MAP7 and MUCL1 are biomarkers of Vitamin D3-induced tolerogenic dendritic cells in multiple sclerosis patients

The administration of autologous tolerogenic dendritic cells (tolDC) has become a promising alternative for the treatment of autoimmune diseases, such as multiple sclerosis (MS). Specifically, the use of vitamin D3 for the generation of tolDC (vitD3-tolDC) constitutes one of the most widely studied...

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Detalhes bibliográficos
Autores: Navarro-Barriuso, Juan|||0000-0003-2884-4961, Mansilla Lopez, Maria Jose|||0000-0002-5044-6313, Quirant, Bibiana|||0000-0002-3875-8074, Ardiaca-Martínez, Alicia, Teniente Serra, Aina|||0000-0003-3440-804X, Presas Rodríguez, Sílvia|||0000-0001-8545-2476, Ten Brinke, Anja, Ramo-Tello, Cristina|||0000-0001-8643-5053, Martínez Cáceres, Eva María|||0000-0002-6762-8025
Formato: artículo
Fecha de publicación:2019
País:España
Recursos:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:224181
Acesso em linha:https://ddd.uab.cat/record/224181
https://dx.doi.org/urn:doi:10.3389/fimmu.2019.01251
Access Level:acceso abierto
Palavra-chave:Tolerogenic dendritic cells
Multiple sclerosis
Biomarkers
Vitamin D3
Immune tolerance
Descrição
Resumo:The administration of autologous tolerogenic dendritic cells (tolDC) has become a promising alternative for the treatment of autoimmune diseases, such as multiple sclerosis (MS). Specifically, the use of vitamin D3 for the generation of tolDC (vitD3-tolDC) constitutes one of the most widely studied approaches, as it has evidenced significant immune regulatory properties, both in vitro and in vivo. In this article, we generated human vitD3-tolDC from monocytes from healthy donors and MS patients, characterized in both cases by a semi-mature phenotype, secretion of IL-10 and inhibition of allogeneic lymphocyte proliferation. Additionally, we studied their transcriptomic profile and selected a number of differentially expressed genes compared to control mature and immature dendritic cells for their analysis. Among them, qPCR results validated CYP24A1, MAP7 and MUCL1 genes as biomarkers of vitD3-tolDC in both healthy donors and MS patients. Furthermore, we constructed a network of protein interactions based on the literature, which manifested that MAP7 and MUCL1 genes are both closely connected between them and involved in immune-related functions. In conclusion, this study evidences that MAP7 and MUCL1 constitute robust and potentially functional biomarkers of the generation of vitD3-tolDC, opening the window for their use as quality controls in clinical trials for MS.