The emergence of SARS-CoV-2 variants is jeopardizing the effectiveness of current vaccines and limiting the application of monoclonal antibody-based therapy for COVID-19 (refs. 1,2). Here we analysed the memory B cells of five naive and five convalescent people vaccinated with the BNT162b2 mRNA vaccine to investigate the nature of the B cell and antibody response at the single-cell level. Almost 6,000 cells were sorted, over 3,000 cells produced monoclonal antibodies against the spike protein and more than 400 cells neutralized the original SARS-CoV-2 virus first identified in Wuhan, China. The B.1.351 (Beta) and B.1.1.248 (Gamma) variants escaped almost 70% of these antibodies, while a much smaller portion was impacted by the B.1.1.7 (Alpha) and B.1.617.2 (Delta) variants. The overall loss of neutralization was always significantly higher in the antibodies from naive people. In part, this was due to the IGHV2-5;IGHJ4-1 germline, which was found only in people who were convalescent and generated potent and broadly neutralizing antibodies. Our data suggest that people who are seropositive following infection or primary vaccination will produce antibodies with increased potency and breadth and will be able to better control emerging SARS-CoV-2 variants.
Twenty months after the beginning of the COVID-19 pandemic, with 252 million people infected, 5 million deaths and 7.2 billion vaccine doses administered, the world is still struggling to control the virus. In most developed countries, vaccines have vastly reduced severe disease, hospitalization and deaths, but they have not been able to control the infections that are fuelled by new and more infectious variants. A large number of studies so far have shown that protection from infection is linked to the production of neutralizing antibodies against the spike (S) protein of the virus3,4,5,6. This is a metastable, trimeric class 1 fusion glycoprotein, composed of the S1 and S2 subunits, and mediates virus entry, changing from a prefusion to postfusion conformation after binding to the human angiotensin-converting enzyme 2 (ACE2) receptor and heparan sulfates on the host cells7. Potent neutralizing antibodies recognize the S1 subunit of each monomer, which includes the receptor-binding domain (RBD) and N-terminal domain (NTD) immunodominant sites8. The large majority of neutralizing antibodies bind to the receptor-binding motif, within the RBD, and a smaller fraction targets the NTD5,9. Neutralizing antibodies against the S2 subunit have been described; however, they have very low potency5,10. Neutralizing antibodies generated after infection derive in large part from germline IGHV3-53 and the closely related IGHV3-66 with very few somatic mutations11,12. From June 2020, the virus started to generate mutations that allowed the virus to evade neutralizing antibodies, to become more infectious, or both. Some of the mutant viruses completely replaced the original SARS-CoV-2 first detected in Wuhan, China. The most successful variant viruses are B.1.1.7 (Alpha), B.1.351 (Beta), B.1.1.248 (Gamma) and B.1.617.2 (Delta), which have been named variants of concern (VoCs)13. The Delta variant is currently spreading across the globe and causing large concerns also in fully vaccinated populations. It is therefore imperative to understand the molecular mechanisms of the immune response to vaccination to design better vaccines and vaccination policies. Several investigators have shown that vaccination of people who are convalescent can yield neutralizing antibodies that can be up to a thousand-fold higher than those induced by infection or vaccination, suggesting that one way of controlling the pandemic may be the induction of a hybrid immunity-like response using a third booster dose14,15,16,17,18. At the single-cell level, here we compared the nature of the neutralizing antibody response against the original virus first detected in Wuhan and the VoCs in naive and convalescent participants who were immunized with the BNT162b2 mRNA vaccine.
