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I型干扰素可增强自然杀伤细胞产生γ干扰素的能力。

Type I interferons enhance production of IFN-gamma by NK cells.

作者信息

Hunter C A, Gabriel K E, Radzanowski T, Neyer L E, Remington J S

机构信息

Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia 19104-6008, USA.

出版信息

Immunol Lett. 1997 Oct;59(1):1-5. doi: 10.1016/s0165-2478(97)00091-6.

Abstract

In murine models, challenge with different viral and parasitic infection is closely associated with the production of type I interferons (IFN-alpha/beta) and NK cell production of interferon-gamma (IFN-gamma). Therefore, we wished to determine if IFN-alpha/beta had a role in the regulation of NK cell production of IFN-gamma. IFN-alpha/beta alone stimulated low levels of IFN-gamma production by purified populations of IL-2 activated NK cells but in combination with IL-12 resulted in the production of significant levels of IFN-gamma. Interestingly, maximal production of IFN-gamma by NK cells stimulated with IL-2 plus IFN-alpha/beta was dependent on endogenous tumor necrosis factor-alpha (TNF-alpha). Further studies revealed that TNF-alpha enhanced the ability of IFN-alpha/beta to stimulate production of IFN-gamma by NK cells. In contrast to the stimulatory effect of IFN-alpha/beta on NK cell production of IFN-gamma, IFN-alpha/beta inhibited IL-2 induced proliferation of NK cells. This inhibitory effect was not reversed by the addition of neutralizing antibodies specific for IFN-gamma or TNF-alpha. These data demonstrate that the type I interferons enhance NK cell production of IFN-gamma and suggest that they may be important in the regulation of NK cell production of IFN-gamma during infection.

摘要

在小鼠模型中,用不同的病毒和寄生虫感染进行攻击与I型干扰素(IFN-α/β)的产生以及NK细胞产生干扰素-γ(IFN-γ)密切相关。因此,我们希望确定IFN-α/β是否在调节NK细胞产生IFN-γ中发挥作用。单独的IFN-α/β只能刺激经IL-2激活的纯化NK细胞群体产生低水平的IFN-γ,但与IL-12联合使用时则会导致产生显著水平的IFN-γ。有趣的是,用IL-2加IFN-α/β刺激的NK细胞产生IFN-γ的最大值依赖于内源性肿瘤坏死因子-α(TNF-α)。进一步的研究表明,TNF-α增强了IFN-α/β刺激NK细胞产生IFN-γ的能力。与IFN-α/β对NK细胞产生IFN-γ的刺激作用相反,IFN-α/β抑制了IL-2诱导的NK细胞增殖。添加针对IFN-γ或TNF-α的中和抗体并不能逆转这种抑制作用。这些数据表明I型干扰素增强了NK细胞产生IFN-γ的能力,并表明它们在感染期间调节NK细胞产生IFN-γ可能很重要。

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