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抑制性免疫受体酪氨酸激活基序:生死攸关之事。

Inhibitory ITAMs: a matter of life and death.

作者信息

Pinheiro da Silva Fabiano, Aloulou Meryem, Benhamou Marc, Monteiro Renato C

机构信息

INSERM U699, University of Paris 7, Paris F-75018, France.

出版信息

Trends Immunol. 2008 Aug;29(8):366-73. doi: 10.1016/j.it.2008.05.001. Epub 2008 Jul 2.

Abstract

The balance between activating and inhibitory signals is essential to control immune responses to microorganisms. Innate and adaptive immune responses are regulated by receptors that signal through either an immunoreceptor tyrosine-based activation motif (ITAM) or an immunoreceptor tyrosine-based inhibitory motif (ITIM). When clustered, these motifs are, respectively, responsible for activating and inhibitory signals. Recently, the concept of inhibitory ITAM (ITAM(i)) has emerged as a new means to negatively control the immune response. In this Opinion, we will discuss the ability of Escherichia coli to evade the immune system by eliciting ITAM(i) function through FcgammaRIII (CD16) on phagocytes leading to uncontrolled systemic infection and sepsis. Elucidating such mechanisms will open opportunities for specific therapeutic manipulation of ITAM(i)-based signaling pathways.

摘要

激活信号与抑制信号之间的平衡对于控制针对微生物的免疫反应至关重要。固有免疫反应和适应性免疫反应由通过基于免疫受体酪氨酸的激活基序(ITAM)或基于免疫受体酪氨酸的抑制基序(ITIM)发出信号的受体调节。这些基序聚集时,分别负责激活信号和抑制信号。最近,抑制性ITAM(ITAM(i))的概念已成为一种对免疫反应进行负调控的新方式。在本观点文章中,我们将讨论大肠杆菌通过引发吞噬细胞上的FcγRIII(CD16)的ITAM(i)功能来逃避免疫系统,从而导致不受控制的全身感染和败血症的能力。阐明此类机制将为基于ITAM(i)的信号通路的特异性治疗性干预创造机会。

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