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        Chapter Nucleated Red Blood Cells Contribute to the Host Immune Response Against Pathogens

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        Author(s)
        Nombela, Ivan
        Chico, Veronica
        Puente-Marin, Sara
        Ortega-Villaizan, M.
        Collection
        European Research Council (ERC); EU collection
        Language
        English
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        Abstract
        It has recently come to light that nucleated red blood cells (RBCs) of fish, amphibians, reptiles and birds are multifunctional cells, because in addition to being involved in gas exchange and transport, it has also been reported that they respond to pathogens by means of (i) phagocytosis, (ii) antigen presentation, (iii) production of cytokines and antimicrobial peptides, (iv) regulation of complement system, and (v) exerting paracrine molecular communication with other immune cells and modulating their functions. Similarly, human cord blood nucleated RBCs have been shown to exert a regulatory function in the innate immune response, by means of the suppression of the production of inflammatory cytokines. This chapter comprises the study of the implications of nucleated RBCs as mediators of both branches of immune system (innate and adaptive immune responses).
        URI
        https://library.oapen.org/handle/20.500.12657/49316
        Keywords
        nucleated red blood cells, erythrocytes, immune response, cytokines, antimicrobial peptides, virus, antigen presentation
        DOI
        10.5772/intechopen.80545
        Publisher
        InTechOpen
        Publisher website
        https://www.intechopen.com/
        Publication date and place
        2019
        Grantor
        • H2020 European Research Council - 639249 - BLOODCELLSCROSSTALK Research grant informationFind all documents
        Classification
        Medical microbiology and virology
        Rights
        https://creativecommons.org/licenses/by/3.0/
        • Imported or submitted locally

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        • If not noted otherwise all contents are available under Attribution 4.0 International (CC BY 4.0)

        Credits

        • logo EU
        • This project received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement No 683680, 810640, 871069 and 964352.

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