key: cord-0745467-0tzr3e55
authors: Milazzo, Laura; Pezzati, Laura; Oreni, Letizia; Kullmann, Cristina; Lai, Alessia; Gabrieli, Arianna; Bestetti, Giovanna; Beschi, Cristian; Conti, Federico; Ottomano, Cosimo; Gervasoni, Cristina; Meroni, Luca; Galli, Massimo; Antinori, Spinello; Ridolfo, Anna Lisa
title: Impact of prior infection status on antibody response to the BNT162b2 mRNA COVID-19 vaccine in healthcare workers at a COVID-19 referral hospital in Milan, Italy
date: 2022-01-27
journal: Hum Vaccin Immunother
DOI: 10.1080/21645515.2021.2002639
sha: f5aeabf0ea09130a8332e2be04f3d5124f324e89
doc_id: 745467
cord_uid: 0tzr3e55

In Italy, SARS-CoV-2 vaccination campaign prioritized healthcare workers (HCWs) to receive two doses of BNT162b2 vaccine, irrespective of a previous SARS-CoV-2 infection. In this real-life study, we compared the humoral response to BNT162b2 vaccine in HCWs with and without a previous SARS-CoV-2 infection. Of the 407 HCWs enrolled, 334 (82.1%) were SARS-CoV-2-naive and 73 (17.9%) SARS-CoV-2-experienced. Post-vaccine humoral response was detectable in more than 98% of HCWs. Overall, the median level of anti-S IgG in SARS-COV-2-experienced HCWs was twice as high as those of SARS-CoV-2-naive subjects (24641.0 AU/mL [IQR: 15273.0–>40000.0] versus 13053.8 [IQR: 7303.3–20105.8]; p < .001), irrespective of the time elapsed from SARS-CoV-2 previous infection. In a subgroup of SARS-CoV-2-naive and -experienced subjects who received only one dose of the vaccine, the latter showed 32 times higher levels of anti-S IgG compared to the former. Although no serious adverse events have been reported, mild to moderate side effects occurred more frequently after the first dose in the SARS-CoV-2-experienced than in naive subjects (67% versus 42%, respectively; p < .001). Notably, post-vaccination anti-SARS-CoV-2 spike IgG levels ≥20,000 AU/mL were independently associated with the risk of fever ≥38°C (adjusted odds ratio [aOR] 5.122, 95% CI 2.368–11.080, p < .0001). Our study showed high responsiveness of BNT162b2 vaccine and a relationship between levels of antibody response and reactogenicity. It suggests that a single dose of mRNA vaccine might evoke effective protection in SARS-CoV-2-experienced subjects.

The pandemic of the coronavirus disease 19 due to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that started in China in late 2019 has rapidly become an unprecedented global health challenge. 1 With continuing cases and deaths from the pandemic, researchers worldwide raced to develop COVID-19 vaccines. The application of new vaccine techniques mainly based on mRNA and adenoviral vector platforms has led to the rapid development of anti-SARS-CoV-2 vaccine candidates. At the end of 2020, the results of phase 3 clinical trials on vaccines targeting the spike (S) proteins of SARS-CoV-2 demonstrated their ability to induce robust humoral and cellular immune responses and showed 95% efficacy at preventing Covid-19 illness, including severe disease. [2] [3] [4] [5] [6] [7] Since then, the rapid implementation of mass SARS-CoV-2 vaccination has become a global healthcare priority for curbing the epidemic.

COVID-19 vaccination campaign in Italy started on 27 December 2020 as soon as the BNT162b2 (Pfizer-BioNTech) vaccine, an mRNA-based COVID-19 vaccine, was approved for emergency use. 8 Initial targeted population included healthcare workers (HCW) to whom two doses of BNT162b2 vaccine were recommended, irrespectively of a previous SARS-CoV-2 infection and regardless of some concerns on the indication of prioritizing vaccination in subjects with preexisting natural immunity. 9 The main objective of the study was to compare the humoral response to BNT162b2 vaccine in HCWs with and without a previous SARS-CoV-2 infection. As a secondary objective, we explored the association between previous SARS-CoV-2 infection and the frequency and severity of postvaccination symptoms.

The study was conducted at the Luigi Sacco University Hospital (LSUH) that has served as a main COVID-19 referral center for the metropolitan area of Milan, Italy, since the start of the pandemic. 10 From 28 December 2020, LSUH offered the BNT162b2 mRNA-based vaccine to all its 1500 healthcare workers (HCWs) including nurses, doctors, healthcare technicians, health service assistants, cleaners, laboratory staff, and administrative staff. HCWs enrolled into the vaccination program were invited to participate in a pre-and post-vaccination serosurvey on a voluntary basis, and those who agreed gave the written informed consent to the storage of their anonymized data in a protected database. The study was approved by the ethical committee of the University of Milan (Comitato Etico Università degli Studi di Milano, n. 23/21) and conducted in compliance with Good Clinical Practice guidelines and the Declaration of Helsinki.

