Cargando…

Vitamin D increases programmed death receptor-1 expression in Crohn’s disease

Background: Vitamin D modulates inflammation in Crohns disease (CD). Programmed death (PD)-1 receptor contributes to the maintenance of immune tolerance. Vitamin D might modulate PD-1 signalling in CD. Aim: To investigate PD-1 expression on T cell subsets in CD patients treated with vitamin D or pla...

Descripción completa

Detalles Bibliográficos
Autores principales: Bendix, Mia, Greisen, Stinne, Dige, Anders, Hvas, Christian L., Bak, Nina, Jørgensen, Søren P., Dahlerup, Jens F., Deleuran, Bent, Agnholt, Jørgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421837/
https://www.ncbi.nlm.nih.gov/pubmed/28412753
http://dx.doi.org/10.18632/oncotarget.15489
_version_ 1783234660156833792
author Bendix, Mia
Greisen, Stinne
Dige, Anders
Hvas, Christian L.
Bak, Nina
Jørgensen, Søren P.
Dahlerup, Jens F.
Deleuran, Bent
Agnholt, Jørgen
author_facet Bendix, Mia
Greisen, Stinne
Dige, Anders
Hvas, Christian L.
Bak, Nina
Jørgensen, Søren P.
Dahlerup, Jens F.
Deleuran, Bent
Agnholt, Jørgen
author_sort Bendix, Mia
collection PubMed
description Background: Vitamin D modulates inflammation in Crohns disease (CD). Programmed death (PD)-1 receptor contributes to the maintenance of immune tolerance. Vitamin D might modulate PD-1 signalling in CD. Aim: To investigate PD-1 expression on T cell subsets in CD patients treated with vitamin D or placebo. Methods: We included 40 CD patients who received 1200 IU vitamin D3 for 26 weeks or placebo and eight healthy controls. Peripheral blood mononuclear cells (PBMCs) and plasma were isolated at baseline and week 26. The expressions of PD-1, PD-L1, and surface activation markers were analysed by flow cytometry. Soluble PD-1 plasma levels were measured by ELISA. Results: PD-1 expression upon T cell stimulation was increased in CD4(+)CD25(+int) T cells in vitamin D treated CD patients from 19% (range 10 39%) to 29% (11 79%)(p = 0.03) compared with placebo-treated patients. Vitamin D treatment, but not placebo, decreased the expression of the T cell activation marker CD69 from 42% (31 62%) to 33% (19 - 54%)(p = 0.01). Soluble PD-1 levels were not influenced by vitamin D treatment. Conclusions: Vitamin D treatment increases CD4(+)CD25(+int) T cells ability to up-regulate PD-1 in response to activation and reduces the CD69 expression in CD patients.
format Online
Article
Text
id pubmed-5421837
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-54218372017-05-10 Vitamin D increases programmed death receptor-1 expression in Crohn’s disease Bendix, Mia Greisen, Stinne Dige, Anders Hvas, Christian L. Bak, Nina Jørgensen, Søren P. Dahlerup, Jens F. Deleuran, Bent Agnholt, Jørgen Oncotarget Research Paper: Immunology Background: Vitamin D modulates inflammation in Crohns disease (CD). Programmed death (PD)-1 receptor contributes to the maintenance of immune tolerance. Vitamin D might modulate PD-1 signalling in CD. Aim: To investigate PD-1 expression on T cell subsets in CD patients treated with vitamin D or placebo. Methods: We included 40 CD patients who received 1200 IU vitamin D3 for 26 weeks or placebo and eight healthy controls. Peripheral blood mononuclear cells (PBMCs) and plasma were isolated at baseline and week 26. The expressions of PD-1, PD-L1, and surface activation markers were analysed by flow cytometry. Soluble PD-1 plasma levels were measured by ELISA. Results: PD-1 expression upon T cell stimulation was increased in CD4(+)CD25(+int) T cells in vitamin D treated CD patients from 19% (range 10 39%) to 29% (11 79%)(p = 0.03) compared with placebo-treated patients. Vitamin D treatment, but not placebo, decreased the expression of the T cell activation marker CD69 from 42% (31 62%) to 33% (19 - 54%)(p = 0.01). Soluble PD-1 levels were not influenced by vitamin D treatment. Conclusions: Vitamin D treatment increases CD4(+)CD25(+int) T cells ability to up-regulate PD-1 in response to activation and reduces the CD69 expression in CD patients. Impact Journals LLC 2017-02-18 /pmc/articles/PMC5421837/ /pubmed/28412753 http://dx.doi.org/10.18632/oncotarget.15489 Text en Copyright: © 2017 Bendix et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper: Immunology
Bendix, Mia
Greisen, Stinne
Dige, Anders
Hvas, Christian L.
Bak, Nina
Jørgensen, Søren P.
Dahlerup, Jens F.
Deleuran, Bent
Agnholt, Jørgen
Vitamin D increases programmed death receptor-1 expression in Crohn’s disease
title Vitamin D increases programmed death receptor-1 expression in Crohn’s disease
title_full Vitamin D increases programmed death receptor-1 expression in Crohn’s disease
title_fullStr Vitamin D increases programmed death receptor-1 expression in Crohn’s disease
title_full_unstemmed Vitamin D increases programmed death receptor-1 expression in Crohn’s disease
title_short Vitamin D increases programmed death receptor-1 expression in Crohn’s disease
title_sort vitamin d increases programmed death receptor-1 expression in crohn’s disease
topic Research Paper: Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421837/
https://www.ncbi.nlm.nih.gov/pubmed/28412753
http://dx.doi.org/10.18632/oncotarget.15489
work_keys_str_mv AT bendixmia vitamindincreasesprogrammeddeathreceptor1expressionincrohnsdisease
AT greisenstinne vitamindincreasesprogrammeddeathreceptor1expressionincrohnsdisease
AT digeanders vitamindincreasesprogrammeddeathreceptor1expressionincrohnsdisease
AT hvaschristianl vitamindincreasesprogrammeddeathreceptor1expressionincrohnsdisease
AT baknina vitamindincreasesprogrammeddeathreceptor1expressionincrohnsdisease
AT jørgensensørenp vitamindincreasesprogrammeddeathreceptor1expressionincrohnsdisease
AT dahlerupjensf vitamindincreasesprogrammeddeathreceptor1expressionincrohnsdisease
AT deleuranbent vitamindincreasesprogrammeddeathreceptor1expressionincrohnsdisease
AT agnholtjørgen vitamindincreasesprogrammeddeathreceptor1expressionincrohnsdisease