Iron overload and immunity

被引:101
作者
Porto, Graca
De Sousa, Maria
机构
[1] Inst Mol & Cellular Biol, P-8234150 Oporto, Portugal
[2] Abel Salazar Inst Biomed Sci, Oporto, Portugal
[3] Santo Antonio Gen Hosp, P-8234150 Oporto, Portugal
关键词
iron; iron overload; innate immunity; adaptive immunity;
D O I
10.3748/wjg.v13.i35.4707
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Progress in the characterization of genes involved in the control of iron homeostasis in humans and in mice has improved the definition of iron overload and of the cells affected by it. The cell involved in iron overload with the greatest effect on immunity is the macrophage. Intriguing evidence has emerged, however, in the last 12 years indicating that parenchymal iron overload is linked to genes classically associated with the immune system. This review offers an update of the genes and proteins relevant to iron metabolism expressed in cells of the innate immune system, and addresses the question of how this system is affected in clinical situations of iron overload. The relationship between iron and the major cells of adaptive immunity, the T lymphocytes, will also be reviewed. Most studies addressing this last question in humans were performed in the clinical model of Hereditary Hemochromatosis. Data will also be reviewed demonstrating how the disruption of molecules essentially involved in adaptive immune responses result in the spontaneous development of iron overload and how they act as modifiers of iron overload. (C) 2007 WJG. All rights reserved.
引用
收藏
页码:4707 / 4715
页数:9
相关论文
共 99 条
[1]   Decreased liver hepcidin expression in the Hfe knockout mouse [J].
Ahmad, KA ;
Ahmann, JR ;
Migas, MC ;
Waheed, A ;
Britton, RS ;
Bacon, BR ;
Sly, WS ;
Fleming, RE .
BLOOD CELLS MOLECULES AND DISEASES, 2002, 29 (03) :361-366
[2]   Anomalies of the CD8(+) T cell pool in haemochromatosis: HLA-A3-linked expansions of CD8(+)CD28(-) T cells [J].
Arosa, FA ;
Oliveria, L ;
Porto, G ;
DaSilva, BM ;
Kruijer, W ;
Veltman, J ;
DeSousa, M .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1997, 107 (03) :548-554
[3]   DECREASED CD8-P56LCK ACTIVITY IN PERIPHERAL-BLOOD T-LYMPHOCYTES FROM PATIENTS WITH HEREDITARY HEMOCHROMATOSIS [J].
AROSA, FA ;
DASILVA, AJ ;
GODINHO, IM ;
TERSTEEGE, JCA ;
PORTO, G ;
RUDD, CE ;
DESOUSA, M .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1994, 39 (05) :426-432
[4]  
Barton James C, 2005, BMC Blood Disord, V5, P5, DOI 10.1186/1471-2326-5-5
[5]   Variations in the Nrampi gene and susceptibility to tuberculosis in West Africans [J].
Bellamy, R ;
Ruwende, C ;
Corrah, T ;
McAdam, KPWJ ;
Whittle, HC ;
Hill, AVS .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (10) :640-644
[6]   Expression of iron transport proteins divalent metal transporter-1, Ferroportin-1, HFE and transferrin receptor-1 in human monocyte-derived dendritic cells [J].
Brinkmann, Martin ;
Teuffel, Regina ;
Laham, Nihay ;
Ehrlich, Rachel ;
Decker, Patrice ;
Lemonnier, Francois A. ;
Pascolo, Steve .
CELL BIOCHEMISTRY AND FUNCTION, 2007, 25 (03) :287-296
[7]   Inappropriately high iron regulatory protein activity in monocytes of patients with genetic hemochromatosis [J].
Cairo, G ;
Recalcati, S ;
Montosi, G ;
Castrusini, E ;
Conte, D ;
Pietrangelo, A .
BLOOD, 1997, 89 (07) :2546-2553
[8]   T-cell receptor repertoire in hereditary hemochromatosis:: A study of 32 hemochromatosis patients and 274 healthy subjects [J].
Cardoso, C ;
Porto, G ;
Lacerda, R ;
Resende, D ;
Rodrigues, P ;
Bravo, F ;
Oliveira, JC ;
Justiça, B ;
de Sousa, M .
HUMAN IMMUNOLOGY, 2001, 62 (05) :488-499
[9]   HFE, the MHC and hemochromatosis:: Paradigm for an extended function for MHC class I [J].
Cardoso, CS ;
de Sousa, M .
TISSUE ANTIGENS, 2003, 61 (04) :263-275
[10]  
CARDOSO CS, 2005, BOCA RATON, P281