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用于体外免疫调节和体内减轻特应性皮炎的 BCL-2 多菌株益生菌

BCL-2 Multi-Strain Probiotics for Immunomodulation In Vitro and In Vivo Alleviation of Atopic Dermatitis.

作者信息

Sung MinKyung, Sim Seongrok, Lim Ahyoung, Moon Jin Seok, Jeon JongIk, Heo Keon, Kwak Woongkwon, Park Myeong Soo, Kwak Jungki, Park EunYoung, Yoon Seokmin

机构信息

Lotte R&D Center, Seoul 07594, Republic of Korea.

Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul 02841, Republic of Korea.

出版信息

Microorganisms. 2025 Aug 21;13(8):1950. doi: 10.3390/microorganisms13081950.

Abstract

Atopic dermatitis (AD) is a chronic inflammatory disorder with immune imbalance, including elevated IgE levels and mast cell activation mediated by Th2 cytokines, leading to allergic inflammation and impaired skin barrier function. Current treatment limitations highlight the need for safer and more effective AD alternatives. We aimed to evaluate the therapeutic effects of multi-strain probiotics, BCL-2 (comprising LRCC5264 and RAPO), in alleviating AD clinical signs and elucidate its underlying immunomodulatory mechanisms. In vitro, BCL-2 treatment significantly reduced IL-4 secretion in RBL-2H3 cells, with higher inhibitory effects than single-strain treatment. In vivo, BCL-2 (10-10 CFU/day) was orally administered for 28 days to AD-induced Nc/Nga mice. BCL-2 treatment improved the clinical signs and histopathological features of AD, including epidermal hypertrophy, hyperkeratosis, and mast cell infiltration ( < 0.05). It also reduced neutrophil and eosinophil counts and modulated cytokine and chemokine profiles, notably decreasing IL-17, IL-5, IL-6, TNF-α, IL-1β, TARC, and eotaxin, while increasing IL-10, IFN-γ, and IL-12 ( < 0.05). Among the tested concentrations, 10 CFU exhibited the most effective immune modulation with no adverse effects on body weight. These findings demonstrate the therapeutic potential of BCL-2 in AD; however, further studies are required to validate its clinical relevance.

摘要

特应性皮炎(AD)是一种伴有免疫失衡的慢性炎症性疾病,包括免疫球蛋白E(IgE)水平升高以及由辅助性T细胞2(Th2)细胞因子介导的肥大细胞活化,导致过敏性炎症和皮肤屏障功能受损。目前治疗方法的局限性凸显了对更安全、更有效的AD替代疗法的需求。我们旨在评估多菌株益生菌BCL-2(由LRCC5264和RAPO组成)在减轻AD临床症状方面的治疗效果,并阐明其潜在的免疫调节机制。在体外,BCL-2处理显著降低了大鼠嗜碱性粒细胞白血病细胞株2H3(RBL-2H3)细胞中白细胞介素-4(IL-4)的分泌,其抑制作用高于单菌株处理。在体内,将BCL-2(10¹⁰ 菌落形成单位/天)口服给予AD诱导的Nc/Nga小鼠28天。BCL-2处理改善了AD的临床症状和组织病理学特征,包括表皮肥厚、角化过度和肥大细胞浸润(P<0.05)。它还减少了中性粒细胞和嗜酸性粒细胞计数,并调节了细胞因子和趋化因子谱,显著降低了IL-17、IL-5、IL-6、肿瘤坏死因子-α(TNF-α)、IL-1β、胸腺和活化调节趋化因子(TARC)和嗜酸性粒细胞趋化因子,同时增加了IL-10、干扰素-γ(IFN-γ)和IL-12(P<0.05)。在所测试的浓度中,10¹⁰ 菌落形成单位表现出最有效的免疫调节作用,且对体重无不良影响。这些发现证明了BCL-2在AD中的治疗潜力;然而,需要进一步研究来验证其临床相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/12388198/78c50128c8d4/microorganisms-13-01950-g001.jpg

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