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Cited by 334Trace Elements in HealthIron Metabolism and DisordersNutrition and Health in Aging

The DOI matches its Crossref record; 158 of the 159 references it cites were found in a registry or an index.

The immune system and the impact of zinc during aging

Open access
Haase, Hajo, Rink, Lothar·2009·Immunity & Ageing
DOI 10.1186/1742-4933-6-9PMC PMC2702361
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Abstract

The trace element zinc is essential for the immune system, and zinc deficiency affects multiple aspects of innate and adaptive immunity. There are remarkable parallels in the immunological changes during aging and zinc deficiency, including a reduction in the activity of the thymus and thymic hormones, a shift of the T helper cell balance toward T helper type 2 cells, decreased response to vaccination, and impaired functions of innate immune cells. Many studies confirm a decline of zinc levels with age. Most of these studies do not classify the majority of elderly as zinc deficient, but even marginal zinc deprivation can affect immune function. Consequently, oral zinc supplementation demonstrates the potential to improve immunity and efficiently downregulates chronic inflammatory responses in the elderly. These data indicate that a wide prevalence of marginal zinc deficiency in elderly people may contribute to immunosenescence.

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Crossref · 10.1186/1742-4933-6-9

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Figures

Figure 1 Zinc as a signal molecule for immune cells. Zinc homeostasis is tightly controlled by three mechanisms: (A) Transport through the plasma membrane by zinc transporters from the ZnT (SLC A30) or ZIP (SLC A39) families. (B) Buffering by metallothionein. (C) Reversible transport by ZnT and ZIP proteins into or out of zincosomes, and storage bound to ligands that form a zinc sink. Zinc signals, i.e., changes in the intracellular concentration of free zinc, control immune cell signal transduction by regulating the activity of major signaling molecules, including kinases, phosphatases, and transcription factors. One representative example for each group is given. (TCR, T cell receptor; MKP, MAPK phosphatase; MTF-1, metal-response element binding transcription factor-1).
Figure 1 Zinc as a signal molecule for immune cells. Zinc homeostasis is tightly controlled by three mechanisms: (A) Transport through the plasma membrane by zinc transporters from the ZnT (SLC A30) or ZIP (SLC A39) families. (B) Buffering by metallothionein. (C) Reversible transport by ZnT and ZIP proteins into or out of zincosomes, and storage bound to ligands that form a zinc sink. Zinc signals, i.e., changes in the intracellular concentration of free zinc, control immune cell signal transduction by regulating the activity of major signaling molecules, including kinases, phosphatases, and transcription factors. One representative example for each group is given. (TCR, T cell receptor; MKP, MAPK phosphatase; MTF-1, metal-response element binding transcription factor-1).CC BY · PubMed Central
Figure 2 Disturbed B-cell function in ageing. In general, the numbers of B cells and specific antibodies (e.g., in response to vaccination) decrease with age, while total and unspecific immunoglobulin and autoantibodies increase. Some B cell clones expand, resulting in higher probability for lymphocyte malignancies.
Figure 2 Disturbed B-cell function in ageing. In general, the numbers of B cells and specific antibodies (e.g., in response to vaccination) decrease with age, while total and unspecific immunoglobulin and autoantibodies increase. Some B cell clones expand, resulting in higher probability for lymphocyte malignancies.CC BY · PubMed Central
Figure 3 Influence of zinc on age-related changes of immune function. Aging leads to an increase in pro-inflammatory cytokines and modulates the TH1–TH2 balance toward a TH2 response by reducing the TH-1 cytokines IFN-α and -γ and increasing IL-10. This reduces T cell help for immunoglobulin class switch and causes unspecific activation of B cells. Zinc counteracts the effects on [a] pro-inflammatory cytokines [27], [b] IFN-α [73], [c] IFN-γ [92], and [d] IL-10 [93].
Figure 3 Influence of zinc on age-related changes of immune function. Aging leads to an increase in pro-inflammatory cytokines and modulates the TH1–TH2 balance toward a TH2 response by reducing the TH-1 cytokines IFN-α and -γ and increasing IL-10. This reduces T cell help for immunoglobulin class switch and causes unspecific activation of B cells. Zinc counteracts the effects on [a] pro-inflammatory cytokines [27], [b] IFN-α [73], [c] IFN-γ [92], and [d] IL-10 [93].CC BY · PubMed Central

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Research works printed but not linked: 1

  1. Kaplan J, Hess JW, Prasad AS: Impaired interleukin-2 production in the elderly: Association with mild zinc deficiency. J Trace Elem Exp Med. 1988, 1: 3-8.

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Metadata

Authors
Haase, H., & Rink, L.
Affiliations
RWTH Aachen University (DE)
Corresponding author
Rink, Lothar
ORCID
Venue
Immunity & Ageing
Publisher
Springer Science and Business Media LLC
Published
2009-06-12
Volume
6
Issue
1
Pages
9-9
ISSN
1742-4933 (ISSN-L)
DOI
10.1186/1742-4933-6-9
PMC
PMC2702361
OpenAlex
W2124890716
Cited by
334
References
157
Citations by year
2026: 14 · 2025: 20 · 2024: 18 · 2023: 14 · 2022: 30 · 2021: 38 · 2020: 31 · 2019: 18 · 2018: 13 · 2017: 17 · 2016: 16 · 2015: 13 · 2014: 17 · 2013: 16 · 2012: 28
FWCI
19.04
Type
journal article
Language
en
Open access
Licence
Locations
  • Immunity & Ageing (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
  • RWTH Publications (RWTH Aachen) (submittedVersion, cc-by)
Topics
  • Health Sciences › Nursing › Nutrition and Dietetics › Trace Elements in Health
  • Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
  • Health Sciences › Medicine › Physiology (medical) › Nutrition and Health in Aging
Keywords
zinc, zinc deficiency, immunosenescence, aging, innate immunity, adaptive immunity, thymus, T helper cells, Th2 shift, vaccine response, oral zinc supplementation, chronic inflammation, older adults

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