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Immune response in relation to zinc status, sex and antioxidant defence in Italian elderly population: the ZENITH study

Abstract

Objective:

Evaluation of some immune markers in Italian elderly population in relation to zinc status, gender and antioxidant defence.

Design:

Observational study.

Setting:

Italian population.

Subjects:

Apparently healthy, free-living subjects, 56 men and 52 women, aged 70–85 y, enrolled in Italy.

Methods:

Lymphocytes were unstimulated or stimulated with the mitogen phytohemoagglutinin (PHA). The proliferative capacity was measured as incorporation of [3H]-thymidine and reported as stimulation index (SI). Cytokine secretion by lymphocytes was determined by ELISA. The antioxidant enzyme activities were measured using commercial kits.

Results:

Dietary zinc intake, as well as zinc in serum, red blood cells and urine were on the normal range of values and did not show any difference between men and women.

Conclusions:

Only weak differences on immune response between men and women were observed. However, zinc status appears to have more influence on the ability of lymphocytes to proliferate in men than in women.

Sponsorship:

The ZENITH study is supported by the European Commission ‘Quality of Life and Management of Living Resources’ Fifth Framework Programme, Contract No: QLK1-CT-2001-00168.

The proliferative response showed a high variability without significant differences between men and women. The amount of secreted pro- and anti-inflammatory cytokines was similar in men and women. No differences were found in the activity of antioxidant enzymes in lymphocytes, namely superoxide dismutase, glutathione peroxidase and catalase, between men and women.

An association between SI and serum zinc level in men was found. SI resulted negatively correlated with interleukin (IL)-1β (R2=0.036 and P=0.012) and IL-10 (R2=0.34 and P=0.040) only in men. IL-10 of PHA-stimulated lymphocytes was negatively correlated with red blood zinc in men (R2=0.41 and P=0.008), while IL-10 of unstimulated and PHA-stimulated lymphocytes were negatively correlated with serum zinc in women (R2=0.38 and P=0.020; R2=0.31 and P=0.040, respectively). No correlation was observed between immune markers and antioxidant enzyme activities.

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References

  • Ahluwalia N (2004): Aging, nutrition and immune function. J. Nutr. Health Aging 8, 2–61.

    CAS  PubMed  Google Scholar 

  • Andriollo-Sanchez M, Hininger-Favier I, Meunier N, Toti E, Zaccaria M, Brandollini-Bunlon M, Polito A, O’Connor JM, Ferry M, Coudray C & Roussel AM (2005): Zinc intake and status in middle-aged and older European subjects: the ZENITH study. Eur. J. Clin. Nutr. 59, S37–S41.

    Article  CAS  Google Scholar 

  • Bogden JD (2004): Influence of zinc on immunity in the elderly. J. Nutr. Health Aging 8, 48–54.

    CAS  PubMed  Google Scholar 

  • Bradford MM (1976): A rapid and sensitive for the quantitation of microgram quantitites of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248–254.

    Article  CAS  Google Scholar 

  • Chakravarti B & Abraham GN (1999): Aging and T-cell-mediated immunity. Mech. Ageing Dev. 17, 183–206.

    Article  Google Scholar 

  • Chandra RK (1999): Nutrition and immunology: from the clinic to cellular biology and back again. Proc. Nutr. Soc. 58, 681–683.

    Article  CAS  Google Scholar 

  • Douziech N, Seres I, Larbi A, Szikszay E, Roy PM, Arcand M, Dupuis G & Fulop T (2002): Modulation of human lymphocyte proliferative response with aging. Exp. Gerontol. 37, 369–387.

    Article  CAS  Google Scholar 

  • Fabris N, Mocchegiani E & Provinciali M (1997): Plasticity of neuroendocrine interactions during aging. Exp. Gerontol. 32, 415–429.

    Article  CAS  Google Scholar 

  • Finamore A, Roselli M, Merendino N, Nobili F, Vignolini F & Mengheri E (2003): Zinc deficiency suppresses the development of oral tolerance in rats. J. Nutr. 133, 191–198.

    Article  CAS  Google Scholar 

  • Gaillard RC & Spinedi E (1998): Sex– and stress–steroids interactions and the immune system: evidence for a neuroendocrine–immunological sexual dimorphism. Domest. Anim. Endocrinol. 15, 345–352.

    Article  CAS  Google Scholar 

  • Groux H, O’Garra A, Bigler M, Rouleau M, Antonenko S, de Vries JE & Roncarolo MG (1997): A CD4+ T-cell subset inhibits antigen-specific T-cell responses and prevents colitis. Nature 16, 737–742.

    Article  Google Scholar 

  • Hirokawa K, Utsuyama M, Katsura Y & Sado T (1988): Influence of age on the proliferation and peripheralization of thymic T cells. Arch. Pathol. Lab. Med. 112, 13–21.

    CAS  PubMed  Google Scholar 

  • Kraus A, Roth HP & Kirchgessner M (1997): Supplementation with vitamin C, vitamin E or beta-carotene influences osmotic fragility and oxidative damage of erythrocytes of zinc-deficient rats. J. Nutr. 127, 1290–1296.

