IgG titers Decline Post-Vaccination with BNT6112b2 in an Italian Dental Team

Article Information

Livia Barenghi1*, Francesco Romano2, Garagiola Umberto1, Francesco Spadari1

1Department of Biomedical, Surgical and Dental Sciences, University of Milano, Milan, Italy

2European Institute of Medical Studies (EIMS), New Building of Saint Martin, Schembri Street, Hamrun HMR1541, Malta

*Corresponding Author: Livia Barenghi, Department of Biomedical, Surgical and Dental Sciences, University of Milano, Milan, Italy

Received: 18 October 2021; Accepted: 26 October 2021; Published: 28 October 2021


Livia Barenghi, Francesco Romano, Garagiola Umberto, Francesco Spadari. IgG titers Decline Post-Vaccination with BNT6112b2 in an Italian Dental Team. Dental Research and Oral Health 4 (2021): 074-084.

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The occupational risk of dental health care workers for COVID-19 is a burning issue. Currently, the long-lasting efficacy of the induced immunity from SARS-CoV-2 vaccination is largely unknown. Our aim is to study the RDB-IgG response after 1, 4, and 7 months from complete vaccination with BNT6112b2 in an Italian dental team. All 13 dental health care workers (3 men and 10 women) working in a private dental office were enrolled in the frame of scheduled controls for occupational safety. All dental health care workers were aged less than 60 yrs old; the mean age (±DS) was 41.23±9.63 yrs; 2/13 had one medical condition associated with a higher risk of developing severe illness from COVID-19, but none of DHCW were affected with the disease. Antigen tests on nasal swab in detecting the SARSCoV-2 were always negative from December 2020 to September 2021. Any symptoms commonly attributed to COVID-19 were not reported. The vaccination with BNT6112b2 was done on them with two doses according to the authorization protocol. Some female dental health workers (4/13) seem to be non-responders or slightly responders and reported associated pathologies (obesity, hypertension). 7 months after the second dose of vaccine, the RDB-IgG antibodies against SARS-CoV-2 have reduced significantly (94%; P < 0.001) compared to levels 1 month after. More knowledge on occupational risk and on vaccine efficacy in dental health care workers, stringent adoption of standard precautions, and, perhaps, the vaccine boost or new mucosal vaccines seem to be the main strategy in facing COVID-19 pandemic.


COVID-19, Infection, Vaccination, Safety, Workers, Dentistry

COVID-19 articles; Infection articles; Vaccination articles; Safety articles; Workers articles; Dentistry articles

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Article Details

1. Introduction

As Tamim recently stated, “Occupational health professionals have a unique and key role at the interface between work and health”, but their decisions are not always trouble-free in dental settings [1]. The Coronavrus Disease 2019 (COVID-19) risk on dental health care workers (DHCW) and dental patients is a burning issue, based on contradictory and largely unknown evidence [2-5]. It is unclear how the interplay among SARS-CoV-2, host, social behaviour, specific dental procedures and then the worker and environmental contamination by droplets and aerosol, affects infection risk. The rate of COVID-19 in a population seeking oral healthcare reflects the community positivity rate, including a considerable percentage of asymptomatic and afebrile patients [6]. SARS-CoV-2 dispersion parameter, named k, is small, and SARS-CoV-2 transmission, has been highly over-dispersed and propelled by the super-spreading of events. This means that 10–20% of cases cause 80% of secondary infections, and asymptomatic cases are nearly impossible to identify by triage in dental settings [7]. In addition to respiratory apparatus and vascular system, SARS-CoV-2 also resides in oral cavities, saliva, crevicular fluid and dental biofilm, and also influences oral microbiome and different oral manifestations [8]. Currently, it seems that aerosol and fomite contamination do not contributed substantially to transmission [2]. Nevertheless, DHCW work near to, or inside the oral cavity, while avoiding aerosol generating procedures (AGP), is a real tiring job in dentistry.

In general, vaccination has been considered the best defense in the hierarchy of infection prevention control (IPC) and against human error during infection prevention [9]. Vaccination against SARS-CoV-2 generally induces systemic immune responses with dominant IgG responses, while natural infection induces both systemic and mucosal immune responses. Vaccination, with traditional, viral vector, protein and RNA based vaccines, is promising in terms of bringing the COVID-19 pandemic to an end, mainly by lowering the risk of symptomatic COVID-19 and the most serious and deadly consequences of the virus.  Vaccine ability to limit viral transmission between individuals is less well understood [10].

