Th1趋化因子升高。尽管未观察到TARC和MDC的水平有明显变化,但IFN-γ和NB-UVB的组合可进一步提高IP-10和MIG。另一方面,NB-UVB单一疗法未改变Th1或Th2趋化因子的水平。结论:IFN-γ和NB-UVB的组合可升高血清Th1趋化因子,但不影响Th2趋化因子。由于NB-UVB单一疗法不能影响趋化因子水平,因此联合疗法的效果可归因于IFN-γ。考虑到Th1趋化因子在MF早期对肿瘤攻击性T细胞募集的作用,该疗法可能对MF早期起有益作用。

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