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Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy
Published on: December 17, 2019
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Chimeric antigen receptor T-cell therapy for HIV cure
Oscar Alfageme-Abello1, Raphaël Porret, Matthieu Perreau
1Lausanne University Hospital (CHUV), Department of Medicine, Division of Immunology and Allergy, Lausanne, Switzerland.
Current Opinion in HIV and AIDS
|February 9, 2021
Summary
Chimeric antigen receptor (CAR)-T cell therapies show promise for treating HIV. Researchers are developing new anti-HIV CARs targeting viral glycoproteins, with early preclinical success paving the way for clinical trials.
Area of Science:
- Immunology
- Virology
- Biotechnology
Background:
- Chimeric antigen receptor (CAR)-T cell therapies have advanced significantly for hematologic cancers.
- The success of anti-CD19 CAR-T cells has spurred interest in their application for HIV treatment.
Purpose of the Study:
- To review the historical and recent advancements in the development of anti-HIV CARs.
- To discuss the potential of CAR-T cell therapy in managing HIV infection.
Main Methods:
- Development of CARs targeting HIV glycoproteins (gp120/gp41).
- Utilizing CD4+ extracellular domains or variable heavy/light chain (VH/VL) segments from broadly neutralizing antibodies.
- Engineering T cells for multiplexed specificities, enhanced signaling, and HIV resistance.
Main Results:
- New generations of anti-HIV CARs have been developed since the 1990s.
- Preclinical studies in mouse models have shown promising results for novel anti-HIV CAR-T cells.
- Ongoing research focuses on optimizing CAR design for efficacy and safety.
Conclusions:
- Anti-HIV CAR-T cell therapies are progressing towards clinical evaluation.
- Key challenges include controlling the HIV reservoir and minimizing off-target effects.
- Further research is needed to establish the safety and efficacy of CAR-T cells for HIV treatment.
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