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Molecules 2018, 23(5), 1068; https://doi.org/10.3390/molecules23051068

Passive Aβ Immunotherapy: Current Achievements and Future Perspectives

1
Fraunhofer Institute for Cell Therapy and Immunology, Department for Drug Design and Target Validation, 06120 Halle (Saale), Germany
2
Probiodrug AG, 06120 Halle (Saale), Germany
3
Ann Romney Center for Neurologic Diseases, Brigham and Womens’s Hospital, Harvard Medical School, Boston, MA 02116, USA
*
Author to whom correspondence should be addressed.
Received: 29 March 2018 / Revised: 23 April 2018 / Accepted: 25 April 2018 / Published: 3 May 2018
(This article belongs to the Special Issue 25th Anniversary of the Amyloid Hypothesis and Alzheimer Disease)
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Abstract

Passive immunotherapy has emerged as a very promising approach for the treatment of Alzheimer’s disease and other neurodegenerative disorders, which are characterized by the misfolding and deposition of amyloid peptides. On the basis of the amyloid hypothesis, the majority of antibodies in clinical development are directed against amyloid β (Aβ), the primary amyloid component in extracellular plaques. This review focuses on the current status of Aβ antibodies in clinical development, including their characteristics and challenges that came up in clinical trials with these new biological entities (NBEs). Emphasis is placed on the current view of common side effects observed with passive immunotherapy, so-called amyloid-related imaging abnormalities (ARIAs), and potential ways to overcome this issue. Among these new ideas, a special focus is placed on molecules that are directed against post-translationally modified variants of the Aβ peptide, an emerging approach for development of new antibody molecules. View Full-Text
Keywords: amyloid-β; monoclonal antibodies; posttranslational modifications; drug development amyloid-β; monoclonal antibodies; posttranslational modifications; drug development
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Schilling, S.; Rahfeld, J.-U.; Lues, I.; Lemere, C.A. Passive Aβ Immunotherapy: Current Achievements and Future Perspectives. Molecules 2018, 23, 1068.

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