The most important results from the study are presented on this page. The results have been updated until round 6 (autumn 2021).
General information
The first round of the PIENTER Corona Study was in April and May 2020. In total, more than 3200 blood samples were examined in this round. After enlarging the study sample in the second round, in June and July 2020, RIVM examined more than 7300 samples. The third round of the PIENTER Corona Study took place in September and October 2020. The fourth round was in February and March 2021. Both round 3 and round 4 involved about 6500 blood samples. In the fifth round of the PIENTER Corona Study (June/July 2021), RIVM examined nearly 5800 blood samples. Round 6 took place in November and December 2021. New participants were invited during this round, so about 8500 blood samples were included in the 6th round.
In each round, slightly more than half of the blood samples generally came from women. Also, there are usually slightly more older participants than younger ones. This is taken into account in our analyses.
Timeline and (approximate) total number of blood samples per research round in rounds 1 through
Skip chart Timeline and (approximate) total number of blood samples per research round and go to datatableFigure 1: Timeline and (approximate) total number of blood samples per research round in rounds 1 through 6.
*New participants were invited in round 2 and round 6.
Number of participants by age and region
The average age of the participants in the PIENTER Corona Study is about 50 years old. The youngest participant is 1 year old and the oldest participant is 92 years old. The figure below shows the current age distribution of the participants for each region in the Netherlands. The age groups of 70-74 years and 75-79 years had the most participants, and the age groups are evenly distributed across the regions.
Figure 1: Age distribution of participants (round 6) – November/December 2021). The regions shown consist of the following provinces: North = Groningen, Friesland, Drenthe and Overijssel; Midwest = North Holland and Flevoland; Midwest = Utrecht and Gelderland; Southwest = South Holland and Zeeland; Southeast = North Brabant and Limburg. LVC sample = Low Vaccination Coverage, consisting of a few municipalities in the Netherlands where general vaccination coverage (against all kinds of infectious diseases) is lower compared to the rest of the Netherlands.
The number of participants per municipality since round 6 is shown in Figure 2. The larger the blue dot, the more people from this municipality are participating. The distribution of blood samples for each municipality shows some correlation to the population distribution in the Netherlands: more people from the Randstad conurbation took part in the study. The research results are analysed with due consideration of differences in the participants’ gender, age, region and ethnic background.
Figure 2: Number of participants per municipality (round 6 – November/December 2021).
People who have antibodies
The research results show what percentage of the general population in the Netherlands has generated antibodies against the coronavirus (SARS-CoV-2) that causes COVID-19. This allows us to estimate the number of people who have built up immunity to the virus due to infection, and (since the vaccination campaign started in 2021) also due to vaccination. This is known as seroprevalence. During the first round of research in the spring of 2020, this was just under 3%. In the second round in the summer, it rose to 4.5%, reaching approximately 5% during the third round of the study in autumn 2020. In February 2021, seroprevalence had risen to over 14%. At that time, about 2% of the participants had antibodies resulting from vaccination and about 12% had had a coronavirus infection. In the fifth round (summer 2021), nearly 65% of the population had antibodies against the coronavirus in their blood, and about 20% had evidence of a previous coronavirus infection in their blood. In autumn 2021 (round 6), nearly 87% of the population had antibodies against the coronavirus in their blood. At that time, over 25% of the total population turned out to have evidence of a previous infection in their blood.
The increase in the percentage of people with antibodies since previous rounds is mainly due to the start of the vaccination programme in early 2021, and partly due to infection with the Alpha and Delta variants of the virus. Women are slightly more likely to have antibodies than men, and people with a Dutch background or a Western migration background are slightly more likely to have antibodies compared to people with a non-Western migration background. This is primarily due to differences in vaccination coverage.
Age distribution of people who have antibodies
Figure 3 shows the percentage of participants with antibodies distributed across the age groups in the population (from 1 up to 92 years old) since the first wave in 2020. The research results from the PIENTER Corona Study are then extrapolated to the general population. An estimate is provided for the percentage of the Dutch population that has been in contact with the coronavirus in each age group. Since January 2021, people started getting vaccinated against SARS-CoV-2. Due to that fact, since the fourth round in February 2021, a distinction has been made between immunity resulting from infection or from vaccination. This is established by looking at different types of antibodies in combination with information from the questionnaire. In addition, some people also become infected after vaccination.
Similar to the fourth and fifth rounds, the antibody results from the sixth round (November/December 2021) show a combination of vaccination and infections in the population. The older age groups and vulnerable people were the first to receive a COVID-19 vaccination. The younger age groups followed later. During the sixth round of the study, the basic vaccination programme against COVID-19 had been completed for all people aged 12 years and older. That means that everyone in those age groups had had the opportunity to be vaccinated against the coronavirus SARS-CoV-2 by that time.
