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"Cumulative Stress": The Effects of Maternal and Neonatal Oxidative Stress and Oxidative Stress-Inducible Genes on Programming of Atopy.

1. Introduction

Allergic diseases including atopic dermatitis, allergic rhinitis, and asthma are some of the most common chronic diseases in the world [1]. Although extensive epidemiological and laboratory studies have been performed to identify the environmental and immunological causes of atopy, genetic predisposition seems to be the biggest risk factor for allergic diseases [2, 3]. It is known that several foetal adaptive responses to environmental factors are mediated by epigenetic changes which, impacting early-life morbidity, may exercise effects on the immune system, lung development, airway remodelling, allergen predisposition, and atopic and nonatopic inflammation, through numerous pathways [2, 4]. In particular, the onset of atopic diseases may be the result of heritable changes of gene expression, without any alteration in DNA sequences, occurring in response to early (prenatal) or later (perinatal) environmental stimuli [4]. Findings suggest that the establishment of a peculiar epigenetic pattern may also be generated by oxidative stress (OS) and perpetuated by the activation of OS-related genes [5]. Reactive oxygen species (ROS), known to be important cell-signalling molecules [6], could, in fact, set up a positive-feedback loop that induces and perpetuates atopic injury. OS, also influencing T-cell signal transduction and gene expression [7], modulates T-cell polarization toward a T helper- (Th-) 2 cellular subset [8] which might be, in turn, a further source of ROS.

OS is a specific setting also occurring in normal events such as pregnancy and birth.

Pregnancy is a physiological period associated with enhanced OS related to high metabolic turnover and elevated tissue oxygen requirements [9]. During pregnancy, increased oxygen demand augments the rate of production of ROS, and women, even during normal pregnancies, experience elevated serum OS levels [9]. Increased OS levels and reduced antioxidative capacities may contribute to the pathogenesis of perinatal [10, 11] and postnatal disorders [12, 13], such as atopic diseases [14, 15], as newborns are more prone to OS than individuals later in life [16]. Moreover, it has also been reported that OS-related maternal genetics, independently of transmission of specific alleles, may influence a child's atopic risk beginning in the uterus [17, 18].

Also during pregnancy, newborns are also continually exposed to elevated levels of ROS. At birth, newborns transit from a hypoxic intrauterine to a normoxic extrauterine environment. This increased OS further favours neonatal morbidity, also including atopy [14].

Analyzing the role of maternal and neonatal oxidative stress and oxidative stress-inducible genes, the purpose of this review was to summarize what is known about the relationship between maternal and neonatal OS-related genes and the development of atopic diseases.

2. Cumulative Effects of Maternal and Neonatal Oxidative Stress on the Immune System

It is well known that OS occurs early in pregnancy and continues in the postnatal period [12]. In particular, pregnancy is associated with enhanced OS related to high metabolic turnover and elevated tissue oxygen requirements [34]. On the other hand, newborns, exhibiting an accelerated production of free radicals and limited antioxidant protection, are also constitutively vulnerable to OS. Therefore, during pregnancy and intrauterine life, many factors such as hypoxia, inflammation, and infections can easily induce overproduction of free radicals (FRs) [11], exceeding the capacity of defensive mechanisms to neutralize them. The release of FRs leads to the oxidation of lipids, proteins, and polysaccharides and to DNA modifications [7-9, 19] which, in turn, increase the susceptibility of rapidly growing tissues to damage [35], as well as modulation of the immune system [10, 36].

With regard to the immune system, different immunological responses to ROS production have been reported, depending on environmental oxidative status. While normal ROS amounts have been shown to be important for T-cell function and for adequate, beneficial antimicrobial protection [37], high ROS concentrations can negatively modulate immune system responses leading to inhibited T-cell proliferation [37] and to hyporesponsivity to exogenous and/or endogenous activating stimuli [9]. In particular, OS plays a critical role as a secondary messenger in the initiation and amplification of signalling, miming antigenic effects. The antigen receptors are themselves OS-generating enzymes, contributing further to enhancing the cellular "oxidative burst" against exogenous pathogens as well as neighbouring cells [10], causing autoinflammatory and/or allergic diseases [17, 38].

