key: cord-0865327-38l773zn
authors: Huang, Kuan-Ying A.; Tan, Tiong Kit; Chen, Ting-Hua; Huang, Chung-Guei; Harvey, Ruth; Hussain, Saira; Chen, Cheng-Pin; Harding, Adam; Gilbert-Jaramillo, Javier; Liu, Xu; Knight, Michael; Schimanski, Lisa; Shih, Shin-Ru; Lin, Yi-Chun; Cheng, Chien-Yu; Cheng, Shu-Hsing; Huang, Yhu-Chering; Lin, Tzou-Yien; Jan, Jia-Tsrong; Ma, Che; James, William; Daniels, Rodney S.; McCauley, John W.; Rijal, Pramila; Townsend, Alain R.
title: Breadth and function of antibody response to acute SARS-CoV-2 infection in humans
date: 2021-02-26
journal: PLoS Pathog
DOI: 10.1371/journal.ppat.1009352
sha: 81cc4d963b2f004b42a94a9cbb7cc035cd00323a
doc_id: 865327
cord_uid: 38l773zn

Serological and plasmablast responses and plasmablast-derived IgG monoclonal antibodies (MAbs) have been analysed in three COVID-19 patients with different clinical severities. Potent humoral responses were detected within 3 weeks of onset of illness in all patients and the serological titre was elicited soon after or concomitantly with peripheral plasmablast response. An average of 13.7% and 3.5% of plasmablast-derived MAbs were reactive with virus spike glycoprotein or nucleocapsid, respectively. A subset of anti-spike (10 of 32) antibodies cross-reacted with other betacoronaviruses tested and harboured extensive somatic mutations, indicative of an expansion of memory B cells upon SARS-CoV-2 infection. Fourteen of 32 anti-spike MAbs, including five anti-receptor-binding domain (RBD), three anti-non-RBD S1 and six anti-S2, neutralised wild-type SARS-CoV-2 in independent assays. Anti-RBD MAbs were further grouped into four cross-inhibiting clusters, of which six antibodies from three separate clusters blocked the binding of RBD to ACE2 and five were neutralising. All ACE2-blocking anti-RBD antibodies were isolated from two recovered patients with prolonged fever, which is compatible with substantial ACE2-blocking response in their sera. Finally, the identification of non-competing pairs of neutralising antibodies would offer potential templates for the development of prophylactic and therapeutic agents against SARS-CoV-2.

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In late 2019, a novel coronavirus emerged and was identified as the cause of a cluster of respiratory infection cases in Wuhan, China. It spread quickly around the world. In March of 2020 a pandemic was declared by the World Health Organization, the virus was formally named as Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and the resulting disease was named COVID-19. As of 1 April 2021, there have been over 128 million confirmed cases of SARS-CoV-2 infection with over two million deaths (World Health Organization, https:// covid19.who.int/).

There is no fully effective drug for COVID-19. Antibodies neutralise SARS-CoV-2 in vitro, consistent with the induction of neutralising antibodies and protection from disease seen after vaccination [1, 2] , and antibodies may be an effective treatment for COVID-19 in clinical practice. Convalescent plasma is being tested in clinical trials as a therapy for COVID-19 [3, 4] , and may be effective if given early after infection [5] . It was previously used in the treatment of SARS [6] . The virus spike, a trimeric glycoprotein on the viral surface, is a target of neutralising antibodies, and plays a central role in receptor binding and membrane fusion. The spike is composed of two functional subunits; the S1 subunit contains the receptor-binding domain (RBD) that is required for binding to host cell ACE2 receptor and the N-terminal domain (NTD) and the S2 subunit mediates the fusion of the viral and host cell membranes [7] .

B cell responses in COVID-19 patients have been detected concomitantly with follicular helper T cell responses from week one after illness onset [8] . In SARS patients, B cell responses typically arise first against the nucleocapsid protein then, within four to eight days after symptom onset, antibody responses to spike glycoprotein have been found; neutralising antibody responses begin to develop by week two, and most symptomatic patients develop neutralising antibodies by week three [9] . Two serological studies of COVID-19 patients showed anti-SARS-CoV-2 IgG seroconversion at week three after onset and some cross-reactivity to nucleocapsid of SARS [10, 11] .