Evidence from prospective cohorts of 3,950 health care workers (HCW), shows that with full immunization (14 days after second dose), mRNA vaccine was 90% effective against SARS-CoV-2 infections, regardless of symptom status [11]. 14 weeks after complete vaccination with BNT6112b2 (Pfizer/BioNTech) vaccine, 2.6% of the Israeli HCW had breakthrough COVID-19 infections (BCI), 67% of which were mild, and 33% of which were asymptomatic [12]. Among fully vaccinated HCW, the occurrence of BCI was correlated with neutralizing antibody titers during the peri-infection period. Male sex, older age, and hospitalization for COVID-19 have been associated with increased antibody response, while obesity, arthritis and some drugs with reduced antibody response. Antibody titers induced by natural coronavirus infection have been reported to wane over time. Unfortunately, the duration of the induced immunity from SARS-CoV-2 vaccination is largely unknown after many months [13]. Little evidence has been reported on long-lasting efficacy of COVID-19 mRNA vaccines, but it is indicative of a rapid decline of spike antigen specific serum IgG (<23% peak levels within 80 days of the initial shot) in four HCW [14].

Therefore, we investigated the induced immunity in a sample of DHCW, where the occupational risk was homogeneous, by the strict adoption of standard precautions [2].

2. Methods

2.1 Study place and enrolment

This study was conducted in a private dental office (Centro Odontoiatrico del dr. V. Romano, Piazza Castelnuovo 26A, 90141 - Palermo, Italy) located in Sicily, under the guidelines of occupational risk according to Italian Law (mainly Law 81/08), rules, regulations, and local guidance and specific recommendation for COVID-19 prevention in dental offices [15]. The study protocol was approved by the internal board for occupational risk (including the occupational physician), according to Italian Law and health data protection (EU General Data Protection Regulation). DHCW (2 dentists, 8 dental nurses, 2 receptionists) were included after a written informed consent. The study was carried out from January 2021 to September 2021. During dental cares, administrative work and instrument and environmental decontamination, the dental office strictly adopted the up-to-date guidance by CDC and the Italian recommendation  [2,15]. In Sicily, the epidemiologic trend of COVID-19 showed three main peaks on 20 November 2020, 14 January, 14 April  and 25 August 2021, with respectively 1634,1867, 1542 and 1491 new cases/daily and 40,38,20 and 9 deaths/daily for about 4.9 million of inhabitants (mean age =44,4 yrs) [16]. As of 5 September 2021, the total cases and death were respectively 281000 and 6435 for about 4.9 million of inhabitants.

2.2 Vaccination with BNT6112b2

The regional heath government of Sicily  prioritised DHCW for COVID-19 vaccination early, since January 2021. We underline that only on 21 December 2021, did the European Commission grant market authorization for EU-wide use for the vaccine Comirnaty, developed by BioNTech and Pfizer, named BNT6112b2, to prevent COVID-19 in people from 16 years of age. The vaccination with BNT6112b2 was done on DHCW with two doses according to the authorization protocol. The first dose of vaccination was administered from the 9th of January 2021 to the 12th of February 2021, and after 3 weeks, the second dose was administered, from the 30th of January to the 6th of March. As of August 28, 70.88% (equal to 3 million people) of the resident population in Sicily received at least one dose of the anti-COVID-19 vaccine, while 61.71% (over 2.6 million) were completely immunized (i.e. received both doses or the single Janssen dose).

2.3 Analytical methods

Diagnostic analyses were carried out in a highly specialized laboratory (Locorotondo Labs S.R.L. via G. Carducci n.3, 90141 Palermo; https://www.locorotondolabs.it/), authorised by the Sicily Region in accordance with the methods and procedures agreed upon with the National Reference Laboratory of the Istituto Superiore di Sanità. Analyses were performed at 1, 4 and 7 months after the second dose of vaccine.

