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Immunometabolic profiling of patients with multiple sclerosis identifies new biomarkers to predict disease activity during treatment with interferon beta-1a

Authors :
Roberta Lanzillo
Marcello Moccia
Francesco Saccà
Mario Quarantelli
Fortunata Carbone
Carla De Luca Picione
Alessandra Colamatteo
Dario Bruzzese
Antonio Carotenuto
Teresa Micillo
Veronica De Rosa
Vincenzo Brescia Morra
Anna De Rosa
Giuseppe Matarese
Lanzillo, Roberta
Carbone, Fortunata
Quarantelli, Mario
Bruzzese, Dario
Carotenuto, Antonio
DE ROSA, Veronica
Colamatteo, Alessandra
Micillo, Teresa
De Luca Picione, Carla
Sacca', Francesco
DE ROSA, Anna
Moccia, Marcello
Morra, Vincenzo Brescia
Matarese, Giuseppe
Source :
Clinical immunology (Orlando, Fla., Print) 183 (2017): 249–253. doi:10.1016/j.clim.2017.08.011, info:cnr-pdr/source/autori:Lanzillo R.; Carbone F.; Quarantelli M.; Bruzzese D.; Carotenuto A.; De Rosa V.; Colamatteo A.; Micillo T.; De Luca Picione C.; Sacca F.; De Rosa A.; Moccia M.; Brescia Morra V.; Matarese G./titolo:Immunometabolic profiling of patients with multiple sclerosis identifies new biomarkers to predict disease activity during treatment with interferon beta-1a/doi:10.1016%2Fj.clim.2017.08.011/rivista:Clinical immunology (Orlando, Fla., Print)/anno:2017/pagina_da:249/pagina_a:253/intervallo_pagine:249–253/volume:183
Publication Year :
2017
Publisher :
Elsevier, Amsterdam , Paesi Bassi, 2017.

Abstract

Reliable immunologic biomarkers able to monitor disease course during multiple sclerosis (MS) are still missing. We aimed at identifying possible immunometabolic biomarkers able to predict the clinical outcome in MS patients during treatment with interferon (IFN)-beta-1a. We measured in 45 relapsing-remitting (RR) MS patients, blood circulating levels of several immunometabolic markers, at enrolment, and correlated their levels to disease activity and progression over time. Higher levels of interleukin (IL)-6, soluble-CD40-ligand (sCD40L) and leptin at baseline associated with a higher relapse rate and a greater risk of experiencing at least one relapse in the following year. Higher values of soluble tumor necrosis factor receptor (sTNF-R) and leptin at baseline were predictive of a higher number of lesions in the following one-year of follow up. In conclusion, our data suggest that an immunometabolic profiling measuring IL-6, sCD40L, leptin and sTNF-R at baseline, could represent a useful tool to predict disease course in RRMS patients during treatment with IFN-beta-1a.

Details

Language :
English
Database :
OpenAIRE
Journal :
Clinical immunology (Orlando, Fla., Print) 183 (2017): 249–253. doi:10.1016/j.clim.2017.08.011, info:cnr-pdr/source/autori:Lanzillo R.; Carbone F.; Quarantelli M.; Bruzzese D.; Carotenuto A.; De Rosa V.; Colamatteo A.; Micillo T.; De Luca Picione C.; Sacca F.; De Rosa A.; Moccia M.; Brescia Morra V.; Matarese G./titolo:Immunometabolic profiling of patients with multiple sclerosis identifies new biomarkers to predict disease activity during treatment with interferon beta-1a/doi:10.1016%2Fj.clim.2017.08.011/rivista:Clinical immunology (Orlando, Fla., Print)/anno:2017/pagina_da:249/pagina_a:253/intervallo_pagine:249–253/volume:183
Accession number :
edsair.doi.dedup.....328da3eff9716fd5abcefa635c1253ed
Full Text :
https://doi.org/10.1016/j.clim.2017.08.011