Antibodies may play a role in protection against SARS-CoV-2 infection. The underlying Bcell response leading to the rapid production of plasmablasts (antibody-secreting cells) that secrete antibodies upon natural SARS-CoV-2 exposure/infection is only beginning to be understood [8] . Here, we characterised the infection-induced serological and plasmablast responses and the derived IgG anti-SARS-CoV-2 spike glycoprotein and nucleocapsid monoclonal antibodies (MAbs) from adult patients with laboratory-confirmed COVID-19. The antigenic specificity and breadth of antibodies and the sequence of their variable domains have been characterised in detail. Virus neutralising antibodies were detected that bound epitopes on receptor-binding domain, non-RBD regions of the S1 polypeptide, and the S2 polypeptide of the spike glycoprotein.

Serum IgG antibodies to the virus spike glycoprotein and the isolated RBD were analysed by indirect enzyme-linked immunosorbent and flow cytometry assays in three patients with laboratory-confirmed COVID-19. The clinical characteristics of the three patients studied are shown in S1 Table. Antibodies to spike glycoprotein and RBD were detected in all three patients after week 3 of illness onset ( Fig 1A) . Case A showed a robust response to spike glycoprotein and the isolated RBD by day (D) 22 (D22). Longitudinal sera from case B and C showed lower anti-spike glycoprotein and RBD IgG titres at week 1 or the beginning of week 2 and an elevated titre that peaked at the end of week 2 through week 3 (a peak 50% effective dilution (ED 50 ) titre to RBD 1:1,051 at D18 in case B and 1:588 at D14 in case C). Case B had prolonged fever and developed pneumonia at the end of week 2, which was followed by a robust increase of anti-spike glycoprotein and RBD IgG titres at week 3 ( Fig 1A, S1 Table) . By contrast, case C experienced a two-day course of febrile illness and reduction of all symptoms within the first week, followed by anti-spike glycoprotein and RBD IgG titres that peaked earlier at the end of week 2 ( Fig 1A, S1 Table) .

An increased frequency of circulating plasmablasts was detected in all three patients (healthy adults baseline less than 1%) [8] (Fig 1B) . In case A, a plasmablast response containing a substantial IgG subset was detected at the end of week 2 (D14), followed by a high serological titre at week 3 (D22). Case B had a robust plasmablast response at the end of week 2 (D14) but the IgG plasmablast subset continued to rise, dominated at week 3 (D18), but then subsided at the beginning of week 4 (D22), which is compatible with high anti-spike glycoprotein and RBD IgG serological titres at week 3. Case C produced a significant early plasmablast response at the end of week 1 (D6), the IgG plasmablast subset dominated at the same time, and both the plasmablast response and its IgG subsets subsided at the end of week 2 (D14).

Circulating plasmablasts were identified and used to generate human IgG monoclonal antibodies (MAbs) from the three patients (Fig 2A) . A total of 219 plasmablast-derived IgG MAbs were produced, of which 40 (5 of 50 from case A, 27 of 131 from case B, 8 of 38 from case C) were shown to bind spike glycoprotein or nucleocapsid antigens of SARS-CoV-2 by one or more of the following: staining of spike glycoprotein, RBD and NTD-expressing cells, ELISA, or immunofluorescence and specific virus neutralisation ( Table 1) . Averages of 13.7±6.8% (6.0-18.4%) and 3.5±0.8% (2.6-4.0%) of plasmablast-derived IgG MAbs were reactive with virus spike glycoprotein and nucleocapsid, respectively.

MAbs bound to virus antigens as assessed by immunofluorescence of SARS-CoV-2-infected Vero E6 cells (S1 Fig, Table 1 ), suggesting that the majority of anti-spike glycoprotein human antibodies recognise complex conformational epitopes on the virus glycoprotein.

Moderate binding was observed for a subset (4 of 9) of anti-S2 MAbs with full-length spike glycoprotein ectodomain in the indirect ELISA but bound strongly to the isolated S2 subunit ( Fig 2B) . All anti-S2 MAbs bound to the MDCK-SIAT1 cells transduced to express the prefusion-stabilized spike antigen (S2 Fig) .

Ten of 32 anti-SARS-CoV-2 spike glycoprotein MAbs cross-reacted with the glycoproteins of other betacoronaviruses, including SARS, Middle East Respiratory Syndrome coronavirus (MERS) or human common cold coronavirus OC43 in ELISA (Table 1) , suggesting the presence of conserved epitopes on the spike glycoproteins of betacoronaviruses [12] [13] [14] .

