CCR4+ Skin-Tropic Phenotype as a Feature of Central Memory CD8+ T Cells in Healthy Subjects and Psoriasis Patients

The chemokine receptor CCR4 has emerged as a skin-homing molecule important for the migration of T cells from the blood to the dermis. From our previous data on psoriasis patients, CCR4 memory T cells emerged as a putative recirculating population between skin and blood. Here we focused our attentio...

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Published inFrontiers in immunology Vol. 11; p. 529
Main Authors Casciano, Fabio, Diani, Marco, Altomare, Andrea, Granucci, Francesca, Secchiero, Paola, Banfi, Giuseppe, Reali, Eva
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 03.04.2020
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Summary:The chemokine receptor CCR4 has emerged as a skin-homing molecule important for the migration of T cells from the blood to the dermis. From our previous data on psoriasis patients, CCR4 memory T cells emerged as a putative recirculating population between skin and blood. Here we focused our attention on the expression of CCR4 and skin-tropic molecules in the different stages of memory T cell differentiation. We analyzed the chemokine receptor profile in CD8 and CD4 CD45RA CCR7 (T ) and CD45RA CCR7 (T ) cells. Subpopulations were further divided on the basis of CD62L expression, and the distribution among the subsets of the skin-homing molecule CLA (Cutaneous Lymphocyte Antigen) was evaluated. The characterization was performed on peripheral blood mononuclear cells isolated from 21 healthy subjects and 24 psoriasis patients. The results indicate that (i) the skin-homing CCR4 marker is mainly expressed in T cells, (ii) CCR4 T cells also express high level of CLA and that (iii) the more differentiated phenotype T expresses CXCR3 and CCR5 but lower level of CCR4 and CLA. This indicates that progressive stages of memory T cell differentiation have profoundly different chemokine receptor patterns, with CD8 T displaying a marked skin-tropic phenotype CLA CCR4 . Differential skin-tropic phenotype between T and T cells was observed in both healthy subjects and psoriasis patients. However, patients showed an expanded circulating population of CD8 T cells with phenotype CCR4 CXCR3 that could play a role in the pathophysiology of psoriasis and possibly in disease recurrence.
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Reviewed by: Michio Tomura, Osaka Ohtani University, Japan; James Edward Pease, Imperial College London, United Kingdom
Edited by: Carlo Riccardi, University of Perugia, Italy
This article was submitted to Autoimmune and Autoinflammatory Disorders, a section of the journal Frontiers in Immunology
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2020.00529