Literature DB >> 32450508

BMI influences CD20 kinetics in multiple sclerosis patients treated with ocrelizumab.

E Signoriello1, S Bonavita2, A Di Pietro2, G Abbadessa2, F Rossi2, G Miele2, S Casertano2, G Lus2.   

Abstract

OBJECTIVES: Ocrelizumab (OCR) is a humanized monoclonal antibody targeting CD20 antigen exposed on B cells surface. Kinetic of B-cells repopulation after depletion therapy shows high intra and inter-individual variability. The aim of this study was to explore the influence of Body Mass Index (BMI) on kinetic of B-cell repopulation after treatment with OCR and on treatment response.
METHODS: 108 Multiple Sclerosis (MS) patients were enrolled at the time of the first dose of OCR administration and prospectively evaluated. Clinical, instrumental activity and disability progression were analyzed. According to B cells count, patients were divided into two groups: with fast (FR) and with slow (SR) repopulation rate, respectively.
RESULTS: Significant reduction of disease activity was observed in all patients and a stabilization of disease was obtained in progressive patients. Patients with FR had higher BMI compared to patients with a SR (p<0.001). Contrariwise no correlation between repopulation rate and treatment effectiveness was disclosed.
CONCLUSIONS: In a real world setting we confirmed the effectiveness of OCR in relapsing remitting and progressive patients; patients with higher BMI had a FR. This suggests considering BMI for administration schedule although further investigations with longer follow up could improve treatment protocol and patient selection.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  BMI; CD20 kynetics; Multiple sclerosis; Ocrelizumab; progression

Mesh:

Substances:

Year:  2020        PMID: 32450508     DOI: 10.1016/j.msard.2020.102186

Source DB:  PubMed          Journal:  Mult Scler Relat Disord        ISSN: 2211-0348            Impact factor:   4.339


  6 in total

1.  Seroconversion following COVID-19 vaccination: can we optimize protective response in CD20-treated individuals?

Authors:  David Baker; Amy MacDougall; Angray S Kang; Klaus Schmierer; Gavin Giovannoni; Ruth Dobson
Journal:  Clin Exp Immunol       Date:  2022-05-12       Impact factor: 4.330

2.  Seroconversion following COVID-19 vaccination: Can we optimize protective response in CD20-treated individuals?

Authors:  David Baker; Amy MacDougall; Angray S Kang; Klaus Schmierer; Gavin Giovannoni; Ruth Dobson
Journal:  Clin Exp Immunol       Date:  2021-11-18       Impact factor: 5.732

3.  Product review on MAbs (alemtuzumab and ocrelizumab) for the treatment of multiple sclerosis.

Authors:  Tereza Gabelić; Barbara Barun; Ivan Adamec; Magdalena Krbot Skorić; Mario Habek
Journal:  Hum Vaccin Immunother       Date:  2021-10-20       Impact factor: 4.526

4.  Long-term immunological consequences of anti-CD20 therapies on humoral responses to COVID-19 vaccines in multiple sclerosis: an observational study.

Authors:  Tobias Moser; Ciara O'Sullivan; Ferdinand Otto; Wolfgang Hitzl; Georg Pilz; Kerstin Schwenker; Cornelia Mrazek; Elisabeth Haschke-Becher; Eugen Trinka; Peter Wipfler; Andrea Harrer
Journal:  Ther Adv Neurol Disord       Date:  2022-04-22       Impact factor: 6.430

5.  CD19 B cell repopulation after ocrelizumab, alemtuzumab and cladribine: Implications for SARS-CoV-2 vaccinations in multiple sclerosis.

Authors:  David Baker; Amy MacDougall; Angray S Kang; Klaus Schmierer; Gavin Giovannoni; Ruth Dobson
Journal:  Mult Scler Relat Disord       Date:  2021-12-04       Impact factor: 4.808

Review 6.  COVID-19 vaccine-readiness for anti-CD20-depleting therapy in autoimmune diseases.

Authors:  D Baker; C A K Roberts; G Pryce; A S Kang; M Marta; S Reyes; K Schmierer; G Giovannoni; S Amor
Journal:  Clin Exp Immunol       Date:  2020-08-01       Impact factor: 4.330

  6 in total

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