Each of 32 anti-spike glycoprotein MAbs was encoded by a unique set of heavy chain VDJ and light chain VJ rearrangements in the variable domain (S2 Table) . Fourteen of 32 SARS--CoV-2 spike-reactive MAb genes possessed low numbers of somatic mutations resulting in 0 or 1 amino acid substitutions suggesting a de novo B cell response to the SARS-CoV-2 virus in humans. Six of the 32 MAb genes possessed � 20 nucleotide mutations, and these crossreacted on other beta-coronaviruses, including OC43. Of the nine anti-S2 antibodies five cross-reacted on OC43 virus and three of these also cross-reacted on MERS (Table 1 ). All five cross-reactive anti-S2 antibodies had high rates of somatic mutation (25±5), indicating a memory phenotype.

The CDR3 length varied among anti-spike glycoprotein antibodies (S2 Table) . No significant differences were found between anti-S2 and anti-S1 or anti-RBD subsets. Among anti-S2 MAbs, a significantly longer heavy chain CDR3 length was found in the cross-reactive group compared to the specific group (Cross-reactive 20±2 versus Specific 12±4, p = 0.02, two-tailed Mann-Whitney test; Fig 2C) , indicating that a long CDR3 may play a role in antigen binding, which is also found in several broadly reactive human MAbs against human immunodeficiency virus and influenza virus [15, 16] .

The relationship of the binding activity to CDR3 length of anti-RBD MAbs was further characterised in detail. Using MDCK-SIAT1 cells transduced to express the RBD at the cell surface (by linkage to a transmembrane domain from Influenza haemagglutinin) and flow cytometry, binding activities of the anti-RBD MAbs were shown to vary with 50% binding concentration from 0. 10 

The 32 anti-spike glycoprotein MAbs were systematically examined by plaque reduction neutralisation (PRNT) assay for neutralisation of wild-type SARS-CoV-2 virus (see methods, Table 1 ). A total of 14 neutralising antibodies distributed between different regions of the spike glycoprotein were identified: 5 of 10 to RBD, 3 of 13 to S1 (non-RBD), 6 of 9 to S2. The EC 50 concentrations, as a measure of potency, ranged from 0.05 to~133 nM (8 ng/ml-20 μg/ml).

The binding activity of post-infection sera IgG with SARS-CoV-2 spike glycoprotein in an ELISA and SARS-CoV-2 RBD assessed by flow cytometry on transduced cells, among enrolled patients. Each experiment was repeated twice. Values are presented as mean ± standard error of the mean. Two sera from healthy adults (one collected at day 28 post 2018-19 influenza vaccination and one collected from an influenza-infected patient 9 days after symptom onset) in 2018 were included as controls. Linear regression was used to determine the 50% end-point dilution (ED 50 Neutralisation of anti-RBD antibodies was corroborated by a microneutralisation test that 

Potent neutralising antibodies to the RBD of SARS-CoV-2 spike glycoprotein were identified and we then analysed the blockade of the ACE2-RBD interaction by anti-RBD antibodies in two assays (Fig 3, Table 1 ), including an assay that we reported previously [17, 18] . In the first assay unlabelled MAbs in at least 10-fold excess were mixed with biotin labelled ACE2-Fc and binding to the RBD, displayed on RBD-VLP [19] bound to an ELISA plate ( Fig 3A, S7 Fig) .

The RBD-VLP was used to display the RBD on the plate, because direct binding of RBD to the ELISA plate resulted in loss of ACE2 binding (S7 Fig) . Anti-RBD neutralising antibodies FI 3A and FI 1C, as well as the unlabelled ACE2-Fc, strongly inhibited the binding of labelled ACE2-Fc to RBD. A partial inhibition was detected by anti-RBD antibodies FD 11A, FD 5D and FI 4A. Another unlabelled nanobody VHH72-Fc in excess inhibited the binding of labelled ACE2-Fc to RBD in this assay. VHH72-Fc binds in the Class 4 region of the RBD [20] , and competes for binding with the characterised MAbs CR3022 and EY 6A (Table 1 ) [21] [22] [23] . The structure of VHH72-Fc bound to RBD is known [24] and its footprint on the RBD does not overlap that of ACE2, so inhibition is thought to occur by steric hindrance.

In the second assay, we employed MDCK-SIAT1 cells overexpressing full-length human ACE2 as a transmembrane protein. Unlabelled antibodies or ACE2-Fc were mixed in excess with biotinylated RBD, and binding of RBD was detected with Streptavidin-HRP in ELISA ( Fig 3B) . The results of this assay mostly mirrored those of the first assay and confirmed that in this orientation anti-RBD neutralising antibodies FD 11A and FD 5D competed in excess with soluble RBD for binding to ACE2 (Fig 3B) . In addition, anti-RBD neutralising antibody EY 6A competed with RBD for ACE2 binding. The binding pattern of EY 6A is analogous to a previously described antibody CR3022 (Table 1) [21] [22] [23] . These two antibodies are known to bind to the same region of RBD away from the ACE2 binding site, but they influence the binding kinetics of RBD to ACE2, presumably through steric effects [18] .