2.4 IgG Immunoassay

IgG (sCOVG) antibodies to SARS-CoV-2 were evaluated by Atellica® IM* assay (Siemens, Germany). This test was authorized for emergency use by the FDA, for use by authorized laboratories. It is a chemiluminescent immunoassay intended for qualitative and semi-quantitative detection of IgG antibodies to SARS-CoV-2 in human serum and plasma (lithium heparin), using the Atellica IM Analyzer. The Atellica IM* assay detects IgG antibodies to the S1 RBD antigen, known to be an important component of the spike (S)-protein. The analytic performance (Positive percent agreement =95,58%; negative percent agreement=99-90%) from the manufacturer seems in line with real clinical performance [17,18]. RBD-based antibody tests are appropriate for testing at 6-8 months after SARS-CoV-2 infection. The sensitivity of Siemens tests was similar 4-10 weeks and 6-8 months after infection [18]. The analytical reference value is > 1 (U/mL).

2.5 SARSCoV-2 antigen test

SARSCoV-2 antigen was evaluated by immunoassay (Panbio™ COVID-19 Ag Rapid Test Device) on nasal swabs  at 1, 4 and 7 months. The Panbio™ COVID-19 Ag test (Abbot, USA) has a specificity of 100% and a sensitivity of 93.8% (for subjects with Ct values ≤ 30) among asymptomatic subjects, representing a viable alternative to RT-PCR when molecular testing is not readily available or too expensive. Mutations in the more transmissible forms of SARS-CoV-2 virus are located far from the target regions of the Abbott COVID-19 tests and should not pose a threat to assay performance and our study.

2.6 Statistical methods and software

Statistical analyses were performed using Excel software version 97-2003 for Windows software. The means of IgG levels after 1, 4 and 7 months days were compared by using Paired T Test. All tests were considered significant if  P-value was ≤0.05.

3. Results

All DHCW of the dental office were enrolled. There were 13 (3 men and 10 women) enrolled DHCW (Table). All DHCW aged less than 60 years old; the mean age (±DS) was 41.23±9.63 yrs; 2/13 had a medical condition associated with higher risk of developing severe illness from COVID19, but  none of DHCW were affected with COVID-19.

Tests on nasal swabs in detecting the SARSCoV-2 spike antigen were always negative from December 2020 to September 2021. The SARS CoV-2 Antigen Test is adequate for screening asymptomatic individuals. No symptoms commonly attributed to COVID-19 were reported. Temporary lay-offs of DHCW were in line with previous years, and were not caused by, or attributed to  COVID-19. The vaccination with BNT6112b2 was done on DHCW with two doses according to the authorization protocol. The vaccine immunity response, by RBD-IgG level, is reported in Figures 1,2 and Table 1.

We don’t have RDB-IgG level of three DHCW at four months. After 4 months of the second dose of vaccine, the mean antibody level against SARS-CoV-2 is significantly reduced (80%; P < 0.001) compared to levels 1 month after (Table). After 7 months of the second dose of vaccine, the mean antibody level against SARS-CoV-2 is significantly reduced (94%; P < 0.001) compared to levels 1 month after (Table). Our data is in line with 50% reduction of  anti-RBD antibodies and anti-trimeric spike IgG in HCW,  three months after the first dose [19]. The exponential decay  calculated by mean RBD-IgG levels at 1,4,7 months (R2=0.985), follows the formula y=308,9e-1,41x. The half life of IgG is 36 days and 47 days, calculated between 1-4 months and 4-7 months,  respectively. Four DHCW (signed with 2,4,8,11) seem to be non-responders or slightly responders and reported associated pathologies (obesity, hyperthension) (Figure 1); however, they continued to work in the dental office without problems during this study. Only one female (DHCW n° 5) reported contact with someone with suspected or confirmed COVID-19 infection, and needed to quarantine during the study. She was not never diseased or asymptomatic, but her antibodies levels were the highest, being 163,88, 44.11 and 16.46 U/mL respectively at 1, 4 and 7 months after complete vaccination. It is known that prior SARS-CoV-2 exposure is independently associated with higher IgG levels, after vaccination in HCW [20].


Figure 1: RDB-IgG levels in 10 DHCW at 1,4, 7 months after 2nd dose of vaccine BNT6112b2.


Figure 2: RDB-IgG levels in 10 DHCW at 1,4, 7 months after 2nd dose of vaccine BNT6112b2.

Time after the 2nd dose

1 month

4 months

7 months


Number of DHCW





Age (mean±SD)

41.23±9.63 yrs


Sex (F/M)





Age (mean±SD) of females



Age (mean±SD) of males



RBD-IgG level (mean ± SD) (U/mL) 





P value


P .

