In vitro and clinical immunomodulatory effects of a novel Pentaherbs concoction for atopic dermatitis

外周血单个核细胞 植物血凝素 肿瘤坏死因子α 免疫学 趋化因子 医学 特应性皮炎 细胞因子 逆转录聚合酶链式反应 药理学 体外 淋巴细胞 化学 炎症 信使核糖核酸 生物化学 基因
作者
Ting Fan Leung,K. Y. Wong,Chun Kwok Wong,Kwok‐Pui Fung,Christopher Wai Kei Lam,Tai Fai Fok,Ping Chung Leung,Kam‐Lun Ellis Hon
出处
期刊:British Journal of Dermatology [Oxford University Press]
卷期号:158 (6): 1216-1223 被引量:36
标识
DOI:10.1111/j.1365-2133.2008.08502.x
摘要

Our group recently reported a randomized and placebo-controlled clinical trial on the efficacy of a twice-daily concoction of five herbal ingredients (Pentaherbs formulation, PHF) in treating children with atopic dermatitis (AD).To investigate the immunomodulatory effects that may be induced by PHF treatment.We investigated the effects of PHF on cytotoxicity and proliferation of phytohaemagglutinin (PHA)- and staphylococcal enterotoxin B (SEB)-stimulated peripheral blood mononuclear cells (PBMC) isolated from buffy coat of blood donors. PHF-induced immunomodulation for five inflammatory mediators in cultured PBMC was measured by reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assay. The effects of a 3-month, open-label study of PHF on circulating inflammatory mediators in children with AD were also assessed.PHF at up to 1 mg mL(-1) dose-dependently suppressed PBMC proliferation. The addition of PHF to cultured PBMC reduced supernatant concentrations of brain-derived neurotrophic factor (BDNF), interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha in response to PHA, and BDNF and thymus and activation-regulated chemokine (TARC) following SEB stimulation. PHF increased epithelial cell-derived neutrophil activating peptide-78 levels in culture supernatants. At the RNA level, PHF suppressed the transcription of BDNF, TARC, IFN-gamma and TNF-alpha. Twenty-eight children with AD were treated with PHF for 3 months, and their mean plasma concentrations of BDNF and TARC decreased significantly from 1798 pg mL(-1) and 824 pg mL(-1) at baseline to 1378 pg mL(-1) and 492 pg mL(-1) (P = 0.002 and 0.013, respectively) upon study completion.PHF possesses in vitro and in vivo immunomodulatory properties that may mediate the clinical efficacy observed in AD treatment.
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