In the second half of November 2021, the booster campaign also started, starting with older people and other risk groups. Around the time of round 6, children under 12 years old were not yet eligible for vaccination. For that reason, there was a major difference in people with antibodies when comparing age groups up to 12 years old and groups above that age (Figure 3, orange line). In all age groups from 12 years and older, the percentage of people with antibodies was 90% or higher.
From round 2 through round 5, there was a similar trend in the percentage of people who showed evidence of infection (Figure 3, from light green to dark green dotted line). In every round, young adults showed the highest percentage of infections, relatively speaking, followed by people aged 50-59 years; this percentage was lowest in the oldest age groups. In the sixth round (Figure 3, black dotted line), there was a relatively large increase in the percentage of infections among children and adolescents, from primary school age up to young adults, with a peak rising above 40% in people aged 20-29 years. The percentage of people with antibodies from infection was still lowest in the oldest age groups, at 20%.
Figure 3: Percentage of people who have antibodies by age over time (rounds 2-6). The dotted lines (light green to black) show the percentage of people who have antibodies due to infection in round 2 (June/July 2020) up to and including round 6 (November/December 2021). The orange line shows total seroprevalence after infection and vaccination in round 6 (November/December 2021).
People who have antibodies due to infection and/or vaccination by region
The study is also investigating the distribution of the virus throughout the Netherlands. Figure 4 shows the percentage of participants per GGD region that had the virus since the first wave. A lighter colour (light orange) means a lower percentage per region on average, while a darker colour (dark red) means a higher percentage per region on average.
During the first wave (round 2 – June/July 2020 and round 3 – September/October 2020), the prevalence of antibodies from infection was significantly lower in the northern provinces than in the central regions, and much lower compared to the south of the Netherlands. Although seroprevalence was still highest in the southern provinces after the second wave (round 4 – February/March 2021), it was clearly distributed more evenly across the entire country. A similar pattern was observed after the third wave (round 5 – June/July 2021), with the strongest increases in the GGD regions of Zuid-Limburg, Utrecht, Fryslân and Hollands-Noorden.
During the fourth wave (round 6 – November/December 2021), the occurrence of antibodies due to infection continued to differ between northern and southern regions. The GGD regions of Amsterdam, Zeeland, Zuid-Limburg, Hart voor Brabant and West-Brabant had the highest percentages. The GGD regions of West-Brabant, Zaanstreek/Waterland and Twente had the largest relative increases between round 5 and round 6.
Figure 4: Percentage of people who have antibodies due to infection, over time (rounds 2 through 6 – June/July 2020 through November/December 2021), by GGD region.
Figure 5 illustrates the total percentage of people who have antibodies due to infection and vaccination in the sixth round (November/December 2021) (on a scale of 80 to 100%), by GGD region. The total percentage of people with antibodies differs between GGD regions. Relatively speaking, the GGD regions of Limburg-Noord, IJsselland, Fryslân and Flevoland had the lowest percentages and the GGD regions of Twente, Hollands-Midden, Kennemerland and Zeeland had the highest percentages.
Figure 5: Total percentage of people who have antibodies due to infection and/or vaccination in round 6 (November/December 2021) (scale 80-100%), by GGD region.
Antibodies after vaccination with various vaccines
The Netherlands started vaccinating against the coronavirus SARS-CoV-2 in January 2021. So far, four vaccines have mainly been used in the Netherlands: Pfizer/BioNTech (Comirnaty), Moderna (Spikevax), AstraZeneca/Oxford (Vaxzevria) and Janssen. This study examined antibody levels after vaccination, comparing the results for these four vaccines. We looked at antibodies after full vaccination, i.e. 14 days or more after the second dose of Pfizer, Moderna and AstraZeneca or 14 days or more after one dose of Janssen.
Nearly all adults aged 18-64 years had antibodies in their blood after full vaccination. That was the case in 99-100% of participants who received Pfizer, Moderna or AstraZeneca. The few who did not produce antibodies were vulnerable people with an underlying health condition (such as organ transplants or cardiovascular disease). Not everyone had antibodies in the blood 14 days after vaccination with Janssen (95%), but antibody levels increased over time and by 28 days had risen to 98%.
Figure 6 shows the levels of antibodies for each of the four vaccines at 14 days or more after 1 and 2 vaccinations in adults aged 18 to 64 years. Two groups are displayed here: people who were infected with the coronavirus before vaccination (orange clouds) and people who were not (purple clouds). In the group that had had a coronavirus infection before vaccination, a strong increase in antibodies was visible after only one COVID-19 vaccination. This was the case for all four vaccines. In people who had a previous infection, the levels of antibodies did not increase further after a second vaccination with Pfizer, Moderna or AstraZeneca (i.e., there is almost no difference between the orange clouds per type of vaccine).
