How Type I Interferons Work in Multiple Sclerosis and Other Diseases: Some Unexpected Mechanisms

被引:64
作者
Reder, Anthony T. [1 ]
Feng, Xuan [1 ]
机构
[1] Univ Chicago, Dept Neurol, Chicago, IL 60637 USA
关键词
REGULATORY T-CELLS; DOUBLE-BLIND; ALPHA-INTERFERON; IFN-BETA; VITAMIN-D; THERAPY; RISK; PLACEBO; EXPRESSION; RESPONSES;
D O I
10.1089/jir.2013.0158
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Type I interferons (IFNs) are important in innate and adaptive immunity. They are used to treat virus infections, cancer, and multiple sclerosis (MS). There are 5 type I IFN families in humans-IFN-alpha with 13 subtypes, plus IFN-beta, epsilon, kappa, and omega. Because their receptor binding affinities vary, these IFNs have different gene induction profiles and quite variable therapeutic effects. IFN-alpha subtypes may each be specific for certain viruses, but can be neurotoxic. IFN-beta induces IFN-alpha, plus has additional direct effects on target cells. IFN-beta was the first therapy approved that could change the course of MS. It has broader specificity than IFN-alpha, enhances cognition in MS, and may be neuroprotective and can potentially enhance fertility in women. Priming the IFN signaling system with an injection of IFN-beta can enhance subnormal type I IFN signals in MS. Many other commonly used drugs and vitamins may potentiate clinical benefits of IFN-beta.
引用
收藏
页码:589 / 599
页数:11
相关论文
共 109 条
[1]   Abnormal levels of interferon-gamma receptors in active multiple sclerosis are normalized by IFN-β therapy:: Implications for control of apoptosis [J].
Ahn, J ;
Feng, X ;
Patel, N ;
Dhawan, N ;
Reder, AT .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2004, 9 :1547-1555
[2]  
Amezcua L, 2013, ECTRIMS, P1097
[3]   CIMETIDINE AS AN IMMUNOMODULATOR IN SUBACUTE SCLEROSING PANENCEPHALITIS - A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY [J].
ANLAR, B ;
GUCUYENER, K ;
IMIR, T ;
YALAZ, K ;
RENDA, Y .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1993, 12 (07) :578-581
[4]   SUPPRESSOR CELL-FUNCTION IN MULTIPLE-SCLEROSIS - CORRELATION WITH CLINICAL-DISEASE ACTIVITY [J].
ANTEL, JP ;
ARNASON, BGW ;
MEDOF, ME .
ANNALS OF NEUROLOGY, 1979, 5 (04) :338-342
[5]   ACTIVATED SUPPRESSOR-CELL FUNCTION IN SEVERELY DISABLED PATIENTS WITH MULTIPLE-SCLEROSIS [J].
ANTEL, JP ;
FREEDMAN, MS ;
BRODOVSKY, S ;
FRANCIS, GS ;
DUQUETTE, P .
ANNALS OF NEUROLOGY, 1989, 25 (02) :204-207
[6]   Mechanisms of action of adrenocorticotropic hormone and other melanocortins relevant to the clinical management of patients with multiple sclerosis [J].
Arnason, Barry G. ;
Berkovich, Regina ;
Catania, Anna ;
Lisak, Robert P. ;
Zaidi, Mone .
MULTIPLE SCLEROSIS JOURNAL, 2013, 19 (02) :130-136
[7]   Interferon β-1b directly modulates human neural stem/progenitor cell fate [J].
Arscott, W. Tristram ;
Soltys, John ;
Knight, Julia ;
Mao-Draayer, Yang .
BRAIN RESEARCH, 2011, 1413 :1-8
[8]   Vitamin D as an Early Predictor of Multiple Sclerosis Activity and Progression [J].
Ascherio, Alberto ;
Munger, Kassandra L. ;
White, Rick ;
Koechert, Karl ;
Simon, Kelly Claire ;
Polman, Chris H. ;
Freedman, Mark S. ;
Hartung, Hans-Peter ;
Miller, David H. ;
Montalban, Xavier ;
Edan, Gilles ;
Barkhof, Frederik ;
Pleimes, Dirk ;
Radue, Ernst-Wilhelm ;
Sandbrink, Rupert ;
Kappos, Ludwig ;
Pohl, Christoph .
JAMA NEUROLOGY, 2014, 71 (03) :306-314
[9]   INITIAL LESION IN EXPERIMENTAL ALLERGIC NEURITIS [J].
ASTROM, KE ;
WEBSTER, HDF ;
ARNASON, BG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1968, 128 (03) :469-&
[10]   T helper type 1 and 17 cells determine efficacy of interferon-β in multiple sclerosis and experimental encephalomyelitis [J].
Axtell, Robert C. ;
de Jong, Brigit A. ;
Boniface, Katia ;
van der Voort, Laura F. ;
Bhat, Roopa ;
De Sarno, Patrizia ;
Naves, Rodrigo ;
Han, May ;
Zhong, Franklin ;
Castellanos, Jim G. ;
Mair, Robert ;
Christakos, Athena ;
Kolkowitz, Ilan ;
Katz, Liat ;
Killestein, Joep ;
Polman, Chris H. ;
Malefyt, Rene de Waal ;
Steinman, Lawrence ;
Raman, Chander .
NATURE MEDICINE, 2010, 16 (04) :406-U21