Moreover, it has been suggested that OS, leading to secretion of a variety of proinflammatory cytokines and chemokines [38], elicits a polarized immune response which is closely associated with a breakdown in immune tolerance [39]. In particular, when immunoglobulin- (Ig-) E binds to specific membrane receptors, peripheral blood is activated to produce more superoxide and hydrogen peroxide ([H.sub.2][O.sub.2]), contributing to elevated environmental OS and sterile inflammation [40] in upper and lower airways [41-43], and in the skin [44]. Furthermore, immune cells, because of higher production of ROS, are themselves particularly sensitive to OS, creating a vicious circle for the production of proinflammatory mediators and supporting a prooxidant status [9]. The activation of both the redox-sensitive transcription factor nuclear factor-kappa B (NF-[kappa]B) and activator protein(AP-) 1 and the release of proinflammatory proteins involved in immune response (e.g., interleukin- (IL-) 1, IL-6, tumour necrosis factor- (TNF-) [alpha], and interferon- (INF-) [alpha], as well as [H.sub.2][O.sub.2]) are critical events in immunity, promoting stimulus-specific genes expression [17, 38]. These findings confirm the evidence that foetal immune response is prenatally influenced [45] and that the activation of maternal and neonatal OS-inducible genes may influence a child's atopic risk, early in the uterus [46, 47] (Tables 1, 2, and 3).

3. Epigenetic Effects on Atopic Predisposition

Epigenetics refers to information that is heritable through cell division. Epigenetic mechanisms include DNA methylation, chromatin remodelling and noncoding RNA, histone variations, and posttranslational histone modifications [48]. Epigenetic alterations can occur prenatally, perinatally, and later in life during developmental stages, with unique susceptibility to the effects of environmental exposures [48]. Uterine life is the most critical time in developmental programming; when negative environmental exposures occur, the foetal structure and its functions are irreversibly modified and subjects can be predisposed to several diseases, including allergy [49]. T-cellular differentiation into Th1, Th2, Th17, and Treg is influenced by changes in DNA/histone methylation and/or histone acetylation in naive T-cells and in cytokine promoter regions. Thus, the well-known correlation between epigenetic modifications and Th lineage has led to hypothesize that triggers inhibit Th1 and T regulatory cell differentiation, promote Th2-response, and could favour the risk of atopic predisposition [50]. Although the mechanism of this process is not fully understood, environmental changes, such as microbial burden [51], dietary changes [52, 53], and environmental pollutants [54], appear essential to initiate the cascade of epigenetic modifications that stabilize Th2 gene expression [55]. It is also likely that effects of environmental triggers are also mediated by oxidative stress which, by NF-[kappa]B-induced expression of proinflammatory cytokines and methylation-mediated changing, can induce histone modifications and chromatin remodelling of proinflammatory genes, exercising further implications on foetal immune programming, atopic predisposition, and increased IgE production following allergen sensitization [49, 56].

4. Cumulative Effects of Oxidative Stress-Inducible Genes on the Immune System

Genetic linkage and transmission alleles analyses have highlighted the important role of oxidative stress-inducible genes on the neonatal immune system response [26, 57]. In particular, the concurrent presence of higher ROS levels and antigenic exposure has been reported to alter the methylation of T helper genes [58]. All these changes impair the differentiation of T helper cells, increasing the risk of allergic sensitization [58]. More recently, changes in the expression of small noncoding regulator microRNAs have also been suggested as being critical for mediation of imbalanced responses to allergens [59]. However, to date, it is still unclear what genes and pathways are active during pregnancy and/or at birth and which systems are down- and/or upregulated in response to perinatal OS.

There is increasing evidence that ROS, also at physiologic concentrations, might, acting as cell-signalling mediators and promoting a shift toward a Th2-skewed immune response [17, 38], play additional roles in the onset of allergic disorders [17, 38].

The lung, due to its anatomy, provides an extensive surface area available to interact with all sources of reactive [O.sub.2] species, and a large variety of lung diseases, including allergic asthma, may be induced by ROS [26, 43]. In particular, pulmonary epithelial cells of alveolar structure appear to be the principle target for oxidant injury which, inhibiting cellular cycle progression, promotes a delayed reepithelialization process and irreversible cellular damage [60]. Moreover, airway inflammatory cells, such as macrophages [61], eosinophils, and peripheral blood monocytes [40], are themselves a likely source of ROS production [62]. Confirming these findings, studies have shown higher [H.sub.2][O.sub.2], nitric oxide, and superoxide levels in exhaled gases from asthmatic patients than from control subjects [63-66]. A prooxidant status also induces a wide range of biological and molecular damage in the lung. Increased release of isoprostanes and ethane, both in epithelial and in endothelial cell membranes, as well as diminished activity of proteins, such as [alpha]1-protease inhibitor, ascorbate, [alpha]-tocopherol, and superoxide dismutase (SOD), has been reported [67].

Acting on other targets, such as airway smooth muscle, inducing acetylcholine-mediated contraction [68], mucin secretion [69], and nitric oxide- (NO-) mediated neurogenic inflammation [69], ROS can also impair broncho- and vasoregulation [70, 71].

Finally, large-scale genome-wide association studies (GWAS) have demonstrated that genetic susceptibility to allergic asthma is also determined by complex interactions between genes involved in OS, such as glutamate cysteine ligase (GCLM), glutathione peroxidase (GPX1), catalase (CAT), myeloperoxidase (MPO), NADPH oxidase (CYBA, p22phox subunit), NAD(P)H, quinone oxidoreductase type 1 (NQO1), and microsomal epoxide hydrolase (EPHX1) [26] (Table 1).