B cell response in COVID-19 vaccinees
We enrolled ten donors who were vaccinated with the BNT162b2 mRNA vaccine: five of them were healthy people who were naive to SARS-CoV-2 infection at vaccination (seronegative) and the other five had recovered from SARS-CoV-2 infection before vaccination (seropositive). Participant details are summarized in Extended Data Table 1. Blood collection occurred at an average of 48 and 21 days after the last vaccination dose for participants who were seronegative and seropositive, respectively (Extended Data Table 1). This difference may affect the frequency of circulating B cells and the serum activity of participants who are seronegative and seropositive analysed in this study. We initially analysed the frequency of circulating B cell populations between our groups. Participants who were seropositive showed a 2.46-fold increase in S-protein-specific CD19+CD27+IgD−IgM− memory B cells compared with participants who were seronegative and an overall 10% higher count of CD19+CD27+IgD−IgM− memory B cells (Extended Data Fig. 1a–c). Conversely, participants who were seronegative showed a 2.3-fold higher frequency of CD19+CD27+IgD−IgM+ memory B cells than participants who were seropositive. No differences were found in the numbers of CD19+CD27+IgD−IgM+ S protein+ memory B cells between the two groups assessed in this study (Extended Data Fig. 1a–c). Following the analyses of memory B cells, we characterized the polyclonal response of these donors by testing their binding response to the S protein trimer, RBD, NTD and the S2 domain, and subsequently by testing their neutralization activity against the original SARS-CoV-2 virus first detected in Wuhan (Extended Data Fig. 2). Plasma from participants who were seropositive showed a higher binding activity to the S protein and all tested domains than plasma from participants who were seronegative (Extended Data Fig. 2a–d). In addition, participants who were seropositive showed a tenfold-higher neutralization activity against the original SARS-CoV-2 virus detected in Wuhan than in participants who were seronegative (Extended Data Fig. 2e, f).
Isolation of neutralizing antibodies
To better characterize the B cell immune response, we single-cell-sorted antigen-specific memory B cells using the SARS-CoV-2 S protein antigen identified in Wuhan as bait, which was encoded by the mRNA vaccine. The single-cell sorting strategy was performed as previously described5. In brief, the prefusion S protein trimer-specific (S protein+), class-switched memory B cells (CD19+CD27+IgD−IgM−) were single-cell-sorted and then incubated for 2 weeks to naturally produce and release monoclonal antibodies (mAbs) into the supernatant. A total of 2,352 and 3,532 S protein+ memory B cells were sorted from vaccinees who were seronegative and seropositive, respectively (Extended Data Table 2). Of these, 944 (40.1%) and 2,299 (65.1%), respectively, were released in the supernatant mAbs, recognizing the S protein prefusion trimer in enzyme-linked immunosorbent assay (ELISA) (Fig. 1a, Extended Data Table 2). These mAbs were then tested in a cytopathic effect-based microneutralization assay (CPE-MN) with the original live SARS-CoV-2 virus detected in Wuhan at a single point dilution (1:5) to identify SARS-CoV-2 neutralizing human monoclonal antibodies (nAbs). This first screening identified a total of 411 nAbs, of which 71 derived from participants who were seronegative and 340 were from participants who were seropositive (Fig. 1b, Extended Data Table 2). Overall, the fraction of S-protein-specific B cells producing nAbs were 7.5% for participants who were seronegative and 14.8% for participants who were seropositive. Following this first screening, all nAbs that were able to neutralize the SARS-CoV-2 virus detected in Wuhan were tested by CPE-MN against major VoCs, including B.1.1.7 (Alpha), B.1.351 (Beta) and B.1.1.248 (Gamma) to understand the breadth of neutralization of nAbs elicited by the BNT162b2 mRNA vaccine. At the time of this assessment the B.1.617.2 (Delta) variant had not yet spread globally and therefore was not available for screening. Participants who were seropositive had an overall higher percentage of nAbs neutralizing the VoCs than participants who were seronegative. The average frequency of nAbs from participants who were seropositive neutralizing the Alpha, Beta and Gamma variants was 80.6% (n = 274), 39.4% (n = 134) and 62.0% (n = 211), respectively, compared with 70.4% (n = 50), 22.5% (n = 16) and 43.6% (n = 31), respectively, in participants who were seronegative (Fig. 1c, Extended Data Table 2).
