Next Article in Journal
Major Role of S-Glycoprotein in Providing Immunogenicity and Protective Immunity in mRNA Lipid Nanoparticle Vaccines Based on SARS-CoV-2 Structural Proteins
Next Article in Special Issue
Questionable Immunity to Mumps among Healthcare Workers in Italy—A Cross-Sectional Serological Study
Previous Article in Journal
Flow Cytometry-Based Measurement of Antibodies Specific for Cell Surface-Expressed Folded SARS-CoV-2 Receptor-Binding Domains
Previous Article in Special Issue
Key Learnings from the Development and Early Use of Global Guidance on the Integration of COVID-19 Vaccination into Broader Health Systems
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Diphtheria and Tetanus Immunity Status among Greek Adults: Results from a Nationwide Seroprevalence Study

by
Dimitrios Papagiannis
1,*,
Eleftherios Thireos
2,
Anargiros Mariolis
3,
Antonios Katsioulis
1,
Ioannis Ch. Lampropoulos
4,
Ioanna Tsiaousi
5,
Kostantina Gartzonika
6,
Niki Malliaraki
7,
Foteini Malli
4,
Erasmia C. Rouka
1,
Georgios Marinos
8,
Emmanouil K. Symvoulakis
9,
Georgios Rachiotis
10 and
Konstantinos I. Gourgoulianis
11
1
Public Health & Vaccines Laboratory, Faculty of Nursing, School of Health Sciences, University of Thessaly, 41110 Larissa, Greece
2
National Health System of Greece, Primary Health Center of Vari, 16672 Athens, Greece
3
National Health System of Greece, Primary Health Center, 23062 Areopolis, Greece
4
Respiratory Disorders Lab, Faculty of Nursing, University of Thessaly, 41110 Larissa, Greece
5
Private Primary Health Sector, Queen Sophia Avenue 123, 11521 Athens, Greece
6
Microbiology Department, Faculty of Medicine, School of Health Sciences, University of Ioannina, 45110 Ioannina, Greece
7
Laboratory of Clinical Chemistry-Biochemistry, University Hospital of Heraklion, 71003 Crete, Greece
8
Department of Hygiene, Epidemiology and Medical Statistics, School of Medicine, National and Kapodistrian University of Athens, 11527 Athens, Greece
9
Department of Social Medicine, Faculty of Medicine, University of Crete, 71003 Heraklion, Greece
10
Department of Hygiene and Epidemiology, Medical Faculty, School of Health Science, University of Thessaly, 42200 Larissa, Greece
11
Department of Respiratory Medicine, Faculty of Medicine, School of Health Sciences, University of Thessaly, BIOPOLIS, 41110 Larissa, Greece
*
Author to whom correspondence should be addressed.
Submission received: 17 February 2024 / Revised: 27 March 2024 / Accepted: 28 March 2024 / Published: 2 April 2024
(This article belongs to the Special Issue Promoting Vaccination in the Post-COVID-19 Era)

Abstract

:
Diphtheria and tetanus could lead to serious morbidity. We aimed to evaluate immunity levels by measuring specific IgG antibodies for diphtheria and tetanus in serum samples from a nationally expanded sample of the Greek population. A geographically stratified sampling approach based on regional units (NUTS level 2) was applied by considering variables such as age group (30–80+) and sex. In total, 1201 persons (47.7% males and 52.3% females) participated in the survey. Bivariate analysis revealed a negative relationship between diphtheria and tetanus median antibody titers and age. The overall seropositivity rate for diphtheria IgG antibodies (≥0.10 IU/mL) was estimated at 31.5%. Regarding tetanus, the total seropositivity rate was estimated at 59.5% (tetanus IgG antibodies ≥0.10 IU/mL). Logistic regression analysis indicated that age groups <40 years and 40–59 years were independently associated with tetanus seropositivity. Logistic regression also revealed that male sex and being aged 60–69 years were independent risk factors for diphtheria-related seropositivity. Lastly, being resident of some regions was an independent risk factor for both diphtheria- and tetanus-related seropositivity. The present study shows that Greek adults are still not completely immune to diphtheria and tetanus. It is likely possible to achieve optimal immunization coverage by implementing serviceable public health initiatives after comprehending real community needs.

1. Introduction

The bacterium Corynebacterium diphtheriae (C. Diphtheriae) may cause a severe disease, and this disease is vaccine preventable. Humans are the only reservoir for C. Diphtheriae [1]. Diphtheria was a frequent source of sickness and mortality in the days before vaccinations were available. The disease’s epidemiology was altered by the implementation of widespread baby vaccination campaigns, and a notable decline in prevalence was seen globally [2].
According to the European Centre for Disease Prevention and Control (ECDC), 281 cases were reported in Europe in 2022. More specifically, the majority of cases were in Germany (206), though cases also occurred in Belgium (37), Czechia (10), Slovakia (9), the Netherlands (9), Sweden (5), Latvia (3), Norway (1) and Spain (1). Furthermore, two deaths, reported in 2023, occurred in Belgium and Latvia [3]. Greece has been proclaimed diphtheria free since 1994 since the last autochthonous case of the disease was detected in 1982 [4,5]. The latest recorded case of diphtheria occurred in Greece in November 2019 and affected an 8-year-old boy who had pulmonary hypertension and mosaic Down syndrome as underlying disorders [5].
Clostridium tetani (C. tetani) toxigenic strains are the source of the acute infectious illness tetanus. The environment is full of C. tetani spores, which can enter the body through tissue damage such as puncture wounds or infected skin wounds. The disease can strike at any age, and, even in cases where intensive care is provided, it has a high case fatality rate at any age [6,7]. A large percentage of tetanus occurrences globally are related to birth or delivery. These cases typically occur in low-income nations and are typically connected with unvaccinated women and their newborn children after unsanitary births or abortions, as well as because of inadequate postnatal hygiene practices [8]. For the year 2018, twenty-six member countries of the EU reported ninety-two tetanus cases, of which half were labeled as confirmed, and Italy accounted for nearly half of all registered cases [9].
The incidence of this dangerous disease has significantly decreased as a result of tetanus vaccination. Tetanus-related deaths have decreased by 99% from the time before vaccinations. During the period 2004–2021, the number of tetanus cases reported through the mandatory notification system in Greece was ninety-three. The notification rate during the period 2004–2021 ranged between 0.02/100,000 population and 0.10/100,000 population, while the mean rate over the period 2004–2021 was 0.05 cases per 100,000 population [9]. Elimination of environmental exposure to tetanus is impossible, especially for some people like farm workers. Vaccination against tetanus has been assessed as the most effective intervention. Furthermore, the disease of tetanus is notably resource consuming. The average direct cost of care for tetanus patients is estimated to be substantial in the USA [10]. In addition, residents of low- and middle-income countries are at a higher risk of neonatal tetanus, particularly in locations like rural and urban slums where sanitary home births are widespread and maternal tetanus toxoid immunization and antenatal care service coverage are typically insufficient [11,12]. Tetanus has also a high fatality rate within the adult population. As a systematic review reported, the fatality rate is estimated to be 45.5% in African countries [13].
Many studies have been carried out to estimate the adult population’s vaccination coverage against tetanus and diphtheria in Greece [14,15], but very little is known about the seroprevalence, particularly at a national level [16]. Incidence in less developed countries also decreased after the launch of the World Health Organization (WHO) Expanded Programme on Immunization in 1974. The vaccination coverage of the first three doses for both diseases in Greece approaches 99% in infants [17]. There are differences in the Greek immunization schedule, number of doses given overall and type of vaccine used and included in the program. The Greek national healthcare system covers the cost of the vaccines included in the standard childhood immunization program, as well as booster doses for adults. The Greek immunization schedule is recommended and not mandatory [18].
In addition, information on the regional distribution of diphtheria- and tetanus-related seroprevalence for adults in Greece is not available. Consequently, there is a sparsity of relevant data on the seroprevalence of diphtheria and tetanus among the Greek general population.
In the present study, we aimed to investigate the immune responses to diphtheria and tetanus in Greek adults by using ELISA to detect specific IgG antibodies resistant to diphtheria and tetanus.

