State Key Laboratory for Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Research Units of Discovery of Unknown Bacteria and Function (2018 RU010), Chinese Academy of Medical Sciences, Beijing, China.
Respiratory Department, Beijing University of Chinese Medicine Third Affiliated Hospital, Beijing, China.
Front Immunol. 2022 Jan 26;12:828887. doi: 10.3389/fimmu.2021.828887. eCollection 2021.
Probiotics can modulate immune responses to resist influenza infection. This study aims to evaluate the anti-viral efficacy of .
C57BL/6J mice were infected with influenza virus together with treatment of PBS vehicle, , or oseltamivir respectively. Anti-influenza potency of and the underlying mechanism were determined by measuring survival rate, lung viral load and pathology, gene expression and production of cytokines and chemokines, and analysis of gut microbiota.
Administration of increased (by 30%) the survival of influenza-infected mice, and improved their weight loss, lung pathology, lung index, and colon length compared to the vehicle control group. treatment reduced (by 61%) the viral load of lung tissue and increased expression of type 1 interferon more rapidly at day 3 postinfection. At day 7 postinfection, dorei-treated mice showed lower local (lung) and systemic (serum) levels of interferon and several proinflammatory cytokines or chemokines (IL-1β, IL-6, TNF-α, IL-10, MCP-1 and IP-10) with a efficacy comparable to oseltamivi treatment. treatment also altered gut microbiota as indicated by increased levels of Bacteroides, Prevotella, and Lactobacillus and decreased levels of Escherichia, Shigella, and Parabacteroides.
has anti-influenza effect. Its working mechanisms involve promoting earlier interferon expression and down-regulating both local and systemic inflammatory response. changes the composition of gut microbiota, which may also contribute to its beneficial effects.
益生菌可以调节免疫反应以抵抗流感感染。本研究旨在评估.
C57BL/6J 小鼠与 PBS 载体、. 或奥司他韦一起感染流感病毒。通过测量存活率、肺部病毒载量和病理学、基因表达和细胞因子和趋化因子的产生以及分析肠道微生物群,来确定. 的抗流感效力及其潜在机制。
与载体对照组相比,. 给药增加(增加 30%)了流感感染小鼠的存活率,并改善了它们的体重减轻、肺部病理学、肺部指数和结肠长度。. 治疗在感染后第 3 天更快地降低(降低 61%)肺部组织的病毒载量,并更快地增加 I 型干扰素的表达。在感染后第 7 天,. 处理的小鼠表现出较低的局部(肺部)和全身(血清)水平的干扰素和几种促炎细胞因子或趋化因子(IL-1β、IL-6、TNF-α、IL-10、MCP-1 和 IP-10),其疗效与奥司他韦治疗相当。. 处理还改变了肠道微生物群,表现为双歧杆菌、普雷沃氏菌和乳酸杆菌水平升高,而大肠杆菌、志贺氏菌和副拟杆菌水平降低。
具有抗流感作用。其作用机制涉及促进干扰素的早期表达和下调局部和全身炎症反应。 改变了肠道微生物群的组成,这也可能有助于其有益效果。