As the primary cell of interface between internal and external environments, nasal mucosal epithelial cells are known to initiate the release of a cascade of proinflammatory mediators through redoxpathways [20]. Moreover, these cells also exhibit the capacity to upregulate an effective antioxidant defence [20]. However, natural allergen exposure agents show the ability to interfere with oxidant/antioxidant balance, enhancing OS and upper airway inflammation [72].

Although it has been hypothesized that the role of OS in allergic rhinitis is similar to that of asthma, the exact underlying mechanism is still not understood. However, it has been reported that OS, playing a critical role in allergic asthma, can also contribute to the onset of allergic rhinitis and to enhancing the asthma-rhinitis link, as expression of united airways disease [73].

It has been widely assessed that the loss of antioxidant activities characterizes patients affected by allergic rhinitis. Studies reported that decreased activities of both antioxidant enzyme paraoxonase (PON1) [74] and reduced glutathione [20] are inversely correlated to plasma total oxidant status and to severity of disease [20]. Consequently, increased nasal fraction of exhaled NO (FENO), 8-isoprostane, leukotriene(LT-) B4, and PGE2 levels was detected in patients with allergic rhinitis [75]. An impaired function and distribution of superoxide anion, NADPH oxidase (NOX)1, and NOX4 in allergic nasal rhinitis has also been noted, as further confirmation of the possible influence of OS on the development of allergic rhinitis [76] (Table 2).

The ability to interfere with the immune system allows ROS to induce and perpetuate skin injury, also in atopic dermatitis. In particular, authors reported that ROS, acting mainly on keratinocytes and partially on lymphocytes [77], induce oxidative protein damage in the stratum corneum, leading to the disruption of barrier functions and the exacerbation of atopic dermatitis [78]. Therefore, in response to a variety of oxidant reactants, the skin upregulates transactivating AP-1 components such as Fos and Jun, whereas it downregulates anti-inflammatory components [79]. Precisely, it has been suggested that upregulation of AP-1 may be associated with a defect in ceramide generation which could result in enhanced protein kinase-C activation, leading to excessive release of proinflammatory cytokines by keratinocytes [79]. Generally, peroxisome proliferator-activated receptors (PPARs), amemberofthe nuclearfactorfamily, also influence the biological activity of keratinocytes. To be precise, PPAR isoform-[alpha] (PPAR-[alpha]) counteracts the inflammatory response by inhibition of the expression of proinflammatory genes, as well as cytokines and metalloproteases. PPAR-[alpha] activation also induces antioxidant enzymes (catalase, SOD) which would reduce oxidative damage and inflammatory response [21].

The oxidant/antioxidant balance is also altered in atopic dermatitis. ROS reduce the physiological antioxidant levels of a number of compounds, such as [alpha]-tocopherol (VE), ubiquinol-10 (CoQH2-10), ascorbic acid (VC), and glutathione (GSH), in the epidermis and dermis and thus impair the cellular redox system [80]. Evidence of enhanced protein and lipid-oxidative damage was also found in atopic dermatitis patients, as demonstrated by the increase of carbonyl moieties both in lesional and in nonlesional skin, along with higher activity of SOD, an effective scavenger of ROS [81]. Recent experimental studies support a role for oxidative/antioxidative imbalance also in the shift toward a Th2-skewed immune response, probably NO-mediated [38]. Accordingly, the administration of antioxidants to human T-cells culture downregulated Th2 polarization, with a decrease in the expression of IL-4 and IL-5, and simultaneous skewing toward a Th1- phenotype [38]. Finally, data suggest epigenetic changes linked to the development of atopic dermatitis through OS-mediated immune dysregulation [82] (Table 3).

5. Conclusions

To date, the exact underlying mechanisms of atopic disease are still not understood. Recently, more attention has been given to the critical role of OS-inducible genes in the pathogenesis of atopic diseases. However, in spite of much evidence linking atopic predisposition, inflammatory status, and maternal and neonatal OS, much more remains to be investigated. Moreover, a genomic approach would clarify the role of oxidant/antioxidant pathways, in order to better understand the pathogenesis of atopic diseases and identify innovative therapeutic strategies.

Competing Interests

The authors have declared no conflict of interests.

Authors' Contributions

All authors had equally contributed to the manuscript.


