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      The hemochromatosis protein HFE 20 years later: An emerging role in antigen presentation and in the immune system

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          Abstract

          Introduction

          Since its discovery, the hemochromatosis protein HFE has been primarily defined by its role in iron metabolism and homeostasis, and its involvement in the genetic disease termed hereditary hemochromatosis (HH). While HH patients are typically afflicted by dysregulated iron levels, many are also affected by several immune defects and increased incidence of autoimmune diseases that have thereby implicated HFE in the immune response. Growing evidence has supported an immunological role for HFE with recent studies describing HFE specifically as it relates to MHC I antigen presentation.

          Methods/Results

          Here, we present a comprehensive overview of the relationship between iron metabolism, HFE, and the immune system to better understand the origin and cause of immune defects in HH patients. We further describe the role of HFE in MHC I antigen presentation and its potential to impair autoimmune responses in homeostatic conditions, a mechanism which may be exploited by tumors to evade immune surveillance.

          Conclusion

          Overall, this increased understanding of the role of HFE in the immune response sets the stage for better treatment and management of HH and other iron‐related diseases, as well as of the immune defects related to this condition.

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          Most cited references124

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          Inhibiting glycolytic metabolism enhances CD8+ T cell memory and antitumor function.

          Naive CD8+ T cells rely upon oxidation of fatty acids as a primary source of energy. After antigen encounter, T cells shift to a glycolytic metabolism to sustain effector function. It is unclear, however, whether changes in glucose metabolism ultimately influence the ability of activated T cells to become long-lived memory cells. We used a fluorescent glucose analog, 2-NBDG, to quantify glucose uptake in activated CD8+ T cells. We found that cells exhibiting limited glucose incorporation had a molecular profile characteristic of memory precursor cells and an increased capacity to enter the memory pool compared with cells taking up high amounts of glucose. Accordingly, enforcing glycolytic metabolism by overexpressing the glycolytic enzyme phosphoglycerate mutase-1 severely impaired the ability of CD8+ T cells to form long-term memory. Conversely, activation of CD8+ T cells in the presence of an inhibitor of glycolysis, 2-deoxyglucose, enhanced the generation of memory cells and antitumor functionality. Our data indicate that augmenting glycolytic flux drives CD8+ T cells toward a terminally differentiated state, while its inhibition preserves the formation of long-lived memory CD8+ T cells. These results have important implications for improving the efficacy of T cell-based therapies against chronic infectious diseases and cancer.
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            Protein-glycan interactions in the control of innate and adaptive immune responses.

            The importance of protein glycosylation in the migration of immune cells throughout the body has been extensively appreciated. However, our awareness of the impact of glycosylation on the regulation of innate and adaptive immune responses is relatively new. An increasing number of studies reveal the relevance of glycosylation to pathogen recognition, to the modulation of the innate immune system and to the control of immune cell homeostasis and inflammation. Similarly important is the effect of glycan-containing 'information' in the development of autoimmune diseases and cancer. In this review, we provide an overview of these new directions and their impact in the field of glycoimmunology.
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              A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation.

              Iron absorption by the duodenal mucosa is initiated by uptake of ferrous Fe(II) iron across the brush border membrane and culminates in transfer of the metal across the basolateral membrane to the portal vein circulation by an unknown mechanism. We describe here the isolation and characterization of a novel cDNA (Ireg1) encoding a duodenal protein that is localized to the basolateral membrane of polarized epithelial cells. Ireg1 mRNA and protein expression are increased under conditions of increased iron absorption, and the 5' UTR of the Ireg1 mRNA contains a functional iron-responsive element (IRE). IREG1 stimulates iron efflux following expression in Xenopus oocytes. We conclude that IREG1 represents the long-sought duodenal iron export protein and is upregulated in the iron overload disease, hereditary hemochromatosis.
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                Author and article information

                Contributors
                alexandre.reuben@gmail.com
                rejean.lapointe1@videotron.ca
                Journal
                Immun Inflamm Dis
                Immun Inflamm Dis
                10.1002/(ISSN)2050-4527
                IID3
                Immunity, Inflammation and Disease
                John Wiley and Sons Inc. (Hoboken )
                2050-4527
                19 April 2017
                September 2017
                : 5
                : 3 ( doiID: 10.1002/iid3.2017.5.issue-3 )
                : 218-232
                Affiliations
                [ 1 ] Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM) Montréal, Québec Canada
                [ 2 ] Département de Médicine Université de Montréal Montréal, Québec Canada
                [ 3 ] Institut du Cancer de Montréal Montréal, Québec Canada
                Author notes
                [*] [* ] Correspondence

                Alexandre Reuben or Réjean Lapointe, Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, Québec, Canada. Tel: 514‐890‐8000 extn. 25489; Fax: 514‐412‐7591; E‐mail: alexandre.reuben@ 123456gmail.com (A.R.); rejean.lapointe1@ 123456videotron.ca (R.L.)

                Article
                IID3158
                10.1002/iid3.158
                5569368
                28474781
                22e3519b-709f-43a6-9dac-6af4d327d70d
                © 2017 The Authors. Immunity, Inflammation and Disease Published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 12 December 2016
                : 30 January 2017
                : 10 February 2017
                Page count
                Figures: 5, Tables: 1, Pages: 15, Words: 10667
                Categories
                Review
                Review
                Custom metadata
                2.0
                iid3158
                September 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.1.8 mode:remove_FC converted:24.08.2017

                antigen processing and presentation,hereditary hemochromatosis,hfe,mhc

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