key: cord-0883599-poctq8wj authors: Lenicek Krleza, Jasna; Zrinski Topic, Renata; Stevanovic, Vladimir; Lukic-Grlic, Amarela; Tabain, Irena; Misak, Zrinjka; Roic, Goran; Kaic, Bernard; Mayer, Dijana; Hruskar, Zeljka; Barbic, Ljubo; Vilibic-Cavlek, Tatjana title: Seroprevalence of SARS-CoV-2 infection among children in Children’s Hospital Zagreb during the initial and second wave of COVID-19 pandemic in Croatia date: 2021-04-15 journal: Biochem Med (Zagreb) DOI: 10.11613/bm.2021.020706 sha: 9842c3aa6401109f7a4e4494df727f77f99c7167 doc_id: 883599 cord_uid: poctq8wj INTRODUCTION: The study aimed to investigate the prevalence and titres of anti-SARS-CoV-2 antibodies in children treated at the Children’s Hospital Zagreb in the first and the second wave of the COVID-19 pandemic. Statistical significance of difference at two time points was done to determine how restrictive epidemiological measures and exposure of children to COVID-19 infection affect this prevalence in different age groups. MATERIALS AND METHODS: At the first time point (13th to 29th May 2020), 240 samples and in second time point (24th October to 23rd November 2020), 308 serum samples were tested for anti-SARS-CoV-2 antibodies by enzyme-linked immunosorbent assay (ELISA) and electrochemiluminescence immunoassay (ECLIA). Confirmation of results and titre determination was done using virus micro-neutralization test. Subjects were divided according to gender, age and epidemiological history. RESULTS: Seroprevalence of anti-SARS-CoV-2 antibodies differs significantly in two time points (P = 0.010). In first time point 2.9% of seropositive children were determined and in second time point 8.4%. Statistically significant difference (P = 0.007) of seroprevalence between two time points was found only in a group of children aged 11-19 years. At the first time point, all seropositive children were asymptomatic with titre < 8. At the second time point, 69.2% seropositive children were asymptomatic with titre ≥ 8. CONCLUSIONS: The prevalence of anti-SARS-CoV-2 antibodies was significantly lower at the first time point than at the second time point. Values of virus micro-neutralization test showed that low titre in asymptomatic children was not protective at the first time point but in second time point all seropositive children had protective titre of anti-SARS-CoV-2 antibodies. In December 2019, a novel coronavirus emerged in Wuhan, China (1) . The virus was named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and disease COVID-19. Due to a rapid spread and possibility of causing severe and life-threatening infections, it has attracted worldwide attention. On 11 th March 2020, the World Health Organization Lenicek Krleza J. et al. Seroprevalence of SARS-CoV-2 infection in children system accordingly (3) . With the gradual relaxing of restrictive measures in May and during the summer, the number of new COVID-19 cases gradually increased daily, but in September and October, this number dramatically and exponentially increased in many countries, especially in Europe. It was difficult to talk about the new (or the second) wave of epidemic since the virus had not disappeared at any moment and practically the first wave has not "finished". However, many states introduced new different restrictive measures in September and October 2020 due to the "new" wave of COVID-19. In Croatia, despite a significant daily increase in the number of new cases, new restrictive measures were introduced in late November (4) . Incidence data of COVID-19 in the paediatric population are available from epidemiological reports of countries with the highest number of cases. Reports show a small proportion of children (0-19 years) in the total number of patients. In China, children under 18 amounted to 2-5%, Italy 1.2%, United States 7.3%, and in Australia 4% of all COV-ID-19 positive cases (5) (6) (7) (8) (9) . The first multinational and multicentre study on children with COVID-19 in Europe during the initial peak of the pandemic, which was conducted in 82 tertiary and quaternary paediatric units in 25 European countries, showed that COVID-19 is generally a mild disease in children, including infants, and a proportion of 8% of those COVID-19 positive children developed a severe illness that required intensive care support and prolonged mechanical ventilation. Several predisposing factors for intensive care support have been identified, and it is confirmed that death is rare in children (10) . All these data suggest that children show clinical symptoms less often than adults, and they also have a milder illness, recover faster and have a better prognosis. The role of asymptomatic or subclinical infection in human-to-human transmission of the virus is not fully understood. Due to mild or asymptomatic infections, children are not included in the routine molecular testing (reverse transcriptase polymerase chain reaction; RT-PCR) for COVID-19 and according to existing data, it is impossible to accurately determine the number of infected children (11) . Generally, mildly affected or asymptomatic persons are not routinely tested and included in the COVID-19 reports and