Potency and breadth against variants
To better characterize and understand the potency and breadth of coverage of all nAbs against the SARS-CoV-2 virus detected in Wuhan, we aimed to express all the 411 nAbs previously identified as IgG1. We were able to recover and express 276 antibodies for further characterization, 224 (89.8%) from participants who were seropositive and 52 (10.2%) from participants who were seronegative. Initially, antibodies were tested for binding against the RBD, NTD and the S2 domain of the original SARS-CoV-2 Sprotein identified in Wuhan. Overall, no major differences were observed in nAbs that recognized the RBD and NTD, whereas nAbs that were able to bind to the S protein only in its trimeric conformation (that is, not able to bind single domains) were almost threefold higher in participants who were seronegative than in participants who were seropositive (Extended Data Fig. 3). None of the tested nAbs targeted the S2 domain. nAbs were then tested by CPE-MN in serial dilution to evaluate their 100% inhibitory concentration (IC100) against the SARS-CoV-2 virus detected in Wuhan and the VoCs. At this stage of the study, the B.1.617.2 (Delta) virus had spread globally, and we were able to obtain the live virus for our experiments. Overall, nAbs isolated from vaccinees who were seropositive had a significantly higher potency than those isolated from vaccinees who were seronegative. The IC100 geometric mean in participants who were seropositive was 2.87-fold, 2.17-fold, 1.17-fold, 1.43-fold and 1.92-fold lower than in participants who were seronegative for the virus detected in Wuhan, and the Alpha, Beta, Gamma and Delta VoCs, respectively (Fig. 2). In addition, a bigger fraction of nAbs from participants who were seropositive retained the ability to neutralize the VoCs. Indeed, when nAbs were individually tested against all VoCs, the ability to neutralize the Alpha, Beta, Gamma and Delta variants was lost by 14%, 61%, 61% and 29% of the antibodies from participants who were seropositive versus 32%, 78%, 75% and 46% of those from participants who were seronegative, respectively (Fig. 2). Finally, a major difference between participants who were seronegative and seropositive was found in the class of nAbs with medium/high potency (IC100 of 11–100 ng ml−1 and 101–1,000 ng ml−1) against all variants. Indeed, nAbs in these ranges from participants who were seropositive constitute 71.0%, 62.5%, 23.7%, 22.8% and 53.1% of the whole nAb repertoire, whereas nAbs from seronegative donors were 48.1%, 38.5%, 17.3%, 17.3% and 34.6% against the SARS-CoV-2 virus detected in Wuhan and the Alpha, Beta, Gamma and Delta VoCs respectively (Fig. 2).
Functional gene repertoire
The analysis of the immunoglobulin G heavy chain variable (IGHV) and joining (IGHJ) gene rearrangements of 58 and 278 sequences recovered from participants who were seronegative and seropositive, respectively, showed that they use a broad range of germlines and share the most abundant germlines. In particular, both groups predominantly used the IGHV1-69;IGHJ4-1 and IGHV3-53;IGHJ6-1 germlines, which were shared by three out five participants per group (Fig. 3a). In addition, the IGHV3-30;IGHJ6-1 and IGHV3-33;IGHJ4-1 germlines, which were more abundant in donors who were seronegative, and the IGHV1-2;IGHJ6-1 germline, which was mainly expanded in vacinees who were seropositive, were also used with high frequency in both groups. Only the IGHV2-5;IGHJ4-1 germline was seen to be predominantly expanded only in donors who were seropositive (Fig. 3a). Despite the fact that selected germlines were boosted following vaccination, no major clonal families were identified, and the biggest family observed contained only four antibodies. To better characterize these predominant gene families, we evaluated their neutralization potency and breadth against SARS-CoV-2 and VoCs. In this analysis, we could not evaluate IGHV3-33;IGHJ4-1 nAbs, as only three of these antibodies were expressed, but we included the IGHV3-53 closely related family IGHV3-66;IGHJ4-1, as this family was previously described to be mainly involved in the neutralization of the SARS-CoV-2 virus11,19. A large part of nAbs deriving from these predominant germlines had a very broad range of neutralization potency against the original SARS-CoV-2 virus detected in Wuhan, with the IC100 spanning from less than 10 to over 10,000 ng ml−1 (Fig. 3b–g). However, many of them lost the ability to neutralize SARS-CoV-2 VoCs. The loss of neutralizing activity occurred for most germlines and it was moderate against the Alpha and Delta variants, whereas the loss was marked against the Beta and Gamma variants (Fig. 3b–g). A notable exception was the IGHV2-5;IGHJ4-1 germline, which was present only in nAbs of participants who were seropositive, that showed potent antibodies able to equally neutralize all SARS-CoV-2 VoCs (Fig. 3d). Finally, we evaluated the CDRH3 length and V-gene somatic hypermutation levels for all nAbs retrieved from participants who were seronegative and seropositive and for predominant germlines. Overall, the two groups show a similar average CDRH3 length (15.0 amino acids and 15.1 amino acids for participants who were seronegative and seropositive, respectively); however, participants who were seropositive showed almost twofold-higher V-gene mutation levels than participants who were seronegative (Extended Data Fig. 4). As for predominant gene-derived nAbs, we observed heterogenous CDRH3 length, with the only exception of IGHV3-53;IGHJ6-1 nAbs, and higher V-gene mutation levels in predominant germlines from participants who were seropositive than in germlines from participants who were seronegative (Extended Data Fig. 5).
