Zinc-metallothioneins and ageing

MT are a group of low-molecular-weight metal-binding proteins that have high affinity for zinc (k _d (constant of dissociation) 1·4×10⁻¹³ m)⁽Reference Krezel, Hao and Maret¹³⁾. MT exist in different isoforms characterized by the length of amino acid chain: isoforms I, II, III and IV mapped on chromosome 16 in man and on chromosome 8 in mice with complex polymorphisms⁽Reference Mocchegiani, Costarelli and Giacconi⁹⁾. The more common isoforms are I and II; the isoform III is a brain-specific member and the isoform IV is restricted to squamous epithelia. MT contain 20 cysteines, all in reduced form, and bind seven zinc atoms through mercaptide bonds that have the spectroscopy characteristics of metal thiolate clusters⁽Reference Krezel, Hao and Maret¹³⁾. MT distribute intracellular zinc as zinc undergoes rapid inter- and intracluster exchange⁽Reference Krezel, Hao and Maret¹³⁾. The redox properties of MT and their effect on zinc in the clusters are crucial for the protective role of MT in the presence of ionizing and UV radiations, heavy toxic metals (mercury and cadmium), lipid peroxidation, reactive oxygen species, oxidative stress caused by anticancer drugs and conditions of hyperoxia⁽Reference Sato and Kondoh¹⁴⁾. This protective role of MT has been especially studied in young–adult MT knockout mice (null mice) for short periods of exposure to toxic metals or in the presence of zinc excess or zinc deficiency⁽Reference Kelly, Quaife and Froelick¹⁵⁾. Therefore, the protective role of MT is evident in transient stress conditions, as it may occur in the young–adult age, in which the chronic status (by stress or inflammation) is a rare event⁽Reference Mocchegiani, Costarelli and Giacconi⁹⁾. In contrast, this role may be questionable in ageing, because the stress-like condition and the inflammation by high IL-6 are chronic⁽Reference Mocchegiani, Costarelli and Giacconi⁹⁾. Since IL-6 affects MT gene expression⁽Reference Mocchegiani, Giacconi and Cipriano¹⁶⁾, these proteins may turn off from protective to harmful agents in ageing following the ‘Antagonistic Pleiotropy Theory of Ageing'⁽Reference Williams and Day¹⁷⁾. Despite MT increase in ageing, a limited release of zinc by MT occurs suggesting one of the possible causes of the impaired immune response⁽Reference Mocchegiani, Costarelli and Giacconi⁹⁾. In contrast, in the presence of lower stress and inflammatory condition, as it occurs in centenarians, MT production is low, coupled with satisfactory intracellular zinc ion availability⁽Reference Mocchegiani, Giacconi and Cipriano¹⁶⁾. Since IL-6 acts through its sub-unit receptor gp130, the relative lower gene expression of gp130 in centenarians⁽Reference Moroni, Di Paolo and Rigo¹⁸⁾ may imply that a quota of IL-6 is inactive in very old age. As a result, the satisfactory immune performance, metabolic harmony and antioxidant activity allow a good healthy status in centenarians⁽Reference Mocchegiani, Giacconi and Cipriano¹⁶⁾. Therefore, the interrelationships among stress/inflammatory/immune status, MT and zinc are pivotal in order to achieve successful ageing. However, this role remains to be clearly established taking also into account that MT may play different roles in different organs. In this regard, recent findings in cardiac-specific MT transgenic mice suggest that the expression of MT in cardiocytes may alleviate ageing-induced cardiac contractile defects and oxidative stress prolonging the lifespan⁽Reference Yang, Doser and Fang¹⁹⁾. In addition, Daf-2 (gene of insulin receptor-like protein-2) mutant nematodes, other than a longevity phenotype, display an altered expression of MT which, in turn, seem to interact with the insulin signalling pathway⁽Reference Barsyte, Lovejoy and Lithgow²⁰⁾. Therefore, even if the specific function of MT in ageing is still a matter of discussion, these last reports, associated with recent findings on the possible role played by MT in modulating energy metabolism⁽Reference Feng, Cai and Pierce²¹⁾, strongly suggest that MT is pivotal for maintaining the health status. On the other hand, polymorphisms of MT1A (A/C at position +647) are involved in successful ageing⁽Reference Cipriano, Malavolta and Costarelli²²⁾.