Read more in the published scientific article describing these results and other conclusions
Figure 6: Levels of antibodies at 14 days or more after vaccination with Pfizer (Comirnaty), Moderna (Spikevax), AstraZeneca (Vaxzevria) and Janssen in adults aged 18-64 years. A distinction is made between people who are infected with the coronavirus before vaccination (orange clouds) and people who are not (purple clouds). The dots above the dotted line indicate that the person has antibodies. The black lines in the clouds indicate the median level for that group: half of the people have a value above the black line, and the other half below it.
Duration of the presence of antibodies after infection and/or vaccination
It has become apparent from the PIENTER Corona Study that 90% of the people whose blood samples were found to contain SARS-CoV-2 antibodies still had antibodies in their blood nearly 18 months later. This involves IgG antibodies. These are the most important type of antibodies, since they provide long-term protection. The research results also show that the antibodies grew stronger over time. They were more effective in binding to the virus, so fewer antibodies were needed to achieve the same protection. Read more in the published scientific article describing these results for up to 7 months post infection and other conclusions.
Figure 7 shows persistent antibody levels over time in different age groups, up to 16 months after infection. Since this figure only looks at antibodies produced after infection, and since many people have been vaccinated by now, there were fewer people with antibodies after infection at the later dates on the chart. Antibody levels drop shortly after infection, but the decrease slows over time, so many people continue to have antibodies for a long time.
Figure 7: Antibody levels after infection, in people of various ages who have not received a vaccination. This looks at the levels of antibodies against the spike protein of the virus, which is also in the vaccine, and can be compared to the virus. 100 in this figure corresponds to 102 in Figures 6, 8 and 9 and 10,000 to 104.
Figure 8 shows the antibody levels over time in different age groups for three different vaccines (Pfizer, Moderna and AstraZeneca). For all vaccines, antibody levels decrease over time. This holds true for all age groups. It is interesting to note that younger people have more antibodies than older people after vaccination with the Pfizer vaccine.
Figure 8: Antibody levels over time, after two vaccinations, for three different vaccines in different age groups. Information is only displayed for age groups for which data has been recorded in sufficient numbers to show significant trends. Only people who have not been infected with the virus have been included in this figure.
Table 1 shows the percentage of people with antibodies after completing basic vaccination. Before booster vaccinations were available, the standard practice was to administer 2 vaccinations with Pfizer/BioNTech, Moderna or AstraZeneca, or 1 vaccination with Janssen. Nearly everyone still had antibodies 100-200 days after these vaccinations. The number of people with antibodies decreases gradually with age.
Table 1. The percentage of people with antibodies by age group, after completing basic vaccination with Pfizer, Moderna, AstraZeneca (2 vaccinations) or Janssen (1 vaccination).
Vaccine |
Number of vaccinations |
Age (years) |
Number of participants |
% positive after 100-200 days |
---|---|---|---|---|
Comirnaty (Pfizer/BioNTech) |
2 |
12 – 40 |
264 |
100 |
40 – 65 |
779 |
99.7 |
||
65 – 93 |
930 |
98.6 |
||
Spikevax (Moderna) |
2 |
12 – 40 |
74 |
100 |
40 – 65 |
181 |
100 |
||
65 – 93 |
9 |
100 |
||
Vaxzevria (AstraZeneca) |
2 |
12 - 40 |
41 |
100 |
40 - 65 |
363 |
98.1 |
||
65 - 93 |
123 |
98.4 |
||
Janssen |
1 |
12 - 40 |
58 |
100 |
40 - 65 |
114 |
96.5 |
||
65 - 93 |
1 |
- |
Only people who have not been infected with the SARS-CoV-2 virus have been included in this figure.
Figure 9 shows the antibody levels after vaccination with Pfizer, Moderna and AstraZeneca in people who had a SARS-CoV-2 infection before they were vaccinated. People who had first had an infection (Figure 9, red lines) had more antibodies after vaccination than people who had not been infected before vaccination (Figure 9, black lines). This holds true for all three vaccines, but antibody levels shortly after vaccination vary between vaccines. Also, people who had an infection before being vaccinated retain more antibodies over time (Figure 9, the red lines show less rapid decrease than the black lines). Future analyses will also look at the effect of booster vaccinations and the effect of infections after vaccination.
Figure 9. The course of antibody levels after vaccination with Pfizer, Moderna and AstraZeneca in people who did (red lines) or did not (black lines) have a SARS-CoV-2 infection before they were vaccinated.