The ten anti-RBD MAbs were then divided into cross-inhibiting groups as described for human MAbs to Ebola [25] by assessing competition of unlabelled antibodies at 10-fold (or greater) excess over a biotin labelled target antibody by ELISA. Included as controls were the VHH72-Fc [24] and H11-H4-Fc [17] nanobodies linked to the hinge and Fc region of human

A total of 219 IgG monoclonal antibodies were produced from COVID-19 patients (50 from case A, 131 from case B, 38 from case C). An average of 13.7±6.8% and 3.5±0.8% of antibodies were reactive with spike glycoprotein (S) and nucleocapsid (N) antigens of SARS-CoV-2, respectively. The data are presented as specificity, number of antibodies, and the percentage of total antibodies isolated from each patient. (B) The binding activity of anti-SARS-CoV-2 MAbs with spike glycoprotein, RBD and the S2 subunit in ELISA. Anti-influenza H3 MAb BS-1A and anti-SARS RBD CR3022 were included as controls. Each experiment was repeated twice. The OD 450 values are presented as mean ± standard error of the mean. Panels (C) and (D) show numbers of variable domain mutations in MAb genes and variation in MAb CDR3 lengths among anti-S2 and anti-N MAbs, respectively. Antibodies that strongly cross-react with at least one betacoronavirus (SARS or MERS or OC43) were defined as cross-reactive MAbs. CDR3 length and mutation numbers are presented as mean ± standard error of the mean (anti-S2, specific, n = 4 versus cross-reactive, n = 5; anti-N, specific, n = 3 versus cross-reactive, n = 5). The two-tailed Mann-Whitney test was performed to compare the mutations between two groups. � p < 0.05; D, = Day; ns, nonsignificant; CR, cross-reactive.

https://doi.org/10.1371/journal.ppat.1009352.g002 a The specificity of antibody was tested using flow cytometry with MDCK-SIAT1 cells expressing the spike glycoprotein, RBD and NTD. CR3022 is a SARS and SARS-CoV-2 RBD cross-reactive human MAb and BS-1A is an anti-influenza H3 human MAb.

b The antibody was assessed by immunofluorescence of wild-type SARS-CoV-2-infected Vero E6 cells.

c A sample (10 μg/ml) was considered positive when the measured extinction is at least 3 times the OD value of the negative control in the ELISA with SARS-CoV-2, SARS, MERS and OC43 spike proteins. CR3022 is an anti-SARS and SARS-CoV-2 RBD human MAb and BS-1A is an anti-influenza H3 human MAb. The OD value � 1.00, 0.50-0.99, or � 0.49 is highlighted in deep green, green and light green, respectively.

d The PRNT assay was performed with wild-type SARS-CoV-2 (see methods) and the 50% effective concentration (EC 50 ) was determined using linear regression analysis.

e ACE2-blocking activity of anti-RBD antibody compared to ACE2-Fc (see methods): +, partial; ++, IC 50 > ACE2-Fc; +++, IC 50~= ACE2-Fc; ++++, IC 50 < ACE2-Fc. � Memory phenotype.

Abbreviations: MAb, monoclonal antibody; FCM, flow cytometry; IFA, immunofluorescence; S, spike; RBD, receptor-binding domain; NTD, N-terminal domain;

PRNT, plaque reduction neutralisation assay; ACE2, Angiotensin-Converting Enzyme 2.

https://doi.org/10.1371/journal.ppat.1009352.t001

IgG1, CR3022 and S309 human IgG1 antibodies [21, 26] . These four control molecules have characterised binding footprints on the RBD defined by crystal structures [17, 22, 24, 26] , as does EY 6A [18] . Also included was the protease domain (residues 18-615) of ACE2 linked to the Fc region of human IgG1 (ACE2-Fc dimer). The ten antibodies formed four cross-inhibiting clusters (Table 2) , represented by antibodies EY 6A (cluster 1, equivalent to Class 4 of Barnes et al, which included CR3022 and VHH72), FI 3A (cluster 2, equivalent to Classes 1 and 2 of Barnes et al, which included H11-H4), FD 11A (cluster 3, equivalent to Class 3 of Barnes et al, which included S309) and FJ 10B (cluster 4, not represented in the Barnes classification) [20] . Cluster 2 is composed of antibodies in the Barnes Classes 1 and 2 that have overlapping binding footprints and cross inhibit each other's binding [20] . The strongest inhibitors of ACE2-Fc binding were in clusters 2 and 3 (Tables 1 and 2 ). Neutralising antibodies were detected in clusters 1, 2 and 3, with the strongest antibodies FI 3A and FD 11A being in clusters 2 and 3 (Tables 1 and 2). The sites of binding of the clusters of antibodies to the RBD and the ACE2 binding site are represented on a diagram of the RBD represented as in the shape of a squirrel, as an aide memoire for orientation in S8 Fig.