RDB-IgG level at 7 months vs 1 month


RDB-IgG level at 4 months vs 1 month


RDB-IgG level at 7 months vs 4 month


Table 1: Characteristics of the enrolled DHCP and vaccine immunity response after two doses of vaccine BNT6112b2, by RBD-IgG level

6. Discussion

Vaccination and the application of standard precautions are the two main preventive measures against COVID-19 for DHCW.  The challenges are open because the rate of infection is the highest in DHCW, at 26% , while in HCW it’s at 14.5%. These figures are respectively about 5 and 3 fold higher than the local population [5] or significant [4].  The estimated incidence rate ratio against any SARS-CoV-2 infection and asymptomatic or symptomatic/contact SARS-CoV-2 infection was 0.16 (0.10-0.25 95% CI) in vaccinated hospital employers (HE) compared to those not vaccinated HE [21]. The cumulative incidence of positive tests for symptoms or known exposure is 5-fold lower in vaccinated HE, compared to unvaccinated HE.  By mathematical modeling, the transmission probability of corona virus was estimated to be between 0 and 99,4% in three different dental scenarios, and driven mainly by patient infectiousness, indoor air quality, and slightly limited by respiratory protection [22]. Despite the fact that the pandemic led to unprecedented attention on infection prevention (IP), we have to underline that: a) different National Laws and European guidelines on IP often raise differing levels of awareness, and operational choice in UE [23]; lapses, errors, and the use of counterfeit products (mainly PPE, hand sanitizer products, “gray market” disinfectants) were frequent even before COVID-19 [24]. International guidelines (USA CDC, UK NHS etc) continue to recommend the application of standard IP measures, and in particular the use of a filtering facepiece respirator (N95, FFP). That said, data from a 6-month longitudinal study from June to November 2020, shows that only about 60% of dentists always wore FFP and eye protection by performing AGP. Additionally, the extended use (no change every patients) of respiratory protection is adopted by 75% of dentists [3]. During AGP, the evidence-based recommendation to use air turbine at 60-80 rpm to avoid aerosol production is largely unknown.  DHCW are considered fully vaccinated 2 weeks after their second dose in a 2-dose series, such as the Pfizer or Moderna vaccines. Post-dose 2, BNT162b2 vaccine efficacy (VE) in preventing COVID-19 (ClinicalTrials.gov number, NCT04368728), peaked at 96.2% during the interval from 7 days to <2 months post-dose 2, and then showed an average decline of ~6% every 2 months [25].

Long term vaccine efficacy is very important for DHCW occupational safety and for establishing the "levels of protection" determined by FDA approved clinical laboratory assays, even if at present, the CDC does not recommend measuring post vaccination titers for COVID-19. Data by different analytical methods, antigen target, and intra-individual immune response have contributed to an unclear picture around this topic.

Here, we show the spike RBD-IgG response to BNT162b2 vaccine in a homogeneous sample of DHCW, with concurrent antigen test negative for COVID-19 from nasal swabs (Figure 1,2 and Table). RBD-IgG level dropped by 94 % after 7 months. As expected, IgG decrease by vaccination is higher than the roughly 10-20% of  the maximum concentration observed 1 year after the natural infection [26]. We evaluated serum anti–RBD IgG because of antibodies against SARSCoV-2 spike and receptor binding domain (RBD) are known to decline moderately over 8 months after infection, according to several other reports [27,28], and have an estimated half life (t1/2) of  83 days (95% CI: 62 to 126 days) [27]. In healthy volunteers, a decrease in anti-RBD antibody after its peak in "2nd dose" group was significant only on

In convalescent plasma donors, the antibody decay is bi-phasic, with a more pronounced decrease during the first 6 months following the onset of symptoms. The antibodies half life for spike-RDB and nucleocapisde are respectively 62, and 47 days at a 0-6 months interval following symptom onset, while at 212 and 100 days at

6 months or more, following symptom onset [30]. Our data after vaccination (Figure 2), shows an increased exponential decay of RdB-IgG and shorter  t1/2: 36 and 47 days calculated between 1-4 months and 4-7 months, respectively. 