2. Materials and Methods

2.1. Sampling Method

Details on the methodology and the sampling methods have been previously published [19]. In brief, a geographically stratified sampling plan was based on the distribution of the population within the thirteen (13) regions of Greece (Eurostat’s NUTS-2). This sampling plan was applied in order to produce a representative sample, taking into consideration the proportions of specific age groups in the Greek general population (30–39, 40–49, 50–59, 60–69, 70–79 and 80+ years) and sex. The required minimum sample size was determined to be 1100 participants based on the assumption of an expected prevalence of 50% for tetanus and diphtheria antibodies, with a precision of ±3%, a confidence level of 95% and a power of 80% [20]. In the present study, we were able to report data from all 13 regions of Greece, including the South Aegean region. The samples were derived from healthy individuals who visited health facilities for routine screening and reasons unrelated to both diseases. The vaccination status for diphtheria and for tetanus was not taken as a criterion for participants in this study. Exclusion criteria were age under 30 years old and residence and symptomatic status. Each prospective participant was informed about the aims and procedures of the study and could then freely choose whether to participate or not. During September 2021 to March 2023, blood samples were collected from a nationwide network of general practitioners (GPs), including microbiological laboratories of private and public hospitals and primary healthcare facilities. The research protocol complied with ethical standards described in the Declaration of Helsinki [21] and received approval from the ethical committee of the University of Thessaly (protocol number 49/4 June 2021).

2.2. Laboratory Examination

The enzyme-linked immunosorbent assay (ELISA) was employed for measuring diphtheria and tetanus antibodies from serum samples [22,23]. We used the SERION ELISA with 99% Sensitivity and Specificity (Institute Virion/Serion GmbH Würzburg, Würzburg, Germany), diphtheria IgG test and tetanus IgG test for detection of human IgG antibodies in serum directed against tetanus and diphtheria toxin. Antibody activity test results were measured in international units (IU)/mL. A level of tetanus antibodies <0.01 IU/mL was defined as offering “no immune protection or seronegative”, an antibody level between 0.01 and 0.1 IU/mL was marked as offering “basic protection or low seropositivity” and a level ≥0.1 IU/mL was defined as offering “full protection” [24]. Diphtheria IgG antibody levels <0.01 IU/mL were considered as offering seronegative susceptibility, levels of 0.01–0.099 IU/mL were considered as providing “basic protection” and levels above 0.1 IU/mL were considered to offer “full protection” against diphtheria [25,26].

2.3. Statistical Analysis

Variables were checked for normality of distribution (application of Kolmogorov–Smirnoff test). Medians with interquartile range (1st quartile–3rd quartile) were presented. Absolute and relative frequencies were used. A Chi-squared test or Fisher’s exact test was used for the univariate analysis of prevalence of diphtheria and tetanus seropositivity by sex, age group and region of residence. A Mann–Whitney test or Kruskal–Wallis test was performed to reveal any differences among groups of non-normally distributed quantitative variables. Pairwise comparisons were used for age groups for both endpoints (diphtheria and tetanus seropositivity). Two models of logistic regression analysis were adopted in order to explain risk factors independently associated with the likelihood of seropositivity for both endpoints (diphtheria and tetanus seropositivity).
Logistic regression analysis was performed using the Wald test. Sex, age group and region of residence were included as independent variables (factors) and diphtheria or tetanus antibody levels as dependent variables. The level of statistical significance was set at p-value < 0.05. All analyses were performed using IBM SPSS Statistics software version 29.0 (IBM Corp., Armonk, NY, USA).