Zinc-metallothioneins and inflammatory/immune response in ageing

For a prompt immune response against stressor agents and inflammation, macrophages produce some cytokines, such as IL-1, IL-6, interferon (IFN)-α, TNF-α, which in turn provoke a new synthesis of MT in the liver, but at the same time, an alteration in the zinc status⁽Reference Mocchegiani, Costarelli and Giacconi⁹⁾. These findings clearly suggest the existence of interplay between MT and the immune system. MT act both as a reservoir of zinc during zinc deficiency and as a zinc buffering protein in the presence of excessive amount of zinc in order to prevent zinc toxicity⁽Reference Kelly, Quaife and Froelick¹⁵⁾. Therefore, MT are protective agents with also the task to prevent zinc deficiency during an inflammatory status. Under inflammatory conditions, MT in the extra-cellular environment may support the beneficial movement of leucocytes to the site of inflammation representing a ‘danger signal’ for the immune cells and modifying the character of the immune response when cells sense cellular stress. However, high MT produced in chronic inflammation may alter the normal chemotactic response that regulates leucocyte trafficking⁽Reference Yin, Knecht and Lynes²³⁾. Taking into account that zinc ions attract leucocytes by promoting the chemotactic response⁽Reference Hujanen, Seppa and Virtanen²⁴⁾, high MT might thus be dangerous for the immune response during chronic inflammation. Moreover, (1) the existence of high MT and low zinc ion availability in the atrophic thymus from old mice⁽Reference Mocchegiani, Giacconi and Muti²⁵⁾, (2) the presence of high MT in lymphocytes from old people and Down's syndrome subjects (premature ageing) coupled with impaired innate immunity⁽Reference Mocchegiani, Giacconi and Cipriano¹⁶⁾ and (3) the occurrence of atrophic thymus in young stressed mice over-expressing MT⁽Reference Mocchegiani, Giacconi and Cipriano²⁶⁾, further suggest this dangerous role played by MT in immune response during ageing. Additionally, elevated levels of extra-cellular MT, as found in chronic inflammatory sites, can cause a dramatic decrease in cytotoxic T lymphocyte activity against allogeneic target cells, reduce the proliferative response of CTLL-2 (IL-2 dependent cytotoxic T-lymphocyte cell line) cells to cytokines, and decrease the level of MHC Class I and CD8 molecules⁽Reference Youn and Lynes²⁷⁾. Or paradoxically, high levels of MT induced by antigenic stimuli may allow an iper-activation of the immune system with subsequent deleterious effect, as it occurs in revertant CD4 T-cells from older individuals⁽Reference Lee, Cui and Czesnikiewicz-Guzik²⁸⁾. Therefore, high MT may be considered as a consequence of the intracellular zinc dyshomeostasis further supporting its task as a specific ‘danger signal’ for the efficiency of the immune system in ageing. Anyway, high MT may be harmful in ageing. This role may be largely due to the increased zinc influx within the cells during acute or chronic inflammation that, in turn, provokes increased MT with concomitant decrement in intracellular labile zinc, because a majority of the zinc ions are buffered by MT⁽Reference Malavolta, Cipriano and Costarelli²⁹⁾. This phenomenon is observed in old people (aged up to 70–75 years.), but not in very old people (>80 years), in whom both MT and intracellular labile zinc are low perhaps due to lower dietary zinc intake or cellular senescence phenomena⁽Reference Malavolta, Cipriano and Costarelli²⁹⁾. Subsequently, the immune efficiency is diminished or altered in ageing and in very old age. This effect may be worsened by the fact that MT are not efficient donors of zinc in ageing⁽Reference Mocchegiani, Giacconi and Cipriano¹⁶⁾. On the other hand, high MT induce down-regulation of many other biological functions related to zinc, such as metabolism, gene expression and signal transduction⁽Reference Mocchegiani, Costarelli and Giacconi⁹⁾.