the number of infections is probably underestimated. In this context, seroprevalence studies are important in the assessment of the extent of infection in the population. As the WHO recommended, monitoring changes in the seroprevalence over time is also crucial to predict dynamics and plan adequate public health measures (12) . Testing for specific antibodies has far greater potential than molecular testing to detect a past asymptomatic patients or patients with mild symptoms of infection. Antibodies most commonly become detectable 1-3 weeks after symptom onset, at which time evidence suggests that infectiousness likely is greatly decreased and that some degree of immunity has developed (13) . Existing commercial assays generally detect SARS-CoV-2 immunoglobulin (Ig)A, IgM and IgG class antibodies separately or total antibodies specific for the nucleocapsid or spike protein of the virus (11). Children's Hospital Zagreb (CHZ) is a general hospital for children aged 0 to 19 years whose primary role is not the treatment of COVID-19 and the aim of this study was to investigate the prevalence and titres of anti-SARS-CoV-2 antibodies in children treated at the CHZ in the first and the second wave of the COVID-19 pandemic. A statistical significance of the difference of anti-SARS-CoV-2 prevalence at two time points was done to determine how restrictive epidemiological measures and exposure of children to COVID-19 infection affect this prevalence in children of different age groups. The results of this study represent a contribution to the assessment of the extent of COVID-19 infection in the population, but also help in monitoring seroprevalence changes to predict dynamics and planning appropriate public health measures in Croatian pandemic conditions. All blood samples of children which arrived at the Department of Laboratory Diagnostics of CHZ that Samples collected during the first and second time points came from independent groups of subjects. During the first time point, the number of subjects was defined according to the protocol of multi-center study of anti-SARS-CoV-2 antibodies seroprevalence in the general population where 240 samples were collected in CHZ and tested in Croatian Institute of Public Health (CIPH). At second time point, the CHZ proposed, collected, and determined the samples collected during one month at the peak of the second wave (N = 308). All subjects were divided according to gender and age into three groups: (i) < 1 year; (ii) 1-10 years and (iii) 11-19 years. The reason for this age-based classification is the exposure of children to the SARS-CoV-2 virus, which varies according to the age of the child. The assumption is that the newborns and infants are mostly at home with their families, while older children are mostly exposed to the virus in kindergarten and school. In addition to the school exposure, teenagers are exposed due to a more intense social life. According to the epidemiological history, the subjects were classified as (i) negative, (ii) potentially positive and (iii) positive for COVID-19. Table 1 shows the criteria for distribution to groups of children according to epidemiological history. Table 2 . Potentially positive children and children suspected for SARS-CoV-2 infection were not considered as an exclusion criteria in order for the level of infection in the general population would not be underestimated. Informed consent was obtained from parents of all children included in the study. CIPH and CHZ Ethics Committee approved this study. Patient's venous blood was collected in a tube with clot activator and gel separator (Vacuette, Greiner Bio-One GmbH, Austria). Centrifugation of the blood samples was applied according to the manufacturer's recommendation (2000xg, 10 min-utes), the samples were forwarded for analysis and immediately after analysis (maximum 4 hours after centrifugation) the remaining serum was separated into labelled plastic tubes and stored at -20 °C until analysis (maximum 3 weeks). Blood sampling for outpatients were performed in fasting state in the morning from 8 to 10 am, but for day hospital and hospital departments, patient's blood samples were collected throughout the day in fasting and non-fasting state. Therefore, all lipaemic samples were not included in this study. In addition, haemolysed and icteric samples were also excluded from the study. Serological testing during the first and second waves of the COVID-19 pandemic was done by dif- (14) . The methods showed good comparability and the results of both methods were confirmed using virus micro-neutralization test (mVNT). The results of mVNT were defined as final. The result of sample testing is given either as reactive or non-reactive as well as in the form of a cutoff index (COI; signal sample/cut-off). Samples results with COI < 1.0 is negative for anti-SARS-CoV-2 antibodies and COI ≥ 1.0 is positive for anti-SARS-CoV-2 antibodies. Verification of the ECLIA method was done according to the American Society for Microbiology recommendations and protocol (14) . The first, initial wave of the pandemic was marked by a total lockdown, and samples were collected when the first