Affiliation:
1. “Peter Gorer” Department of Immunobiology, School of Immunology & Microbiological Sciences King's College London London UK
2. British Heart Foundation Centre, School of Cardiovascular Medicine and Sciences King's College London London UK
Abstract
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.
Funder
British Heart Foundation
King's Health Partners
LUPUS UK
National Institute for Health and Care Research
Wellcome Trust
Subject
Cell Biology,Histology,Pathology and Forensic Medicine
Cited by
5 articles.
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