However, the limited capability of MT in zinc release is still an unresolved problem in ageing, especially with regard to the precise mechanism involved. The zinc release from MT under oxidative stress conditions is accompanied by more MT disulfide bond formation⁽Reference Feng, Benz and Cai³⁰⁾. But, an intriguing point is that also nitric oxide (NO) provokes the zinc release by MT, via s-nitrosylation of MT cysteines (i.e. the transfer of an NO group to cysteine sulfhydryl groups on MT molecule), and Zn²⁺⁺ release is sufficiently mild to allow the reconstitution of MT through Zn²⁺⁺ rebinding⁽Reference Zangger, Oz and Haslinger³¹⁾. During inflammation, hepatocytes respond to cytokines by up-regulating inducible NO synthase, which generates a large amount of NO from arginine with concomitant enhanced MT⁽Reference Spahl, Berendji-Grun and Suschek³²⁾. NO promotes zinc release from MT, which in turn may repress inducible NO synthase in an autocrine way⁽Reference Zangger, Oz and Haslinger³¹⁾. However, despite inducible NO synthase increases in ageing, the release of zinc by MT is very limited. NO donors and zinc fluorescent probes are useful tools in order to study the zinc release from MT and to evaluate the intracellular labile zinc in ageing. Using a methodology recently developed in our laboratory⁽Reference Malavolta, Costarelli and Giacconi³³⁾, the NO-induced release of zinc can be preserved at least in non-agenarians carrying MT1A polymorphism favourable to the longevity⁽Reference Cipriano, Malavolta and Costarelli²²⁾. Moreover, a flow cytometric assay for the measurement of intracellular labile zinc shows that the intracellular concentration of labile zinc in resting cells were estimated to be 0·17 nM in monocytes and 0·35 nM in lymphocytes (CD4+)⁽Reference Haase, Hebel and Engelhardt³⁴⁾. The combination of these two novel methodological procedures will permit to study in depth the cause of limited zinc release from MT in ageing and, at the same time, to evaluate the amount of intracellular labile zinc. Anyway, a limited zinc release from MT exists in ageing with an emphasis after 70 years of age⁽Reference Malavolta, Cipriano and Costarelli²⁹⁾. The recent discovery of a novel polymorphism of MT (−209A/G MT2A) may indirectly support this assumption. Old subjects carrying AA genotype display high MT, low intracellular zinc ion availability, enhanced IL-6 and impaired innate immune response with subsequent possible risk to develop atherosclerosis and diabetes type-2⁽Reference Giacconi, Cipriano and Muti³⁵⁾. Therefore, MT might have a different role in immunosenescence, fitting thus with the concept that several genes/proteins that increase fitness early in life may have negative effects later in life⁽Reference Williams and Day¹⁷⁾.

