Addressing Safety Liabilities of TfR Bispecific Antibodies That Cross the Blood-Brain Barrier

Author:

Couch Jessica A.1,Yu Y. Joy2,Zhang Yin3,Tarrant Jacqueline M.1,Fuji Reina N.1,Meilandt William J.2,Solanoy Hilda2,Tong Raymond K.4,Hoyte Kwame5,Luk Wilman5,Lu Yanmei5,Gadkar Kapil1,Prabhu Saileta1,Ordonia Benjamin A.1,Nguyen Quyen1,Lin Yuwen1,Lin Zhonghua6,Balazs Mercedesz6,Scearce-Levie Kimberly2,Ernst James A.4,Dennis Mark S.3,Watts Ryan J.2

Affiliation:

1. Development Sciences, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.

2. Neurodegeneration Labs, Department of Neuroscience, Genentech Inc., South San Francisco, CA 94080, USA.

3. Antibody Engineering, Genentech Inc., South San Francisco, CA 94080, USA.

4. Protein Chemistry, Genentech Inc., South San Francisco, CA 94080, USA.

5. Biochemical and Cellular Pharmacology, Genentech Inc., South San Francisco, CA 94080, USA.

6. Translational Immunology, Genentech Inc., South San Francisco, CA 94080, USA.

Abstract

The safety of therapeutic bispecific antibodies that use TfR for delivery to the brain can be improved by reducing affinity for TfR and eliminating antibody effector function.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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