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In Vivo Immunogenicity Screening of Tumor-Derived Extracellular Vesicles by Flow Cytometry of Splenic T Cells
Published on: September 23, 2021
Exploring the potential of the convergence between extracellular vesicles and CAR technology as a novel immunotherapy
Ofir Bar1, Angel Porgador1, Tomer Cooks1
1The Shraga Segal Department of Microbiology, Immunology and Genetics, Faculty of Health Sciences Ben-Gurion University Beer-Sheva Israel.
Abstract:
Cancer therapy is a dynamically evolving field, witnessing the emergence of innovative approaches that offer a promising outlook for patients grappling with persistent disease. Within the realm of therapeutic exploration, chimeric antigen receptor (CAR) T cells as well as CAR NK cells, have surfaced as novel approaches, each possessing unique attributes and transformative potential. Immune cells engineered to express CARs recognizing tumour-specific antigens, have shown remarkable promise in treating terminal cancers by combining the precision of antibody specificity with the potent cytotoxic function of T cells. However, their application in solid tumours is still in its nascent stages, presenting unique major challenges. On the same note, CAR NK cells offer a distinct immunotherapeutic approach, utilizing CARs on NK cells, providing advantages in safety, manufacturing simplicity, and a broader scope for cancer treatment. Extracellular vesicles (EVs) have emerged as promising therapeutic agents due to their ability to carry crucial biomarkers and biologically active molecules, serving as vital messengers in the intercellular communication network. In the context of cancer, the therapeutic potential of EVs lies in delivering tumour-suppressing proteins, nucleic acid components, or targeting drugs with precision, thereby redefining the paradigm of precision medicine. The fusion of CAR technology with the capabilities of EVs has given rise to a new therapeutic frontier. CAR T EVs and CAR NK EVs, leveraging the power of EVs, have the potential to alleviate challenges associated with live-cell therapies. EVs are suggested to reduce the side effects linked to CAR T cell therapy and hold the potential to revolutionize the penetrance in solid tumours. EVs act as carriers of pro-apoptotic molecules and RNA components, enhancing immune responses and thereby expanding their therapeutic potential. In this review article, we navigate dynamic landscapes, with our objective being to evaluate comparative efficacy, safety profiles, manufacturing complexities, and clinical applicability.
Insights
Chimeric antigen receptor (CAR) T and CAR NK cell therapies are evolving, with extracellular vesicles (EVs) offering a new frontier. CAR T EVs and CAR NK EVs may overcome challenges in solid tumor treatment and reduce side effects.
Area of Science:
- Oncology
- Immunotherapy
- Biotechnology
Background:
- Chimeric antigen receptor (CAR) T cells and CAR NK cells show promise in cancer therapy.
- Challenges remain, particularly in solid tumors, regarding safety and efficacy.
- Extracellular vesicles (EVs) are emerging as novel drug delivery systems for targeted cancer treatment.
Purpose of the Study:
- To review and compare the efficacy, safety, manufacturing, and clinical applicability of CAR T EVs and CAR NK EVs.
- To explore the potential of EVs in overcoming limitations of live-cell CAR immunotherapies.
- To evaluate the role of EVs in enhancing cancer treatment precision and reducing side effects.
Main Methods:
- Review of current literature on CAR T cells, CAR NK cells, and extracellular vesicles in cancer therapy.
- Comparative analysis of CAR T EVs and CAR NK EVs based on published data.
- Evaluation of safety profiles, manufacturing processes, and clinical trial outcomes.
Main Results:
- CAR T EVs and CAR NK EVs offer potential advantages over traditional CAR T cell therapy, including improved tumor penetration and reduced toxicity.
- EVs can be engineered to deliver therapeutic payloads, enhancing immune responses and targeting cancer cells.
- Early findings suggest EVs may mitigate side effects associated with live-cell immunotherapies.
Conclusions:
- CAR T EVs and CAR NK EVs represent a promising advancement in cancer immunotherapy, potentially addressing current limitations.
- Further research and clinical trials are necessary to fully establish the therapeutic potential and optimize the application of CAR-EVs.
- This approach holds significant promise for redefining precision medicine in oncology.
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