Two blood samples for each participant were obtained: the first within the 7 days preceding the administration of the first vaccine dose (baseline sample), and the second after 28-30 days from the first dose of vaccine (post-vaccination sample), regardless of the receipt of the second dose. Participants were asked to complete a questionnaire that, in addition to demographic and occupational data, included questions concerning whether they had experienced symptoms possibly related to SARS-CoV-2 infection (fever, myalgia, fatigue, sore throat, conjunctivitis, gastrointestinal symptoms, anosmia/dysgeusia, cough, and dyspnea) and/or they have ever had a PCR test on nasopharyngeal swab and/or a serological test positive SARS-CoV-2. At the post-vaccination survey participants were also asked to report any new symptoms or diagnosis of SARS-CoV-2 infection and any side effects that occurred after the first and/or the second vaccination dose. HWCs were asked to define their side effect(s) as follows: mild (negligible symptom(s)), moderate (symptom(s) not requiring specific medical intervention), intense (symptom(s) requiring medications or impacting on the daily activities) and referred them at the high intensity experienced from the first dose to the post-vaccination questionnaire. In the case of fever or hypertension, specifically, HCWs were asked to indicate if fever was <38°C (moderate) or ≥38°C (intense) and weather the diastolic blood pressure was <100 mmHg (moderate) or ≥100 mmHg (intense).

New SARS-CoV-2 infections diagnosed between the two observation time points were considered to be prevaccination if they occurred within 5 days from first dose of vaccine administration. 11

Plasma samples were stored at −20°C until serological tests were performed.

In order to capture possible asymptomatic infections and to assess the persistence of specific antibodies in previously infected subjects, baseline samples were screened for antibodies against the SARS-CoV-2 nucleocapsid protein (anti-N IgG) using the Abbott chemiluminescent microparticle immunoassay (Abbott, Abbott Park, Illinois, USA) and for IgG antibodies against the receptor-binding domain (RBD) of the viral S1 spike protein (anti-S IgG), which levels showed a strong correlation with neutralizing activity, 12,13 using the SARS-CoV-2 IgG II Quant assay (Abbott, Abbott Park, Illinois, USA). The assay cutoff is ≥50 AU/ml, with linear quantification of detected results from 50 to 40,000 AU/ml reported by the manufacturer. 14 This same assay was also used to quantify the magnitude of anti-S IgG response in post-vaccination samples.

For the purpose of our analyses the study population was divided in two groups: a) HCWs without a prior history of SARS-CoV-2 infection and resulted negative at the baseline anti-N IgG and anti-S IgG screening test (SARS-CoV-2-naive), and b) HCWs with a previous infection documented by a positive PCR test on a nasopharyngeal (NF) swab and/or a positive serologic test or resulted positive to our baseline N/ S-IgG screening test (SARS-CoV-2-experienced).

The descriptive statistics include proportions for categorical variables, and median values and interquartile range (IQR) for continuous variables. The baseline characteristics of SARS-CoV-2 -naive and SARS-CoV-2-experienced HCWs were compared using the χ 2 or the Fisher's exact test where necessary for categorical variables and the nonparametric Mann-Whitney test for continuous variables.

The Mann-Whitney test or the Kruskal-Wallis with Dunn's test for pairwise multiple-comparison procedure were used to compare post-vaccination anti-S IgG levels between HCWs according to the following characteristics: a) being SARS-CoV-2 -naive and SARS-CoV-2 -experienced; b) having been diagnosed with SARS-CoV-2 infection for less or more than 6 months, c) having received one or two vaccine doses, and d) being male and female. Differences in anti-S IgG levels according to age strata was also evaluated by using the Cuzick's trend test. Nonparametric analysis of the correlation between pre-and postvaccination anti-S IgG levels in SARS-CoV-2-experienced subjects was assessed by Spearman's rank correlation coefficient r s .

The frequency of post-vaccination symptoms, overall and grade 3 systemic events, was compared between SARS-CoV-2naive and SARS-CoV-2-experienced HCWs. In case of statistically significant difference in the frequency of grade 3 systemic events between the two groups, we applied multivariable logistic regression model, adjusting for age, sex and postvaccination anti-S IgG levels. All statistics were conducted using SAS, version 9.4 and p-values < .05 were considered to be statistically significant.