3. Results

Of the 1201 total participants from the 13 regional districts in Greece (NUTS level 2 districts), 573 were male (47.7%) and 628 were female (52.3%) (Table 1). The levels for IgG tetanus antibodies ranged from 0.01 IU/mL to 1.31 IU/mL, with median 0.20 IU/mL and IQR 0.03–0.53 IU/mL, and, for diphtheria, IgG antibodies ranged between 0.00 IU/mL and 0.69 IU/mL with median 0.05 IU/mL and IQR 0.02–0.13 IU/mL. Regarding the sample distribution, in accordance with the census of 2011, most participants originated from the region of Attica (38.80%), while participants from North Aegean and Ionian Islands accounted for 1.75% (Table 1, Figure 1).
We recorded that the estimated overall seroprotective rate for diphtheria IgG antibodies ≥0.10 IU/mL was 31.5%. We report differences among age groups, with the age groups <40 having the highest prevalence of protective antibodies for diphtheria in comparison to older groups (p-value = 0.023) in both sexes. Regarding tetanus, we recorded the total seroprotective rate for 715 participants (59.5%) with tetanus IgG antibodies ≥0.10 IU/m. As previously reported for diphtheria, the age groups <40 exhibited significant differences in comparison to the rest of the age groups in terms of having seroprotective antibodies against tetanus (p-value < 0.001) (Table 2).
Of the total 573 male participants, 201 (35.1%) had seroprotective titers against diphtheria in comparison to 177 females (28.2%) (p-value = 0.010). Slight differences for protective antibodies were recorded for tetanus among male and female subjects. Specifically, 357 men (62.3%) had protective antibodies ≥0.10 IU/m in comparison to 358 females (57%) (p-value = 0.062) (Table 2).
The majority of diphtheria IgG antibodies varied between 0.001 and 0.20 IU/mL. IgG antibodies protective against diphtheria were highest in the age groups <40, and the lowest proportion was recorded in the age group >80 (Table 2) (Figure 2). IgG antibodies decreased by age group. Significant differences in antibody levels were found between the younger (30–49 years) and the oldest (60–80 years) participants (Figure 3). This observation was more pronounced in regions with commonly low antibody levels, such as West Greece, which had a mean concentration of 0.06 IU/mL, in comparison to, for example, Eastern Macedonia and Thrace with 0.13 IU/mL and Ionian Islands with 0.14 IU/mL. We recorded the highest proportion of antibodies <0.01 IU/mL in the age group of 60–69, with a total proportion of 24.90%, followed by the age group of 70–79 with 19.80%.
Diphtheria IgG antibodies were significantly higher (p-values = 0.002) in males (median = 0.06 IU/mL with IQR: 0.02–0.16 IU/mL) in comparison with females (median = 0.04 IU/mL with IQR: 0.02–0.12 IU/mL) (Mann–Whitney test) (Figure 4). The median concentration values for IgG diphtheria declined as the age increased for all regions and both sexes (Figure 2 and Figure 4).

3.1. Univariate Analysis

Univariate analysis found that diphtheria and tetanus seropositivity was significantly associated with male gender. This also was the case for age. Furthermore, bivariate analysis detected a negative relationship between diphtheria and tetanus median antibody titers (Spearman’s correlation coefficient for diphtheria mean antibody titers and age = −0.102, p < 0.001; Spearman’s correlation coefficient for tetanus-related median titers and age = −0.210, p < 0.001). With respect to the distribution of diphtheria and tetanus median antibody titers by region, we report a considerable variation for both outcomes (p < 0.001 for tetanus-related antibodies, and p = 0.0062 for diphtheria; Kruskal–Wallis test).
Tetanus IgG antibody titers <0.01 IU/mL were considered seronegative. When considering the antibodies for tetanus, we recorded that 92 out of the 1201 samples were under the cut off of 0.01 IU/mL, and the total proportion of sera with levels below 0.01 IU/mL was 7.6%. The vast majority of tetanus IgG antibodies varied between 0.001 and 0.20 IU/mL. Tetanus mean IgG antibody titer values were usually increased in men versus women. Tetanus IgG antibodies were significantly higher (p-values = 0.009) in males (median = 0.23 IU/mL with IQR: 0.03–0.56 IU/mL) in comparison with females (median = 0.16 IU/mL with IQR: 0.03–0.49 IU/mL) (Mann–Whitney test) (Figure 4). As reported previously for the diphtheria antibodies, significant differences in mean tetanus antibody titer levels were found between the younger (30–59 years) and older (60–80 years) participants for tetanus too (Figure 5). The regions with the lowest mean titer of IgG antibodies were the regions of Epirus and West Greece, and the regions with the highest were the regions of Eastern Macedonia and Thrace followed by the region of Central Greece (Figure 6).
In pairwise comparisons between age groups, the younger ages had the highest titers of IgG antibodies against both diseases. Especially for diphtheria, age groups <40 and 40–49 exhibited significant differences in comparison to the 60–69, 70–79 and 80+ age groups (Figure 7). Similar results were recorded for the age groups <40 for tetanus antibodies in comparison to the 50–59 and 60–69 age groups. Significant differences were recorded for the age group of 60–69 compared with participants with age >80 (Figure 7).

3.2. Logistic Regression Analysis of Diphtheria- and Tetanus-Related Seropositivity

Logistic regression analysis has shown that men were more likely to be positive for diphtheria antibodies (OR = 1.39; 95% CI: 1.09–1.79; p = 0.009) than women. The age group of 60–69 years was significantly less likely to be positive for diphtheria antibodies compared to the age group of 80+ years (OR = 0.49; 95% CI: 0.30–0.80; p = 0.005). The Central Macedonia region was significantly less likely than the Attica region to be associated with positivity for diphtheria antibodies (OR = 0.61; 95% CI: 0.42–0.91; p = 0.014). In addition, the West Greece region was significantly less likely than the Attica region to show a considerable prevalence of diphtheria antibodies (OR = 0.35; 95% CI:0.18–0.70; p = 0.003) (Table 3).

3.3. Seropositivity of Antibodies Specific to Tetanus Toxoid

According to the logistic regression results, gender was not an independent predictor of antibody seropositivity related to the specific tetanus toxoid (OR = 1.26; 95% CI: 0.99–1.60; p = 0.058). The age groups >40 years were significantly more likely than the age group 80+ years to be positive for antibodies specific to the tetanus toxoid (OR = 2.73; 95% CI: 1.72–4.33; p < 0.001). The age group of 40–49 years was more likely than the age group of 80+ years to be positive for specific tetanus toxoid antibodies (OR = 2.90; 95% CI: 1.86–4.54; p < 0.001). Additionally, the age group of 50–59 years was significantly more likely than the age group of 80+ years to be positive for tetanus antibodies (OR = 1.56; 95% CI: 1.01–2.43; p = 0.045). Those from the Epirus region were significantly less likely than those from the Attica region to be positive for tetanus antibodies (OR = 0.43; 95% CI: 0.21–0.87; p = 0.019). Additionally, those from West Greece were significantly less likely than those from Attica to be positive for tetanus antibodies (OR = 0.38; 95% CI: 0.22–0.66; p = 0.001), as shown in Table 4.