Five neutralising anti-RBD MAbs partially or completely blocked the interaction between RBD and ACE2 (Tables 1 and 2, Fig 3) . The most potent neutralising antibodies were ACE2 blockers (FI 3A in cluster 2, and FD 11A in cluster 3), and bound independently of each other to the RBD (Fig 3C) . MAb EY 6A has been shown to alter the binding kinetics of the interaction without full inhibition [18] and it had a moderate effect on ACE2 binding in the assay where ACE2 was expressed at the cell surface. These three MAbs bound independently of each other indicating the existence of at least three neutralisation-sensitive epitopes within the RBD ( Fig 3C) .

All five neutralising MAbs to the RBD (EY 6A, FI 3A, FI 1C, FD 11A, FD 5A) had V gene sequences close to germline (S2 Table) , indicating the development of de novo anti-RBD neutralising antibodies upon natural SARS-CoV-2 infection in humans.

The ability of convalescent sera to block soluble RBD for binding to cell-expressed ACE2 was assessed. Both convalescent sera from case A (D22) and case B (D26) exhibited detectable ACE2-blocking activities ( Fig 3D) . This serological activity is compatible with the isolation of potent ACE2-blocking antibodies from both patients (Table 1) . By contrast, the D18 serum from case C showed minimal ACE2-blocking activity. Both cases A and B had prolonged fever and the development of pneumonia during hospitalization (S1 Table) , which suggests that the development of ACE2-blocking antibody response in the convalescent stage is likely associated with clinical severity after infection.

Six of nine MAbs specific for S2 showed moderate neutralisation in the PRNT assay ( Table 1) . The antibodies FB 1E, FJ 4E and EW 9C, are moderately neutralising (EC 50 .33 nM), cross-react on the spike glycoprotein from the common cold betacoronavirus OC43, and show sequence characteristics of memory cells with high numbers of somatic mutations. This indicates that memory B cells, likely primed by an endemic or epidemic betacoronavirus related to OC43, can give rise to antibodies that neutralise SARS-CoV-2, albeit modestly. The other three neutralising antibodies specific for S2, FD 10A, FG 7A and FM 1A were close to germline in sequence (S2 Table) and did not cross-react strongly with other betacoronaviruses (Table 1) . 

Thirteen MAbs were defined that bound the S1 region and three, close to germline in sequence, were neutralising. FJ 1C showed neutralisation (EC 50 

A set of 8 anti-SARS-CoV-2 nucleocapsid MAbs were derived from circulating plasmablasts in the naturally infected subjects (Table 3, [18, 21, 24] were coloured in magenta. The epitopes recognized by H11-H4 (cluster 2 MAb) [17] were overlapping with ACE2-binding site and coloured in blue. The epitopes recognized by S309 (cluster 3 MAb) [26] were coloured in yellow. (D) Convalescent sera were analysed in the ACE2-blocking (ACE2 anchored) assay. Experiments were performed in triplicate. Anti-RBD antibody FD 11A and anti-influenza H3 antibody BS 1A were included as controls. Data are presented as mean ± standard error of the mean. IC 50 , 50% inhibitory concentration.

https://doi.org/10.1371/journal.ppat.1009352.g003 

CoV in ELISA. This suggested cross-reactivity of the antibody response to epitopes in nucleocapsids of betacoronaviruses following natural infection with SARS-CoV-2. The 8 MAbs were evolved from 7 clonal groups defined by their heavy chain VDJ and light chain VJ rearrangements (S3 Table) . Those cross-reactive with SARS-CoV carried more nucleotide and amino acid substitutions than SARS-CoV-2-specific MAbs in their variable domains, but this trend did not reach statistical significance (Cross-reactive heavy 24±19 nt versus specific heavy 8±14 nt, p = 0.45; Cross-reactive heavy 13±10 aa versus specific heavy 5 ±8 aa, p = 0.45; two-tailed Mann-Whitney test; Fig 2D) .

