Precision targeting of autoantigen-specific B cells in muscle-specific tyrosine kinase myasthenia gravis with chimeric autoantibody receptor T cells.
Sangwook OhXuming MaoSilvio M VieiraJinmin LeeDarshil PatelEun Jung ChoiAndrea AlvaradoEbony Cottman-ThomasDamian MasedaPatricia Y TsaoChristoph T EllebrechtSami L KhellaDavid P RichmanKevin C O'ConnorUri HerzbergGwendolyn K BinderMichael C MiloneSamik BasuAimee S PaynePublished in: Nature biotechnology (2023)
Muscle-specific tyrosine kinase myasthenia gravis (MuSK MG) is an autoimmune disease that causes life-threatening muscle weakness due to anti-MuSK autoantibodies that disrupt neuromuscular junction signaling. To avoid chronic immunosuppression from current therapies, we engineered T cells to express a MuSK chimeric autoantibody receptor with CD137-CD3ζ signaling domains (MuSK-CAART) for precision targeting of B cells expressing anti-MuSK autoantibodies. MuSK-CAART demonstrated similar efficacy as anti-CD19 chimeric antigen receptor T cells for depletion of anti-MuSK B cells and retained cytolytic activity in the presence of soluble anti-MuSK antibodies. In an experimental autoimmune MG mouse model, MuSK-CAART reduced anti-MuSK IgG without decreasing B cells or total IgG levels, reflecting MuSK-specific B cell depletion. Specific off-target interactions of MuSK-CAART were not identified in vivo, in primary human cell screens or by high-throughput human membrane proteome array. These data contributed to an investigational new drug application and phase 1 clinical study design for MuSK-CAART for the treatment of MuSK autoantibody-positive MG.
Keyphrases
- tyrosine kinase
- high throughput
- myasthenia gravis
- mouse model
- epidermal growth factor receptor
- skeletal muscle
- multiple sclerosis
- systemic lupus erythematosus
- cell therapy
- drug delivery
- stem cells
- single cell
- randomized controlled trial
- cancer therapy
- big data
- drug induced
- electronic health record
- adverse drug
- double blind