Kim Min-Soo, Kim Jin-Eung, Yoon Yeo-Sang, Seo Jae-Gu, Chung Myung-Jun, Yum Do-Young
R&D Center, Cell Biotech Co., Ltd., Gimpo, Korea.
Toxicol Res. 2016 Apr;32(2):149-58. doi: 10.5487/TR.2016.32.2.149. Epub 2016 Apr 30.
Atopic dermatitis (AD) is a chronic inflammatory skin disease with a complex etiology that encompasses immunologic responses. AD is frequently associated with elevated immunoglobulin (Ig) E levels, and common environmental factors contribute to its pathogenesis. Several recent studies have documented the role of specific lactic acid bacteria in the treatment and prevention of AD in humans and mice. In this study, the efficacy of Duolac ATP, a probiotic preparation, was determined in a mouse model with AD-like skin lesions. Alterations in the cytokine levels and histological staining suggested the alleviation of AD. The in vivo test showed that T helper (Th)2 cytokines, IgE, interleukin (IL)-4, and IL-5, were significantly downregulated, whereas Th1 cytokines, IL-12p40 and interferon (IFN)-γ, were upregulated in all groups of mice treated with Duolac ATP compared to that observed in the group of mice treated with 1-chloro-2,4-dinitrobenzene (DNCB) alone. Moreover, the scratch score decreased in all mice treated with Duolac ATP. Staining of the dorsal area of the mice in each group with hematoxylin and eosin and toluidine blue further confirmed the alleviation of AD in mice orally treated with Duolac ATP. These results suggest that Duolac ATP inhibits the development of AD-like skin lesions in NC/Nga mice by suppressing the Th2 cell response and increasing the Th1 cell response. Thus, Duolac ATP is beneficial and effective for the treatment of AD-like skin lesions.
特应性皮炎(AD)是一种病因复杂的慢性炎症性皮肤病,涉及免疫反应。AD常与免疫球蛋白(Ig)E水平升高相关,常见环境因素也参与其发病机制。最近的几项研究记录了特定乳酸菌在人类和小鼠AD治疗与预防中的作用。在本研究中,在具有类AD皮肤病变的小鼠模型中测定了益生菌制剂多乐可ATP(Duolac ATP)的疗效。细胞因子水平的改变和组织学染色表明AD有所缓解。体内试验显示,与仅用1-氯-2,4-二硝基苯(DNCB)处理的小鼠组相比,用多乐可ATP处理的所有小鼠组中,辅助性T(Th)2细胞因子、IgE、白细胞介素(IL)-4和IL-5均显著下调,而Th1细胞因子IL-12p40和干扰素(IFN)-γ上调。此外,用多乐可ATP处理的所有小鼠的搔抓评分均降低。用苏木精和伊红以及甲苯胺蓝对每组小鼠的背部区域进行染色,进一步证实了口服多乐可ATP的小鼠AD得到缓解。这些结果表明,多乐可ATP通过抑制Th2细胞反应和增强Th1细胞反应来抑制NC/Nga小鼠类AD皮肤病变的发展。因此,多乐可ATP对类AD皮肤病变的治疗有益且有效。