    Article  CAS  Google Scholar 

  • Levings MK & Roncarolo MG (2005): Phenotypic and functional differences between human CD4+CD25+ and type 1 regulatory T cells. Curr. Top. Microbiol. Immunol. 293, 303–326.

    CAS  PubMed  Google Scholar 

  • Losonczy G, Kriston T, Szabo A, Muller V, Harvey J, Hamar P, Heeman V & Baylis C (2000): Male gender predisposes to development of endotoxic shock in the rat. Cardiovasc. Res. 47, 183–191.

    Article  CAS  Google Scholar 

  • Malaguarnera L, Ferlito L, Imbesi RM, Gulizia GS, Di Mauro S, Maugeri D, Malaguarnera M & Messina A (2001): Immunosenescence: a review. Arch. Gerontol. Geriatr. 32, 1–14.

    Article  CAS  Google Scholar 

  • McClain CJ, McClain M, Barcve S & Boosalis MG (2002): Trace elements and the elderly. Clin. Geriatr. Med. 18, 801–818.

    Article  Google Scholar 

  • Offner PJ, Moore EE & Bi WL (1999): Male gender is a risk factor for major infections after surgery. Arch. Surg. Chicago 134, 935–938.

    Article  CAS  Google Scholar 

  • Olsen NJ & Kovacs WJ (1996): Gonadal steroids and immunity. Endocrinol. Rev. 17, 369–384.

    CAS  Google Scholar 

  • Paganelli R, Scala E, Quinti I & Ansotegui IJ (1994): Humoral immunity in aging. Aging (Milano) 6, 143–150.

    CAS  Google Scholar 

  • Polito A, Meunier N, Andriollo-Sanchez M, Catasta G, Azzini E, Simpson EEA, O’Connor JM, Roussel AM, Ferry M, Coudray C & Maiani G (2005): Screening and recruitment procedure of late-middle aged and older European subjects: the ZENITH study. Eur. J. Clin. Nutr. 59, S8–S12.

    Article  CAS  Google Scholar 

  • Prasad AS (1998): Zinc and immunity. Mol. Cell. Biochem. 188, 63–69.

    Article  CAS  Google Scholar 

  • Prasad AS (2000): Effect of zinc deficiency on Th1 and Th2 cytokine shifts. J. Infect. Dis. 182, S62–S68.

    Article  CAS  Google Scholar 

  • Prasad AS, Fitzgerald JT, Hess JW, Kaplan J, Pelen F & Dardenne M (1993): Zinc deficiency in elderly patients. Nutrition 9, 218–224.

    CAS  PubMed  Google Scholar 

  • Ravaglia G, Forti P, Maioli F, Bastagli L, Facchini A, Mariani E, Savarino L, Sassi S, Cucinotta D & Lenaz G (2000): Effect of micronutrient status on natural killer cell immune function in healthy free-living subjects aged ≥90 y. Am. J. Clin. Nutr. 71, 590–598.

    Article  CAS  Google Scholar 

  • Rink L, Cakman I & Kirchner H (1998): Altered cytokine production in the elderly. Mech. Ageing Dev. 15, 199–209.

    Article  Google Scholar 

  • Ripa S & Ripa R (1995): Zinc and the elderly. Minerva Med. 86, 275–278.

    CAS  PubMed  Google Scholar 

  • Sarkar D & Fisher PB (2005): Molecular mechanisms of aging-associated inflammation. Cancer Lett. 21, 1–11.

    Google Scholar 

  • Sullivan JF, Jetton MM, Hahn HK & Burch RE (1980): Enhanced lipid peroxidation in liver microsomes of zinc-deficient rats. Am. J. Clin. Nutr. 33, 51–56.

    Article  CAS  Google Scholar 

  • Valle B & Falchuk KH (1993): The biochemical basis of zinc. Physiol. Rev. 73, 79–118.

    Article  Google Scholar 

  • Windmill KF & Lee VM (1998): Effects of castration on the lymphocytes of the thymus, spleen and lymph nodes. Tissue Cell 30, 104–111.

    Article  CAS  Google Scholar 

Download references

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Correspondence to E Mengheri.

Additional information

Guarantor: E Mengheri.

Contributors: AF performed experiments and data analysis on immune response, CD performed experiments and data analysis on antioxidant enzyme activities, DP contributed to experiments on immune response, MD was responsible for study design and execution of antioxidant experiments, AP was responsible for subjects recruitment and assisted statistical analysis, EV contributed to subjects recruitment and performed erythrocyte preparation, AR performed blood collection, CC was the Zenith study coordinator, EM was responsible for study design, execution and data analysis of immune response experiments and for the preparation of this paper. All authors contributed to finalization of the manuscript.

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Finamore, A., Devirgiliis, C., Panno, D. et al. Immune response in relation to zinc status, sex and antioxidant defence in Italian elderly population: the ZENITH study. Eur J Clin Nutr 59 (Suppl 2), S68–S72 (2005). https://doi.org/10.1038/sj.ejcn.1602302

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