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ABSTRACT: Aim
To clarify the role of Eomesodermin (EOMES) to serve as a disease-relevant biomarker and the intracellular molecules underlying the immunophenotype shifting of CD4+T subsets in amyotrophic lateral sclerosis (ALS).Methods
The derivation and validation cohorts included a total of 148 ALS patients and 101 healthy controls (HCs). Clinical data and peripheral blood were collected. T-cell subsets and the EOMES expression were quantified using multicolor flow cytometry. Serum neurofilament light chain (NFL) was measured. In 1-year longitudinal follow-ups, the ALSFRS-R scores and primary endpoint events were further recorded in the ALS patients of the validation cohort.Results
In the derivation cohort, the CD4+EOMES+T-cell subsets were s
SUBMITTER: Chen S
PROVIDER: S-EPMC11017423 | biostudies-literature | 2024 Apr
REPOSITORIES: biostudies-literature