Gender and sex hormones in multiple sclerosis pathology and therapy

被引:80
作者
Nicot, Arnaud [1 ,2 ]
机构
[1] Fac Med Pierre & Marie Curie Paris6, UMR S 546, INSERM, F-75013 Paris, France
[2] Univ Paris 06, F-75013 Paris, France
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2009年 / 14卷
关键词
Estradiol; Estriol; Progesterone; Testosterone; Neuroinflammation; EAE; Experimental Allergic Encephalomyelitis; TMEV; Th1; Th2; Autoimmune disease; Dendritic cell; Treg; Review; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; ESTROGEN-RECEPTOR-ALPHA; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; ACTIVATED PROTEIN-KINASE; CENTRAL-NERVOUS-SYSTEM; BLOOD-BRAIN-BARRIER; REGULATORY T-CELLS; TUMOR-NECROSIS-FACTOR; NATURAL-KILLER-CELLS; INDUCED DEMYELINATING DISEASE;
D O I
10.2741/3543
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
Several lines of evidence indicate that gender affects the susceptibility and course of multiple sclerosis (MS) with a higher disease prevalence and overall better prognosis in women than men. This sex dimorphism may be explained by sex chromosome effects and effects of sex steroid hormones on the immune system, blood brain barrier or parenchymal central nervous system (CNS) cells. The well known improvement in disease during late pregnancy has also been linked to hormonal changes and has stimulated recent clinical studies to determine the efficacy of and tolerance to sex steroid therapeutic approaches. Both clinical and experimental studies indicate that sex steroid supplementation may be beneficial for MS. This could be related to anti-inflammatory actions on the immune system or CNS and to direct neuroprotective properties. Here, clinical and experimental data are reviewed with respect to the effects of sex hormones or gender in the pathology or therapy of MS or its rodent disease models. The different cellular targets as well as some molecular mechanisms likely involved are discussed.
引用
收藏
页码:4477 / 4515
页数:39
相关论文
共 442 条
[1]  
AHMADI K, 2005, AM J IMMUNOL, V1, P48
[2]   Supraoptimal peptide major histocompatibility complex causes a decrease in Bcl-2 levels and allows tumor necrosis factor α receptor II-mediated apoptosis of cytotoxic T lymphocytes [J].
Alexander-Miller, MA ;
Derby, MA ;
Sarin, A ;
Henkart, PA ;
Berzofsky, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (08) :1391-1399
[3]   More severe neurologic deficits in SJL/J male than female mice following Theiler's virus-induced CNS demyelination [J].
Alley, J ;
Khasabov, S ;
Simone, D ;
Beitz, A ;
Rodriguez, M ;
Njenga, MK .
EXPERIMENTAL NEUROLOGY, 2003, 180 (01) :14-24
[4]   Recent use of oral contraceptives and the risk of multiple sclerosis [J].
Alonso, A ;
Jick, SS ;
Olek, MJ ;
Ascherio, A ;
Jick, H ;
Hernán, MA .
ARCHIVES OF NEUROLOGY, 2005, 62 (09) :1362-1365
[5]  
Alves SE, 1998, J COMP NEUROL, V391, P322, DOI 10.1002/(SICI)1096-9861(19980216)391:3<322::AID-CNE3>3.3.CO
[6]  
2-S
[7]  
[Anonymous], 1999, Neurology, V53, P457
[8]   Th2 bias of CD4+ NKT cells derived from multiple sclerosis in remission [J].
Araki, M ;
Kondo, T ;
Gumperz, JE ;
Brenner, MB ;
Miyake, S ;
Yamamura, T .
INTERNATIONAL IMMUNOLOGY, 2003, 15 (02) :279-288
[9]   Mechanism of progesterone neuroprotection of rat cerebellar Purkinje cells following oxygen-glucose deprivation [J].
Ardeshiri, A. ;
Kelley, M. H. ;
Korner, I. P. ;
Hurn, P. D. ;
Herson, P. S. .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2006, 24 (09) :2567-2574
[10]  
Arnal JF, 2007, ARCH MAL COEUR VAISS, V100, P554