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Monitoring CD49d Receptor Occupancy: A Method to Optimize and Personalize Natalizumab Therapy in Multiple Sclerosis Patients
Author(s) -
PuñetOrtiz Joan,
HervásGarcía José Vicente,
TenienteSerra Aina,
CanoOrgaz Antonio,
Mansilla Maria José,
QuirantSánchez Bibiana,
NavarroBarriuso Juan,
FernándezSanmartín Marco A.,
PresasRodríguez Silvia,
RamoTello Cristina,
MartínezCáceres Eva María
Publication year - 2018
Publication title -
cytometry part b: clinical cytometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.646
H-Index - 61
eISSN - 1552-4957
pISSN - 1552-4949
DOI - 10.1002/cyto.b.21527
Subject(s) - natalizumab , dosing , medicine , multiple sclerosis , progressive multifocal leukoencephalopathy , flow cytometry , oncology , immunology
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