4. Discussion

Despite the high vaccination coverage in infants and young children in Greece, the present study demonstrates that a substantial portion of participants remain susceptible to vaccine-preventable diseases such as diphtheria and tetanus. In the present nationwide seroprevalence study, we present results with an overall positivity rate for IgG antibodies against tetanus in an adult population group in Greece different from that in a previous study conducted across European countries including Greece [16]. These differences may be related to differences in the methodological approaches between the two studies in terms of the geographical aspects of sample selection and different demographic background (e.g., age) of the participants. Our results differ from those of a study in Italy, which reported that a significant minority (22%) of Italian construction workers were inadequately protected against tetanus [27].
Determining how long vaccine-induced immunity lasts is essential for making well-informed decisions on the optimal interval between booster shots. Tetanus IgG antibodies decreased with an eleven-year half-life in longitudinal trials with a small number of participants [28]. We present results that indicated a reduction in the mean titer of antibodies by age group. The results for the immunity status of the adults of the present study reflectively support data published by the National Public Health Organization (EODY) about the age and gender distribution of tetanus incidence. Especially for the period 2004–2021, the disease presented the highest frequency of occurrence in the age group >65 years old, with a mean annual notification rate of 0.16 cases per 100,000 population. This notification rate is higher than that of the other age groups (5–14, 25–44 and 45–64), in which it did not exceed 0.04 cases per 100,000 population. No cases have been reported in children below the age of 4 years old, and these data are supported by the high vaccination rates for this age. The mean annual notification rate for men was equal to that for women (0.05/100,000 population) [9]. Of the 93 cases that were documented between 2004 and 2021, 58 patients (62.4%) had not ever had a vaccination. Only ten cases—four with one dose of the vaccine, two with two doses and one with three doses—were reported to have had tetanus vaccinations according to the EODY’s analysis of the data. In four cases, there was no information available regarding the number of doses administered. There was no information provided regarding the vaccination status in 23 instances. Most of the cases, particularly in the over-65 age group, were unvaccinated [9].
With the passing of years, the immunological response to the tetanus vaccination seems to diminish. Comparative research has shown that adolescents often produce higher antibody levels than adults. Most adult immunizations contribute and sustain protective levels of antibodies for many years despite the decline in immunogenicity. The importance of booster doses has been supported by evidence from many studies in the past. American soldiers received booster shots after wounds in addition to two or three rounds of the primary vaccine series [10]. Out of twelve million injured US army participants, only twelve cases of tetanus were reported [10]. Soldiers across the board (0.44 per 100,000) were compared to 70 of the 520,000 injured in the Second World War (13.4 per 100,000), and only four of the twelve had received all of their main vaccinations [11]. The data of the present study support the necessity for booster vaccinations against tetanus in Greek adults and indicate that an important proportion of the Greek adult population is susceptible. Many studies have repeatedly reported insufficient antibody concentrations against both tetanus and diphtheria (<0.1 IU/mL) in adults, particularly in the elderly [19,20,21,22,23,24,25,26,27,28,29,30,31]. Our results agree with previous studies that the concentration of protective antibodies decreases with increasing age.
Regarding immunity against diphtheria, we recorded a large proportion of participants with limited protection against the disease (67.3%), while 31.50% had antibodies within the protective level. Similar results for diphtheria, showing a low level of protection, were reported for Greece by a European study conducted six years before the present study [32]. Results from a study among immunized healthy Slovak adults assessed the long-term pattern of humoral immunity in the case of diphtheria, with only 21% of individuals found to have seroprotective antibodies ≥0.1 IU/mL before the booster immunization [33].
Completely vaccinated individuals seldom catch the disease, and even when they do, outbreaks in communities highly exposed to the toxin-producing C. diphtheriae are uncommon [34]. However, illness in those who have received vaccinations is typically moderate, with fewer sequelae and no fatalities. We present data showing that, in most regions, diphtheria-specific IgG antibodies decreased by age group. People between the ages of 40 and 59 had inadequate levels of seroprotection against diphtheria according to recent seroprevalence research carried out in 16 European nations [16]. This emphasizes how crucial it is to receive booster shots containing the diphtheria toxoid after the immunization campaign. Adults should receive booster doses at different intervals, and it is critical to ensure that everyone is vaccinated against diphtheria. Results for these special age groups reported in a previous study in Greece showed very low vaccination coverage for tetanus and diphtheria [14].
Another finding of this cross-sectional seroprevalence study (secondary analysis data) was the significant differences in antibody levels between the age cohorts when comparing the younger (30–49 years) to the older (60–80 years) participants. A study in Vietnam found significant variation between the age groups of 21–30 and 31–40 compared to the age group of 60+ years (p < 0.05) [35]. In countries where routine vaccination rates are low, diphtheria is nevertheless endemic. The regular repetition of booster immunizations can help to sustain full protection of the population and enhance the herd immunity. The outbreak in the former Soviet Union in the recent past was caused by a number of circumstances, including a lack of population immunity, a weak socioeconomic infrastructure and a delayed public health response [36,37]. Greece has a low overall incidence and a high childhood immunization rate against tetanus and diphtheria toxoids [4,5]. Compared to booster vaccinations for the adult population [14], Greece has a higher vaccination rate for newborns [3], including both the first and third doses of the diphtheria, tetanus toxoid and pertussis vaccines.
The WHO reports that preschool-age and school-age children are most frequently vulnerable to diphtheria when they are either unvaccinated or have not received enough vaccinations. The amount of diphtheria antitoxin obtained and the length of protection are influenced by the formulation of the diphtheria toxoid and the timing of vaccination delivery [38]. Regarding the tetanus toxoid, the ability to evoke booster responses even after intervals of 20 years or more shows that immunological memory is persistent. Data from serological surveys indicate that adults and teenagers who want to maintain high antibody levels that can last for decades must take booster doses [39]. The American guideline panel on vaccination practices, the Advisory Committee on Immunization Practices, advises the Centers for Disease Control and Prevention to prescribe booster doses for adults every ten years [40].
It is believed that a significant factor contributing to the increased incidence and prevalence of chronic illnesses such as metabolic, neurological and cardiovascular disorders is the aging immune system, or immunosenescence. These illnesses frequently manifest clinically in the elderly population as multimorbidity, which raises the risk of organ failure and mortality. As immunosenescence progresses, older persons are also more vulnerable to infectious infections. In practical terms, this means that vaccination schedules should be modified to account for the immunological responses that are observed in clinical studies with elderly participants.
The published research demonstrates that the two sexes respond differently to immunological stimuli in terms of both innate and adaptive immunity, yet this is not taken into account when developing recommended vaccination schedules for any age. The persistence of gender differences in the innate immune system in older adults has not received enough attention, yet some studies indicate that females continue to produce more inflammatory proteins than males do [41]. In the present study, we recorded gender differences in the level of immunity for both diphtheria and tetanus. Univariate analysis found that diphtheria and tetanus seropositivity was significantly associated with male gender. One explanation is that a booster dose was given to the men on entrance to the military corps. According to the Greek army, vaccinations against tetanus diphtheria and pertussis at the introduction to the army are mandatory, independent of the immunological status of the subjects. Similar results regarding gender and tetanus antibodies are presented by Weinberger et al. This is probably due to vaccination during military service or more frequent booster vaccinations after injuries [32].
The present study has several limitations. Taking into consideration that our sample was based on a non-probability sampling method, we may underline that the seroprevalence figures from the present sample of participants might not represent the prevalence of tetanus and diphtheria for the whole country. It is difficult to discern between the particular humoral immune responses brought on by vaccinations and those brought on by infection. Furthermore, it was unknown whether the subjects had received any vaccinations. Another limitation of the study is that we did not include immigrants in the population study. The migrants leaving countries with poor immunization programs or where vaccinations have been interrupted may represent a new risk group in host countries. A study conducted in six European countries depicted that 22.3% of the participants were without protective antibodies for tetanus [42].
Despite these drawbacks, our study has the advantage of being the first to offer some estimates of the nationwide seroprevalence of tetanus and diphtheria IgG antibodies among adults in Greece using stratified sampling, and the findings may be useful as recently reported information for policymakers and health professionals in planning future campaigns to prevent these diseases.

