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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)
            Language
            English
            Show full item record
            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://doab-dev.siscern.org/handle/20.500.12854/195636
            Keywords
            nucleated red blood cells, erythrocytes, immune response, cytokines, antimicrobial peptides, virus, antigen presentation; thema EDItEUR::M Medicine and Nursing::MK Medical specialties, branches of medicine::MKF Pathology::MKFM Medical microbiology and virology
            DOI
            10.5772/intechopen.80545
            Publisher
            InTechOpen
            Publication date and place
            2019
            Grantor
            • H2020 European Research Council
            • OAPEN harvesting collection

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              This project received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 871069.

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