Targeting B cells in multiple sclerosis

Research output: Contribution to journalReviewResearchpeer-review

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Targeting B cells in multiple sclerosis. / Sellebjerg, Finn; Weber, Martin S.

In: Current Opinion in Neurology, Vol. 34, No. 3, 2021, p. 295-302.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Sellebjerg, F & Weber, MS 2021, 'Targeting B cells in multiple sclerosis', Current Opinion in Neurology, vol. 34, no. 3, pp. 295-302. https://doi.org/10.1097/WCO.0000000000000938

APA

Sellebjerg, F., & Weber, M. S. (2021). Targeting B cells in multiple sclerosis. Current Opinion in Neurology, 34(3), 295-302. https://doi.org/10.1097/WCO.0000000000000938

Vancouver

Sellebjerg F, Weber MS. Targeting B cells in multiple sclerosis. Current Opinion in Neurology. 2021;34(3):295-302. https://doi.org/10.1097/WCO.0000000000000938

Author

Sellebjerg, Finn ; Weber, Martin S. / Targeting B cells in multiple sclerosis. In: Current Opinion in Neurology. 2021 ; Vol. 34, No. 3. pp. 295-302.

Bibtex

@article{031d4175a24448ef95a85845b4dad925,
title = "Targeting B cells in multiple sclerosis",
abstract = "PURPOSE OF REVIEW: Treatments targeting B cells are increasingly used for patients with multiple sclerosis (MS). We review the mechanisms of action, clinical effectiveness and safety of treatment, with emphasis on recently published studies. RECENT FINDINGS: Several monoclonal antibodies targeting the surface molecule CD20 on B cells are approved or being developed for treatment of MS. Overall, they seem comparable in terms of strongly suppressing radiological disease activity and relapse biology. Novel approaches include anti-CD19 antibody therapy and treatment with oral drugs targeting Bruton's tyrosine kinase (BTK). The main safety issue with persistent B cell depletion is an increased risk of infections - possibly including an increased risk of severe COVID-19. Vaccine responses are also blunted in patients treated with anti-CD20 antibodies. Lower doses or longer infusion intervals may be sufficient for control of disease activity. Whether this might also improve the safety of treatment and increase vaccination responses remains to be determined. SUMMARY: Available data support the widespread use of therapies targeting B cells in MS. Whether novel approaches targeting CD19 or BTK will have advantages compared to anti-CD20 antibody therapy remains to be established. Furthermore, trials investigating alternative dosing regimens for anti-CD20 antibody treatment are warranted.",
author = "Finn Sellebjerg and Weber, {Martin S.}",
note = "Publisher Copyright: Copyright {\textcopyright} 2021 Wolters Kluwer Health, Inc. All rights reserved.",
year = "2021",
doi = "10.1097/WCO.0000000000000938",
language = "English",
volume = "34",
pages = "295--302",
journal = "Current Opinion in Neurology",
issn = "1350-7540",
publisher = "Lippincott Williams & Wilkins, Ltd.",
number = "3",

}

RIS

TY - JOUR

T1 - Targeting B cells in multiple sclerosis

AU - Sellebjerg, Finn

AU - Weber, Martin S.

N1 - Publisher Copyright: Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

PY - 2021

Y1 - 2021

N2 - PURPOSE OF REVIEW: Treatments targeting B cells are increasingly used for patients with multiple sclerosis (MS). We review the mechanisms of action, clinical effectiveness and safety of treatment, with emphasis on recently published studies. RECENT FINDINGS: Several monoclonal antibodies targeting the surface molecule CD20 on B cells are approved or being developed for treatment of MS. Overall, they seem comparable in terms of strongly suppressing radiological disease activity and relapse biology. Novel approaches include anti-CD19 antibody therapy and treatment with oral drugs targeting Bruton's tyrosine kinase (BTK). The main safety issue with persistent B cell depletion is an increased risk of infections - possibly including an increased risk of severe COVID-19. Vaccine responses are also blunted in patients treated with anti-CD20 antibodies. Lower doses or longer infusion intervals may be sufficient for control of disease activity. Whether this might also improve the safety of treatment and increase vaccination responses remains to be determined. SUMMARY: Available data support the widespread use of therapies targeting B cells in MS. Whether novel approaches targeting CD19 or BTK will have advantages compared to anti-CD20 antibody therapy remains to be established. Furthermore, trials investigating alternative dosing regimens for anti-CD20 antibody treatment are warranted.

AB - PURPOSE OF REVIEW: Treatments targeting B cells are increasingly used for patients with multiple sclerosis (MS). We review the mechanisms of action, clinical effectiveness and safety of treatment, with emphasis on recently published studies. RECENT FINDINGS: Several monoclonal antibodies targeting the surface molecule CD20 on B cells are approved or being developed for treatment of MS. Overall, they seem comparable in terms of strongly suppressing radiological disease activity and relapse biology. Novel approaches include anti-CD19 antibody therapy and treatment with oral drugs targeting Bruton's tyrosine kinase (BTK). The main safety issue with persistent B cell depletion is an increased risk of infections - possibly including an increased risk of severe COVID-19. Vaccine responses are also blunted in patients treated with anti-CD20 antibodies. Lower doses or longer infusion intervals may be sufficient for control of disease activity. Whether this might also improve the safety of treatment and increase vaccination responses remains to be determined. SUMMARY: Available data support the widespread use of therapies targeting B cells in MS. Whether novel approaches targeting CD19 or BTK will have advantages compared to anti-CD20 antibody therapy remains to be established. Furthermore, trials investigating alternative dosing regimens for anti-CD20 antibody treatment are warranted.

U2 - 10.1097/WCO.0000000000000938

DO - 10.1097/WCO.0000000000000938

M3 - Review

C2 - 33782253

AN - SCOPUS:85106069911

VL - 34

SP - 295

EP - 302

JO - Current Opinion in Neurology

JF - Current Opinion in Neurology

SN - 1350-7540

IS - 3

ER -

ID: 272125663