Synthetic Biology in the Engineering of CAR-T and CAR-NK Cell Therapies: Facts and Hopes

Author:

Clubb Justin D.1ORCID,Gao Torahito A.1ORCID,Chen Yvonne Y.123ORCID

Affiliation:

1. 1Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, Los Angeles, California.

2. 2Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, California.

3. 3Parker Institute for Cancer Immunotherapy Center at UCLA, Los Angeles, California.

Abstract

Abstract The advent of modern synthetic-biology tools has enabled the development of cellular treatments with engineered specificity, leading to a new paradigm in anticancer immunotherapy. T cells have been at the forefront of such development, with six chimeric antigen receptor–modified T-cell products approved by the FDA for the treatment of hematologic malignancies in the last 5 years. Natural killer (NK) cells are innate lymphocytes with potent cytotoxic activities, and they have become an increasingly attractive alternative to T-cell therapies due to their potential for allogeneic, “off-the-shelf” applications. However, both T cells and NK cells face numerous challenges, including antigen escape, the immunosuppressive tumor microenvironment, and potential for severe toxicity. Many synthetic-biology strategies have been developed to address these obstacles, most commonly in the T-cell context. In this review, we discuss the array of strategies developed to date, their application in the NK-cell context, as well as opportunities and challenges for clinical translation.

Funder

Cancer Research Institute

National Institutes of Health

Mark Foundation For Cancer Research

National Science Foundation

Parker Institute for Cancer Immunotherapy

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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