A summary of current NKG2D-based CAR clinical trials

Author:

Curio Sophie12ORCID,Jonsson Gustav3ORCID,Marinović Sonja45

Affiliation:

1. Department of Life Sciences, Imperial College London, London, UK

2. The University of Queensland Diamantina Institute, The University of Queensland, Woolloongabba, QLD 4102, Australia

3. Institute of Molecular Biotechnology of the Austrian Academy of Sciences, Vienna, Austria

4. Laboratory for Personalized Medicine, Division of Molecular Medicine, Ruder Boskovic Institute, Zagreb, Croatia

5. Department of Histology and Embryology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia

Abstract

Summary Cancer immunotherapies have significantly improved patient survival and treatment options in recent years. Nonetheless, the success of immunotherapy is limited to certain cancer types and specific subgroups of patients, making the development of new therapeutic approaches a topic of ongoing research. Chimeric antigen receptor (CAR) cells are engineered immune cells that are programmed to specifically eliminate cancer cells. Ideally, a CAR recognizes antigens that are restricted to tumor cells to avoid off-target effects. NKG2D is an activating immunoreceptor and an important player in anti-tumor immunity due to its ability to recognize tumor cells and initiate an anti-tumor immune response. Ligands for NKG2D are expressed on malignant or stressed cells and typically absent from healthy tissue, making it a promising CAR candidate. Here, we provide a summary of past and ongoing NKG2D-based CAR clinical trials and comment on potential pitfalls.

Funder

Wellcome Trust

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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