5. Conclusions

The present study shows that Greek adults are still not longitudinally immune to diphtheria and tetanus. It is likely that optimal immunization coverage could be achieved by implementing sensible public health initiatives. In order to maintain protection into old age, these measures would need to incorporate a lifelong perception through public health and primary-care-driven education on vaccinations as repeated booster shots throughout maturity are required. Our study findings about regional differences serve as a call for uniform vaccination incentives throughout Greece. Apart from personalized motivational support, enhancing public awareness of the advantages and disadvantages of vaccinations could potentially boost adherence to immunization protocols. Generally, antibodies were higher in some regions than others, but, interestingly, variations between regions were not proportionally similar. The local vaccination policies followed by the physicians of primary healthcare or occupational health settings could be an explanation for this variation. This is surprising because combo vaccinations are advised to prevent both tetanus and diphtheria. Despite the prescription for combined immunizations, it appears that this suggestion is not always followed, and it is possible that solo tetanus vaccinations are occasionally used.

Author Contributions

Conceptualization, D.P., I.T., E.K.S. and G.R.; methodology, D.P. and A.K.; software, D.P., I.C.L. and A.K.; validation, D.P., E.T., A.M., K.G., N.M., E.C.R., F.M., G.M., E.K.S., G.R. and K.I.G.; formal analysis, D.P., I.C.L. and A.K.; investigation, D.P., E.T., A.M. and I.T.; data curation, D.P., E.T., A.M., K.G., N.M. and A.K.; writing—original draft preparation, D.P. and A.K.; writing—review and editing, D.P., E.K.S. and G.R.; supervision, D.P. and K.I.G.; project administration, D.P. All authors have read and agreed to the published version of the manuscript.

Funding

The primary research was funded by the Special Account for Research Grants, University of Thessaly (no. 6093).

Institutional Review Board Statement

The study was approved by the Ethics Committee of the University of Thessaly (protocol number 49/4 June 2021).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data that support the findings of this study are available on request from the corresponding author.