S protein epitope mapping
To map the regions of the S protein recognized by the identified nAbs, we used a competition assay with four known antibodies: J08, which targets the top loop of the receptor-binding motif5; S309, which binds to the RBD but outside of the RMB region20; 4A8, which recognizes the NTD21; and L19, which binds to the S2 domain5 (Extended Data Fig. 6). The nAbs identified in this study were pre-incubated with the original SARS-CoV-2 S protein detected in Wuhan, and subsequently the four nAbs labelled with different fluorophores were added as a single mix. For one of the four fluorescently labelled nAbs, 50% signal reduction was used as a threshold for positive competition. The vast majority of nAbs from both seronegative (50.0%; n = 26) and seropositive (51.3%; n = 115) vaccinees competed with J08 (Extended Data Fig. 7a, Extended Data Table 3). For vaccinees who were seronegative, the second most abundant population was composed of nAbs that did not compete with any of the four fluorescently labelled nAbs (25.0%; n = 13), followed by nAbs targeting the NTD (17.3%; n = 9). As for vaccinees who were seropositive, the second most abundant population was composed of nAbs that competed with S309 (21.4%; n = 48), followed by nAbs that competed with 4A8 (15.6%; n = 35) and not-competing nAbs (11.6%; n = 26). None of our nAbs competed with the S2-targeting antibody L19 (Extended Data Fig. 7a, Extended Data Table 3). nAbs that competed with J08, which are likely to bind to the receptor-binding motif, derived from several germlines, including the predominant IGHV3-53;IGHJ6-1 (10.6%; n = 14), IGHV1-69;IGHJ4-1 (8.3%; n = 11) and IGHV1-2;IGHJ6-1 (6.8%; n = 9) germlines (Extended Data Fig. 7b). By contrast, those that competed with S309 derived mostly from the IGHV2-5;IGHJ4-1 germline (13.7%; n = 7), which were isolated exclusively from vaccinees who were seropositive (Extended Data Fig. 7c). As for NTD-directed nAbs, the non-predominant gene family IGHV1-24;IGHJ6-1 was the most abundant, confirming what was reported in previous studies22 (Extended Data Fig. 7d). Finally, for nAbs that did not compete with any of the known antibodies used in our competition assay, the non-predominant gene families IGHV1-69;IGHJ3-1 (9.7%; n = 3) and IGHV1-69;IGHJ6-1 (9.7%; n = 3) were the most abundant (Extended Data Fig. 7e).
Our study analysed the repertoire of B cells producing neutralizing antibodies following vaccination of naive and previously infected people at the single-cell level. The most important conclusion from this work is that people who are previously exposed to SARS-CoV-2 infection respond to vaccination with more B-cell-producing antibodies that are not susceptible to escape variants and that have higher neutralization potency. This can be explained in part by the increased number of somatic mutations and by the fact that participants who are seropositive expand potent antibodies derived from the IGHV2-5;IGHJ4-1 germline, which were not described in naive vaccinees18. One limitation of our study is that we did not include people who received a third booster dose of vaccine. Despite this limitation, we believe that our conclusions are likely to be extendable to people who are seronegative, as a third vaccine dose could lead to a hybrid immunity-like response as neutralizing antibodies following infection and vaccination derive mostly from the same immunodominant germlines11,12,17,18,19. Our analysis suggests that a booster dose of vaccine will increase the frequency of memory B cells producing potent neutralizing antibodies that are not susceptible to escape variants and will allow better control of this pandemic. The massive variant escape from predominant germlines, such as IGHV3-53, IGHV3-66, IGHV3-30 and IGHV1-69, and the presence of antibodies deriving from the IGHV2-5 germline that are resistant to variants, suggest that the design of vaccines that preferentially promote or avoid the expansion of selected germlines can generate broad protection against SARS-CoV-2 variants. Germline-targeting vaccination, which has been pioneered in the HIV field23,24, may be a promising strategy to fight the COVID-19 pandemic.
Enrolment of COVID-19 vaccinees and human sample collection
This work results from a collaboration with the Azienda Ospedaliera Universitaria Senese, Siena (IT) that provided samples from donors vaccinated against COVID-19, of both sexes, who gave their written consent. The study was approved by the Comitato Etico di Area Vasta Sud Est (CEAVSE) ethics committees (Parere 17065 in Siena) and conducted according to good clinical practice in accordance with the declaration of Helsinki (European Council 2001, US Code of Federal Regulations, ICH 1997). This study was unblinded and not randomized. No statistical methods were used to predetermine sample size.
