Bath Psoralen Plus UVA Therapy Suppresses Keratinocyte-Derived Chemokines in Pathogenetically Relevant Cells

Psoriasis is a chronic inflammatory proliferative skin disease involving various types of chemokines regulating immune cell migration, localization, and activation. Bath psoralen plus UVA (PUVA) treatment is an established phototherapy for psoriasis, but its effects on chemokine levels remain unknow...

Full description

Bibliographic Details
Main Authors: Yoshifumi Kanayama, Kan Torii, Kyoko Ikumi, Akimichi Morita
Format: Article
Language:English
Published: Elsevier 2021-09-01
Series:JID Innovations
Online Access:http://www.sciencedirect.com/science/article/pii/S2667026721000278
_version_ 1819121537550123008
author Yoshifumi Kanayama
Kan Torii
Kyoko Ikumi
Akimichi Morita
author_facet Yoshifumi Kanayama
Kan Torii
Kyoko Ikumi
Akimichi Morita
author_sort Yoshifumi Kanayama
collection DOAJ
description Psoriasis is a chronic inflammatory proliferative skin disease involving various types of chemokines regulating immune cell migration, localization, and activation. Bath psoralen plus UVA (PUVA) treatment is an established phototherapy for psoriasis, but its effects on chemokine levels remain unknown. We investigated the levels of 22 serum chemokines in 20 patients with psoriasis first treated with bath PUVA therapy between 2007 and 2011 in a single center and analyzed the associations between the chemokines and disease severity (PASI) before and after therapy to investigate the mechanisms of action of bath PUVA therapy. Before bath PUVA therapy, the PASI scores correlated with the serum levels of CCL17 (r = 0.581), CCL18 (r = 0.462), CCL19 (r = 0.477), and CXCL16 (r = 0.524). After bath PUVA, the serum levels of CCL17, CCL22, CXCL1, and CXCL9 were significantly decreased. Heatmap clustering and network analysis based on statistically significant Spearman correlations among the chemokines showed distinctive changes in the chemokine signature. Our findings revealed that the levels of several chemokines correlated with the disease state of psoriasis. Furthermore, bath PUVA therapy reduced the secretion of keratinocyte-derived chemokines that induce the migration of immune cells important for psoriasis pathogenesis, partly revealing the mechanism of the therapeutic activity.
first_indexed 2024-12-22T06:38:08Z
format Article
id doaj.art-0eb546174b194f61a50cb1f5295b0541
institution Directory Open Access Journal
issn 2667-0267
language English
last_indexed 2024-12-22T06:38:08Z
publishDate 2021-09-01
publisher Elsevier
record_format Article
series JID Innovations
spelling doaj.art-0eb546174b194f61a50cb1f5295b05412022-12-21T18:35:30ZengElsevierJID Innovations2667-02672021-09-0113100027Bath Psoralen Plus UVA Therapy Suppresses Keratinocyte-Derived Chemokines in Pathogenetically Relevant CellsYoshifumi Kanayama0Kan Torii1Kyoko Ikumi2Akimichi Morita3Department of Geriatric and Environmental Dermatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, JapanDepartment of Geriatric and Environmental Dermatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, JapanDepartment of Geriatric and Environmental Dermatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, JapanDepartment of Geriatric and Environmental Dermatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan; Correspondence: Akimichi Morita, Department of Geriatric and Environmental Dermatology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan.Psoriasis is a chronic inflammatory proliferative skin disease involving various types of chemokines regulating immune cell migration, localization, and activation. Bath psoralen plus UVA (PUVA) treatment is an established phototherapy for psoriasis, but its effects on chemokine levels remain unknown. We investigated the levels of 22 serum chemokines in 20 patients with psoriasis first treated with bath PUVA therapy between 2007 and 2011 in a single center and analyzed the associations between the chemokines and disease severity (PASI) before and after therapy to investigate the mechanisms of action of bath PUVA therapy. Before bath PUVA therapy, the PASI scores correlated with the serum levels of CCL17 (r = 0.581), CCL18 (r = 0.462), CCL19 (r = 0.477), and CXCL16 (r = 0.524). After bath PUVA, the serum levels of CCL17, CCL22, CXCL1, and CXCL9 were significantly decreased. Heatmap clustering and network analysis based on statistically significant Spearman correlations among the chemokines showed distinctive changes in the chemokine signature. Our findings revealed that the levels of several chemokines correlated with the disease state of psoriasis. Furthermore, bath PUVA therapy reduced the secretion of keratinocyte-derived chemokines that induce the migration of immune cells important for psoriasis pathogenesis, partly revealing the mechanism of the therapeutic activity.http://www.sciencedirect.com/science/article/pii/S2667026721000278
spellingShingle Yoshifumi Kanayama
Kan Torii
Kyoko Ikumi
Akimichi Morita
Bath Psoralen Plus UVA Therapy Suppresses Keratinocyte-Derived Chemokines in Pathogenetically Relevant Cells
JID Innovations
title Bath Psoralen Plus UVA Therapy Suppresses Keratinocyte-Derived Chemokines in Pathogenetically Relevant Cells
title_full Bath Psoralen Plus UVA Therapy Suppresses Keratinocyte-Derived Chemokines in Pathogenetically Relevant Cells
title_fullStr Bath Psoralen Plus UVA Therapy Suppresses Keratinocyte-Derived Chemokines in Pathogenetically Relevant Cells
title_full_unstemmed Bath Psoralen Plus UVA Therapy Suppresses Keratinocyte-Derived Chemokines in Pathogenetically Relevant Cells
title_short Bath Psoralen Plus UVA Therapy Suppresses Keratinocyte-Derived Chemokines in Pathogenetically Relevant Cells
title_sort bath psoralen plus uva therapy suppresses keratinocyte derived chemokines in pathogenetically relevant cells
url http://www.sciencedirect.com/science/article/pii/S2667026721000278
work_keys_str_mv AT yoshifumikanayama bathpsoralenplusuvatherapysuppresseskeratinocytederivedchemokinesinpathogeneticallyrelevantcells
AT kantorii bathpsoralenplusuvatherapysuppresseskeratinocytederivedchemokinesinpathogeneticallyrelevantcells
AT kyokoikumi bathpsoralenplusuvatherapysuppresseskeratinocytederivedchemokinesinpathogeneticallyrelevantcells
AT akimichimorita bathpsoralenplusuvatherapysuppresseskeratinocytederivedchemokinesinpathogeneticallyrelevantcells