Vitamin C and Immune Function.

Anitra C Carr, Silvia Maggini

Journal: Nutrients 2018;9(11):1211

PMID: 29099763

Plain Language Summary

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Vitamin C is essential to immune function and performs several crucial roles supporting cellular function in both the innate and adaptive immune system. Low storage capacity means a regular intake of a minimum 100-200mg of Vit C daily is necessary for adequate plasma levels. A potent antioxidant, Vit C can readily donate electrons as part of its immuno-protective role protecting against oxidative damage. VitC is a cofactor for the transportation of fatty acids into the cell mitochondria as well as numerous gene regulatory enzymes, including those involved in the cardiovascular response to infection. Structurally, Vit C supports barrier integrity and wound healing and concentrations of the vitamin accumulate in the epidermis. White leukocyte cells actively accumulate intracellular stores of Vit C indicating an important role in immune signalling. Neutrophils use Vit C to help migration to infection sites in the body and it enhances the differentiation and proliferation of B- and T-cells. Vit C has been shown to moderate inflammatory cytokines and reduce infection severity and longevity. Specifically, supplementation with high dose Vit C appears to be able to both prevent and ameliorate respiratory and systemic infections such as pneumonia. In summary, optimal levels of Vit C are necessary for proper immune function and resistance to infections.

Abstract

Vitamin C is an essential micronutrient for humans, with pleiotropic functions related to its ability to donate electrons. It is a potent antioxidant and a cofactor for a family of biosynthetic and gene regulatory enzymes. Vitamin C contributes to immune defense by supporting various cellular functions of both the innate and adaptive immune system. Vitamin C supports epithelial barrier function against pathogens and promotes the oxidant scavenging activity of the skin, thereby potentially protecting against environmental oxidative stress. Vitamin C accumulates in phagocytic cells, such as neutrophils, and can enhance chemotaxis, phagocytosis, generation of reactive oxygen species, and ultimately microbial killing. It is also needed for apoptosis and clearance of the spent neutrophils from sites of infection by macrophages, thereby decreasing necrosis/NETosis and potential tissue damage. The role of vitamin C in lymphocytes is less clear, but it has been shown to enhance differentiation and proliferation of B- and T-cells, likely due to its gene regulating effects. Vitamin C deficiency results in impaired immunity and higher susceptibility to infections. In turn, infections significantly impact on vitamin C levels due to enhanced inflammation and metabolic requirements. Furthermore, supplementation with vitamin C appears to be able to both prevent and treat respiratory and systemic infections. Prophylactic prevention of infection requires dietary vitamin C intakes that provide at least adequate, if not saturating plasma levels (i.e., 100-200 mg/day), which optimize cell and tissue levels. In contrast, treatment of established infections requires significantly higher (gram) doses of the vitamin to compensate for the increased inflammatory response and metabolic demand.

Address: Department of Pathology, University of Otago, Christchurch, P.O. Box 4345, Christchurch 8140, New Zealand. [email protected].; Bayer Consumer Care Ltd., Peter-Merian-Strasse 84, 4002 Basel, Switzerland. [email protected].
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