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Keywords
Immunology, Autoimmunity, CAAR T cells, B cells
Abstract
- Graves’ Disease (GD) is the 4th most common autoimmune disease in the United States.
- GD is characterized by autoreactive B cells releasing anti-thyroid stimulating hormone receptor (TSHR) Ab that bind to TSHR, causing an overexpression of hormones.
- Excessive hormonal release leads to hyperthyroidism, causing a variety of metabolic issues.
- No cure exists, only limited effectiveness of treatments, including chemotherapy, radiation, or thyroidectomy.
- Chimeric antigen receptors (CAR) T cell therapy has been effective in treating blood cancers.
- Modifying this therapy by engineering T cells that replace the antigen as the T cell receptor will selectively target autoreactive B cells, namely chimeric autoantibody receptor (CAAR) T cell therapy.
- By using TSHR as the binding domain, we believe that our CAAR T cell that will be able to eliminate anti-TSHR B cells in GD.
BYU ScholarsArchive Citation
Demars, Kimbal; Cheever, Abigail; Kang, Chloe; Lindsay, Hunter; Hansen, Mackenzie; O'Neill, Kim; and Weber, Scott, "Engineering Chimeric Autoantibody Receptor T cells (CAAR): a potential cure for Graves' Disease" (2025). Library/Life Sciences Undergraduate Poster Competition 2025. 54.
https://scholarsarchive.byu.edu/library_studentposters_2025/54
Document Type
Article
Publication Date
2025
Language
English
College
Life Sciences
Department
Microbiology and Molecular Biology
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