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Monitoring CD49d Receptor Occupancy: A Method to Optimize and Personalize Natalizumab Therapy in Multiple Sclerosis Patients.
Puñet-Ortiz, Joan; Hervás-García, José Vicente; Teniente-Serra, Aina; Cano-Orgaz, Antonio; Mansilla, Maria José; Quirant-Sánchez, Bibiana; Navarro-Barriuso, Juan; Fernández-Sanmartín, Marco A; Presas-Rodríguez, Silvia; Ramo-Tello, Cristina; Martínez-Cáceres, Eva María.
Afiliação
  • Puñet-Ortiz J; Division of Immunology, Germans Trias i Pujol University Hospital and Research Institute, Campus Can Ruti, Badalona, Spain.
  • Hervás-García JV; Department of Cellular Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, Spain.
  • Teniente-Serra A; Department of Neuroscience, Multiple Sclerosis Unit, University Hospital Germans Trias i Pujol, Badalona, Spain.
  • Cano-Orgaz A; Division of Immunology, Germans Trias i Pujol University Hospital and Research Institute, Campus Can Ruti, Badalona, Spain.
  • Mansilla MJ; Department of Cellular Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, Spain.
  • Quirant-Sánchez B; Neurology Service, Consorci Sanitari del Maresme, Mataró, Spain.
  • Navarro-Barriuso J; Division of Immunology, Germans Trias i Pujol University Hospital and Research Institute, Campus Can Ruti, Badalona, Spain.
  • Fernández-Sanmartín MA; Department of Cellular Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, Spain.
  • Presas-Rodríguez S; Division of Immunology, Germans Trias i Pujol University Hospital and Research Institute, Campus Can Ruti, Badalona, Spain.
  • Ramo-Tello C; Department of Cellular Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, Spain.
  • Martínez-Cáceres EM; Division of Immunology, Germans Trias i Pujol University Hospital and Research Institute, Campus Can Ruti, Badalona, Spain.
Cytometry B Clin Cytom ; 94(2): 327-333, 2018 03.
Article em En | MEDLINE | ID: mdl-28378895
ABSTRACT

BACKGROUND:

In natalizumab-treated relapsing-remitting MS (RRMS) patients, various extended interval dosing strategies are under evaluation to minimize severe treatment-associated side effects, mainly progressive multifocal leukoencephalopathy development. Up to now, it has not been presented any approach, even in form of assay design, to determine the optimal percentage of CD49d receptor occupancy (RO) associated with a favorable clinical, radiological, and immunological response.

METHODS:

A multiparametric quantitative flow cytometry method was settled to measure CD49d RO on peripheral blood lymphocytes. The analytical protocol was tested in a 6-month follow-up from 19 RRMS patients treated with the natalizumab standard dosing of every 4 weeks or an extended-interval dosing of every 6 weeks.

RESULTS:

Extended natalizumab dose schedule promoted an increase of CD49d molecules per cell surface and a reduction of CD49d RO levels. The reduction observed on CD49d RO was not only depending on dose schedule but also on individual parameters such as body mass. Interestingly, individual clinical outcome was apparently the same between the different dose schedules or even better with the extended interval dosing.

CONCLUSIONS:

Following up CD49d RO levels with a well-regulated monitoring work scheme is crucial to further identify over-/under-treated patients and to define a safe, personalized natalizumab regimen. © 2017 International Clinical Cytometry Society.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Integrina alfa4 / Anticorpos Monoclonais Humanizados / Natalizumab / Esclerose Múltipla Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Integrina alfa4 / Anticorpos Monoclonais Humanizados / Natalizumab / Esclerose Múltipla Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article