Of the 1550 HCWs who were offered COVID-19 vaccination, 407 participated in the study: 334 (82.1%) SARS-CoV-2-naive and 73 (17.9%) SARS-CoV-2-experienced HCWs. The baseline characteristics of SARS-CoV-2-naive and SARS-CoV-2experienced HCWs are shown in Table 1 . SARS-CoV-2experienced HCWs were more frequently males than SARS-CoV-2-naive, but there were no between-groups differences according to age and occupational category. SARS-CoV-2experienced HCWs included 21 individuals without a history of infection who resulted positive to baseline anti-S IgG test but had no report of positive PCR on a NF swab. Overall, of the 73 SARS-CoV-2-experienced HCWs, 93.2% resulted positive for anti-SARS-CoV-2 spike IgG at baseline, while in 49.3% of them baseline anti-N IgG were negative. The median interval between SARS-CoV-2 diagnosis and enrollment resulted significantly longer in these subjects compared to those who tested anti-N IgG positive (258 days [IQR 166-289] versus 75 days [IQR 70-90], respectively, p = .007).

All participants received the first dose of BNT162b2 mRNA COVID-19 vaccine. After 28-30 days from the first dose administration, 326 (97.6%) of SARS-CoV-2-naive HCWs had completed their 2-dose vaccination schedule, while 8 (2.4%) had the second dose delayed for personal reasons (4 were unwell and 4 had familiar commitments and were rescheduled). Among SARS-CoV-2-experienced HCWs, 60 (82.2%) had received the second dose, while 13 (17.8%) declined it.

At this post-vaccination time point, anti-S IgG were detectable in more than 98% of HCWs. Overall, the median levels of anti-S IgG in SARS-CoV-2-experienced HCWs increased from 871.9 AU/mL [IQR: 233.9-2767.9] at baseline (Table 1) (Figure 1a) . Moreover, anti-S IgG levels among SARS-CoV-2-experienced HCWs who had completed a 2-dose course of vaccination did not significantly differ between subjects who had been diagnosed with SARS-CoV-2 infection for less than 6 months (n = 40) and those who had been diagnosed for more than 6 months (n = 20) (Figure 1b) .

No statistically significant difference was found in postvaccination anti-S IgG levels according to sex, while a significant decreasing trend was shown with increasing of age (p = .021) among SARS-CoV-2-naive subjects.

Finally, in the timespan between the two plasma samples we did not observe any symptomatic infection except one subject who resulted positive to nasopharyngeal swab one day after the first dose and was considered a pre-vaccine infection, thus included in SARS-CoV-2 experienced-HCWs.

At least one side effect was reported by 245 (73.4%) and 63 (86.3%) of SARS-CoV-2-naive and SARS-CoV-2-experienced subjects (p = .019), respectively, none requiring hospitalization ( Table 2 ). Symptoms after both first and second dose of vaccine were reported by 98 and 23 SARS-CoV-2-naive and -experienced participants, respectively. Overall, a higher number of SARS-CoV-2 naive HCWs reported side effects after the second vaccine dose than after the first dose, while no significant difference emerged in the number of SARS-CoV-2-experienced subjects reporting side effects after the first or second vaccine dose.

The most common side effect was localized injection-site pain, followed by fatigue, fever, muscle pain, joint pain, nausea and very rarely skin rash and blood hypertension. Systemic intense (grade 3) events were more frequent in SARS-CoV-2experienced than in SARS-CoV-2-naive vaccine recipients, but no significant association between the frequency of grade 3 events and the time elapsed from the diagnosis of SARS-CoV -2 infection was seen (Figure 2) . Table 3 shows the multivariable logistic regression analysis of the factors associated with the odds of developing a systemic grade 3 event after vaccine exposure. Post-vaccination anti-SARS-CoV-2 spike IgG levels ≥20,000 AU/mL was independently associated with the risk of fever ≥38°C (adjusted odds ratio [aOR] 5.122, 95% CI 2.368-11.080, p < .0001).

Moreover, to be SARS-COV-2-naive was independently associated with a reduced likelihood of presenting fatigue (adjusted odds ratio [aOR] 0.281, 95% CI 0.084-0.935, p = .038). 

In this study we have assessed the neutralizing antibody response to BNT162b2 mRNA COVID-19 vaccine in previously infected and uninfected HCWs. The vaccine resulted effective and well tolerated, with no severe side effects reported.

In accordance with previous reports [15] [16] [17] [18] [19] [20] vaccination of individuals with previous SARS-CoV-2 infection lead to anti-S IgG levels at least twice as high as SARS-CoV-2naive subjects, irrespective of the loss of SARS-CoV-2 N antibodies and of the time elapsed from infection diagnosis. Notably, in patients with a confirmed date of SARS-CoV-2 infection, over a median of 80 days [IQR, 72-257] from the diagnosis, 49.3% of subjects resulted negative for anti-N IgG though 86% of them still had anti-SARS-CoV-2 spike IgG antibodies. Participants with anti-N IgG loss had an older SARS-CoV-2 infection compared with subjects with detectable N IgG. This finding confirms previous observation on SARS-CoV-2 antibody kinetic 21 that showed IgG titers to RBD, S1 and N antigens to start their decrease in patients after the first month from the onset of symptoms, particularly in asymptomatic infection or mild disease. We also confirmed anti-N-antibodies to have a shorter postinfection persistence than anti-S-antibodies 22 , thus making the N-specific antibodies detection to estimate SARS-CoV-2 seroprevalence of low utility.