Acknowledgments

The authors would like to thank the GPs and health professionals who participated and helped with sample collection for this study as follows: Anna Tzanavari, Meropi Saloustrou, Eleftheria Mpifsa, Ioanna Panagiotara, Michael Dandoulakis, Ioulia Kolovou, Pavlos Sklavounos, Kyriaki Zamagia, Diomideia Papadopoulou, Eleni Sidiropoulou, Anastasios Koukaliotis, Ioanna Gemeliari, Clairi Korogianaki, Botia Glykidou, Doukas Zeibekis, Ioanna Kotsiri, Gkini, Maria, Anastasia Lemonidou and Konstantina Tyblalexi.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Centers for Disease Control and Prevention (CDC). The Pink Book: Diphtheria. Atlanta: CDC. 2021. Available online: https://www.cdc.gov/vaccines/pubs/pinkbook/dip.html (accessed on 18 November 2023).
  2. Clarke, K.E.; MacNeil, A.; Hadler, S.; Scott, C.; Tiwari, T.S.; Cherian, T. Global Epidemiology of Diphtheria, 2000–2017. Emerg. Infect. Dis. 2019, 25, 1834–1842. [Google Scholar] [CrossRef]
  3. ECDC. Epidemiological Update: Diphtheria Cases in Europe. Available online: https://www.ecdc.europa.eu/en/news-events/epidemiological-update-diphtheria-cases-europe (accessed on 8 March 2024).
  4. WHO. Global Health Observatory Data Repository. Diphtheria Reported Cases by Country. Available online: https://apps.who.int/gho/data/view.main.1540_41?lang=en (accessed on 3 November 2023).
  5. Georgakopoulou, T.; Tryfinopoulou, K.; Doudoulakakis, A.; Nikolaou, F.; Magaziotou, I.; Flountzi, A.; Fry, N.K.; Litt, D.J.; Damala, M.; Spiliopoulou, I.; et al. A patient with respiratory toxigenic diphtheria in Greece after more than 30 years. Epidemiol. Infect. 2020, 148, e274. [Google Scholar] [CrossRef]
  6. Roper, M.H.; Vandelaer, J.H.; Gasse, F.L. Maternal and neonatal tetanus. Lancet 2007, 370, 1947–1959. [Google Scholar] [CrossRef]
  7. World Health Organization. Tetanus Vaccines: WHO position Paper—February 2017. Wkly. Epidemiol. Rec. 2017, 92, 53–76. Available online: http://apps.who.int/iris/bitstream/10665/254582/1/WER9206.pdf (accessed on 18 November 2023).
  8. ECDC. Tetanus. Annual Epidemiological Report for 2018. Available online: https://www.ecdc.europa.eu/sites/default/files/documents/Tetanus_AER_2018_Report.pdf (accessed on 18 November 2023).
  9. Greek National Public Health Organization. Epidemiological Data for Tetanus in Greece, 2004–2021. Available online: https://eody.gov.gr/wp-content/uploads/2019/01/tetanus-2004-2021-eng.pdf (accessed on 29 November 2023).
  10. Roper, M.H.; Wassilak, S.G.F.K.; Scobie, M.H.; Ridpath, A.D.; Orenstein, W.A. In Chapter 58. Tetanus toxoid. In Vaccines, 7th ed.; Plotkin, S.A., Orenstein, W.A., Offit, P.A., Edwards, K.M., Eds.; Saunders/Elsevier: Philadelphia, PA, USA, 2018; pp. 1052–1079. [Google Scholar]
  11. Singh, A.; Pallikadavath, S.; Ogollah, R.; Stones, W. Maternal tetanus toxoid vaccination and neonatal mortality in rural north India. PLoS ONE 2012, 7, e48891. [Google Scholar] [CrossRef] [PubMed]
  12. Kyu, H.H.; Shannon, H.S.; Georgiades, K.; Boyle, M.H. Association of Urban Slum Residency with Infant Mortality and Child Stunting in Low and Middle Income Countries. BioMed Res. Int. 2013, 2013, 12. [Google Scholar] [CrossRef]
  13. Woldeamanuel, Y.W.; Andemeskel, A.T.; Kyei, K.; Woldeamanuel, M.W.; Woldeamanuel, W. Case fatality of adult tetanus in Africa: Systematic review and meta-analysis. J. Neurol. Sci. 2016, 368, 292–299. [Google Scholar] [CrossRef]
  14. Papagiannis, D.; Rachiotis, G.; Mariolis, A.; Zafiriou, E.; Gourgoulianis, K.I. Vaccination Coverage of the Elderly in Greece: A Cross-Sectional Nationwide Study. Can. J. Infect. Dis. Med. Microbiol. 2020, 2020, 5459793. [Google Scholar] [CrossRef] [PubMed]
  15. Maltezou, H.C.; Lourida, A.; Katragkou, A.; Grivea, I.N.; Katerelos, P.; Wicker, S.; Syrogiannopoulos, G.A.; Roilides, E.; Theodoridou, M. Attitudes regarding occupational vaccines and vaccination coverage against vaccine-preventable diseases among healthcare workers working in pediatric departments in Greece. Pediatr. Infect. Dis. J. 2012, 31, 623–625. [Google Scholar] [CrossRef] [PubMed]
  16. Berbers, G.; van Gageldonk, P.; van de Kassteele, J.; Wiedermann, U.; Desombere, I.; Dalby, T.; Toubiana, J.; Tsiodras, S.; Ferencz, I.P.; Mullan, K.; et al. Circulation of pertussis and poor protection against diphtheria among middle-aged adults in 18 European countries. Nat. Commun. 2021, 12, 2871. [Google Scholar] [CrossRef]
  17. WHO. Diphtheria Tetanus Toxoid and Pertussis (DTP) Vaccination Coverage). Available online: https://immunizationdata.who.int/pages/coverage/dtp.html?CODE=GRC&ANTIGEN=&YEAR (accessed on 7 March 2024).
  18. Greek Government. Child and Adult Immunization. Available online: https://www.gov.gr/en/sdg/healthcare/public-preventive-healthcare-measures/general/child-and-adult-immunisation (accessed on 7 March 2024).
  19. Papagiannis, D.; Thireos, E.; Mariolis, A.; Katsioulis, A.; Gartzonika, K.; Malliaraki, N.; Agnantis, C.; Tsaras, K.; Malli, F.; Rouka, E.C.; et al. Pertussis Prevalence in Adult Population in Greece: A Seroprevalence Nationwide Study. Vaccines 2022, 10, 1511. [Google Scholar] [CrossRef] [PubMed]
  20. Macfarlane, S.B. Conducting a Descriptive Survey: Choosing a Sampling Strategy. Trop. Dr. 1997, 27, 14–21. [Google Scholar] [CrossRef]
  21. World Medical Association. World Medical Association Declaration of Helsinki: Ethical principles for medical research involving human subjects. JAMA 2013, 310, 2191–2194. [Google Scholar] [CrossRef]
