"Peter Gorer" Department of Immunobiology, School of Immunology & Microbiological Sciences, King's College London, London, UK.
British Heart Foundation Centre, School of Cardiovascular Medicine and Sciences, King's College London, London, UK.
Cytometry A. 2023 May;103(5):362-367. doi: 10.1002/cyto.a.24720. Epub 2023 Feb 5.
The 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.
该面板是为监测人类 CD4 常规和调节性 T 细胞亚群归巢能力和功能多样性的变化而开发和优化的。该分析仅基于新鲜分离的外周血单核细胞(PBMC)表面标志物的表达,以最大程度地减少由于通透化或冻融过程引起的任何变化。我们包括了基于 CD45RA、CCR7、CD25、CD28 和 CD95 在常规和调节性 T 细胞中的表达来评估幼稚和记忆群体分布的标记物。使用 CCR4、CCR6、CCR10、CXCR3 和 CXCR5 对主要功能亚群进行鉴定。最后,使用 CLA、CCR3、CCR5 和整合素 β7 评估这些亚群对皮肤、气道、肠道和炎症病变的归巢能力。该面板已在健康供体和过敏性鼻炎或自身免疫性疾病患者的新鲜分离 PBMC 上进行了测试。