Department of Neurology, Inflammatory Disorders of Nervous System and Neurooncology, University of Müenster, Domagkstr. 13, 48149 Müenster, Germany.
Cell Mol Life Sci. 2011 Feb;68(3):407-16. doi: 10.1007/s00018-010-0582-5. Epub 2010 Nov 18.
The central nervous system (CNS) is considered an immune-privileged organ that maintains an adaptable immune surveillance system. Dysregulated immune function within the CNS contributes to the development of brain tumor growth, and robust immune activation results in excessive inflammation. Human lymphocyte antigen-G (HLA-G) proteins with tolerogenic immunoreactivity have been implicated in various pathophysiological processes including immune surveillance, governing homeostasis and immune regulation. In this review, we describe the wealth of evidence for the involvement of HLA-G in the CNS under physiological and pathological conditions. Further, we review regulatory functions that may be applicable as beneficial strategies in the therapeutic manipulation of immune-mediated CNS immune responses. Additionally, we try to understand how this molecule cooperates with other CNS-resident cells to maintain normal immune homeostasis, while still facilitating the development of the appropriate immune responses.
中枢神经系统(CNS)被认为是一个免疫特权器官,它维持着适应性免疫监视系统。CNS 内失调的免疫功能导致脑肿瘤生长,而强烈的免疫激活会导致过度炎症。具有免疫耐受性的人类淋巴细胞抗原-G(HLA-G)蛋白已被牵涉到多种病理生理过程中,包括免疫监视、维持内环境稳定和免疫调节。在这篇综述中,我们描述了 HLA-G 在生理和病理条件下参与 CNS 的大量证据。此外,我们还回顾了可能作为治疗性干预 CNS 免疫反应的有益策略的调节功能。此外,我们还试图了解该分子如何与其他中枢神经系统驻留细胞合作,以维持正常的免疫内环境稳定,同时仍促进适当免疫反应的发展。