Zinc transporters, zinc signalling, inflammatory/immune response and ageing

Zinc transporter proteins also appear to be specifically involved in regulating cellular zinc homeostasis via influx, efflux or vesicular sequestration with a task in maintaining intracellular zinc concentration in a narrow physiological range in order to avoid cellular zinc toxicity or deficiency when extra-cellular zinc concentration changes⁽Reference Cousins, Liuzzi and Lichten¹²⁾. Two families of zinc transporters have been identified. The ZnT family decreases cytoplasmic zinc concentration by secretion, sequestration or efflux, whereas the ZIP family increases cytoplasmic zinc influx or release of stored zinc⁽Reference Cousins, Liuzzi and Lichten¹²⁾. Therefore, the balance of zinc transporter families is fundamental in maintaining an optimal intracellular zinc homeostasis as well as the zinc signalling. In this context, ZIP7 releases Zn from the endoplasmic reticulum controlling tyrosine phosphorylation⁽Reference Taylor, Vichova and Jordan³⁶⁾, and lysosomal ZIP8 is required for IFN-γ expression in T-cells⁽Reference Aydemir, Liuzzi and McClellan³⁷⁾. ZIP6 is implicated in the zinc signalling required for revertant CD4 T-cell proliferation, via activation of NF-κB and subsequent pro-inflammatory cytokine productions⁽Reference Lee, Cui and Czesnikiewicz-Guzik²⁸⁾. The zinc signal via ZIP6 is also responsible for MT2A induction which, in turn, mediates a negative feedback to down-regulate this signal. The relevance of the zinc signals in regulating inflammatory signalling, via NF-κB, was also observed in monocytes treated with lipopolysaccharide⁽Reference Haase, Ober-Blobaum and Engelhardt³⁸⁾, suggesting the relevance of zinc transporters and zinc signalling in modulating the immune response, especially in ageing because of the likely reduced zinc dietary intake and intestinal malabsorption⁽Reference Mocchegiani, Costarelli and Giacconi⁹⁾.

However, a paucity of data exists regarding the role played by zinc transporters in ageing. After an increase from the birth up to the adult age in some tissues, significant decrements of both ZnT and ZIP families in peripheral leucocytes from elderly women have been observed, in particular the sub-types ZnT1 and ZIP1⁽Reference Andree, Kim and Kirschke³⁹⁾. Taking into account that ZIP family increases cytoplasmic zinc influx⁽Reference Cousins, Liuzzi and Lichten¹²⁾, an intriguing point is that IL-6 up-regulates the ZIP14 gene expression in the liver, which is in turn responsible for the hypozincaemia that accompanies the acute phase response to inflammation and infection⁽Reference Liuzzi, Lichten and Rivera¹⁰⁾. Since chronic inflammation by high IL-6, hypozincaemia and risk of infections are common in old age⁽Reference Mocchegiani, Giacconi and Cipriano¹⁶⁾, the possible alterations of the zinc transporters in ageing coupled with the inability of MT in zinc release, might induce synergistic deleterious effects on immune efficiency with the subsequent emergence of some age-related diseases.

Rationale for zinc supplementation in ageing: in vitro studies

Since the crude zinc balance is negative in old mice and human individuals⁽Reference Mocchegiani, Muzzioli and Giacconi⁴⁰⁾, zinc supplementations in old mice and in the elderly have been carried out in order to restore the immune efficiency. The scientific rationale for in vivo zinc supplementation finds consistent support by in vitro data in immune cells. When peripheral blood mononuclear cells are stimulated with zinc, IL-1, IL-6 and TNF-α, soluble IL-2 receptor and IFN-γ are released⁽Reference Haase and Rink⁴¹⁾. However, the effect of zinc on monocytes may depend on external stimulation. In fact, zinc inhibits lipopolysaccharide-induced TNF-α and IL-1-β release from both primary human monocytes and monocytic cell lines through the inhibition of cyclic nucleotide phosphodiesterase activity⁽Reference Haase and Rink⁴¹⁾, suggesting that zinc may also display some anti-inflammatory properties. The dose of zinc used is also a critical variable. In a serum-free culture medium, the concentration of zinc ≥100 μM stimulates monocytes, but prevents T-cell activation, perhaps owing to a lower intracellular zinc content in T-cells than in monocytes⁽Reference Haase and Rink⁴¹⁾.

Treatment with zinc in vitro generally also displays beneficial effects on cell survival, but the effect largely depends upon the cell type and the dose of zinc used. It seems that both apoptosis prevention and induction are mediated by pathways involving zinc and/or zinc-dependent enzymes⁽Reference Fraker and Lill-Elghanian⁸⁾. Therefore, the modulation of the intracellular zinc homeostasis plays a key role not only in preventing apoptosis, when oxidative stress or chronic inflammation are low, but also in inducing apoptosis especially when oxidative stress and cellular damage is high in order to down-regulate the immune response and to eliminate virally infected or malignant cells. Induction of apoptosis by zinc signalling in damaged cells, via activation of p53 pathway, is evident in young–adult age and in very old age⁽Reference Ostan, Alberti and Bucci⁴²⁾, perhaps owing to a preserved regulation of zinc homeostasis in both classes of age⁽Reference Mocchegiani, Giacconi and Cipriano¹⁶⁾.

