Hepcidin-Mediated Hypoferremia Disrupts Immune Responses to Vaccination and Infection.
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Frost Joe N, Tan Tiong Kit, Abbas Munawar, Wideman Sarah K, Bonadonna Michael, Stoffel Nicole U, Wray Katherine, Kronsteiner Barbara, Smits Gaby, Campagna Dean R, Duarte Tiago L, Lopes José M, Shah Akshay, Armitage Andrew E, Arezes João, Lim Pei Jin, Preston Alexandra E, Ahern David, Teh Megan, Naylor Caitlin, Salio Mariolina, Gileadi Uzi, Andrews Simon C, Dunachie Susanna J, Zimmermann Michael B, van der Klis Fiona R M, Cerundolo Vincenzo, Bannard Oliver, Draper Simon J, Townsend Alain R M, Galy Bruno, Fleming Mark D, Lewis Marie C, Drakesmith Hal
Аннотация
METHODS: We used a hepcidin mimetic and several genetic models to examine the effect of low iron availability on T cells in vitro and on immune responses to vaccines and viral infection in mice. We examined humoral immunity in human patients with raised hepcidin and low serum iron caused by mutant TMPRSS6. We tested the effect of iron supplementation on vaccination-induced humoral immunity in piglets, a natural model of iron deficiency.
FINDINGS: We show that low serum iron (hypoferremia), caused by increased hepcidin, severely impairs effector and memory responses to immunizations. The intensified metabolism of activated lymphocytes requires the support of enhanced iron acquisition, which is facilitated by IRP1/2 and TFRC. Accordingly, providing extra iron improved the response to vaccination in hypoferremic mice and piglets, while conversely, hypoferremic humans with chronically increased hepcidin have reduced concentrations of antibodies specific for certain pathogens. Imposing hypoferremia blunted the T cell, B cell, and neutralizing antibody responses to influenza virus infection in mice, allowing the virus to persist and exacerbating lung inflammation and morbidity.
CONCLUSIONS: Hypoferremia, a well-conserved physiological innate response to infection, can counteract the development of adaptive immunity. This nutrient trade-off is relevant for understanding and improving immune responses to infections and vaccines in the globally common contexts of iron deficiency and inflammatory disorders.
FUNDING: Medical Research Council, UK.