Gas6/TAM system as potential biomarker for multiple sclerosis prognosis.
Humans
Male
Female
Biomarkers
/ blood
Axl Receptor Tyrosine Kinase
Adult
Intercellular Signaling Peptides and Proteins
/ blood
Receptor Protein-Tyrosine Kinases
/ blood
c-Mer Tyrosine Kinase
Prognosis
Middle Aged
Multiple Sclerosis
/ diagnosis
Proto-Oncogene Proteins
/ blood
Prospective Studies
Severity of Illness Index
Gas6
TAM receptors
biomarker
inflammation
multiple sclerosis
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2024
2024
Historique:
received:
29
12
2023
accepted:
03
04
2024
medline:
15
5
2024
pubmed:
15
5
2024
entrez:
15
5
2024
Statut:
epublish
Résumé
The protein growth arrest-specific 6 (Gas6) and its tyrosine kinase receptors Tyro-3, Axl, and Mer (TAM) are ubiquitous proteins involved in regulating inflammation and apoptotic body clearance. Multiple sclerosis (MS) is the most common inflammatory demyelinating disease of the central nervous system leading to progressive and irreversible disability if not diagnosed and treated promptly. Gas6 and TAM receptors have been associated with neuronal remyelination and stimulation of oligodendrocyte survival. However, few data are available regarding clinical correlation in MS patients. We aimed to evaluate soluble levels of these molecules in the cerebrospinal fluid (CSF) and serum at MS diagnosis and correlate them with short-term disease severity. In a prospective cohort study, we enrolled 64 patients with a diagnosis of clinical isolated syndrome (CIS), radiological isolated syndrome (RIS) and relapsing-remitting (RR) MS according to the McDonald 2017 Criteria. Before any treatment initiation, we sampled the serum and CSF, and collected clinical data: disease course, presence of gadolinium-enhancing lesions, and expanded disability status score (EDSS). At the last clinical follow-up, we assessed EDSS and calculated MS severity score (MSSS) and age-related MS severity (ARMSS). Gas6 and TAM receptors were determined using an ELISA kit (R&D Systems) and compared to neurofilament (NFLs) levels evaluated with SimplePlex™ fluorescence-based immunoassay. At diagnosis, serum sAxl was higher in patients receiving none or low-efficacy disease-modifying treatments (DMTs) Our data suggest a protective role of Gas6 and its receptors in patients with MS and suitable severity disease biomarkers.
Identifiants
pubmed: 38745659
doi: 10.3389/fimmu.2024.1362960
pmc: PMC11091300
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1362960Informations de copyright
Copyright © 2024 D’Onghia, Colangelo, Bellan, Tonello, Puricelli, Virgilio, Apostolo, Minisini, Ferreira, Sozzi, Vincenzi, Cantello, Comi, Pirisi, Vecchio and Sainaghi.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.