Experiments in thymocytes also support this point of view, since media supplemented with zinc from 50 up to 150 μM prevents old thymocyte apoptosis induced by dexamethasone or serum deprivation⁽Reference Provinciali, Di Stefano and Stronati⁴³⁾, whereas the direct introduction of free zinc, as zinc-pyrithone, inside thymocytes provokes apoptosis because of inducing permanent oxidative stress and irreversible damage⁽Reference Mann and Fraker⁴⁴⁾, thus activating pro-apoptotic pathways. Therefore, zinc supplementation, not exceeding the physiological dose, may be of benefit in ageing either in preventing apoptosis of undamaged immune cells or in reducing the inflammation with a possible prevention of the appearance of age-related diseases.

Effect of zinc supplementation on inflammatory/immune response in ageing

The elderly

With regard to the elderly, inconsistent data exist on the beneficial effect of zinc supplementation on the immune efficiency, due to different doses and duration of zinc treatment. Although zinc was used at the dose recommended by RDA (10–25 mg/d with different length of treatment; Table 1) in the majority of the studies, Prasad et al.⁽Reference Prasad, Fitzgerald and Hess⁴⁹⁾ and Boukaiba et al.⁽Reference Boukaiba, Flament and Acher⁵⁰⁾ have found an increment of thymulin activity and improvement in response to skin-test antigens and taste acuity; Bogden et al.⁽Reference Bogden, Oleske and Lavenhar⁵¹⁾ have reported some benefit exclusively for increased lymphocyte mitogen proliferative response; Cakman et al.⁽Reference Cakman, Kirchner and Rink⁵²⁾ have found enhanced IFN-γ production by leucocytes; Fortes et al.⁽Reference Fortes, Forastiere and Agabiti⁵³⁾ report an increased number of cytotoxic T lymphocytes; Hodkinson et al.⁽Reference Hodkinson, Kelly and Alexander⁵⁴⁾ describe no effect on some markers of immunity (natural killer cells) or inflammation (C-reactive protein), but only increased the ratio of CD4/CD8 T lymphocytes at month 6; Kahmann et al.⁽Reference Kahmann, Uciechowski and Warmuth⁵⁵⁾ report reduced levels of activated T-cells and basal IL-6 release from peripheral blood mononuclear cells and improved T-cell response. Using higher doses of zinc, 40–220 mg/d with different lengths of treatment (Table 1), Duchateau et al.⁽Reference Duchateau, Delepesse and Vrijens⁵⁶⁾ and Sandstead et al.⁽Reference Sandstead, Henriksen and Greger⁵⁷⁾ have observed an improvement in response to skin-test antigens and taste acuity; an improved delayed type hypersensitivity reaction has been also found in a limited number of subjects by Cossack⁽Reference Cossack⁵⁸⁾ and by Wagner et al.⁽Reference Wagner, Jernigan and Bailey⁵⁹⁾; Prasad et al.⁽Reference Prasad, Beck and Bao⁶⁰⁾ found improved IL-2 mRNA. Other studies⁽Reference Bogden, Oleske and Lavenhar^61–Reference Stewart-Knox, Simpson and Parr⁶³⁾ report no effects on various immune functions after zinc supplementation, perhaps due to high dose of zinc used for too long a period (Table 1).

Table 1. Zinc supplementation studies in human elderly and old mice: effect upon the immune functions

DTH, delayed type hypersensitivity reaction; (C), control group without supplementation; (P), placebo; (Z), zinc supplementation; PHA, phytohaemagglutinin; PBMC, peripheral blood mononuclear cells; NK, natural killer; CRP, C-reactive protein.