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Sara Manti, (1) Lucia Marseglia, (2) Gabriella D'Angelo, (2) Caterina Cuppari, (1) Erika Cusumano, (2) Teresa Arrigo, (1) Eloisa Gitto, (2) and Carmelo Salpietro (1)

(1) Unit of Pediatric Genetics and Immunology, Department of Pediatrics, University of Messina, 98125 Messina, Italy

(2) Neonatal and Pediatric Intensive Care Unit, Department of Pediatrics, University of Messina, 98125 Messina, Italy

Correspondence should be addressed to Sara Manti;

Received 25 January 2016; Revised 27 May 2016; Accepted 22 June 2016

Academic Editor: Daniela Giustarini
Table 1: Oxidative stress-inducible genes and allergic asthma.

Gene                    Clinical relevance                 References

Glutathione             GSTs conjugate endogenous             [19]
S-transferases          by products of OS with
M1 (GSTM1) and          glutathione, enabling
P1 (GSTP1)              rapid elimination and
                        thus defending tissues
                        against oxidant damage;
                        common polymorphisms
                        exist in genes coding
                        for various GSTs including
                        glutathione S-transferases
                        M1 (GSTM1) and P1 (GSTP1)

Antioxidant             They are associated with           [11, 20,
defence enzymes         allergic and nonallergic              21]
(ADE)                   asthma, inducing increased
Glutamate cysteine      oxidative stress status
ligase (GCLM)
peroxidase (GPX1)
Myeloperoxidase (MPO)
NADPH oxidase
(CYBA, p22phox
NAD(P)H: quinone
type 1 (NQO1)
Microsomal epoxide
hydrolase (EPHX1)
Glutamate cysteine
ligase (GCLM)

Tumor necrosis          It may have a protective              [22]
factor G-308A           role in asthma pathogenesis,
                        depending on airway
                        oxidative stress levels

Methylenetetra-         In addition to foetal smoke           [23]
hydrofolate             exposure, it seems to be              [24]
reductase (MTHFR)       associated with lower airway          [25]
ORM1-like 3 (ORMDL3)    responsiveness, lung
Gasdermin A and         function, and increased risk
B (GSDM)                of transient wheezing, a
                        phenotype of childhood

Antioxidant enzyme      It is inversely correlated            [26]
paraoxonase (PON1)      to plasma total oxidant
                        status and to severity
                        of asthma

Nuclear factor (NF),    It has been found to be               [27]
erythroid-derived       a critical regulator in
2-related factor        protecting cells and
2 (NRF2)                tissues under highly
                        oxidative microenvironments,
                        including airways that
                        interface with the external
                        environment and are exposed
                        to pollutants and other
                        oxidant stressors

Toll-like receptor      It is associated with                 [28]
4 (Tlr4)                [O.sub.3]-induced lung
                        inflammation and increased
                        airway hyperpermeability

Heme oxygenase-         In addition to ozone                  [29]
1 (HMOX-1)              exposure, it is responsible
                        for the onset of allergic

Transforming            This genotype is associated           [30]
growth factor-          with an increased risk of
(TGF-) beta1            asthma in addition to
C-509T polymorphism     maternal smoking exposure
                        in the uterus or to
                        traffic-related emissions

Arginases               It may play an important              [31]
(ARG1 and ARG2)         role in asthma pathogenesis
                        through effects on
                        nitrosative stress

Table 2: Oxidative stress-inducible genes and allergic rhinitis.

Gene                 Clinical relevance           References

Glutathione          It may exert protective         [19]
S-transferases-      effects in allergic
(GSTs-) 1            rhinitis, decreasing
polymorphism         oxidative stress status

Tumour necrosis      They are associated           [22, 28]
factor (TNF)         with a higher risk of
rs1800629            allergic rhinitis
Toll-like receptor
4 (Tlr4) rs1927911

Table 3: Oxidative stress-inducible genes and atopic dermatitis.

Gene                      Clinical relevance           References

Glutathione               It is associated                [19]
S-transferases-           with atopic dermatitis
(GSTs-) 1                 susceptibility in a
polymorphism              Korean population

MicroRNA-223 or           It predisposes the              [32]
hypomethylation           host to development
of the thymic             of atopic dermatitis
stromal lymphopoietin     when combined with
(TSLP) gene 59-CpG        exposure to
island (CGI)              oxidative stress

Tumour necrosis           It is linked to                 [22]
factor (TNF)              oxidative stress-
promoter region           mediated atopic
(TNF-a-308G/A)            dermatitis
and linked

Nitric oxide              It is related to                [33]
polymorphism              clinical and functional
(T276 (276C/T, nNOS) +    manifestations of
C186 (-186A/C, nNOS) +    bronchial asthma and
X (CCTTT), nNOS + G954    atopic dermatitis
(-954G/C, iNOS) +220
(TAAA), niNOS + G894
(894C/G, eNOS) + a
(VNTR), eNOs)
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Author:Manti, Sara; Marseglia, Lucia; D'Angelo, Gabriella; Cuppari, Caterina; Cusumano, Erika; Arrigo, Tere
Publication:Oxidative Medicine and Cellular Longevity
Date:Jan 1, 2016
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