We detected a robust and rapid plasmablast response encoding diverse anti-spike glycoprotein and anti-nucleocapsid antibody populations within 3 weeks of onset of illness in COVID-19 patients. The concomitant serologic response occurred as early as the first week after illness onset, with gradually increasing levels of SARS-CoV-2 spike glycoprotein-and RBD-binding IgG antibodies from the second to third week after symptom onset. The kinetics of plasmablast and virus-specific serologic responses was observed to vary between subjects. Consecutive samples from donor B showed a highly expanded plasmablast subset at the time of progression into pneumonia, followed by class-switching to an IgG-predominant plasmablast response until week three of illness. On the other hand, donor C presented with mild symptoms and produced an early plasmablast response with class-switching at the end of first week of symptom onset. Thevarajan et al demonstrated a similar kinetic of B cell response in a mild COVID-19 case, in whom the peripheral plasmablast response and the SARS-CoV-2-binding IgG antibodies peaked at day eight, soon after the disappearance of fever [8] . An early classswitching phenotype of the humoral response was also noted within the first week of onset in paediatric patients who mainly experienced mild illness after SARS-CoV-2 infection, although the immunological basis for this phenotype is unclear [27] . Both peak plasmablast frequency and serologic titre for spike glycoprotein were higher in donor B, who presented with severe symptoms, than in donor C. Similar observations on the serologic titre and clinical severity have been reported by others [10] . Such plasmablast response may originate from naïve or memory B cells, although its fate remains largely undetermined in humans [28, 29] . The IgG spike-specific plasmablasts that are detectable as soon as at the end of first week and become dominant after the second week of onset are further characterised in the study and these cells may represent either a rapid class-switching in the germinal center or a recall memory [30] [31] [32] .

In this study, a substantial subset of plasmablast-derived anti-S2 (five of nine, 56%) crossreacted with human betacoronavirus OC43. Cross-reactivity among betacoronaviruses has also been reported in polyclonal sera [12] [13] [14] . Human coronavirus OC43, discovered in the 1960s, is one of the major betacoronaviruses that cause common colds in the community [33, 34] , and severe respiratory infections in elderly and immunocompromised individuals [12, 35] . Epidemiologic surveys reveal that OC43 infection can occur in early childhood, and that OC43 seropositivity reaches nearly 90% in adults [36, 37] . The S2 component of SARS--CoV-2 spike glycoprotein shares 43~89% amino acid identity with SARS, MERS and OC43, and, similarly, the amino acid sequence of SARS-CoV-2 nucleocapsid protein of is 34~90% homologous to those of other betacoronaviruses (S11 Fig and S12 Fig) , suggesting the presence of conserved epitopes on these antigens.

The presence of pre-existing immune memory to betacoronavirus that cross-react with SARS-CoV-2 is supported by the accumulation of somatic mutations in the genes encoding cross-reactive antibodies isolated from COVID-19 patients (Fig 2C, S2 Table) . This situation is reminiscent of re-exposure to immunogenic epitopes shared by closely related viruses leading to induction of broadly cross-reactive antibodies in patients infected with influenza, dengue or Zika viruses [38] [39] [40] .

The 32 MAbs that bound to the spike glycoprotein were systematically tested for neutralisation (summarised in Table 1 ). Results established that neutralising epitopes were present on the RBD, S1-NTD, S1-non NTD/RBD, and S2 regions of the spike glycoprotein. The range of neutralisation EC 50 titres against live SARS-CoV-2 reported in the literature for human and murine monoclonal antibodies span at least three orders of magnitude, from ng/ml to μg/ml [41, 42] . Our results reflect the range of values in in vitro potency. The relationship between the EC 50 value in neutralisation assays and therapeutic potential is not established, although antibodies to the RBD with EC 50 in the nanogram range have shown therapeutic activity in small animal models [43] [44] [45] . The majority of the most strongly neutralising antibodies were close to germline in sequence, showing that full affinity maturation is not required in order to achieve SARS-CoV-2 virus neutralisation. We made a similar observation for antibodies induced by an Ebola vaccine [25] , and this has been observed in other collections of monoclonal antibodies to SARS-CoV-2 [7, [42] [43] [44] [45] [46] [47] [48] [49] .