The chosen method for checking vaccine-immune response is adequate. In addition, RBD-binding antibodies are commonly referred to as "neutralizing" antibodies, since binding to the virus precludes its attachment and the entry into the host cell. Low titers of S-specific IgG and neutralizing antibody have been hypotized markers of breakthrough infection [31]. The quantitative values of antibodies against the RBD of the S-Protein of SARS-CoV-2 showed a good correlation to virus neutralization titers (Spearman’s r=0.843, 95%CI: 0.785- 0.885, p<0.0001) [32] and are expected to be suitable for monitoring the humoral immune response to vaccination with BNT162b2 vaccine. Pfizer reported that the BNTl62b2, which encoded the full-length stabilized S glycoprotein, elicited dose-dependent SARS-CoV-2 neutralizing antibody titers comparable or higher than those elicited by a defined panel of convalescent SARS-CoV-2 serum samples, and is also effective against Delta and Kappa variants [33]. When neutralising antibodies alone are insufficient, reinfection with SARS-CoV-2 can be limited by non-neutralising antibodies and T cells [34].

The main limitation of our study was the small size population, mainly of the female sex; nevertheless, the sample is very homogeneous for the occupational risk and the restricted age range of DHCW. In addition, it lacks of neutralization studies, mucosal IgA response, and T-cell response studies, that would have needed a very specialized laboratory and high cost. Unfortunately, the predictive power of circulating RBD IgG for assessing T cell memory was poor, so any speculation should be worrisome [27].


In conclusion, more knowledge is needed to evaluate the long-term VE because of the following factors:

  1. it is known that in nonhuman primates, even low circulating neutralizing (antibody titers 1:20) were associated with a substantial degree of protection against COVID-19.
  2. it is largely unknown the degree to which mucosal antibodies, including salivary highly effective secreted dimeric antibodies, elicited by vaccines can prevent infection [10]. Adenovirus-vectored vaccines seem to be potentially less effective than the mRNA vaccines.
  3. after SARS-CoV-2 infection, the immune system seems to produce around 50% lower amounts of IgG and IgA in women compared to men; this has been related to the higher risk of adverse COVID-19 outcome in men through a stronger (inflammatory) response.
  4. the immunological memory depends not only on antibodies, but also on the cellular immunity (memory B cells, memory CD4+ T cells, and/or memory CD8+T cells) [35]. RDB-specific CD8+ and S-specific IgG+ memory cells have been found to be involved in  VE at long term, that is approximately 7 months after natural infection [36]. Nevertheless, specific memory B cells are extremely scarce even after vaccination  [19,26,37].  But, recent data shows that two months after the second dose of BNT162b2 vaccine, specific antibody levels decline, but highly specific memory B cells continue to increase, thus predicting a sustained protection from COVID-19 [19].

The current strategy for facing COVID-19 outbreak is based on more knowledge of occupational risk, and of vaccine efficacy in DHCW, and the stringent adoption of standard precautions [1-5,9]. A vaccine boost, with intramuscular SARS-CoV-2 vaccines, should be taken into consideration, especially for more vulnerable and non responder DHCW. Infection after vaccination may be caused by the lack of local preventive immunity because of the absence or low levels of mucosal IgA [19]. The new generation mucous vaccines, are in various stages of development and very interesting for dentistry. They could effectively block the transmission of SARS-CoV-2 by the oral epithelial cells and oral mucosa [8] and there, generate antibodies and cellular immunity within the oral mucosa and saliva [10], and then  reduce the danger caused by AGP.


The authors would like to thank Dr Maté Jarai (PhD, Creative Writing Ma Creative Writing Bachelor in Philosophy), for English language revision and Dr Marco Grassini (Degree in Statistical) for statistical analysis.

Competing interests

Until 2018, L. Barenghi had a service agreement with KerrKaVo and was a consultant for DentalTrey il Blog (http://blog.dentaltrey.it/), neither of which gave any input or financial support to the writing of this article. The authors (F Romano, F. Spadari, U. Garagiola) declare that there are no conflicts of interest regarding the publication of this paper.


The work was supported by the Centro Odontoiatrico del dr. V. Romano (Palermo, Italy) [COVR/01/2021], and the Integrated Orthodontic services srl , Lecco (Italy) [IOS/03/2021].


FR conceptualized, planned and run this study. LB wrote the manuscript and prepared figures and the table. All authors contributed to the revision and discussions of the scope of this study and approved the final manuscript.


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