Ly Lan H, McMurray David N
Department of Microbial and Molecular Pathogenesis, Texas A & M System Health Science Center, College Station, Texas, 77843-1114, USA.
Indian J Exp Biol. 2009 Jun;47(6):432-9.
Tumour necrosis factor alpha (TNF-alpha) is a prototypic pro-inflammatory cytokine that has a central role in the initial host response to Mycobacterium tuberculosis infection. It is a key player in granuloma formation, macrophage activation, bacterial killing, and pathology in vivo. However, the exact mechanism has not been completely understood. This review summarizes the TNFalpha data acquired from the 'gold standard' guinea pig animal model of tuberculosis. While production of TNFalpha is widely accepted as beneficial to the host response, we have found that this hypothesis is just one side of the story. TNFalpha can up-regulate and down-regulate some key pro-inflammatory cytokines (IFNgamma, IL-12p40) and differentially modulate macrophage activation and intracellular bacterial growth. Neutralization of TNFalpha in vivo allows an antiinflammatory TGFbeta-mediated response to develop. Furthermore, BCG vaccination modulates TNFalpha responses directly in the pulmonary granulomas to reduce tissue damage. The bipolar nature of TNFalpha should be considered as knowledge of this critical molecule continues to grow.
肿瘤坏死因子α(TNF-α)是一种典型的促炎细胞因子,在宿主对结核分枝杆菌感染的初始反应中起核心作用。它是肉芽肿形成、巨噬细胞活化、细菌杀伤及体内病理过程中的关键因子。然而,确切机制尚未完全明确。本综述总结了从结核病“金标准”豚鼠动物模型中获取的TNF-α相关数据。虽然TNF-α的产生被广泛认为对宿主反应有益,但我们发现这一假设只是事情的一个方面。TNF-α可上调和下调一些关键促炎细胞因子(IFNγ、IL-12p40),并差异调节巨噬细胞活化和细胞内细菌生长。体内中和TNF-α可使抗炎性TGFβ介导的反应得以发展。此外,卡介苗接种可直接调节肺肉芽肿中的TNF-α反应,以减轻组织损伤。随着对这一关键分子的认识不断深入,应考虑TNF-α的双重性质。