Moreover, SARS-CoV-2 neutralizing antibody levels measured after one dose of vaccine in a subgroup of previously infected individuals were similar to those measured after the second dose in naive subjects, confirming a single dose of the vaccine to be likely sufficient for the induction of an effective response in previously infected individuals. [16] [17] [18] [19] [20] This approach might be helpful in widening the vaccine supply, particularly in countries with limited availability and is supported by the recent Italian national recommendations that indicate a one-dose shot in subjects who were diagnosed with SARS-CoV-2 infection between 3 and 6 months before vaccination. 23 We did not observe a different response in neutralizing antibody levels between males and females; however, and consistently with the findings by Abu Jabal, et al. 15 significantly lower antibody levels were observed with increasing age in SARS-CoV-2-naive subjects.

Although no serious adverse events have been reported in our vaccine recipients, in agreement with previous reports, a high number of mild to moderate side effects occurred, particularly after the second dose. 24, 25 In agreement with Krammer et al., 16 symptoms like muscle pain and fatigue were significantly more pronounced in individuals with past SARS-CoV-2 infection than in subjects SARS-CoV-2-naive.

Interestingly, we demonstrated a direct relationship between the onset of fever ≥38°C and high SARS-CoV-2 IgG antibody levels elicited by the vaccination. This finding confirms a strong vaccine reactogenicity to be strictly correlated with antibody response levels. 16 The main limitation of the study is represented by the lack of an available standardized serological test which makes challenging the comparison of our results with those of other studies and to interpret the clinical meaning of quantitative serology response to vaccination and its effectiveness in avoiding infection. Indeed, although anti-spike antibodies levels have been associated with neutralizing activity, 12,13,26 our study was not designed to determine their effects on protection from infection and its clinical consequences. Nevertheless, the incidence decrease of COVID-19 from pre-to post-vaccination has been well established, although positive tests in asymptomatic individuals have been observed following vaccination. [27] [28] [29] [30] However, reliable immune markers like antibody levels that correlate with protection from SARS-CoV-2 are still under investigation. Although several studies to date, including ours, showed that most of vaccinated people develop specific antibodies against SARS-CoV-2, it is not yet defined the range of antibody levels above which individuals are protected from severe COVID-19 and death, or even from infection and transmission. Recently, a threshold of IgG(S-RBD) levels at or above 4,160 AU/mL have been proposed as a surrogate measure of antibody neutralization on a plaque reduction neutralization test, 31 but no association with clinical outcomes have been provided. Moreover, humoral response to SARS-CoV-2 vaccination do not give any insight into other important aspects of immunity, including cellular immune response and further analyses are needed to reliably assess the effectiveness and duration of humoral and cellular immune response.

Other limitations of the study are: 1) despite the large number of participants, the study is limited to HCWs who volunteered to be tested and vaccinated, thus some selection bias might not be excluded, i.e. HCWs with a previous diagnosis of SARS-CoV-2 infection who willingly postpone vaccination; 2) as elderly individuals are under-represented in a working setting like the one described, although statistically significant, the lower antibody levels observed with increasing age may be underestimated and not representative of general population, as well as the lack of extreme ages and of information on co-morbidities.

Finally, we observed a relatively lower seroprevalence of anti-S-IgG antibodies at baseline in our cohort of HCWs, compared to other reports. 32 In a recent metanalysis 33 the overall seroprevalence of SARS-CoV-2 antibodies among HCWs reported by August 2020 was 8.7% with a wide range (from 0% to 45.3%). Our results confirmed the relatively low seroprevalence observed in HCWs at LSUH between March and May 2020 10 and is likely the result of a deep reorganization of our hospital that closed down its routine activities as soon as the number of COVID-19 cases raised in Milan, being a referral Hospital for Infectious Diseases with highly trained personnel to infection control measures.

In conclusion, the BNT162b2 mRNA COVID-19 vaccine induced a high rate of serological response in a large cohort of HCWs with antibody levels higher in HCWs with past COVID-19 diagnosis in whom the levels after the first dose was comparable to the complete vaccination in naive controls. This suggests that a single dose of mRNA vaccine might evoke effective protection in prior SARS CoV-2 infected subjects, although these results need to be confirmed on elderly and fragile population.

No potential conflict of interest was reported by the authors.

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

http://orcid.org/0000-0003-3039-3039 

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