Yarkoni Shai, Kaminitz Ayelet, Sagiv Yuval, Yaniv Isaac, Askenasy Nadir
Target-In Ltd, Petach Tikva, Israel.
Bioessays. 2008 Sep;30(9):875-88. doi: 10.1002/bies.20812.
A large body of evidence on the activity of regulatory T (Treg) cells was gathered during the last decade, and a similar number of reviews and opinion papers attempted to integrate the experimental findings. The abundant literature clearly delineates an exciting area of research but also underlines some major controversies. A linear cause-result interpretation of experimental maneuvers often ignores the fact that the activity of Treg cells is orchestrated with the effector T (Teff) cells within an intricate network of physiological immune homeostasis. Every modulation of the activity of the effector (cytotoxic) immune system revolves to affect the activity of regulatory (suppressive) cells through elaborate feedback loops of negative and positive regulation. The lack of IL-2 production by innate Treg cells makes this cytokine a prime coupler of the effector and suppressive mechanisms. Here we attempt to integrate evidence that delineates the involvement of IL-2 in primary and secondary feedback loops that regulate the activity of suppressive cells within the elaborate network of physiological immune homeostasis.
在过去十年中,积累了大量关于调节性T(Treg)细胞活性的证据,同时也有数量相当的综述和观点论文试图整合这些实验结果。丰富的文献清晰地勾勒出一个令人兴奋的研究领域,但也凸显了一些重大争议。对实验操作进行线性的因果解释往往忽略了这样一个事实,即Treg细胞的活性是在生理免疫稳态的复杂网络中与效应T(Teff)细胞协同调控的。效应(细胞毒性)免疫系统活性的每一次调节都会通过复杂的正负调节反馈回路来影响调节(抑制)细胞的活性。天然Treg细胞缺乏白细胞介素-2(IL-2)的产生,这使得这种细胞因子成为效应机制和抑制机制的主要耦合因子。在这里,我们试图整合相关证据,这些证据描绘了IL-2在调节生理免疫稳态复杂网络中抑制性细胞活性的初级和次级反馈回路中的作用。