Development of Beta-Amyloid-Specific CAR-Tregs for the Treatment of Alzheimer’s Disease

Author:

Saetzler Valerie1ORCID,Riet Tobias12ORCID,Schienke Andrea1,Henschel Pierre1,Freitag Kiara34,Haake Alexander34,Heppner Frank L.34ORCID,Buitrago-Molina Laura Elisa1ORCID,Noyan Fatih1,Jaeckel Elmar15,Hardtke-Wolenski Matthias16ORCID

Affiliation:

1. Department of Gastroenterology, Hepatology, Infectious Diseases & Endocrinology, Hannover Medical School, 30625 Hannover, Germany

2. Department I of Internal Medicine, Tumor Genetics, University Hospital of Cologne and Center for Molecular Medicine Cologne (CMMC), University of Cologne, 50931 Cologne, Germany

3. Department of Neuropathology, Charité-Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt-Universität zu Berlin, 10117 Berlin, Germany

4. German Center for Neurodegenerative Diseases (DZNE) within the Helmholtz Association, 10117 Berlin, Germany

5. Department of Liver Transplantation, Multi Organ Transplant Program, University Health Network, University of Toronto, Toronto, ON M5T 0S8, Canada

6. Institute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, 45147 Essen, Germany

Abstract

Background: Alzheimer’s disease (AD) is a neurodegenerative disease that remains uncured. Its pathogenesis is characterized by the formation of β-amyloid (Aβ) plaques. The use of antigen-specific regulatory T cells (Tregs) through adoptive transfer has shown promise for the treatment of many inflammatory diseases, although the effectiveness of polyspecific Tregs is limited. Obtaining a sufficient number of antigen-specific Tregs from patients remains challenging. Aims and Methods: To address this problem, we used an antibody-like single-chain variable fragment from a phage library and subsequently generated a chimeric antigen receptor (CAR) targeting β-amyloid. Results: The β-amyloid-specific CARs obtained were stimulated by both recombinant and membrane-bound Aβ isolated from the murine brain. The generated CAR-Tregs showed a normal Treg phenotype, were antigen-specific activatable, and had suppressive capacity. Conclusion: This study highlights the potential of CAR technology to generate antigen-specific Tregs and presents novel approaches for developing functional CARs.

Funder

German Research Foundation

Government of Canada’s New Frontiers in Research Fund

European Union’s Horizon 2020 Research and Innovation Program

DFG within the framework of the Open Access Publication Costs Program

Publisher

MDPI AG

Subject

General Medicine

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