Empowering γδ T‐cell functionality with vitamin C

Author:

Kabelitz Dieter12,Cierna Lea1,Juraske Claudia34,Zarobkiewicz Michal1,Schamel Wolfgang W.345,Peters Christian1

Affiliation:

1. Institute of Immunology Christian‐Albrechts University and University Hospital Schleswig‐Holstein Campus Kiel Kiel Germany

2. Institute of Immunology UKSH Campus Kiel Kiel Germany

3. Signalling Research Centres BIOSS and CIBSS, and Faculty of Biology University of Freiburg Freiburg Germany

4. Spemann Graduate School of Biology and Medicine (SGBM) University of Freiburg Freiburg Germany

5. Centre for Chronic Immunodeficiency (CCI) Medical Centre Freiburg Faculty of Medicine, University of Freiburg Freiburg Germany

Abstract

AbstractVitamin C (ascorbic acid) is a potent antioxidant and a cofactor for various enzymes including histone demethylases and methylcytosine dioxygenases. Vitamin C also exerts direct cytotoxicity toward selected tumor cells including colorectal carcinoma. Moreover, vitamin C has been shown to impact immune cell differentiation at various levels including maturation and/or functionality of T cells and their progenitors, dendritic cells, B cells, and NK cells. γδ T cells have recently attracted great interest as effector cells for cell‐based cancer immunotherapy, due to their HLA‐independent recognition of a large variety of tumor cells. While γδ T cells can thus be also applied as an allogeneic off‐the‐shelf product, it is obvious that the effector function of γδ T cells needs to be optimized to ensure the best possible clinical efficacy. Here we review the immunomodulatory mechanisms of vitamin C with a special focus on how vitamin C enhances the effector function of γδ T cells. We also discuss future directions of how vitamin C can be used in the clinical setting to boost the efficacy of adoptive cell therapies.

Funder

Deutsche Forschungsgemeinschaft

Deutscher Akademischer Austauschdienst

Publisher

Wiley

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