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Association of vitamin A deficiency with decrease in TNF-α expressing CD3-CD56+ NK cells in Ghanaians
Yi Jiang1, Francis Obuseh, William Ellis
1Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL.
Insights
Vitamin A deficiency in children is linked to fewer tumor necrosis factor-alpha (TNF-α) expressing Natural Killer (NK) cells. This reduction in immune cells may explain increased susceptibility to infections in deficient individuals.
Area of Science:
- Immunology
- Nutritional Science
- Public Health
Background:
- Low vitamin A levels correlate with increased infection risk and severity in children.
- Limited data exists on vitamin A deficiency's impact on human cellular immune subsets and cytokine production.
Purpose of the Study:
- To characterize cellular immune subsets and their cytokine production in vitamin A deficient versus sufficient individuals.
- To investigate the relationship between plasma vitamin A levels and cellular immune status.
Main Methods:
- Cross-sectional study in Ghana.
- Analysis of peripheral blood mononuclear cells (PBMCs) for cellular phenotypes and intracellular cytokine expression.
- Comparison between vitamin A deficient and sufficient participants.
Main Results:
- Vitamin A deficiency was associated with a significant decrease in TNF-α expressing CD3-CD56+ NK cells.
- No significant differences were observed in CD4+ T cell proliferation or IFN-γ and IL-4 production between groups.
- Findings align with animal studies showing reduced NK cell activity in vitamin A deficiency.
Conclusions:
- Reduced TNF-α expressing NK cells in vitamin A deficiency may contribute to impaired resistance to infections.
- Further research is needed to fully elucidate the role of vitamin A in immune cell function.
Abstract:
Although low plasma vitamin A concentrations are associated with increased incidence or severity of infections such as respiratory tract infection and measles in children, there is a paucity of data on the effect of vitamin A deficiency on the distribution of, and cytokine production by, the different cellular immune subsets in humans. We conducted a cross-sectional study in a district in Ghana to characterize cellular subsets and functional capacity of peripheral blood mononuclear cells from vitamin A deficient and vitamin A sufficient (normal) individuals, and evaluated the relationships between vitamin A concentration in plasma and cellular immune status. We measured the percentages of selected cellular phenotypes and intracellular cytokine expression and describe the differential cellular subset distributions and alterations in cytokine expression in participants with normal and deficient vitamin A concentrations. The major change observed in the constitution of cellular subsets was a decrease in TNF-α expressing CD3-CD56+ NK cells in those with vitamin A deficiency compared with normal individuals. CD4+ T cell proliferation and production of IFN-γ and IL-4 were not statistically different between the two groups. These results support previous studies that demonstrated decreased NK cell activity in vitamin A deficient animals. The decrease in TNF-α expressing NK cells observed in vitamin A deficient individuals in this study could help to explain the decreased resistance to infections observed in those with vitamin A deficiency.
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