The RBDs of SARS and SARS-CoV-2 are known to contain neutralising epitopes [18, [41] [42] [43] [44] [45] [46] [47] [48] [49] [50] [51] , and vaccines based on the RBD of SARS and SARS-CoV-2 induce strong neutralising antibodies that are protective in animal models [52] [53] [54] . There is a tendency for the most potent neutralising antibodies to be those that block the binding of the RBD to its receptor ACE2 [41] [42] [43] [44] [45] [46] [47] [48] [49] [50] [51] [55] [56] [57] . Previous structural studies demonstrated that potent antibodies with footprints overlapping that of ACE2 are composed of two major subgroups (named Class 1 and Class 2 by Barnes et al) [20] , one with representative Vh3-53 gene usage and short CDR3 binding to the RBD in an up conformation and the other binding RBDs in both up and down conformations and even adjacent RBDs [20, 58] . Potent MAb FI 3A shares similar characteristics with the first subgroup described above. Occasional antibodies that do not occupy the ACE2 footprint or weakly block ACE2 binding, i.e., S309, FD 11A and EY 6A, can be almost as potent, perhaps through spike trimer cross-linking or triggering a conformational change in the spike glycoprotein that renders it non-functional [7, 18, 26, 49] .

We characterise MAbs targeting the RBD that can be arranged into four cross-inhibiting clusters ( Table 2 ). Three of these MAb clusters (represented by EY 6A, FI 3A and FD 11A) demonstrate neutralisation of SARS-CoV-2 to some level, while those in the fourth (represented by FM 7B) did not neutralise. This suggests that three neutralising antibodies may be able to bind to the RBD simultaneously. The most potent neutralising MAbs fall in two clusters and interfere strongly with ACE2 binding, which may be exploited therapeutically. For instance, antibodies FI 3A in cluster 2 (EC 50 8.67 nM) and FD 11A in cluster 3 (EC 50 0.05 nM) could be combined to limit possible selection of neutralisation-resistant variants. This principle has been demonstrated in recent studies [45, 47, 59] .

Neutralisation by human MAbs to the S1-NTD of SARS-CoV-2 has been described [44, 60] , but their mechanism of action is not known. The range of neutralising EC 50 titres (0.09-51.1 nM) was overlapping with those targeting the RBD, similar to our NTD-specific antibody FJ 1C. Cocktails of antibodies that include a representative to the NTD would further reduce the likelihood of selecting neutralisation-resistant viruses. A second strong binder to the NTD, FD 7C, was not neutralising. Structural comparisons of these two antibodies bound to spike glycoprotein may provide insight into the neutralising action of FJ 1C [60] .

We detected a subset of six MAbs to the S2 region of the spike glycoprotein that neutralised moderately (EC 50 36-133 nM) . Similar results are found in the antibodies to SARS [61] [62] [63] . It has been shown that the neutralizing activity of anti-SARS S2 antibody involves the inhibition of membrane fusion, but the function of anti-SARS-CoV-2 S2 antibodies could be complex and remain undetermined yet [61] [62] [63] [64] [65] . Five of our anti-S2 antibodies were clearly derived from a memory population; showing significant accumulation of somatic mutations in the MAb encoding genes and cross-reactivity for the OC43 common cold virus spike glycoprotein (Fig 2C) . Further investigation is required to ascertain whether such antibodies, that may be weak-or non-neutralising and cross-reactive with common cold viruses, are beneficial or detrimental with respect to COVID-19 disease. Recent evidence is not conclusive on this issue [66, 67] .

Our results have significance for serologic tests employing the N and S2 antigens of SARS--CoV-2. Serologic surveys, some of which are based on these antigens, with sera from donors infected with SARS-COV-2 during the spring and summer months have shown very high specificity (as judged by comparing convalescent sera from COVID-19 patients versus sera collected in the pre-COVID-19 period) (www.gov.uk/government/publications/covid-19-laboratory-evaluations-of-serological-assays). However, if many individuals have memory B cells to the S2 antigen of circulating betacoronaviruses that cross-react with SARS-CoV-2, concurrent winter infections with these viruses might erode the specificity of serologic tests for SARS-CoV-2 that include the S2 antigen. Cross-reactivity of antibodies targeting the S1 subunit or RBD is relatively much lower, so using this antigen is more likely to give a true indication of SARS-CoV-2 specificity.

In summary, COVID-19 patients developed strong anti-SARS-CoV-2 spike glycoprotein and nucleocapsid plasmablast and antibody responses. A panel of IgG MAbs targeted a diverse spectrum of epitopes on the RBD, S1-NTD, non-NTD/RBD S1 and S2 regions of the spike glycoprotein, of which 14 neutralised wild-type viruses with EC 50 s in the range 0.05 to~133 nM. Neutralising activities of the majority of anti-RBD MAbs were linked to ACE2-binding blockade, and non-competing pairs of such MAbs, perhaps combined with a neutralising MAb to the NTD, offer potential formulations for the development of prophylactic and therapeutic agents against SARS-CoV-2. Antibody responses to the S2 component of spike glycoprotein confirm cross-reactivity with a common cold virus.