Risk of infection
Data from the second round of the study (spring 2020) showed that social distancing is an important measure in stopping the spread of the virus. Participants who had followed the recommendation to stay 1.5 metres apart were less likely to have antibodies in their blood during the first wave, while antibodies were found in the blood of 5.5% of the participants who were less compliant with the distancing rule. And antibodies were only found in the blood of 4% of people who did keep their distance during contact with others. Participants who mostly had contact with children under the age of 10 were hardly ever infected during those encounters. Similarly, participants who indicated that they had an occupation involving physical contact with children were not more likely to be infected. However, the size of the group of people who spent time together (within 1.5 metres) proved to be an important predictor of infection. Antibodies were found in the blood of 6.2% of the participants who had attended a meeting or gathering (involving more than 20 people) in an indoor environment during the first wave. This was almost 1.5 times more often than people who had not attended meetings at all (4.2%). Other conclusions drawn from the analyses can be read in the scientific article. (link is external)
The results of the PIENTER Corona Study are presented in scientific articles for publication, so they can be read by everyone. As a result, other countries can also benefit from the research and use key findings in formulating their public health policies. When articles are published online, they will be posted on this page.
Analysis of SARS-CoV-2 seroprevalence and risk factors, as well as symptoms in relation to antibody levels after infection during the first wave (based on data from round 1):
Vos ERA, den Hartog G, Schepp RM, et al. Nationwide seroprevalence of SARS-CoV-2 and identification of risk factors in the general population of the Netherlands during the first epidemic wave.(link is external) Journal of Epidemiology and Community Health. 2020 Nov 28;75(6):489–95.
The effect of social distancing on contact patterns in the population (based on data from rounds 1 and 2):
Backer JA, Mollema L, Vos ER, et al. Impact of physical distancing measures against COVID-19 on contacts and mixing patterns: repeated cross-sectional surveys, the Netherlands, 2016–17, April 2020 and June 2020.(link is external) Eurosurveillance. 2021 Feb;26(8):2000994.
Estimated asymptomatic SARS-CoV-2 infections in the population (based on data from the PIENTER3 study, and from PIENTER Corona Study rounds 1 and 2):
McDonald SA, Miura F, Vos ERA, et al. Estimating the asymptomatic proportion of SARS-CoV-2 infection in the general population: Analysis of nationwide serosurvey data in the Netherlands.(link is external) European Journal of Epidemiology. 2021 Jul;36(7):735-739.
The effect of social distancing measures on SARS-CoV-2 infection after the first wave (based on data from round 2):
Vos ERA, van Boven M, den Hartog G, et al. Associations between measures of social distancing and SARS-CoV-2 seropositivity: a nationwide population-based study in the Netherlands(link is external). Clinical Infectious Diseases. 2021 Dec 16;73(12):2318-2321.
Duration of immunity and binding strength of SARS-CoV-2 antibodies more than six months after infection (based on data from rounds 1-3):
den Hartog G, Vos ERA, van den Hoogen LL, et al. Persistence of antibodies to SARS-CoV-2 in relation to symptoms in a nationwide prospective study.(link is external) Clinical Infectious Diseases. 2021 Dec 16;73(12):2155-2162.
Use of antibodies to identify breakthrough infections after vaccination (using data from round 4):
van den Hoogen LL, Smits G, van Hagen CCE, et al. Seropositivity to Nucleoprotein to detect mild and asymptomatic SARS-CoV-2 infections: A complementary tool to detect breakthrough infections after COVID-19 vaccination?(link is external) Vaccine. 2022 Apr 1;40(15):2251-2257.
The antibody response after vaccination (using data from round 5):
van den Hoogen LL, Verheul MK, Vos ERA et al. SARS-CoV-2 Spike S1-specific IgG kinetic profiles following mRNA or vector-based vaccination in the general Dutch population show distinct kinetics.(link is external) Scientific Reports. 2022 Apr 8;12(1):5935.
Laboratory method for measuring SARS-CoV-2 antibodies:
den Hartog G, Schepp RM, Kuijer M, et al. SARS-CoV-2–Specific Antibody Detection for Seroepidemiology: A Multiplex Analysis Approach Accounting for Accurate Seroprevalence. (link is external) The Journal of Infectious Diseases. 2020 Oct 1;222(9):1452-1461.
RIVM previously published an article on the scientific background of the PIENTER3 study:
Verberk JDM, Vos RA, Mollema L, et al. (link is external)Third national biobank for population-based seroprevalence studies in the Netherlands, including the Caribbean Netherlands. (link is external) BMC Infectious Diseases. 2019 May;19(1):470.