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Updated: Feb 7, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Increased CCL18 plasma levels are associated with neurodegenerative MRI outcomes in multiple sclerosis patients
Nicole Ziliotto1, Francesco Bernardi2, Dejan Jakimovski3
1Department of Life Sciences and Biotechnology, University of Ferrara, Italy; Buffalo Neuroimaging Analysis Center, Department of Neurology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, NY, USA.
Background:
Chemokine ligands and co-stimulatory factors are involved in macrophage activation and differentiation processes that could contribute to multiple sclerosis (MS) pathogenesis.
Objective:
To investigate associations of C-C motif Ligand 18 (CCL18), C-C motif ligand 5 (CCL5) and soluble Cluster of Differentiation 86 (sCD86) with clinical and MRI measures in MS patients.
Methods:
Plasma levels of CCL18, CCL5 and sCD86 were evaluated in 138 MS patients (85 relapsing-remitting, RR-MS; 53 progressive, P-MS), and in 42 age- and sex-matched healthy individuals (HI). All subjects underwent standardized 3T MRI and clinical examinations. Multiple regression analysis of MRI outcomes as dependent variables was performed with age, gender, having P-MS, and plasma proteins as predictor variables.
Results:
Higher CCL18 plasma levels were found in P-MS (median = 51.5, IQR = 41.0-63.6 ng/mL) compared to RR-MS (median = 43.0, IQR = 29.1-55.0 ng/mL, p = 0.014) and to HI (median = 41.3, IQR = 30.9-54.1 ng/mL, p = 0.009). Disease-modifying treatments altered CCL5 (p = 0.036) and sCD86 (p < 0.001) levels. Higher CCL18 levels were associated with increased lateral ventricular volume (p = 0.006) and T2 lesion volume (LV) (p = 0.034), and decreased grey matter (p = 0.006), thalamic (p = 0.007) and cortical (p = 0.01) volumes.
Conclusions:
Our results provide evidence that higher CCL18 plasma levels are associated with more severe inflammatory and neurodegenerative brain MRI outcomes in MS.
Insights
Higher levels of chemokine ligand 18 (CCL18) in the blood are linked to increased inflammation and brain damage in multiple sclerosis (MS) patients. This finding may help identify disease severity and progression in MS.
Area of Science:
- Neuroimmunology
- Biomarker Discovery
Background:
- Macrophage activation and differentiation are implicated in multiple sclerosis (MS) pathogenesis.
- Chemokine ligands and co-stimulatory factors play a role in these processes.
Purpose of the Study:
- To investigate associations between C-C motif Ligand 18 (CCL18), C-C motif ligand 5 (CCL5), and soluble Cluster of Differentiation 86 (sCD86) with clinical and MRI measures in MS patients.
Main Methods:
- Evaluated plasma levels of CCL18, CCL5, and sCD86 in 138 MS patients and 42 healthy individuals.
- Utilized standardized 3T MRI and clinical examinations for all subjects.
- Performed multiple regression analysis with MRI outcomes as dependent variables.
Main Results:
- Higher CCL18 plasma levels were observed in progressive MS (P-MS) compared to relapsing-remitting MS (RR-MS) and healthy individuals.
- Disease-modifying treatments affected CCL5 and sCD86 levels.
- Elevated CCL18 levels correlated with increased lateral ventricular and T2 lesion volumes, and decreased grey matter, thalamic, and cortical volumes.
Conclusions:
- Higher CCL18 plasma levels are associated with more severe inflammatory and neurodegenerative brain MRI outcomes in MS.
- CCL18 may serve as a potential biomarker for disease severity and progression in multiple sclerosis.
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