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      Ascorbic acid supports ex vivo generation of plasmacytoid dendritic cells from circulating hematopoietic stem cells

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          Abstract

          Plasmacytoid dendritic cells (pDCs) constitute a rare type of immune cell with multifaceted functions, but their potential use as a cell-based immunotherapy is challenged by the scarce cell numbers that can be extracted from blood. Here, we systematically investigate culture parameters for generating pDCs from hematopoietic stem and progenitor cells (HSPCs). Using optimized conditions combined with implementation of HSPC pre-expansion, we generate an average of 465 million HSPC-derived pDCs (HSPC-pDCs) starting from 100,000 cord blood-derived HSPCs. Furthermore, we demonstrate that such protocol allows HSPC-pDC generation from whole-blood HSPCs, and these cells display a pDC phenotype and function. Using GMP-compliant medium, we observe a remarkable loss of TLR7/9 responses, which is rescued by ascorbic acid supplementation. Ascorbic acid induces transcriptional signatures associated with pDC-specific innate immune pathways, suggesting an undescribed role of ascorbic acid for pDC functionality. This constitutes the first protocol for generating pDCs from whole blood and lays the foundation for investigating HSPC-pDCs for cell-based immunotherapy.

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          Most cited references68

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          Vitamin C and Immune Function

          Vitamin C is an essential micronutrient for humans, with pleiotropic functions related to its ability to donate electrons. It is a potent antioxidant and a cofactor for a family of biosynthetic and gene regulatory enzymes. Vitamin C contributes to immune defense by supporting various cellular functions of both the innate and adaptive immune system. Vitamin C supports epithelial barrier function against pathogens and promotes the oxidant scavenging activity of the skin, thereby potentially protecting against environmental oxidative stress. Vitamin C accumulates in phagocytic cells, such as neutrophils, and can enhance chemotaxis, phagocytosis, generation of reactive oxygen species, and ultimately microbial killing. It is also needed for apoptosis and clearance of the spent neutrophils from sites of infection by macrophages, thereby decreasing necrosis/NETosis and potential tissue damage. The role of vitamin C in lymphocytes is less clear, but it has been shown to enhance differentiation and proliferation of B- and T-cells, likely due to its gene regulating effects. Vitamin C deficiency results in impaired immunity and higher susceptibility to infections. In turn, infections significantly impact on vitamin C levels due to enhanced inflammation and metabolic requirements. Furthermore, supplementation with vitamin C appears to be able to both prevent and treat respiratory and systemic infections. Prophylactic prevention of infection requires dietary vitamin C intakes that provide at least adequate, if not saturating plasma levels (i.e., 100–200 mg/day), which optimize cell and tissue levels. In contrast, treatment of established infections requires significantly higher (gram) doses of the vitamin to compensate for the increased inflammatory response and metabolic demand.
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            Interferon-alpha induction through Toll-like receptors involves a direct interaction of IRF7 with MyD88 and TRAF6.

            Toll-like receptors (TLRs) are involved in the recognition of microbial pathogens. A subset of TLRs, TLR7, TLR8 and TLR9, induces antiviral responses by producing interferon-alpha (IFN-alpha). Production of IFN-alpha is dependent on the Toll-interleukin-1 receptor domain-containing adaptor MyD88. Here we show that MyD88 formed a complex with the transcription factor IRF7 but not with IRF3. The death domain of MyD88 interacted with an inhibitory domain of IRF7, and this interaction resulted in activation of the IFN-alpha-dependent promoters. Furthermore, the adaptor molecule TRAF6 also bound and activated IRF7. Ubiquitin ligase activity of TRAF6 was required for IRF7 activation. These results indicate that TLR-mediated IFN-alpha induction requires the formation of a complex consisting of MyD88, TRAF6 and IRF7 as well as TRAF6-dependent ubiquitination.
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              The multifaceted biology of plasmacytoid dendritic cells.

              Plasmacytoid dendritic cells (pDCs) are a unique DC subset that specializes in the production of type I interferons (IFNs). pDCs promote antiviral immune responses and have been implicated in the pathogenesis of autoimmune diseases that are characterized by a type I IFN signature. However, pDCs can also induce tolerogenic immune responses. In this Review, we summarize recent progress in the field of pDC biology, focusing on the molecular mechanisms that regulate the development and functions of pDCs, the pathways involved in their sensing of pathogens and endogenous nucleic acids, their functions at mucosal sites, and their roles in infection, autoimmunity and cancer.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Role: Senior Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                02 September 2021
                2021
                : 10
                : e65528
                Affiliations
                [1 ] Department of Biomedicine, Aarhus University Aarhus Denmark
                [2 ] Aarhus Institute of Advanced Studies, Aarhus University Aarhus Denmark
                [3 ] Centre of Molecular Inflammation Research, Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology Trondheim Norway
                [4 ] Clinic of Medicine, St. Olav's University Hospital Trondheim Norway
                [5 ] Department of Obstetrics and Gynaecology, Aarhus University Hospital Aarhus Denmark
                [6 ] Department of Clinical Medicine, Aarhus University Aarhus Denmark
                Medical College of Georgia at Augusta University United States
                Medical College of Georgia at Augusta University United States
                Medical College of Georgia at Augusta University United States
                Author notes
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-0306-1736
                https://orcid.org/0000-0002-7668-2517
                https://orcid.org/0000-0003-1802-9541
                https://orcid.org/0000-0002-6449-6426
                https://orcid.org/0000-0001-8847-9201
                https://orcid.org/0000-0002-7383-0297
                Article
                65528
                10.7554/eLife.65528
                8445615
                34473049
                068f107d-8acc-4c6a-b46c-f117a2bd4123
                © 2021, Laustsen et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 07 December 2020
                : 01 September 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003554, Lundbeckfonden;
                Award ID: R238-2016-3349
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100009388, Aarhus Institute of Advanced Studies, Aarhus Universitet;
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000780, European Union;
                Award ID: 609033
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100003554, Lundbeckfonden;
                Award ID: R238-2016-2708
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004836, Independent Research Fund Denmark;
                Award ID: 8020-00201B
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100009708, Novo Nordisk Fonden;
                Award ID: NNF18OC0053146
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000780, European Union;
                Award ID: 754513
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002808, Carlsbergfondet;
                Award ID: CF17-0129
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002808, Carlsbergfondet;
                Award ID: CF20-0424
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Tools and Resources
                Immunology and Inflammation
                Custom metadata
                Probing of various culture conditions leads to fundamental advances in ex vivo production of plasmacytoid dendritic cells for use in immunotherapy.

                Life sciences
                ascorbic acid,plasmacytoid,pdc,dendritic cells,hematopoietic stem cells,vitamin c,ex,vivo,differentiation,immunotherapy,tlr7,tlr9,chspc,human

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