* The values are given as elemental zinc.

From all these studies, a physiological dose of zinc applied for a long period or high doses of zinc for short periods might induce limited effects on the immune response, perhaps due to zinc accumulation in various organs and tissues with subsequent toxic effect of zinc upon the immune functions⁽Reference Mocchegiani, Costarelli and Giacconi⁹⁾. In this context, it is also useful to remember that high doses of zinc trigger apoptosis of the immune cells in the presence of high-oxidative stress and inflammation⁽Reference Fraker and Lill-Elghanian⁸⁾. Therefore, caution is advised for the management of zinc supplementation with the suggestion to perform the trial for short periods and on alternate cycles only. In our experience, zinc treatment (15 mg Zn²⁺⁺/d for 1 month) in Down's syndrome subjects, the elderly and old infected patients restores thymic endocrine activity, lymphocyte mitogen proliferative response, CD4(+) cell number, NK cell cytotoxicity and DNA repair, as well as thyroid hormones turnover. At the clinical level, significant reductions of relapsing infection occur in Down's syndrome subjects, the elderly and old infected patients⁽Reference Mocchegiani, Muzzioli and Giacconi⁶⁴⁾.

An intriguing point is the increment of zinc transporters after zinc supplementation. Elderly women treated with 22 mg zinc gluconate/d for 27 d display significant increments of ZnT1 gene expression in peripheral leucocytes⁽Reference Andree, Kim and Kirschke³⁹⁾. Such increments of ZnT1 have been also observed in human lymphoblastoid cells adding in vitro 50 or 100 μmol/l zinc⁽Reference Andree, Kim and Kirschke³⁹⁾, further suggesting the relevance of zinc supplementation in affecting the gene expression of zinc transporters and, consequently, the correct maintenance of intracellular zinc homeostasis. Such a mechanism might be important for restoring ZnT8 gene expression in pancreatic vesicles being involved in the aetiology of type-2 diabetes⁽Reference Sladek, Rocheleau and Rung⁶⁵⁾.

Since zinc also affects the cytotoxicity of liver NKT cells bearing T-cell receptor γδ (extrathymic T-cell pathway) with higher production of IFN-γ in old mice⁽Reference Mocchegiani, Giacconi and Cipriano⁶⁶⁾, the presence of satisfactory zinc ion bioavailability coupled with increased NKT cell cytotoxicity and enhanced IFN-γ production in centenarians with respect to the elderly⁽Reference Miyaji, Watanabe and Toma⁶⁷⁾ strengthens the pivotal role of zinc supplementation in maintaining or improving the global immune response (thymic and extrathymic T-cell pathways) and in fighting oxidative stress and inflammation.

However, since zinc also affects MT gene expression⁽Reference Krezel, Hao and Maret¹³⁾, the question arises whether zinc supplementation in old age may further increase MT, causing possible major harmful effects (i.e. still major limited zinc release by MT). This fact may be avoided, because zinc lowers the inflammation and, as such, MT can still be able to release zinc with subsequent good immune performances⁽Reference Mocchegiani, Muzzioli and Giacconi¹¹⁾. Therefore, the potential harmful effect of MT may be excluded during physiological zinc supplementation in ageing.

