Correlation of Peripheral Blood T Cell Subtypes with Clinical Disability Levels in Patients with Multiple Sclerosis
-
By
-
Penju Liu
-
Wei Liu
-
Xiaoting Zhang
-
Peng Yuan
-
July 20, 2026
Clinical Report: Correlation of Peripheral Blood T Cell Subtypes with Clinical Disability Levels in Patients with Multiple Sclerosis
Overview
This study investigates the relationship between peripheral blood T cell subsets and clinical disability in multiple sclerosis (MS) patients. A negative correlation was found between the CD4+/CD8+ ratio and Expanded Disability Status Scale (EDSS) scores.
Background
Multiple sclerosis (MS) is a chronic immune-mediated disorder that leads to significant disability. Understanding the relationship between immune cell profiles and clinical outcomes is crucial for improving disease management. This study aims to clarify the association between T cell subsets and disability levels in MS patients.
Data Highlights
| Parameter | Mean ± SD |
|---|---|
| Age | 35.1 ± 5.8 years |
| EDSS Score | 3.20 ± 1.50 |
| CD4+/CD8+ Ratio | 2.76 ± 1.08 |
Key Findings
- Mean EDSS score of the study cohort was 3.20 ± 1.50.
- Mean CD4+/CD8+ ratio was 2.76 ± 1.08.
- CD4+/CD8+ ratio correlated negatively with EDSS scores (r = −0.345, p = 0.016).
- Stratified analysis showed a progressive decline in CD4+/CD8+ ratio across disability groups (p = 0.050).
- In a covariate-adjusted model, the association between CD4+/CD8+ ratio and EDSS was attenuated (β = −0.350, p = 0.084).
- Exploratory analyses suggested that disease-modifying therapy (DMT) exposure may influence the association.
Clinical Implications
The findings indicate a negative association between the CD4+/CD8+ ratio and clinical disability in MS.
Conclusion
The study highlights a negative association between CD4+/CD8+ ratio and clinical disability in MS.
Related Resources & Content
- Acta Neuropathologica, 2017 -- Characterization of T Cell Phenotypes and Functions in White Matter Lesions of Patients with Multiple Sclerosis
- Brain, 2025 -- Expanded TCR repertoire targeting EBV in multiple sclerosis: implications for disease specificity and therapeutic strategies
- Frontiers in Immunology, 2026 -- Multiple sclerosis patients under treatment with interferon β1-a or ocrelizumab exhibit different T and B cell responses to SARS-CoV-2 vaccine
- NICE, 2026 -- Overview | Multiple sclerosis in adults: management
- AAN, 2024 -- Practice Guideline Recommendations: Disease-modifying Therapies for Adults with Multiple Sclerosis
- Frontiers in Immunology — Relative increase of memory B-cell subsets under s.c. B-cell-depleting therapies in multiple sclerosis
- Correlation Between Peripheral Blood Immune Cell Distribution and Disease Severity and Prognosis in Multiple Sclerosis Patients
- Baseline Expanded Disability Status Scale Score and CD8+ T Cell Levels as Risk Factors for Disability Progression in Multiple Sclerosis
- Overview | Multiple sclerosis in adults: management | Guidance | NICE
- Practice Guideline Recommendations: Disease-modifying Therapies for Adults with Multiple Sclerosis
- Ongoing Guidelines - ean.org
- Antigen specificity of clonally enriched CD8+ T cells in multiple sclerosis | Nature Immunology
- Ozanimod: A Review in Relapsing Forms of Multiple Sclerosis - PubMed
- The Comparative Effectiveness and Tolerability of Sphingosine-1-Phosphate Receptor Modulators in Patients With Multiple Sclerosis: A Network Meta-Analysis of Randomized Controlled Trials - PubMed
- In vivo Effects of Disease-modifying Therapies on Immunological Subsets in Patients with Relapsing-Remitting Multiple Sclerosis - PubMed
Based on findings from:
Association between peripheral blood T cell subsets and clinical disability in multiple sclerosis patients
Penju Liu, Wei Liu, Xiaoting Zhang, Peng Yuan. Frontiers In Neurology, 2026.
https://www.frontiersin.org/journals/neurology/articles/10.3389/fneur.2026.1843351/full
This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.