Department of Neuropathology, University of Freiburg, Breisacher Str. 64, D-79106 Freiburg, Germany.
Trends Mol Med. 2010 Aug;16(8):379-86. doi: 10.1016/j.molmed.2010.06.001. Epub 2010 Jun 28.
Type I interferons (IFN-alpha and IFN-beta) were discovered more than five decades ago and are widely used for the treatment of human autoimmune diseases such as multiple sclerosis (MS). Despite their highly beneficial features, the precise mechanism of action remains speculative. Given the frequent side effects of IFN-alpha/beta therapy, understanding its action in an in vivo setting is vital to further improve this therapeutic approach. Major advances in our understanding of the IFN biology have recently been made and are particularly based on the combination of powerful genome-wide expression analysis in humans with gene-targeting techniques available for basic research. The recent discovery of a novel T-cell subset, Th17 cells, sheds new light on type I IFNs in MS.
I 型干扰素(IFN-α 和 IFN-β)早在五十年前就被发现了,目前被广泛用于治疗多发性硬化症(MS)等人类自身免疫性疾病。尽管它们具有高度的有益特性,但确切的作用机制仍在推测之中。鉴于 IFN-α/β 治疗的频繁副作用,了解其在体内环境中的作用对于进一步改进这种治疗方法至关重要。最近,我们对 IFN 生物学的理解取得了重大进展,这主要是基于对人类进行强大的全基因组表达分析,并结合用于基础研究的基因靶向技术。最近发现的一种新型 T 细胞亚群——Th17 细胞,为 MS 中的 I 型干扰素提供了新的线索。