Single-cell sorting of SARS-CoV-2 S protein+ memory B cells from COVID-19 vaccinees
Peripheral blood mononuclear cells (PBMCs) and the single-cell sorting strategy were performed as previously described5. In brief, PBMCs were isolated from heparin-treated whole blood by density gradient centrifugation (Ficoll-Paque PREMIUM, Sigma-Aldrich). After separation, PBMCs were stained with Live/Dead Fixable Aqua (Invitrogen; Thermo Scientific) diluted 1:500 at room temperature. After 20 min of incubation, cells were washed with PBS and unspecific bindings were saturated with 20% normal rabbit serum (Life Technologies). Following 20 min of incubation at 4 °C, cells were washed with PBS and stained with SARS-CoV-2 S protein labelled with Strep-Tactin XT DY-488 (2-1562-050, iba-lifesciences) for 30 min at 4 °C. After incubation, the following staining mix was used CD19 V421 (1:320; 562440, BD), IgM PerCP-Cy5.5 (1:50; 561285, BD), CD27 PE (1:30; 340425, BD), IgD-A700 (1:15; 561302, BD), CD3 PE-Cy7 (1:100; 300420, BioLegend), CD14 PE-Cy7 (1:320; 301814, BioLegend), CD56 PE-Cy7 (1:80; 318318, BioLegend) and cells were incubated at 4 °C for an additional 30 min. Stained memory B cells were single-cell-sorted with a BD FACS Aria III (BD Biosciences) into 384-well plates containing 3T3-CD40L feeder cells and were incubated with IL-2 and IL-21 for 14 days as previously described25.
ELISA assay with SARS-CoV-2 S protein prefusion trimer
mAbs and plasma binding specificity against the S protein trimer was detected by ELISA as previously described5. In brief, 384-well plates (microplate clear, Greiner Bio-one) were coated with 3 µg/ml of streptavidin (Thermo Fisher) diluted in carbonate-bicarbonate buffer (E107, Bethyl Laboratories) and incubated at room temperature overnight. The next day, plates were incubated for 1 h at room temperature with 3 µg/ml of SARS-CoV-2 S protein diluted in PBS. Plates were then saturated with 50 µl per well of blocking buffer (phosphate-buffered saline and 1% BSA) for 1 h at 37 °C. After blocking, 25 µl per well of mAbs diluted 1:5 in sample buffer (phosphate-buffered saline, 1% BSA and 0.05% Tween-20) was added to the plates and was incubated at 37 °C. Plasma samples derived from vaccinees were tested (starting dilution of 1:10; step dilution of 1:2 in sample buffer) in a final volume of 25 µl per well and were incubated at 37 °C. After 1 h of incubation, 25 µl per well of alkaline phosphatase-conjugated goat anti-human IgG and IgA (Southern Biotech) diluted 1:2,000 in sample buffer was added. Finally, S protein binding was detected using 25 µl per well of PNPP (p-nitrophenyl phosphate; Thermo Fisher) and the reaction was measured at a wavelength of 405 nm by the Varioskan Lux Reader (Thermo Fisher Scientific). After each incubation step, plates were washed three times with 100 µl per well of washing buffer (phosphate-buffered saline and 0.05% Tween-20). Sample buffer was used as a blank and the threshold for sample positivity was set at twofold the optical density (OD) of the blank. Technical duplicates were performed for mAbs and technical triplicates were performed for sera samples.
ELISA assay with RBD, NTD and S2 subunits
Identification of mAbs and plasma screening of vaccinees against RBD, NTD or S2 SARS-CoV-2 protein were performed by ELISA. In brief, 3 µg/ml of RBD, NTD or S2 SARS-CoV-2 protein diluted in carbonate-bicarbonate buffer (E107, Bethyl Laboratories) was coated in 384-well plates (microplate clear, Greiner Bio-one). After overnight incubation at 4 °C, plates were washed three times with washing buffer (phosphate-buffered saline and 0.05% Tween-20) and blocked with 50 µl per well of blocking buffer (phosphate-buffered saline and 1% BSA) for 1 h at 37 °C. After washing, plates were incubated 1 h at 37 °C with mAbs diluted 1:5 in sample buffer (phosphate-buffered saline, 1% BSA and 0.05% Tween-20) or with plasma at a starting dilution of 1:10 and step diluted of 1:2 in sample buffer. Wells with no sample added were consider blank controls. Anti-human IgG–peroxidase antibody (Fab specific) produced in goat (Sigma) diluted 1:45,000 in sample buffer was then added and samples were incubated for 1 h at 37 °C. Plates were then washed, incubated with TMB substrate (Sigma) for 15 min before adding the stop solution (H2SO4 0.2 M). The OD values were identified using the Varioskan Lux Reader (Thermo Fisher Scientific) at 450 nm. Each condition was tested in triplicate and samples tested were considered positive if the OD value was twofold the blank.