strict epidemiological measures gradually mitigated. At this first study point, after mVNT, the final number of COVID-19 seropositive children was 2.9% ( Table 3 ). The second point of the study was marked as the peak of the second wave of the pandemic, and out of 308 children samples examined, 8.4% COVID-19 seropositive children were found. Statistically significant difference was found in the number of seropositive children during the first and the second wave of the COVID-19 pandemic (P = 0.010) ( Table 3 ). About 90% of the examined children were defined as negative according to epidemiological history at both observed time points and a significant difference during the first and second wave of the pandemic was observed only in the group of children with a positive epidemiological history (P = 0.009) ( Table 3) . Lenicek Krleza J. et al. The distribution of results by age/gender groups showed that a statistically significant difference between seropositive children during the first and second wave of the COVID-19 pandemic is found only for the 11-19 age group (P = 0.007) ( Table 4 ). In this age group, at the two time points, proportions of boys and girls are significantly different. Boys during the first wave is significantly higher than in the second wave (P = 0.048) in contrast to girls where proportion of girls in the first wave is significantly less than in the second wave (P = 0.044) (Table 4). Results of the distribution by gender, age, and epidemiological history are presented in Table 4 . The share of seropositive results in group of children with negative epidemiological history during the first wave was 3.2%, and during the second wave of the pandemic it was 6.6%, with P = 0.107. During the first wave of the pandemic, all seropositive children were asymptomatic at the time of anti-SARS-CoV-2 testing. At the second wave, 7/26 children with a positive COVID-19 RT-PCR test were found: 2 children with positive epidemiological history and positive RT-PCR (within 24 hours) and 7 children recovered from COVID-19 from 8 days to 2 months prior to testing and only 5 were seropositive. During the second wave of the pandemic, out of a total of 26 seropositive children, 6 children were hospitalized for treatment of acute or chronic dis-eases, and 4 children were admitted to emergency hospital admission due to acute disease (2 children had a fever > 38 °C with other symptoms: nausea, vomiting/diarrhea, abdominal pain), and 2 children were afebrile (bone fracture, renal colic). Asymptomatic children who underwent triage before entering the day hospital for specialist examination/treatment (7 children) and before arriving at the laboratory for blood sampling (9 children) were seropositive for COVID-19. Only two seropositive children had fever > 38 °C with other symptoms (urological, gastrointestinal and/or other) and 6 children had combination of symptoms (urological, gastrointestinal and/or other) without fever and respiratory symptoms. In total, at the second wave of the pandemic, we found 18/26 seropositive asymptomatic children without the Lenicek Krleza J. et al. symptoms that could be associated with COVID-19 disease (Table 2 ). The results of serological testing for COVID-19 at Children's Hospital Zagreb show a significantly lower seroprevalence in the paediatric population during the first, initial wave, compared to the second wave of the COVID-19 pandemic (2.9% vs. 8.4%, P = 0.010). This significant difference was expected due to the increase of incidence in the country and the second round of seroprevalence study was conducted in order to provide evidence that the increased transmission of infection affected children as well as adults. The first published results of COVID-19 seroprevalence from the end of March to up April 8, 2020 in Wuhan City was 9.6% in the general population and first systematic review of COVID-19 seroprevalence in May 2020 reported a very wide range of seroprevalence: from 0.4 to 59.3% in the general population (18, 19) . There are few published data on the COVID-19 seroprevalence in children and mainly relate to the first wave (from April to May 2020) of the pandemic. Different results in these studies may be due to the type of the studies (the most of published data are case reports or case series), dynamics in new cases per day, the strength of the epidemiological measures applied in countries, and in the definition of age groups (some results are part of the general population report). However, all these data have the same conclusion that COVID-19 seroprevalence in children is low. The results of a study in Switzerland during April and May 2020 show a very low prevalence in children aged 5-9 years (0.8%) compared to children between 10 and 19 years (9.4%) (20) . An extensive Spanish study of COVID-19 seroprevalence in the general population during April and May 2020 reported that children aged 0-19 were represented by 3.9% (21) . US prevalence study of anti-SARS-CoV-2 antibodies in children (age range 0-18 years) without symptoms of COVID-19 disease who were tested at 28 hospitals showed the prevalence varied from 0% to 2.2%, with a pooled prevalence of 