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Prognostic value of natural killer cell/T cell ratios for disease activity in multiple sclerosis
BACKGROUND AND PURPOSE: Natural killer (NK) cells may play a role in multiple sclerosis (MS). Ratios of NK cells to CD4(+) T cells have been proposed as a biomarker for the therapeutic effect of stem cell transplantation in MS. The objectives here were to explore the relevance of this ratio in MS pa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898592/ https://www.ncbi.nlm.nih.gov/pubmed/33326677 http://dx.doi.org/10.1111/ene.14680 |
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author | Mimpen, Max Muris, Anne‐Hilde Rolf, Linda Gerlach, Oliver Kuhle, Jens Hupperts, Raymond Smolders, Joost Damoiseaux, Jan |
author_facet | Mimpen, Max Muris, Anne‐Hilde Rolf, Linda Gerlach, Oliver Kuhle, Jens Hupperts, Raymond Smolders, Joost Damoiseaux, Jan |
author_sort | Mimpen, Max |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Natural killer (NK) cells may play a role in multiple sclerosis (MS). Ratios of NK cells to CD4(+) T cells have been proposed as a biomarker for the therapeutic effect of stem cell transplantation in MS. The objectives here were to explore the relevance of this ratio in MS patients by analysing NK and T cell subsets, as well as their prognostic value for disease activity. METHODS: Baseline peripheral blood mononuclear cells of 50 relapsing–remitting MS patients, participating in our vitamin D supplementation study (SOLARIUM), were analysed with flow cytometry. Disease activity was measured as new magnetic resonance imaging lesions, relapses and mean plasma neurofilament light chain levels after 48 weeks of follow‐up. RESULTS: The proportion of NK cells correlated negatively with CD4(+) T cells (R = −0.335, p = 0.001) and interleukin 17A (IL‐17A(+)) CD4(+) T cells (R = −0.203, p = 0.043). Participants with magnetic resonance imaging activity or relapses displayed lower NK/IL‐17A(+ )CD4(+) T cell ratios (p =0.025 and p = 0.006, respectively). The NK/IL‐17A(+ )CD4(+) T cell ratio correlated negatively with neurofilament light chain levels (R = −0.320, p = 0.050). Vitamin D supplementation did not affect these ratios. CONCLUSIONS: Our data suggest a protective role of an expanded NK cell compartment compared to the CD4(+) T cell subset fractions in relapsing–remitting MS patients. NK/CD4(+) T cell ratios may be a prognostic biomarker for disease activity in MS. |
format | Online Article Text |
id | pubmed-7898592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78985922021-03-03 Prognostic value of natural killer cell/T cell ratios for disease activity in multiple sclerosis Mimpen, Max Muris, Anne‐Hilde Rolf, Linda Gerlach, Oliver Kuhle, Jens Hupperts, Raymond Smolders, Joost Damoiseaux, Jan Eur J Neurol Multiple Sclerosis BACKGROUND AND PURPOSE: Natural killer (NK) cells may play a role in multiple sclerosis (MS). Ratios of NK cells to CD4(+) T cells have been proposed as a biomarker for the therapeutic effect of stem cell transplantation in MS. The objectives here were to explore the relevance of this ratio in MS patients by analysing NK and T cell subsets, as well as their prognostic value for disease activity. METHODS: Baseline peripheral blood mononuclear cells of 50 relapsing–remitting MS patients, participating in our vitamin D supplementation study (SOLARIUM), were analysed with flow cytometry. Disease activity was measured as new magnetic resonance imaging lesions, relapses and mean plasma neurofilament light chain levels after 48 weeks of follow‐up. RESULTS: The proportion of NK cells correlated negatively with CD4(+) T cells (R = −0.335, p = 0.001) and interleukin 17A (IL‐17A(+)) CD4(+) T cells (R = −0.203, p = 0.043). Participants with magnetic resonance imaging activity or relapses displayed lower NK/IL‐17A(+ )CD4(+) T cell ratios (p =0.025 and p = 0.006, respectively). The NK/IL‐17A(+ )CD4(+) T cell ratio correlated negatively with neurofilament light chain levels (R = −0.320, p = 0.050). Vitamin D supplementation did not affect these ratios. CONCLUSIONS: Our data suggest a protective role of an expanded NK cell compartment compared to the CD4(+) T cell subset fractions in relapsing–remitting MS patients. NK/CD4(+) T cell ratios may be a prognostic biomarker for disease activity in MS. John Wiley and Sons Inc. 2020-12-30 2021-03 /pmc/articles/PMC7898592/ /pubmed/33326677 http://dx.doi.org/10.1111/ene.14680 Text en © 2020 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Multiple Sclerosis Mimpen, Max Muris, Anne‐Hilde Rolf, Linda Gerlach, Oliver Kuhle, Jens Hupperts, Raymond Smolders, Joost Damoiseaux, Jan Prognostic value of natural killer cell/T cell ratios for disease activity in multiple sclerosis |
title | Prognostic value of natural killer cell/T cell ratios for disease activity in multiple sclerosis |
title_full | Prognostic value of natural killer cell/T cell ratios for disease activity in multiple sclerosis |
title_fullStr | Prognostic value of natural killer cell/T cell ratios for disease activity in multiple sclerosis |
title_full_unstemmed | Prognostic value of natural killer cell/T cell ratios for disease activity in multiple sclerosis |
title_short | Prognostic value of natural killer cell/T cell ratios for disease activity in multiple sclerosis |
title_sort | prognostic value of natural killer cell/t cell ratios for disease activity in multiple sclerosis |
topic | Multiple Sclerosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898592/ https://www.ncbi.nlm.nih.gov/pubmed/33326677 http://dx.doi.org/10.1111/ene.14680 |
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