Flow cytometry-based competition assay
To classify mAb candidates on the basis of their interaction with S epitopes, we performed a flow cytometry-based competition assay.In detail, magnetic beads (Dynabeads His-Tag, Invitrogen) were coated with histidine-tagged S protein according to the manufacturer’s instructions. Then, 20 µg/ml of coated S protein beads were pre-incubated with unlabelled nAb candidates diluted 1:2 in PBS for 40 min at room temperature. After incubation, the mix beads–antibodies was washed with 100 µl of 1% PBS-BSA. Then, to analyse epitope competition, mAbs that are able to bind to the RBD (J08 and S309), NTD (4A8) or S2 domain (L19) of the S protein were labelled with four different fluorophores (Alexa Fluor 647, 488, 594 and 405) using the Alexa Fluor NHS Ester kit (Thermo Scientific), were mixed and incubated with S protein beads. Following 40 min of incubation at room temperature, the mix beads–antibodies was washed with PBS, resuspended in 150 µl of 1% PBS-BSA and analysed using the BD LSR II flow cytometer (Becton Dickinson). Beads with or without S protein incubated with labelled antibodies mix were used as positive and negative controls, respectively. FACSDiva Software (version 9) was used for data acquisition and analysis was performed using FlowJo (version 10).
SARS-CoV-2 authentic viruses neutralization assay
All SARS-CoV-2 authentic virus neutralization assays were performed in the biosafety level 3 (BSL3) laboratories at Toscana Life Sciences in Siena (Italy) and Vismederi Srl, Siena (Italy). BSL3 laboratories are approved by a certified biosafety professional and are inspected every year by local authorities. To evaluate the neutralization activity of identified nAbs against SARS-CoV-2 and all VoCs and to evaluate the breadth of neutralization of this antibody, CPE-MN was performed5. In brief, for the CPE-based neutralization assay, we co-incubated J08 with a SARS-CoV-2 viral solution containing 100 median tissue culture infectious dose (100 TCID50) of virus, and after 1 h of incubation at 37 °C, 5% CO2. The mixture was then added to the wells of a 96-well plate containing a sub-confluent Vero E6 cell monolayer. Plates were incubated for 3–4 days at 37 °C in a humidified environment with 5% CO2, then examined for CPE by means of an inverted optical microscope by two independent operators. All nAbs were tested at a starting dilution of 1:5 and the IC100 was evaluated based on their initial concentration, while plasma samples were tested starting at a 1:10 dilution. Both nAbs and plasma samples were then step diluted 1:2. Technical duplicates were performed for both nAbs and plasma samples. In each plate, positive and negative controls were used as previously described5.
SARS-CoV-2 virus variants CPE-MN neutralization assay
The SARS-CoV-2 viruses used to perform the CPE-MN neutralization assay were the original SARS-CoV-2 virus first detected in Wuhan (SARS-CoV-2/INMI1-Isolate/2020/Italy: MT066156), SARS-CoV-2 B.1.1.7 (INMI GISAID accession number: EPI_ISL_736997), SARS-CoV-2 B.1.351 (EVAg Cod: 014V-04058), B.1.1.248 (EVAg CoD: 014V-04089) and B.1.617.2 (GISAID ID: EPI_ISL_2029113)26.
