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.
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 CD49dRO 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 CD49dRO levels. The reduction observed on CD49dRO 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 CD49dRO 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.
Authors: Maria A Zingaropoli; Marco Iannetta; Simona Pontecorvo; Elena Anzivino; Carla Prezioso; Donatella Maria Rodio; Manuela Morreale; Alessandra D'Abramo; Alessandra Oliva; Miriam Lichtner; Antonio Cortese; Marco Frontoni; Valeria Pietropaolo; Ada Francia; Claudio M Mastroianni; Vincenzo Vullo; Maria R Ciardi Journal: Biomed Res Int Date: 2018-02-27 Impact factor: 3.411
Authors: Lisa Lohmann; Claudia Janoschka; Andreas Schulte-Mecklenbeck; Svenja Klinsing; Lucienne Kirstein; Uta Hanning; Timo Wirth; Tilman Schneider-Hohendorf; Nicholas Schwab; Catharina C Gross; Maria Eveslage; Sven G Meuth; Heinz Wiendl; Luisa Klotz Journal: Front Immunol Date: 2018-07-09 Impact factor: 7.561
Authors: Gerd Haga Bringeland; Lucius Bader; Nello Blaser; Lisa Budzinski; Axel R Schulz; Henrik E Mei; Kjell-Morten Myhr; Christian A Vedeler; Sonia Gavasso Journal: Cytometry A Date: 2019-01-27 Impact factor: 4.355
Authors: Júlia Granell-Geli; Cristina Izquierdo-Gracia; Ares Sellés-Rius; Aina Teniente-Serra; Silvia Presas-Rodríguez; María José Mansilla; Luis Brieva; Javier Sotoca; María Alba Mañé-Martínez; Ester Moral; Irene Bragado; Susan Goelz; Eva Martínez-Cáceres; Cristina Ramo-Tello Journal: J Pers Med Date: 2021-12-10