L-selectin and skin damage in systemic sclerosis.

<h4>Background</h4>L-selectin ligands are induced on the endothelium of inflammatory sites. L-selectin expression on neutrophils and monocytes may mediate the primary adhesion of these cells at sites of inflammation by mediating the leukocyte-leukocyte interactions that facilitate their...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: James V Dunne, Stephan F van Eeden, Kevin J Keen
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2012
Materias:
R
Q
Acceso en línea:https://doaj.org/article/25bb559a89654f6689e61986cd39892d
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:25bb559a89654f6689e61986cd39892d
record_format dspace
spelling oai:doaj.org-article:25bb559a89654f6689e61986cd39892d2021-11-18T07:05:42ZL-selectin and skin damage in systemic sclerosis.1932-620310.1371/journal.pone.0044814https://doaj.org/article/25bb559a89654f6689e61986cd39892d2012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23028631/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>L-selectin ligands are induced on the endothelium of inflammatory sites. L-selectin expression on neutrophils and monocytes may mediate the primary adhesion of these cells at sites of inflammation by mediating the leukocyte-leukocyte interactions that facilitate their recruitment. L-selectin retains functional activity in its soluble form. Levels of soluble L-selectin have been reported as both elevated and lowered in patients with systemic sclerosis (SSc). This preliminary study seeks to discern amongst these disparate results and to discover whether there is an association between L-selectin concentrations in plasma and skin damage in SSc patients.<h4>Methodology and principal findings</h4>Nineteen cases with limited systemic sclerosis (lSSc) and 11 cases with diffuse systemic sclerosis (dSSc) were compared on a pairwise basis to age- and sex-matched controls. Criteria of the American College of Rheumatology were used to diagnose SSc. Skin involvement was assessed using the modified Rodnan skin score (mRSS). We find no association between mRSS and plasma L-selectin concentration in lSSc cases (p = 0.9944) but a statistically significant negative correlation in dSSc cases (R(2) = 73.11 per cent, p = 0.0008). The interpretation of the slope for dSSc cases is that for each increase of 100 ng/ml in soluble L-selectin concentration, the mRSS drops 4.22 (95 per cent CI: 2.29, 6.16). There was also a highly statistically significant negative correlation between sL-selectin and disease activity (p = 0.0007) and severity (p = 0.0007) in dSSc cases but not in lSSc cases (p = 0.2596, p = 0.7575, respectively).<h4>Conclusions and significance</h4>No effective treatments exist for skin damage in SSc patients. Nor is there a laboratory alternative to the modified Rodnan skin score as is the case for other organs within the body. Modulation of circulating L-selectin is a promising target for reducing skin damage in dSSc patients. Plasma levels of soluble L-selectin could serve as an outcome measure for dSSc patients in clinical trials.James V DunneStephan F van EedenKevin J KeenPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 9, p e44814 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
James V Dunne
Stephan F van Eeden
Kevin J Keen
L-selectin and skin damage in systemic sclerosis.
description <h4>Background</h4>L-selectin ligands are induced on the endothelium of inflammatory sites. L-selectin expression on neutrophils and monocytes may mediate the primary adhesion of these cells at sites of inflammation by mediating the leukocyte-leukocyte interactions that facilitate their recruitment. L-selectin retains functional activity in its soluble form. Levels of soluble L-selectin have been reported as both elevated and lowered in patients with systemic sclerosis (SSc). This preliminary study seeks to discern amongst these disparate results and to discover whether there is an association between L-selectin concentrations in plasma and skin damage in SSc patients.<h4>Methodology and principal findings</h4>Nineteen cases with limited systemic sclerosis (lSSc) and 11 cases with diffuse systemic sclerosis (dSSc) were compared on a pairwise basis to age- and sex-matched controls. Criteria of the American College of Rheumatology were used to diagnose SSc. Skin involvement was assessed using the modified Rodnan skin score (mRSS). We find no association between mRSS and plasma L-selectin concentration in lSSc cases (p = 0.9944) but a statistically significant negative correlation in dSSc cases (R(2) = 73.11 per cent, p = 0.0008). The interpretation of the slope for dSSc cases is that for each increase of 100 ng/ml in soluble L-selectin concentration, the mRSS drops 4.22 (95 per cent CI: 2.29, 6.16). There was also a highly statistically significant negative correlation between sL-selectin and disease activity (p = 0.0007) and severity (p = 0.0007) in dSSc cases but not in lSSc cases (p = 0.2596, p = 0.7575, respectively).<h4>Conclusions and significance</h4>No effective treatments exist for skin damage in SSc patients. Nor is there a laboratory alternative to the modified Rodnan skin score as is the case for other organs within the body. Modulation of circulating L-selectin is a promising target for reducing skin damage in dSSc patients. Plasma levels of soluble L-selectin could serve as an outcome measure for dSSc patients in clinical trials.
format article
author James V Dunne
Stephan F van Eeden
Kevin J Keen
author_facet James V Dunne
Stephan F van Eeden
Kevin J Keen
author_sort James V Dunne
title L-selectin and skin damage in systemic sclerosis.
title_short L-selectin and skin damage in systemic sclerosis.
title_full L-selectin and skin damage in systemic sclerosis.
title_fullStr L-selectin and skin damage in systemic sclerosis.
title_full_unstemmed L-selectin and skin damage in systemic sclerosis.
title_sort l-selectin and skin damage in systemic sclerosis.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/25bb559a89654f6689e61986cd39892d
work_keys_str_mv AT jamesvdunne lselectinandskindamageinsystemicsclerosis
AT stephanfvaneeden lselectinandskindamageinsystemicsclerosis
AT kevinjkeen lselectinandskindamageinsystemicsclerosis
_version_ 1718423903557124096