Zinc supplementation in the elderly on the basis of genetic background

One possible cause of the discrepancy existing in the literature on the effect of zinc supplementation on the immune response in the elderly may be the choice of old subjects who effectively need zinc supplementation in strict relationship with dietary habits and inflammatory status. This assumption is supported by the discovery that old subjects carrying GG genotypes (termed C− carriers) in the IL-6−174G/C locus display increased IL-6 production, low intracellular zinc ion availability, impaired innate immune response coupled with enhanced MT⁽Reference Mocchegiani, Giacconi and Costarelli⁶⁸⁾. By contrast, old subjects carrying GC and CC genotypes (termed C+ carriers) in the same IL-6−174 locus displayed satisfactory intracellular zinc as well as innate immune response. But, the more intriguing finding is that male C+ carriers are more prone to reach centenarian age than C− carriers. Therefore, old C− carriers are likely to benefit more from zinc supplementation than old C+ carriers. The distribution of IL-6−174 genotype is very different among various European countries with large differences between Northern and Southern European countries⁽Reference Mariani, Neri and Cattini⁶⁹⁾. Zinc supplementation in old C− subjects restores NK cell cytotoxicity to values present in old C+ carriers and considerably improves both zinc status, assessed by the percentage increment of granulocyte Zn⁽Reference Mocchegiani, Giacconi and Costarelli⁶⁸⁾, and stress response, assessed by the percentage increment of MT protein as well as Clusterin/apo J and other proteins related to oxidative stress and inflammation⁽Reference Mocchegiani, Giacconi and Cipriano⁴⁸⁾. When the genetic variations for IL-6 polymorphism are also associated with the variations of MT1A+647A/C gene, the plasma zinc deficiency and the altered immune response is more evident⁽Reference Mariani, Neri and Cattini⁶⁹⁾, suggesting that the genetic variations of IL-6 and MT1A are very useful tools for the identification of old people who effectively need zinc supplementation. These results open the hypothesis that the daily requirement of zinc might be different in elderly harbouring a different genetic background. Such a role played by the genetic background on the beneficial effect of zinc supplementation is also evident in keeping the pro-inflammatory cytokine and chemokine productions better under control⁽Reference Mariani, Neri and Cattini⁶⁹⁾ as well as in reducing the gene expression of genes related to the inflammatory status, such as IL-1 and its receptor⁽Reference Mazzatti, Malavolta and White⁷⁰⁾. A comprehensive portrait of the effect of zinc supplementation on zinc status, immune response, cytokines, chemokines and stress-related proteins in old people selected on the basis of IL-6 and MT polymorphisms is provided in Table 2.

Table 2. Effect of zinc supplementation in the elderly in accordance with genetic background and zinc status

MT, metallothionein; ATF2, activating transcription factor 2; CSF2, colony stimulating factor 2; ICAMI, inter-cellular adhesion molecule 1; LTA, lymphotoxin-α; CCL2, chemokine (C-C motif) ligand 2; SELE, E-selectin; VCAM1, vascular cell adhesion molecule 1; MsR, methionine sulfoxide reductase; SOD, superoxide dismutase; dRib, 2-deoxy-D-ribose; MIP-1α, macrophage inflammatory protein 1α; MCP-1, monocyte chemotactic protein-1; RANTES, regulated upon activation normal T-cell expressed and secreted; CMV, cytomegalovirus; ↑↑=strongly increased, ↑=increased, –=not modified, −↑=slightly increased at least in some sub-groups, ↑↓=great inter-individual variability.

Conclusions and future remarks

Even if some controversial findings exist on the ‘real’ necessity of zinc supplementation, the data reported clearly suggest that zinc plays a pivotal role for the immune efficiency required to reach healthy ageing and longevity. However, the major problem for zinc supplementation in old people is related to the choice of old subjects who effectively need zinc supplementation. The sole determination of plasma zinc is not sufficient, because zinc is bound to many proteins. The intracellular zinc ion availability and the zinc release by MT can be used as complementary methods to test the zinc status, as shown in non-agenarians⁽Reference Mocchegiani, Giacconi and Cipriano¹⁶⁾. The polymorphisms of IL-6 and MT1A may be the added value to screen effective old subjects for zinc supplementation in restoring inflammatory/immune response. As a consequence, healthy ageing and longevity may be achieved. The prolonged survival observed in old, nude and neonatal thymectomized zinc-treated mice and the avoidance of infection relapses in old infected patients after zinc supplementation may be in line with this interpretation. However, some points require further investigation. Firstly, the reason of the limited zinc release in ageing and the biochemical mechanism involved, in particular, addressing NO-related intracellular pathways. However, IL-6 and MT1A polymorphisms may form a solid rationale to select old individuals who effectively need zinc supplementation and not the entire old population.