Single-cell RT–PCR and Ig gene amplification and transcriptionally active PCR expression
The whole process for nAbs heavy and light chain recovery, amplification and transcriptionally active PCR (TAP) expression was performed as previously described5. In brief, 5 µl of cell lysate was mixed with 1 µl of random hexamer primers (50 ng/µl), 1 µl of dNTP-Mix (10 mM), 2 µl of 0.1 M DTT, 40 U/µl of RNAse OUT, MgCl2 (25 mM), 5× FS buffer and Superscript IV reverse transcriptase (Invitrogen) to perform RT–PCR. Reverse transcription (RT) reaction was performed at 42 °C for 10 min, 25 °C for 10 min, 50 °C for 60 min and 94 °C for 5 min. Two rounds of PCR were performed to obtain the heavy (VH) and light (VL) chain amplicons. All PCRs were performed in a nuclease-free water (DEPC) in a total volume of 25 µl per well. For PCR I, 4 µl of cDNA were mixed with 10 µM of VH and 10 µM of VL primer-mix, 10 mM of dNTP mix, 0.125 µl of Kapa Long Range Polymerase (Sigma), 1.5 µl of MgCl2 and 5 µl of 5× Kapa Long Range Buffer. The PCR I reaction was performed at 95 °C for 3 min, 5 cycles at 95 °C for 30 s, 57 °C for 30 s, 72 °C for 30 s and 30 cycles at 95 °C for 30 s, 60 °C for 30 s, 72 °C for 30 s and a final extension of 72 °C for 2 min. Nested PCR II was performed as above starting from 3.5 μl of unpurified PCR I product. PCR II products were purified by the Millipore MultiScreen PCRμ96 plate according to manufacturer’s instructions and eluted in 30 μl of nuclease-free water (DEPC). As for TAP expression, vectors were initially digested using restriction enzymes AgeI, SalI and Xho as previously described and PCR II products ligated by using the Gibson Assembly NEB into 25 ng of respective human Igγ1, Igκ and Igλ expression vectors27,28. TAP reaction was performed using 5 μl of Q5 polymerase (NEB), 5 μl of GC Enhancer (NEB), 5 μl of 5X buffer, 10 mM of dNTPs, 0.125 µl of forward/reverse primers and 3 μl of ligation product, using the following cycles: 98 °C for 2 min, 35 cycles 98 °C for 10 s, 61 °C for 20 s, 72 °C for 1 min and 72 °C for 5 min. TAP products were purified under the same PCR II conditions, quantified by the Qubit Fluorometric Quantitation assay (Invitrogen) and used for transient transfection in the Expi293F cell line following the manufacturer’s instructions.
Functional repertoire analyses
The VH and VL sequence reads of nAbs were manually curated and retrieved using CLC sequence viewer (Qiagen). Aberrant sequences were removed from the dataset. Analysed reads were saved in FASTA format and the repertoire analyses were performed using Cloanalyst (http://www.bu.edu/computationalimmunology/research/software/)29,30.
Statistical analysis was assessed with GraphPad Prism Version 8.0.2 (GraphPad Software). Non-parametric Mann–Whitney t-test was used to evaluate statistical significance between the two groups analysed in this study. Statistical significance was shown as *P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001.
Further information on research design is available in the Nature Research Reporting Summary linked to this paper.
Source data are provided with this paper. All data supporting the findings in this study are available within the article or can be obtained from the corresponding author on request. Source data are provided with this paper.
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This work was funded by the European Research Council (ERC) advanced grant agreement number 787552 (vAMRes). This publication was supported by funds from the ‘Centro Regionale Medicina di Precisione’ and by all of the people who answered the call to fight with us in the battle against SARS-CoV-2 with their kind donations on the platform ForFunding (https://www.forfunding.intesasanpaolo.com/DonationPlatform-ISP/nav/progetto/id/3380). This work was funded by COOP ITALIA Soc. Coop. This publication was supported by the European Virus Archive goes Global (EVAg) project, which has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement number 653316. This publication was supported by the COVID-2020-12371817 project, which has received funding from the Italian Ministry of Health. We also acknowledge J. McLellan, for kindly providing the S protein trimer, RBD, NTD and S2 constructs; O. Schwartz, for providing the B.1.617.2 (Delta) SARS-CoV-2 variant; the nursing staff of the operative unit of the department of Medical Sciences, Infectious and Tropical Diseases Unit, Siena University Hospital, Siena, Italy; and all of the donors who are vaccinated against COVID-19 for participating to this study.
R.R. is an employee of the GSK group of companies. E.A., I.P., N.M., P.P., E.P., C.D.S., C.S. and R.R. are listed as inventors of full-length human mAbs described in Italian patent applications no. 102020000015754 filed on 30 June 2020, 102020000018955 filed on 3 August 2020 and 102020000029969 filed on 4 December 2020, and the international patent system number PCT/IB2021/055755 filed on 28 June 2021. All patents were submitted by Fondazione Toscana Life Sciences, Siena, Italy. The remaining authors declare no competing interests.
