Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/29192
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dc.contributor.authorStroukov, W-
dc.contributor.authorMastronicola, D-
dc.contributor.authorAlbany, CJ-
dc.contributor.authorCatak, Z-
dc.contributor.authorLombardi, G-
dc.contributor.authorScottà, C-
dc.date.accessioned2024-06-16T10:35:48Z-
dc.date.available2024-06-16T10:35:48Z-
dc.date.issued2023-02-05-
dc.identifierORCiD: Wladislaw Stroukov https://orcid.org/0000-0001-6942-3667-
dc.identifierORCiD: Daniela Mastronicola https://orcid.org/0000-0002-7922-7499-
dc.identifierORCiD: Cristiano Scottà https://orcid.org/0000-0003-3942-5201-
dc.identifier.citationStroukov, W. et al. (2023) 'OMIP-090: A 20-parameter flow cytometry panel for rapid analysis of cell diversity and homing capacity in human conventional and regulatory T cells', Cytometry Part A, 103 (5), pp. 362 - 367. doi: 10.1002/cyto.a.24720.en_US
dc.identifier.issn1552-4922-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/29192-
dc.descriptionSupporting Information is available online at: https://onlinelibrary.wiley.com/doi/10.1002/cyto.a.24720#support-information-section .-
dc.description.abstractThe panel was developed and optimized for monitoring changes in homing capacity and functional diversity of human CD4+ conventional and regulatory T cell subsets. The analysis was based on expression of only surface markers in freshly isolated peripheral blood mononuclear cells (PBMCs) to reduce at minimum any alteration due to permeabilization or freezing/thawing procedures. We included markers to assess the distribution of naïve and memory populations based on the expression of CD45RA, CCR7, CD25, CD28 and CD95 in both conventional and regulatory T cells. The identification of major functional subsets was performed using CCR4, CCR6, CCR10, CXCR3 and CXCR5. Homing capacity of these subsets to skin, airway tract, gut and inflammatory lesions could finally be assessed with the markers CLA, CCR3, CCR5 and integrin β7. The panel was tested on freshly isolated PBMCs from healthy donors and patients with allergic rhinitis or autoimmune disorders.en_US
dc.description.sponsorshipBritish Heart Foundation, Grant/AwardNumber: FS/16/57/32733; King's HealthPartners; LUPUS UK; National Institute forHealth Research; Biomedical Research Centrebased at Guy's and St Thomas' NHSFoundation Trust and King's College Londonand the NIHR Clinical Research Facility;Wellcome Trust, Grant/Award Number:108874/B/15/Z; BD Biosciences ResearchProgram Award.en_US
dc.format.extent362 - 367-
dc.format.mediumPrint-Electronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherWiley on behalf of International Society for Advancement of Cytometryen_US
dc.rightsCopyright © 2023 The Authors. Cytometry Part A published by Wiley Periodicals LLC on behalf of International Society for Advancement of Cytometry. This is an open access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium,provided the original work is properly cited.-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectcell subpopulationsen_US
dc.subjectcell traffickingen_US
dc.subjecthelper T cellsen_US
dc.subjectinflammationen_US
dc.subjectregulatory T cellsen_US
dc.subjecttissue homingen_US
dc.titleOMIP-090: A 20-parameter flow cytometry panel for rapid analysis of cell diversity and homing capacity in human conventional and regulatory T cellsen_US
dc.typeArticleen_US
dc.date.dateAccepted2023-01-23-
dc.identifier.doihttps://doi.org/10.1002/cyto.a.24720-
dc.relation.isPartOfCytometry Part A-
pubs.issue5-
pubs.publication-statusPublished-
pubs.volume103-
dc.identifier.eissn1552-4930-
dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/legalcode.en-
dc.rights.holderThe Authors-
Appears in Collections:Dept of Life Sciences Research Papers

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