Natalizumab treatment modulates Peroxisome Proliferator-Activated Receptors expression in women with multiple sclerosis

Peroxisome Proliferator-Activated Receptors (PPAR) are transcription factors suggested to be involved in inflammatory lesions of autoimmune encephalomyelitis and multiple sclerosis (MS). Our objective was to assess whether Natalizumab (NTZ) therapy is associated with alterations of PPAR expression i...

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Bibliographic Details
Main Author: Ferret-Sena, Véronique (author)
Other Authors: Silva, Alexandra Maia e (author), Sena, Armando (author), Cavaleiro, Inês (author), Vale, José (author), Derudas, Bruno (author), Chinetti-Gbaguidi, Giulia (author), Staels, Bart (author)
Format: article
Language:eng
Published: 2017
Subjects:
Online Access:http://hdl.handle.net/10400.26/19449
Country:Portugal
Oai:oai:comum.rcaap.pt:10400.26/19449
Description
Summary:Peroxisome Proliferator-Activated Receptors (PPAR) are transcription factors suggested to be involved in inflammatory lesions of autoimmune encephalomyelitis and multiple sclerosis (MS). Our objective was to assess whether Natalizumab (NTZ) therapy is associated with alterations of PPAR expression in MS patients. We analyzed gene expression of PPAR in peripheral blood mononuclear cells (PBMC) as well as blood inflammatory markers in women with MS previously medicated with first-line immunomodulators (baseline) and after NTZ therapy. No differences in PPAR, PPAR/, PPAR, and CD36 mRNA expression were found in PBMC between patients under baseline and healthy controls. At three months, NTZ increased PPAR/ mRNA ( = 0.009) in comparison to baseline, while mRNA expression of PPAR and CD36 (a well-known PPAR target gene) was lower in comparison to healthy controls ( = 0.026 and = 0.028, resp.). Although these trends of alterations remain after six months of therapy, the results were not statistically significant. Osteopontin levels were elevated in patients ( = 0.002) and did not change during the follow-up period of NTZ