0.65% (95%CI: 0.47% to 0.83%) with significant heterogeneity and significantly associated with weekly incidence of COVID-19 in the general population (22) . Also, the study performed at Seattle Children's Hospital during the lockdown in March and April 2020 found only 1% of COVID-19 seropositive children aged 0 to 15 years (23) . Multicentre observational cohort study, conducted between April to July 2020 at 5 UK sites, recruited children of healthcare workers, aged 2-16 years publish that total COVID-19 seroprevalence is 6.9% (95% CI 5.4% to 8.6%, N = 992) and varied between sites. Belfast had significantly lower seroprevalence than all other sites at 0.9% (95% CI 0.2% to 3.3%, N = 215 and P < 0.001), and in London seroprevalence was significantly higher than all other sites at 11.6% (95% CI 7.8% to 16.8%, N = 199 and P = 0.007) (9) . In the Czech Republic, in April 2020, the overall SARS-CoV-2 seroprevalence was estimated not to exceed 1.3%. In July and August, 2020, 200 children (0 to 18 years of age) from paediatric department of a large hospital in Prague were screened for the presence of anti-SARS-CoV-2 antibodies and zero seropositive subjects were found. Therefore, this study reported a low (< 0.5%) cumulative seroprevalence amongst children in Prague during August, 2020 (24) . According to the initial reports (up to 29th May 2020) of the CIPH, there were 2.8% children under 10 and 4.0% children and young adults from 11 to 20 years among all COVID-19 patients in Croatia. Until November 2020, the cumulative number of children up to age 10 was 2.4%, and children and young adults ages 11 to 20 years 9.3% (25, 26) . When we distributed our subjects according to age groups, taking into account variation of epidemiological measures applied (e.g. infants up to 1 year exposed to COVID-19 infection almost exclusively in contact with mother and household, children staying in kindergarten or attending lower grades at primary schools with a minimum distance and mask-wearing, teenage groups attending school mostly online, and outside of-homecontacts with mandatory mask-wearing indoors by public health and social institutions and ensuring social distance), we noted that a significant difference in seroprevalence is shown exclusively in the age group of teenagers. These results refer that regardless of epidemiological measures and exposure to the COVID-19 virus, the seroprevalence of young children is low. The children are mostly asymptomatic or present a mild form of the disease which is consistent with results of other studies (11, 27) . The literature cited several possible reasons related to the protective effect from severe clinical forms of COVID-19 and lethal outcomes in children: virological and epidemiological characteristics in children, the immune system and the matu-ration and low exposure to ACE2 receptors, characteristics of the renin angiotensin system in childhood, as well as the shorter effect of air pollutants on the respiratory system compared to the adult population (11, 27, 28) . The contribution to the assumption of protective mechanisms in children is the case of one 2 months old child, the subject of this study who was considered positive according to the epidemiological history due to a COVID-19 RT-PCR positive mother at birth, but found negative for both COVID -19 (RT-PCR) as well as anti-SARS-CoV-2 antibodies (IgM, IgG). This study has some limitations. Although Children's Hospital Zagreb is a specific children's health institution in the Republic of Croatia where children from all parts of the country are treated, the obtained results of COVID-19 seroprevalence in children cannot be considered representataive at the national level. Our results do not provide an answer on the transmission of COVID-19 disease from children to adults which should be investigated separately when planning epidemiological measures during a pandemic. In conclusion, the prevalence of anti-SARS-CoV-2 antibodies was significantly lower at the first time point than at the second time point. Virus microneutralization test values showed that low titre in asymptomatic children was not protective at the first time point, but all seropositive children in the second wave had a protective titre of anti-SARS-CoV-2 antibodies. According to the results, the determination of anti-SARS-CoV-2 antibodies could be useful for children older than 10 years both in terms of their own protection and in terms of COV-ID-19 transmission. Determination of mVNT in epidemiological circumstances of COVID-19 pandemic plays an important role in the verification of qualitative methods as well as their quantification by providing important epidemiological data on the protection of individuals and population. Also, for commercial quantitative tests, it will be helpful in order to define activity of anti-SARS-CoV-2 antibodies antibody as the limit of protection. 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We are also thankful to Valentina Vidranski, PhD, Sestre Milosrdnice University Hospital Center, for help in providing positive and negative samples necessary for the verification process of the ECLIA method. None declared.