Assessing Blood-Based Biomarkers to Define a Therapeutic Window for Natalizumab

Natalizumab is a monoclonal antibody that binds CD49d. Although it is one of the most effective treatments for Relapsing-Remitting Multiple Sclerosis (RRMS), a dosing regimen has not been optimized for safety and efficacy in individual patients. We aimed to identify biomarkers to monitor Natalizumab...

ver descrição completa

Detalhes bibliográficos
Autores: Granell-Geli, Júlia|||0000-0002-3369-9765, Izquierdo, Cristina, Sellés-Rius, Ares|||0000-0002-9745-7749, Teniente Serra, Aina|||0000-0003-3440-804X, Presas Rodríguez, Sílvia|||0000-0001-8545-2476, Mansilla Lopez, Maria Jose|||0000-0002-5044-6313, Brieva Ruiz, Luis|||0000-0002-5871-6189, Sotoca Fernández, Javier|||0000-0003-3400-1434, Mañé-Martínez, María Alba, Moral, Ester, Bragado, Irene, Goelz, Susan, Martínez Cáceres, Eva María|||0000-0002-6762-8025, Ramo-Tello, Cristina|||0000-0001-8643-5053
Formato: artículo
Fecha de publicación:2021
País:España
Recursos:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:282871
Acesso em linha:https://ddd.uab.cat/record/282871
https://dx.doi.org/urn:doi:10.3390/jpm11121347
Access Level:acceso abierto
Palavra-chave:Biomarker
CD49d
Extended interval dose
Immunomonitoring
Multiple sclerosis
Natalizumab
Personalized dose
SVCAM-1
Descrição
Resumo:Natalizumab is a monoclonal antibody that binds CD49d. Although it is one of the most effective treatments for Relapsing-Remitting Multiple Sclerosis (RRMS), a dosing regimen has not been optimized for safety and efficacy in individual patients. We aimed to identify biomarkers to monitor Natalizumab treatment and to establish a personalized dose utilizing an ongoing longitudinal study in 29 RRMS patients under Natalizumab with standard interval dose (SD) of 300 mg/4 wks or extended interval dose (EID) of 300 mg/6 wks. Blood samples were analyzed by flow cytometry to determine CD49d saturation and expression in several T and B lymphocytes subpopulations. Each patient was analyzed at two different timepoints separated by 3 Natalizumab administrations. Natalizumab and sVCAM-1 levels in serum were also analyzed using ELISA. To determine the reproducibility of various markers, two different timepoints were compared and no significant differences were observed for CD49d expression nor for saturation; SD patients had higher saturation levels (~80%) than EID patients (~60%). A positive correlation exists between CD49d saturation and Natalizumab serum levels. CD49d expression and saturation are stable parameters that could be used as biomarkers in the immunomonitoring of Natalizumab treatment. Moreover, Natalizumab and sVCAM-1 serum levels could be used to optimize an individual's dosing schedule.