| Literature DB >> 26877243 |
Aleksandra Deczkowska1, Kuti Baruch1, Michal Schwartz2.
Abstract
Recent findings have revealed distinct roles for type I and II interferons (IFN-I and IFN-γ) in the recruitment of immune cells to the central nervous system (CNS) and highlighted the importance of this process for brain maintenance and protection/repair. Furthermore, manipulation of IFN-I and IFN-γ pathways in pathological contexts has yielded conflicting results. We discuss these findings, focusing on two distinct conditions; relapsing remitting multiple sclerosis (RRMS) and brain aging. Using these examples, we propose that regulation of immune cell entry to the CNS is a mechanism through which interaction between IFN-I and -II can affect brain function from its anatomical borders. Deviation from homeostatic IFN-I/-II balance may contribute to distinct brain pathologies, resulting from either insufficient immune surveillance of the CNS and loss of immune-dependent protection, or overwhelming leukocyte entry and immune-mediated destruction.Entities:
Keywords: CNS immune surveillance; aging; choroid plexus; interferons; neurodegeneration
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Year: 2016 PMID: 26877243 DOI: 10.1016/j.it.2016.01.006
Source DB: PubMed Journal: Trends Immunol ISSN: 1471-4906 Impact factor: 16.687