Zinc deficiency in humans decreases the activity of serum thymulin (a thymic hormone), which is required for maturation of T-helper cells. T-helper 1 (Th(1)) cytokines are decreased but T-helper 2 (Th(2)) cytokines are not affected by zinc deficiency in humans. This shift of Th(1) to Th(2) function results in cell-mediated immune dysfunction. Because IL-2 production (Th(1) cytokine) is decreased, this leads to decreased activities of natural-killer cell and T cytolytic cells, which are involved in killing viruses, bacteria, and tumor cells. In humans, zinc deficiency may decrease the generation of new CD4+ T cells from the thymus. In cell culture studies (HUT-78, a Th(0) human malignant lymphoblastoid cell line), as a result of zinc deficiency, nuclear factor-kappaB (NF-kappaB) activation, phosphorylation of IkappaB, and binding of NF-kappaB to DNA are decreased and this results in decreased Th(1) cytokine production. In another study, zinc supplementation to humans decreased the gene expression and production of pro-inflammatory cytokines and decreased oxidative stress markers. In HL-60 cells (a human pro-myelocytic leukemia cell line), zinc deficiency increased the levels of TNF-alpha, IL-1beta, and IL-8 cytokines and mRNA. In these cells, zinc induced A20, a zinc finger protein that inhibited NF-kappaB activation via tumor necrosis factor receptor associated factor pathway, and this decreased gene expression of pro-inflammatory cytokines and oxidative stress markers. We conclude that zinc has an important role in cell-mediated immune functions and also functions as antiinflammatory and antioxidant agent.
Zinc: mechanisms of host defense. Publishing Authors By Initials
Zinc: mechanisms of host defense. Journal Published:
PUBLICATION TYPE: Review
Journal: The Journal of nutrition
VOLUME: 137
Page Numbers: 1345-9
Journal Abbreviation:
ISSN: 0022-3166
DAY: 3
MONTH: May
YEAR: 2007
Zinc: mechanisms of host defense. Information
Number of References:
LANGUAGE: eng
NlmUniqueID: 404243
Zinc: mechanisms of host defense. Keywords Mesh Terms:
KEYWORDS: Zinc
MESH TERMS: therapeutic use
Chemical & Substance for Abstract: Zinc: mechanisms of host defense. Information
Substance Name: Zinc
Registry Number: 7440-66-6
Grant and Affiliation Information for Zinc: mechanisms of host defense.
AFFILIATION: Department of Internal Medicine, Division of Hematology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan 48201, USA. prasada@karmanos.org
Country: United States
AGENCY: United States PHS
GRANT: R01 A150698-04
ACRONYM:
MEDLINETA: J Nutr
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