Peer review information Nature thanks the anonymous reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Extended data figures and tables
a, b, The gating strategy shows from left to right: CD19+ B cells; CD19+CD27+IgD-; CD19+CD27+IgD-IgM-/IgM+; CD19+CD27+IgD-IgM-Sprotein+; CD19+CD27+IgD-IgM+Sprotein+ for a healthy donor (used as negative control for S protein staining) and a vaccinated subject. c, The graph shows the frequency of CD19+CD27+IgD-IgM- and IgM+ in seronegative (n=5) and seropositive donors (n=5). d, The graph shows the frequency of CD19+CD27+IgD-IgM- and IgM+ able to bind the SARS-CoV-2 S protein trimer (S protein+) in seronegative (n=5) and seropositive (n=5) donors. Geometric mean and standard deviation are denoted on the graphs. A nonparametric Mann–Whitney t test was used to evaluate statistical significances between groups. Two-tailed p-value significances are shown as *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001. e, The table summarizes the frequencies of the cell population above described for all subjects enrolled in our study.
a–d, Graphs show the ability of plasma samples from seronegative and seropositive vaccinees to bind the S protein trimer, RBD, NTD and S2 domain. Mean and standard deviation are denoted on each graph. Technical triplicates were performed for each experiment. e, The graph shows the neutralizing activity of plasma samples against the original Wuhan SARS-CoV-2 virus. Technical duplicates were performed for each experiment. f, The table summarizes the 100% inhibitory dilution (ID100) of each COVID-19 vaccinee and the geometric mean for seronegative and seropositive donors.
The graph shows the percentage of antibodies that bind specifically the RBD (light orange) or the NTD (cyan) or that did not bind single domains but recognized exclusively the S protein in its trimetric conformation (gray). The number (n) of tested nAbs per donor is reported on top of each bar. Technical duplicates were performed for each experiment.
Extended Data Fig. 4 Heavy chain CDR3 length and somatic hypermutation levels in seronegative and seropositive vaccinees.
a, The graph shows the heavy chain CDR3 length represented in amino acids (aa). b, The graph shows the overall somatic hypermutation level of nAbs isolated from seronegative and seropositive vaccinees. Geometric mean and standard deviation are denoted on the graphs. A nonparametric Mann–Whitney t test was used to evaluate statistical significances between groups. Two-tailed p-value significances are shown as *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.
Extended Data Fig. 5 Heavy chain CDR3 length and somatic hypermutation levels of predominant gene derived nAbs.
a–f, Graphs show the amino acidic heavy chain CDR3 length (left panel) and the somatic hypermutation level (right panel) of nAbs derived from the IGHV1-2;IGHJ6-1 (n = 13), IGHV1-69;IGHJ4-1 (n = 33), IGHV2-5;IGHJ4-1 (n = 7), IGHV3-30;IGHJ6-1 (n = 10), IGHV3-53;IGHJ6-1 (n = 15) and IGHV3-66;IGHJ4-1 (n = 9) gene families. Geometric mean and standard deviation are denoted on the graphs. A nonparametric Mann–Whitney t test was used to evaluate statistical significances between groups. Two-tailed p-value significances are shown as *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.
a, Schematic representation of the epitopes recognized by J08 (dark red), S309 (orange), 4A8 (dark blue) and L19 (gold), mAbs on the S protein surface. b–e, Representative cytometer peaks per each of the four mAbs used for the competition assay. Positive (beads conjugated with only primary labeled antibody) and negative (un-conjugated beads) controls are shown as green and gray peaks, respectively.
a, The bar graph shows the percentage (%) of nAbs competing with J08 (dark red), S309 (orange), 4A8 (dark blue) and L19 (gold), or antibodies that did not compete with any of the previous mAbs (gray). A schematic representation of J08, S309, 4A8 and L19 epitopes on the S protein surface is shown on the left side of the panel. b–e, Graphs show the IGHV-J rearrangement percentage for nAbs that competed against J08, S309, 4A8, or that did not compete with any of these mAbs. The total number (n) of competing nAbs per group is shown on top of each graph.
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Andreano, E., Paciello, I., Piccini, G. et al. Hybrid immunity improves B cells and antibodies against SARS-CoV-2 variants. Nature 600, 530–535 (2021). https://doi.org/10.1038/s41586-021-04117-7
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