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Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy
Published on: December 17, 2019
CAR-T cell therapy in rheumatic diseases: a review article.
Harshwardhan Patil1, Rajath K Bharadwaj1, Nilanjana Dutta2
1Department of Pharmacy Practice, JSS College of Pharmacy, Mysuru, India.
Chimeric antigen receptor (CAR)-T cell therapy, initially for blood cancers, shows promise for autoimmune and rheumatic diseases by targeting specific immune cells. Further research is needed to ensure safety and affordability.
Area of Science:
- Immunology
- Oncology
- Rheumatology
Background:
- CAR-T cell therapy, a revolutionary treatment for hematologic malignancies, is being explored for autoimmune and rheumatic diseases.
- This therapy involves genetically modifying T cells to express chimeric antigen receptors (CARs) for targeted antigen recognition.
Purpose of the Study:
- To review the potential of CAR-T cell therapy in treating autoimmune diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), and systemic sclerosis (SSc).
- To discuss emerging applications in Sjögren's syndrome and dermatomyositis.
- To highlight challenges and future directions for CAR-T therapy in rheumatic diseases.
Main Methods:
- Review of existing literature and studies on CAR-T cell therapy applications in autoimmune and rheumatic conditions.
- Analysis of CAR-T cell mechanisms targeting pathogenic immune cells and disease processes.
- Evaluation of potential benefits, risks, and future research needs.
Main Results:
- CAR-T therapy demonstrates potential in maintaining remission in SLE by targeting autoreactive B cells.
- It shows promise in refractory RA by selectively eliminating disease-driving immune cells.
- For SSc, CAR-T therapy may address B cell dysregulation and fibrotic processes.
Conclusions:
- CAR-T cell therapy offers targeted immunomodulation with potential for long-term remission in refractory rheumatic diseases.
- Challenges include cytokine release syndrome, immune toxicity, and cost.
- Advancements like CAR-Tregs and gene editing, alongside clinical trials, are crucial for establishing efficacy, safety, and feasibility.
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