Vitamin D as an immune modulator in multiple sclerosis, a review

被引:216
作者
Smolders, Joost [1 ]
Damoiseaux, Jan [2 ]
Menheere, Paul [3 ]
Hupperts, Raymond [1 ]
机构
[1] Univ Hosp, Dept Neurol, NL-6202 AZ Maastricht, Netherlands
[2] Univ Hosp, Dept Clin & Expt Immunol, Maastricht, Netherlands
[3] Univ Hosp, Dept Clin Chem, Maastricht, Netherlands
关键词
multiple sclerosis; experimental allergic encephalomyelitis; vitamin D; calcitriol; immune system;
D O I
10.1016/j.jneuroim.2007.11.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The role of vitamin D in calcium homeostasis is well known. More recently vitamin D has become a topic of interest in immune regulation and multiple sclerosis. The main reason for this is the observed geographical distribution of multiple sclerosis. Areas with high sunlight exposure, the principal inducer of vitamin D synthesis, have a relatively low prevalence of multiple sclerosis and vice versa. Furthermore, low levels of the principal vitamin D metabolite (25-hydroxy vitamin D) in the circulation are associated with a high incidence of multiple sclerosis. Other epidemiological evidence also supports the view that vitamin D metabolites have an immune and disease modulating effect in multiple sclerosis. Experimental research in vitro and in animal models has further clarified the interaction of vitamin D metabolites with the immune system. The evidence obtained from these studies strongly supports a model in which vitamin D mediates a shift to a more anti-inflammatory immune response, and in particular to enhanced regulatory T cell functionality. In the current review we link the basic knowledge on vitamin D and immune regulation with the vitamin D related observations in multiple sclerosis. We conclude that there is a sound basis on which to initiate double-blind placebo-controlled trials that not only address the effect of vitamin D on the clinical outcome of multiple sclerosis, but also on the regulatory T cell compartment. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 17
页数:11
相关论文
共 133 条
[1]  
ACHESON E. D., 1960, ACTA PSYCHIATR ET NEUROL SCAND SUPPL, V35, P132, DOI 10.1111/j.1600-0447.1960.tb08674.x
[2]   Alfacalcidol treatment in multiple sclerosis [J].
Achiron, A ;
Barak, Y ;
Miron, S ;
Izhak, Y ;
Faibel, M ;
Edelstein, S .
CLINICAL NEUROPHARMACOLOGY, 2003, 26 (02) :53-53
[3]   Th1/Th2 cytokine patterns and clinical profiles during and after pregnancy in women with multiple sclerosis [J].
Al-Shammri, S ;
Rawoot, P ;
Azizieh, F ;
AbuQoora, A ;
Hanna, M ;
Saminathan, TR ;
Raghupathy, R .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2004, 222 (1-2) :21-27
[4]   Developmental vitamin D deficiency alters brain protein expression in the adult rat:: Implications for neuropsychiatric disorders [J].
Almeras, Lionel ;
Eyles, Darryl ;
Benech, Philippe ;
Laffite, Daniel ;
Villard, Claude ;
Patatian, Angela ;
Boucraut, Jose ;
Mackay-Sim, Alan ;
McGrath, John ;
Feron, Francois .
PROTEOMICS, 2007, 7 (05) :769-780
[5]  
Auer DP, 2000, ANN NEUROL, V47, P276, DOI 10.1002/1531-8249(200002)47:2<276::AID-ANA28>3.0.CO
[6]  
2-1
[7]   Seasonal variation of interferon-γ production in progressive multiple sclerosis [J].
Balashov, KE ;
Olek, MJ ;
Smith, DR ;
Khoury, SJ ;
Weiner, HL .
ANNALS OF NEUROLOGY, 1998, 44 (05) :824-828
[8]   SEASONAL-VARIATION OF MULTIPLE-SCLEROSIS EXACERBATIONS IN ARIZONA [J].
BAMFORD, CR ;
SIBLEY, WA ;
THIES, C .
NEUROLOGY, 1983, 33 (06) :697-701
[9]   In vitro generation of interleukin 10-producing regulatory CD4+ T cells is induced by immunosuppressive drugs and inhibited by T helper type 1 (Th1)- and Th2-inducing cytokines [J].
Barrat, FJ ;
Cua, DJ ;
Boonstra, A ;
Richards, DF ;
Crain, C ;
Savelkoul, HF ;
de Waal-Malefyt, R ;
Coffman, RL ;
Hawrylowicz, CM ;
O'Garra, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (05) :603-616
[10]   DIFFERENTIAL-EFFECTS OF 1,25-DIHYDROXYVITAMIN D3 ON HUMAN-LYMPHOCYTES AND MONOCYTE MACROPHAGES - INHIBITION OF INTERLEUKIN-2 AND AUGMENTATION OF INTERLEUKIN-1 PRODUCTION [J].
BHALLA, AK ;
AMENTO, EP ;
KRANE, SM .
CELLULAR IMMUNOLOGY, 1986, 98 (02) :311-322