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The ratio of circulating CD56 dim NK cells to follicular T helper cells as a promising predictor for disease activity of relapsing-remitting multiple sclerosis.

Authors :
Ding J
Yan X
Zhao C
Zhao D
Jia Y
Ren K
Wang Y
Lu J
Sun T
Zhao S
Li H
Guo J
Source :
Heliyon [Heliyon] 2024 May 18; Vol. 10 (10), pp. e31533. Date of Electronic Publication: 2024 May 18 (Print Publication: 2024).
Publication Year :
2024

Abstract

Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system primarily mediated by CD4 <superscript>+</superscript> T helper cells. This study investigated the dynamic changes of natural killer (NK) cells and follicular T helper (Tfh) cells and their associations in relapsing-remitting MS patients. The findings revealed inverse relationships between NK cells and CD4 <superscript>+</superscript> T cells or Tfh cells. Specifically, CD56 <superscript>dim</superscript> NK cells, not CD56 <superscript>bright</superscript> NK cells, were negatively correlated with CD4 <superscript>+</superscript> T cells and Tfh cells. However, no significant correlations were found between NK cells and sNfL levels or EDSS scores. The ratio of CD56 <superscript>dim</superscript> NK cells to circulating Tfh (cTfh) cells demonstrated superior discriminatory ability in distinguishing relapsing MS patients from healthy controls (HCs) and remitting patients, as determined by receiver operating characteristic (ROC) analysis. Following treatment with immunosuppressants or disease-modifying therapies (DMTs), a significant increase in the CD56 <superscript>dim</superscript> NK/cTfh ratio was observed. These findings suggest that the CD56 <superscript>dim</superscript> NK/cTfh ratio holds promise as a prognostic indicator for clinical relapse and treatment response in MS.<br />Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (© 2024 The Authors.)

Details

Language :
English
ISSN :
2405-8440
Volume :
10
Issue :
10
Database :
MEDLINE
Journal :
Heliyon
Publication Type :
Academic Journal
Accession number :
38803865
Full Text :
https://doi.org/10.1016/j.heliyon.2024.e31533