  22. Kristiansen, M.; Aggerbeck, H.; Heron, I. Improved ELISA for determination of anti-diphtheria and/or anti-tetanus antitoxin antibodies in sera. APMIS 1997, 105, 843–853. [Google Scholar] [CrossRef]
  23. Von Hunolstein, C.; Aggerbeck, H.; Andrews, N.; Berbers, G.; Fievet-Groyne, F.; Maple, P.A.; Ölander, R.M.; Raux, M.; Tischer, A. European sero-epidemiology network: Standardization of the results of diphtheria antitoxin assays. Vaccine 2000, 18, 3287–3296. [Google Scholar] [CrossRef] [PubMed]
  24. Zhang, C.; Hu, W.; Ma, Y.; Li, L.; Si, Y.; Zhang, S. Seroepidemiology of Tetanus among Healthy People Aged 1–59 Years Old in Shaanxi Province, China. Vaccines 2022, 10, 1806. [Google Scholar] [CrossRef]
  25. World Health Organization. The Immunological Basis for Immunization Series. Module 2: Diphtheria, Update 2009. Geneva, Switzerland. 2009. Available online: https://iris.who.int/bitstream/handle/10665/44094/9789241597869_eng.pdf?sequence=1 (accessed on 29 January 2024).
  26. Vitek, C.R.; Wharton, M. Chapter 10. Diphteria toxoid. In Vaccines, 5th ed.; Plotkin, S.A., Orenstein, W.A., Offit, P.A., Eds.; Saunders/Elsevier: Philadelphia, PA, USA, 2008; pp. 139–156. [Google Scholar]
  27. Rapisarda, V.; Bracci, M.; Nunnari, G.; Ferrante, M.; Ledda, C. Tetanus immunity in construction workers in Italy. Occup. Med. 2014, 64, 217–219. [Google Scholar] [CrossRef] [PubMed]
  28. Amanna, I.J.; Carlson, N.E.; Slifka, M.K. Duration of humoral immunity to common viral and vaccine antigens. N. Engl. J. Med. 2007, 357, 1903–1915. [Google Scholar] [CrossRef]
  29. Steger, M.M.; Maczek, C.; Berger, P.; Grubeck-Loebenstein, B. Vaccination against tetanus in the elderly: Do recommended vaccination strategies give sufficient protection. Lancet 1996, 348, 762. [Google Scholar] [CrossRef]
  30. Van Damme, P.; Burgess, M. Immunogenicity of a combined diphtheria-tetanus-acellular pertussis vaccine in adults. Vaccine 2004, 22, 305–308. [Google Scholar] [CrossRef]
  31. Weinberger, B.; Schirmer, M.; Matteucci Gothe, R.; Siebert, U.; Fuchs, D.; Grubeck-Loebenstein, B. Recall responses to tetanus and diphtheria vaccination are frequently insufficient in elderly persons. PLoS ONE 2013, 8, e82967. [Google Scholar] [CrossRef]
  32. Weinberger, B.; Keller, M.; Putzer, C.; Breitenberger, D.; Koller, B.; Fiegl, S.; Moreno-Villanueva, M.; Bernhardt, J.; Franceschi, C.; Voutetakis, K.; et al. Protection against Tetanus and Diphtheria in Europe: The impact of age, gender and country of origin based on data from the MARK-AGE Study. Exp. Gerontol. 2018, 105, 109–112. [Google Scholar] [CrossRef] [PubMed]
  33. Petráš, M.; Oleár, V.; Molitorisová, M.; Dáňová, J.; Čelko, A.M.; Nováková, E. Factors Influencing Persistence of Diphtheria Immunity and Immune Response to a Booster Dose in Healthy Slovak Adults. Vaccines 2019, 7, 139. [Google Scholar] [CrossRef]
  34. Ohuabunwo, C.; Perevoscikovs, J.; Griskevica, A.; Gargiullo, P.; Brilla, A.; Viksna, L.; Glismann, S.; Wharton, M.; Vitek, C. Respiratory diphtheria among highly vaccinated military trainees in Latvia: Improved protection from DT compared with Td booster vaccination. Scand. J. Infect. Dis. 2005, 37, 813–820. [Google Scholar] [CrossRef]
  35. Le, T.V.; Nguyen, V.T.T.; Nguyen, Q.H.; Nguyen, T.T.T.; Duong, T.T.N.; Ly, T.T.T.; Pham, T.N.; Nguyen, V.L.; Vien, C.C. The evaluation of anti-diphtheria toxoid antibodies in healthy population in Kon Tum, Vietnam: A population-based study. IJID Reg. 2022, 3, 171–176. [Google Scholar] [CrossRef]
  36. Galazka, A.M.; Robertson, S.E.; Oblapenko, G.P. Resurgence of diphtheria. Eur. J. Epidemiol. 1995, 11, 95–105. [Google Scholar] [CrossRef]
  37. Galazka, A. Implications of the diphtheria epidemic in the former Soviet Union for immunization programs. J. Infect. Dis. 2000, 181 (Suppl. S1), S244–S248. [Google Scholar] [CrossRef] [PubMed]
  38. WHO. Diphtheria KEY FACTS 2023. Available online: https://www.who.int/news-room/fact-sheets/detail/diphtheria (accessed on 14 February 2024).
  39. Schatz, D.; Ellis, T.; Ottendorfer, E.; Jodoin, E.; Barrett, D.; Atkinson, M. Aging and the immune response to tetanus toxoid: Diminished frequency and level of cellular immune reactivity to antigenic stimulation. Clin. Diagn. Lab. Immunol. 1998, 5, 894–896. [Google Scholar] [CrossRef] [PubMed]
  40. CDC. Recommended Adult Immunization Schedule for Ages 19 Years or Older. 2024. Available online: https://www.cdc.gov/vaccines/schedules/downloads/adult/adult-combined-schedule.pdf (accessed on 14 February 2024).
  41. Furman, D.; Hejblum, B.P.; Simon, N.; Jojic, V.; Dekker, C.L.; Thiebaut, R.; Tibshirani, R.J.; Davis, M.M. Systems analysis of sex differences reveals an immunosuppressive role for testosterone in the response to influenza vaccination. Proc. Natl. Acad. Sci. USA 2014, 111, 869–874. [Google Scholar] [CrossRef]
  42. Affanni, P.; Colucci, M.E.; Capobianco, E.; Bracchi, M.T.; Zoni, R.; Viani, I.; Caruso, L.; Carlone, L.; Arcuri, C.; Veronesi, L. Immunity status against tetanus in young migrants: A seroprevalence study. Acta Biomed. 2020, 91, 77–84. [Google Scholar] [CrossRef]
Figure 1. Country map—sample distribution.
Figure 1. Country map—sample distribution.
Vaccines 12 00378 g001
Figure 2. Distribution of IgG diphtheria antibody titers by age group. O outliers. * extreme outliers. • mean.
Figure 2. Distribution of IgG diphtheria antibody titers by age group. O outliers. * extreme outliers. • mean.
Vaccines 12 00378 g002
