Tzang Bor-Show, Liu Chung-Hsien, Hsu Kuo-Ching, Chen Yi-Hsing, Huang Chih-Yang, Hsu Tsai-Ching
1Institute of Biochemistry, Microbiology and Immunology,Chung Shan Medical University,Taichung 402,Taiwan,ROC.
5Department of Obstetrics and Gynecology,Chung Shan Medical University and Chung Shan Medical University Hospital,Taichung 402,Taiwan,ROC.
Br J Nutr. 2017 Sep;118(5):333-342. doi: 10.1017/S0007114517002112.
Systemic lupus erythematosus (SLE) is an autoimmune disease that is characterised by a dysregulation of the immune system, which causes inflammation responses, excessive oxidative stress and a reduction in the number of cluster of differentiation (CD)4+CD25+forkhead box P3 (FoxP3)+ T cells. Supplementation with certain Lactobacillus strains has been suggested to be beneficial in the comprehensive treatment of SLE. However, little is known about the effect and mechanism of certain Lactobacillus strains on SLE. To investigate the effects of Lactobacillus on SLE, NZB/W F1 mice were orally gavaged with Lactobacillus paracasei GMNL-32 (GMNL-32), Lactobacillus reuteri GMNL-89 (GMNL-89) and L. reuteri GMNL-263 (GMNL-263). Supplementation with GMNL-32, GMNL-89 and GMNL-263 significantly increased antioxidant activity, reduced IL-6 and TNF-α levels and significantly decreased the toll-like receptors/myeloid differentiation primary response gene 88 signalling in NZB/W F1 mice. Notably, supplementation with GMNL-263, but not GMNL-32 and GMNL-89, in NZB/W F1 mice significantly increased the differentiation of CD4+CD25+FoxP3+ T cells. These findings reveal beneficial effects of GMNL-32, GMNL-89 and GMNL-263 on NZB/W F1 mice and suggest that these specific Lactobacillus strains can be used as part of a comprehensive treatment of SLE patients.
系统性红斑狼疮(SLE)是一种自身免疫性疾病,其特征在于免疫系统失调,这会引发炎症反应、过度氧化应激以及分化簇(CD)4⁺CD25⁺叉头框P3(FoxP3)⁺T细胞数量减少。已有人提出补充某些乳酸杆菌菌株对SLE的综合治疗有益。然而,关于某些乳酸杆菌菌株对SLE的作用和机制知之甚少。为了研究乳酸杆菌对SLE的影响,给NZB/W F1小鼠口服副干酪乳杆菌GMNL-32(GMNL-32)、罗伊氏乳杆菌GMNL-89(GMNL-89)和罗伊氏乳杆菌GMNL-263(GMNL-263)。补充GMNL-32、GMNL-89和GMNL-263可显著提高抗氧化活性,降低IL-6和TNF-α水平,并显著降低NZB/W F1小鼠中的Toll样受体/髓样分化初级反应基因88信号通路。值得注意的是,在NZB/W F1小鼠中补充GMNL-263而非GMNL-32和GMNL-89可显著增加CD4⁺CD25⁺FoxP3⁺T细胞的分化。这些发现揭示了GMNL-32、GMNL-89和GMNL-263对NZB/W F1小鼠的有益作用,并表明这些特定的乳酸杆菌菌株可作为SLE患者综合治疗的一部分。