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Basic & Clinical Research on Iron Biology


Iron Biology (IB) stands today as a fast growing field of knowledge, spanning from the basic understanding of cell and systems homeostasis to applications in most medical fields, including hematology, oncology, neurosciences, genetics and immunology. Advances in the IB field in the last decades have placed several immunological players, such as the MHC class I gene HFE and the antimicrobial peptide hepcidin, at the heart of systemic iron homeostasis, supporting the vision of immunity as a process not exclusively devoted to fight against foreign pathogens but as a system controling the internal milieu equilibrium. In this context, human disorders of iron homeostasis became extraordinary models to address the reciprocal interactions between iron and immunity. One such disorder is hereditary hemochromatosis, a MHC class I-linked genetic disease with a high prevalence in Portugal and a special focus of interest in the group. The BCRIB fits the model of a “translational research” group where scientists involved in fundamental research cooperate intimately with practicing clinicians potentiating the capacity of the whole group to elucidate basic principles of iron biology and put forward new approaches to address iron-related disorders. Focusing on the reciprocal interactions between iron, inflammation and immunity, our aim is to improve our knowledge so that it may help to better manage iron-related disorders in general and hereditary hemochromatosis in particular. In this case, we aim at identifying novel genetic modifiers of disease expression acting either as modifiers of the iron levels in the body or as modifiers of the cellular response to the iron induced stress.



1. We recently demonstrated that T lymphocytes are able to take up non-transferrin-bound iron (NTBI), thus acting as circulating “buffers” against systemic iron toxicity (Arezes et al. 2013). This finding offers, for the first time, a mechanistic explanation for the previously described association of iron overload with defective numbers of circulating CD8+ T lymphocytes in hereditary hemochromatosis (HH) patients.

2. We first demonstrated, in the Nrf2-/- mice model, that the antioxidant response coordinated by this transcription factor is essential for the protection of mouse hepatocytes against iron toxicity (Silva-Gomes et al, 2014). Work is ongoing in mice models defective in both Nrf2 and Hfe and in human patients to understand if Nrf2 can be a relevant modifier of HH.

3. The finding that effector memory CD8 T lymphocytes are abnormal in HH (Macedo et al. 2010) was followed by a study of CD8 T cell gene expression in both mice (Hfe-/-) and human models of HH. Preliminary results point to an activated state of those cells in response to iron overload (Costa et al, in preparation) 4. The finding of a novel association of lymphocyte and iron phenotypes with particular MHC-linked microhaplotypes (Cruz et al. 2008) was the starting point to a running deep sequencing study, in collaboration with the Genecore facility at EMBL, aimed at identifying novel genetic determinants of CD8 T cell numbers.

Energy dispersive X-ray (EDX) elemental analysis showing Iron (Fe, green) accumulation in a carbon-rich (C, red) intracellular region of a human monocyte