Figure 3. Distribution of IgG diphtheria antibody titers by region. O outliers. * extreme outliers. • mean.
Figure 3. Distribution of IgG diphtheria antibody titers by region. O outliers. * extreme outliers. • mean.
Vaccines 12 00378 g003
Figure 4. Frequency of IgG antibodies for diphtheria and tetanus by gender. O outliers. * extreme outliers.
Figure 4. Frequency of IgG antibodies for diphtheria and tetanus by gender. O outliers. * extreme outliers.
Vaccines 12 00378 g004
Figure 5. Distribution of IgG tetanus antibody titers by age group. • mean.
Figure 5. Distribution of IgG tetanus antibody titers by age group. • mean.
Vaccines 12 00378 g005
Figure 6. Distribution of IgG tetanus antibody titers by region. O outliers. * extreme outliers. • mean.
Figure 6. Distribution of IgG tetanus antibody titers by region. O outliers. * extreme outliers. • mean.
Vaccines 12 00378 g006
Figure 7. Pairwise age group comparisons and IgG antibodies for tetanus and diphtheria.
Figure 7. Pairwise age group comparisons and IgG antibodies for tetanus and diphtheria.
Vaccines 12 00378 g007
Table 1. Demographic background of the participants.
Table 1. Demographic background of the participants.
VariableN%
Sex
Male57347.7%
Female62852.3%
Total1201100%
Age Group
<4022218.50%
40–4922618.80%
50–5921417.80%
60–6920917.40%
70–7919115.90%
80+13911.60%
Table 2. Univariate analysis of IgG seroprotective diphtheria and tetanus antibodies.
Table 2. Univariate analysis of IgG seroprotective diphtheria and tetanus antibodies.
Diphtheria IgG (U/mL) (Two Groups)Tetanus IgG (U/mL) (Two Groups)
Count 0.10+%Count <0.10%Totalp-Value *Count
0.10+
%Count
0.01–0.09
%Totalp-Value *
SexMale20135.1%37264.9%5730.01035762.3%21637.7%5730.062
Female17728.2%45171.8%628 35857.0%27043.0%628
Age <408741.6%12258.4%209 14971.3%6028.7%209<0.001 **
40–498435.3%15464.7%2380.023 **17272.3%6627.7%238
50–595425.2%16074.8%214 12759.3%8740.7%214
60–694421.1%16578.9%209 10851.7%10148.3%209
70–795930.9%13269.1%191 9248.2%9951.8%191
80+4935.3%9064.7%139 6647.5%7352.5%139
RegionEastern Macedonia, Thrace2436.9%4163.1%650.1804772.3%1827.7%650.001
Central Macedonia4925.0%14775.0%196 12262.2%7437.8%196
West Macedonia1136.7%1963.3%30 2066.7%1033.3%30
Thessaly3037.0%5163.0%81 4656.8%3543.2%81
Epirus1232.4%2567.6%37 1540.5%2259.5%37
Ionian Islands838.1%1361.9%21 1676.2%523.8%21
West Greece1116.4%5683.6%67 2638.8%4161.2%67
Central Greece2339.0%3661.0%59 3864.4%2135.6%59
Peloponnese2236.1%3963.9%61 4167.2%2032.8%61
Attica15232.6%31467.4%466 26757.3%19942.7%466
North Aegean628.6%1571.4%21 1152.4%1047.6%21
South Aegean1031.3%2268.8%32 2165.6%1134.4%32
Crete2030.8%4569.2%65 4569.2%2030.8%65
* Chi-squared test. ** Chi-squared test for trend. Pearson Chi-squared tests.
Table 3. Multivariate analysis of diphtheria IgG (≥0.10 U/mL).
Table 3. Multivariate analysis of diphtheria IgG (≥0.10 U/mL).
FactorsOdds Ratio95% CIp-Value
Sex
Male
1.391.09–1.790.009
Femaleref.
Age group
<40
1.420.90–2.240.135
40–491.060.68–1.650.802
50–590.630.40–1.020.059
60–690.490.30–0.800.005
70–790.830.52–1.330.447
80+ref.
Region
Eastern Macedonia, Thrace
1.120.64–1.940.695
Central Macedonia0.610.42–0.910.014
West Macedonia1.100.50–2.400.815
Thessaly1.150.70–1.890.585
Epirus0.910.44–1.880.791
Ionian Islands1.170.47–2.920.744
West Greece0.350.18–0.700.003
Central Greece1.220.69–2.160.490
Peloponnese1.040.59–1.840.890
North Aegean0.780.29–2.090.625
South Aegean0.840.38–1.850.664
Crete0.820.46–1.460.506
Atticaref.
The reference category is <0.10 IU/mL.
Table 4. Multivariate analysis of tetanus IgG antibodies (≥0.10 IU/mL).
Table 4. Multivariate analysis of tetanus IgG antibodies (≥0.10 IU/mL).
FactorsOdds Ratio95% CIp-Value
Sex1.260.99–1.600.058
Male
Femaleref.
Age group2.731.72–4.33<0.001
<40
40–492.901.86–4.54<0.001
50–591.561.01–2.430.045
60–691.160.75–1.790.509
70–790.990.63–1.540.963
80+ref.
Region1.720.95–3.090.071
Eastern Macedonia, Thrace
Central Macedonia1.040.73–1.490.811
West Macedonia1.290.58–2.870.535
Thessaly0.890.55–1.460.654
Epirus0.430.21–0.870.019
Ionian Islands2.130.75–6.030.154
West Greece0.380.22–0.660.001
Central Greece1.190.66–2.120.563
Peloponnese1.350.76–2.420.307
North Aegean0.730.30–1.790.488
South Aegean1.190.55–2.570.666
Crete1.420.80–2.520.227
Atticaref.
The reference category is 0.01–0.09 IU/mL.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Papagiannis, D.; Thireos, E.; Mariolis, A.; Katsioulis, A.; Lampropoulos, I.C.; Tsiaousi, I.; Gartzonika, K.; Malliaraki, N.; Malli, F.; Rouka, E.C.; et al. Diphtheria and Tetanus Immunity Status among Greek Adults: Results from a Nationwide Seroprevalence Study. Vaccines 2024, 12, 378. https://0-doi-org.brum.beds.ac.uk/10.3390/vaccines12040378

AMA Style

Papagiannis D, Thireos E, Mariolis A, Katsioulis A, Lampropoulos IC, Tsiaousi I, Gartzonika K, Malliaraki N, Malli F, Rouka EC, et al. Diphtheria and Tetanus Immunity Status among Greek Adults: Results from a Nationwide Seroprevalence Study. Vaccines. 2024; 12(4):378. https://0-doi-org.brum.beds.ac.uk/10.3390/vaccines12040378

Chicago/Turabian Style

Papagiannis, Dimitrios, Eleftherios Thireos, Anargiros Mariolis, Antonios Katsioulis, Ioannis Ch. Lampropoulos, Ioanna Tsiaousi, Kostantina Gartzonika, Niki Malliaraki, Foteini Malli, Erasmia C. Rouka, and et al. 2024. "Diphtheria and Tetanus Immunity Status among Greek Adults: Results from a Nationwide Seroprevalence Study" Vaccines 12, no. 4: 378. https://0-doi-org.brum.beds.ac.uk/10.3390/vaccines12040378

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop