Iron Chelators Dictate Immune Cells Inflammatory Ability: Potential Adjuvant Therapy for IBD

被引:23
作者
Chieppa, Marcello [1 ]
Galleggiante, Vanessa [1 ]
Serino, Grazia [1 ]
Massaro, Monica [1 ]
Santino, Angelo [2 ]
机构
[1] Natl Inst Gastroenterol S de Bellis, Inst Res, Castellana Grotte, BA, Italy
[2] CNR, Inst Sci Food Prod, Unit Lecce, Via Monteroni, I-73100 Lecce, Italy
关键词
Iron chelators; immune cells; inflammation; IBD; hemoproteins; iron-chelating drugs; RIBONUCLEOTIDE REDUCTASE INHIBITOR; FACTOR-KAPPA-B; IN-VITRO; BOWEL-DISEASE; EXPERIMENTAL COLITIS; SALMONELLA-ENTERICA; MURINE MACROPHAGES; LIPID-PEROXIDATION; HYDROGEN-PEROXIDE; DEFICIENCY ANEMIA;
D O I
10.2174/1381612823666170215143541
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The importance of hemoproteins for life lies largely in their iron-mediated chemical properties. In the human body, there are about 4 g of iron, a precious resource preserved by sophisticated recycling mechanisms. Iron is also important for pathogen growth, so it is not surprising that immune cells developed mechanisms to reduce iron availability in cases of inflammation. In healthy conditions, macrophages degrade hemoproteins and export iron, while if inflammation develops, they retain cytoplasmic iron to reduce extracellular iron concentrations. Iron-rich macrophages possess a stronger inflammatory ability, which explains the chronic inflammatory response observed in states of iron overload. Inflammatory bowel syndromes are often characterized by intestinal blood loss and consequent anemia, but iron-supplementation therapies may exacerbate the inflammatory response. In chronically transfused patients iron overload is frequently observed; the iron can become toxic and in excess, even fatal if not treated with iron-chelating drugs. Conclusion: In the present review, we discuss the importance of iron homeostasis in states of health and inflammation, focusing on iron and iron-chelation treatment for IBD patients. Oral administration of natural ironchelating chemicals may be an effective adjuvant therapy for IBD patients, acting on numerous aspects of chronic inflammatory syndromes.
引用
收藏
页码:2289 / 2298
页数:10
相关论文
共 163 条
[1]   SERUM NON-TRANSFERRIN-BOUND IRON IN BETA-THALASSEMIA MAJOR PATIENTS TREATED WITH DESFERRIOXAMINE AND L1 [J].
ALREFAIE, FN ;
WICKENS, DG ;
WONKE, B ;
KONTOGHIORGHES, GJ ;
HOFFBRAND, AV .
BRITISH JOURNAL OF HAEMATOLOGY, 1992, 82 (02) :431-436
[2]  
Anderegg G, 1996, J CHEM SOC CHEM COMM, V17, P1194
[3]   IRON CHELATION FOR AMELIORATION OF LIVER ISCHEMIA-REPERFUSION INJURY [J].
Arkadopoulos, Nikolaos ;
Nastos, Constantinos ;
Kalimeris, Konstantinos ;
Economou, Emmanuil ;
Theodoraki, Kassiani ;
Kouskouni, Evangelia ;
Pafiti, Agathi ;
Kostopanagiotou, Georgia ;
Smyrniotis, Vassilios .
HEMOGLOBIN, 2010, 34 (03) :265-277
[4]   Molecular biology of iron acquisition in Saccharomyces cerevisiae [J].
Askwith, CC ;
deSilva, D ;
Kaplan, J .
MOLECULAR MICROBIOLOGY, 1996, 20 (01) :27-34
[5]   OXYGEN RADICALS IN ULCERATIVE-COLITIS [J].
BABBS, CF .
FREE RADICAL BIOLOGY AND MEDICINE, 1992, 13 (02) :169-181
[6]   In vitro and in vivo radiosensitization induced by the ribonucleotide reductase inhibitor-triapine (3-aminopyridine-2-carboxaldehyde-thiosemicarbazone) [J].
Barker, CA ;
Burgan, WE ;
Carter, DJ ;
Cerna, D ;
Gius, D ;
Hollingshead, MG ;
Camphausen, K ;
Tofilon, PJ .
CLINICAL CANCER RESEARCH, 2006, 12 (09) :2912-2918
[7]  
Barton JC, 2007, IDRUGS, V10, P480
[8]   Mucosal Interactions between Genetics, Diet, and Microbiome in Inflammatory Bowel Disease [J].
Basson, Abigail ;
Trotter, Ashley ;
Rodriguez-Palacios, Alex ;
Cominelli, Fabio .
FRONTIERS IN IMMUNOLOGY, 2016, 7
[9]  
Bauerle PA, 1994, ANNU REV IMMUNOL, V12, P79
[10]  
Bäumler AJ, 1998, J BACTERIOL, V180, P1446