Preclinical B cell depletion and safety profile of a brain‐shuttled crystallizable fragment‐silenced CD20 antibody

The BBB hinders mAb-based brain disorder therapies A brain-targeted B-cell-depleting mAb for MS that efficiently crosses the BBB via hTfR1 was developed using Brainshuttle<sup>™</sup> technology (1a and 1b) The Brainshuttle<sup>™</sup>-CD20 mAb was well tolerated (2a and 2b) and displayed B-cell-killing properties (1c), paving the way for future development and clinical translation of TfR1-targetingtherapies for increased brain penetration.

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Publication Details

Journal
Clinical and Translational Medicine
Published
2025-03-01
DOI
https://doi.org/10.1002/ctm2.70178
Citations
1
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
1.36
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article

Preclinical B cell depletion and safety profile of a brain‐shuttled crystallizable fragment‐silenced CD20 antibody

Sylvia Herter, H.‐Christian von Büdingen, Elisa Di Lenarda, Shanon Seger et al.
1 citations
Clinical and Translational Medicine
Monoclonal and Polyclonal Antibodies Research
1.36
article

Preclinical B cell depletion and safety profile of a brain‐shuttled crystallizable fragment‐silenced CD20 antibody

Sylvia Herter, H.‐Christian von Büdingen, Elisa Di Lenarda, Shanon Seger, Vanessa Schumacher, Claudia Senn, Eduard Urich, Martina Stirn, Cordula Jany, Alain C. Tissot, Johannes Auer, Solen Pichereau, Anne Eichinger‐Chapelon, Adrian Roth, Kevin Brady, Michael B. Otteneder, Juliana Bessa, Anja Kipar, Christian Klein, Nadine Stokar‐Regenscheit, Juergen Bachl, Michael Winter, Nicole Clemann, Felix Weber, Robert M. Mader, Mohammed Ullah, Niels Janssen, J. F. Hönig
article en
1 citations

Abstract

The BBB hinders mAb-based brain disorder therapies A brain-targeted B-cell-depleting mAb for MS that efficiently crosses the BBB via hTfR1 was developed using Brainshuttle<sup>™</sup> technology (1a and 1b) The Brainshuttle<sup>™</sup>-CD20 mAb was well tolerated (2a and 2b) and displayed B-cell-killing properties (1c), paving the way for future development and clinical translation of TfR1-targetingtherapies for increased brain penetration.

Clinical and Translational MedicineVol. 15(3)
Roche (Switzerland) (CH), University of Liverpool (GB), University of Zurich (CH), Roche Pharma AG (Germany) (DE)
Good health and well-being
Openalex Percentile: Top 22%
Monoclonal and Polyclonal Antibodies Research
1.36
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