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发酵乳杆菌 CJL-112 通过激活辅助性 T 细胞 1 并引发保护性免疫应答来保护小鼠免受流感病毒感染。

Lactobacillus fermentum CJL-112 protects mice against influenza virus infection by activating T-helper 1 and eliciting a protective immune response.

机构信息

CJ Research Institute of Biotechnology, 92-1, Gayang-dong, Gangseo-gu, Seoul 157-724, South Korea.

CJ Research Institute of Biotechnology, 92-1, Gayang-dong, Gangseo-gu, Seoul 157-724, South Korea.

出版信息

Int Immunopharmacol. 2014 Jan;18(1):50-4. doi: 10.1016/j.intimp.2013.10.020. Epub 2013 Nov 6.

Abstract

We have previously reported that nasally administered Lactobacillus fermentum CJL-112 (CJL-112) efficiently improves resistance against lethal influenza infection in both mice and chicken. The aim of the present study was to understand the underlying mechanisms of the significant anti-influenza activity of this lactobacilli strain. In vitro, co-culturing of the chicken macrophage cell line HD-11 with CJL-112 significantly increased nitric oxide (NO) production. In vivo, CJL-112 was nasally administered to BALB/c mice for 21 days prior to influenza A/NWS/33 (H1N1) virus (IFV) infection. Significant up-regulation of T-helper 1 (Th1) cytokines (IL-2, IFN-γ) was observed, while the levels of T-helper 2 (Th2) cytokines (IL-4, IL-5, IL-10) was either reduced or unchanged than that in control mice were. Furthermore, IgA and specific anti-influenza IgA levels increased significantly in the treated mice than those in untreated mice. Therefore, CJL-112 likely protects the mice against lethal IFV infection via stimulation of macrophages, activation of Th1 and augmentation of IgA production, when directly delivered into the respiratory tract.

摘要

我们之前曾报道过,经鼻腔给予发酵乳杆菌 CJL-112(CJL-112)可有效提高小鼠和鸡对致死性流感感染的抵抗力。本研究旨在了解该乳酸菌菌株具有显著抗流感活性的潜在机制。体外,鸡巨噬细胞系 HD-11 与 CJL-112 共培养可显著增加一氧化氮(NO)的产生。体内,将 CJL-112 经鼻腔给予 BALB/c 小鼠,在感染甲型流感病毒 A/NWS/33(H1N1)之前共给予 21 天。观察到 Th1 细胞因子(IL-2、IFN-γ)的显著上调,而 Th2 细胞因子(IL-4、IL-5、IL-10)的水平要么降低,要么与对照组小鼠相比无变化。此外,与未治疗的小鼠相比,治疗组小鼠的 IgA 和特异性抗流感 IgA 水平显著增加。因此,当直接递送至呼吸道时,CJL-112 可能通过刺激巨噬细胞、激活 Th1 和增强 IgA 产生来保护小鼠免受致死性 IFV 感染。

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