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Eur J Immunol ; 54(7): e2451028, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38616772

ABSTRACT

Vitamin 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.


Subject(s)
Ascorbic Acid , Receptors, Antigen, T-Cell, gamma-delta , Ascorbic Acid/pharmacology , Humans , Receptors, Antigen, T-Cell, gamma-delta/immunology , Receptors, Antigen, T-Cell, gamma-delta/metabolism , Animals , Immunotherapy, Adoptive/methods , T-Lymphocytes/immunology , Neoplasms/immunology , Neoplasms/therapy , Neoplasms/drug therapy , Cell Differentiation/immunology , Cell Differentiation/drug effects
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