The study protocol and informed consent were approved by the ethics committee at the Chang Gung Medical Foundation and the Taoyuan General Hospital, Ministry of Health and Welfare. Written informed consent was received from each participant prior to inclusion in the study. The study and all associated methods were carried out in accordance with the approved protocol, the Declaration of Helsinki and Good Clinical Practice guidelines.

This study was designed to isolate SARS-CoV-2 antigen-specific MAbs from peripheral plasmablasts of humans infected with SARS-CoV-2 and to characterise the antigenic specificity and phenotypic activities of the MAbs. Diagnosis of SARS-CoV-2 infection was based on positive real-time reverse transcriptase polymerase chain reaction results of respiratory samples. . 555787, BD) . The CD3 neg CD19 pos CD20 neg CD27hi CD38 hi IgG pos plasmablasts were gated and isolated in chamber as single cells as previously described [32] .

Sorted single cells were used to produce human IgG MAbs as previously described [32] . Briefly, the variable region genes from each single cell were amplified in a reverse transcriptase polymerase chain reaction (RT-PCR: QIAGEN, Germany) using a cocktail of sense primers specific for the leader region and antisense primers to the Cγ constant region for heavy chain and Cκ and Cλ for light chain. The RT-PCR products were amplified in separate polymerase chain reactions for the individual heavy and light chain gene families using nested primers to incorporate restriction sites at the ends of the variable gene as previously described [32] . These variable genes were then cloned into expression vectors for the heavy and light chains. Plasmids were transfected into the HEK293T cell line for expression of recombinant full-length human IgG MAbs in serum-free transfection medium. A selected panel of MAbs were further expanded and purified.

To determine the individual gene segments employed by VDJ and VJ rearrangements and the number of nucleotide mutations and amino acid replacements, the variable domain sequences were aligned with germline gene segments using the international ImMunoGeneTics (IMGT) alignment tool (http://www.imgt.org/IMGT_vquest/input).

ELISA plates (Corning 96-well Clear Polystyrene High Bind Stripwell Microplate, USA) were coated with 8 μg/ml SARS-CoV-2 antigens (spike glycoprotein extracellular or receptor-binding domains or S2 subunit, or nucleocapsid) or SARS antigen (spike glycoprotein S1 or S2 subunit, or nucleocapsid) or MERS antigen (spike glycoprotein extracellular domain, or nucleocapsid) or human coronavirus OC43 antigen (spike glycoprotein extracellular domain, or nucleocapsid) at 4˚C overnight. Recombinant SARS-CoV-2 proteins were purchased from Sino Biologicals (S1+S2 extracellular domain, 40589-V08B1; RBD, 40592-V08B; S2, 40590-V08B; Nucleocapsid, 40588-V08B) and were produced in the baculovirus-insect cell expression system. Recombinant SARS proteins were purchased from Sino Biologicals (S1, 40150-V08B1; S2, 40150-V08B3; Nucleocapsid, 40143-V08B) and were produced in the baculovirus-insect cell expression system. Recombinant MERS proteins were purchased from Sino Biologicals (S1+S2 extracellular domain, 40069-V08B; Nucleocapsid, 40068-V08B) and were produced in the baculovirus-insect cell expression system. Recombinant coronavirus OC43 proteins were purchased from Sino Biologicals (S1+S2 extracellular domain, 40607-V08B; Nucleocapsid, 40643-V07E). Plates were washed with phosphate-buffered saline containing 0.05% Tween-20 and blocked with 3% bovine serum albumin (BSA) at room temperature for 1 hour on a shaker. Serial dilutions of MAb-containing cell culture supernatant or purified MAb were added and plates were incubated at 37˚C for 1 hour. Plates were washed and incubated with horseradish peroxidase-conjugated rabbit anti-human IgG secondary antibody (Rockland Immunochemicals, USA). Plates were washed and developed with TMB substrate reagent (BD Biosciences, USA). Reactions were stopped with 0.5M hydrochloric acid and absorbances was measured at 450nm on a microplate reader. Non-transfected cell culture supernatant, anti-influenza H3 human IgG MAb BS 1A (in house), anti-SARS spike glycoprotein MAb CR3022 and convalescent serum were used as controls for each experiment.

Reaction yielding an absorbance value above three times the mean absorbance of the negative control BS 1A were considered positive.

MDCK-Spike cells were produced by stably transducing parental MDCK-SIAT1 cells with cDNA expressing full-length SARS-CoV-2 spike glycoprotein. MDCK-RBD cells were produced by, stably transducing MDCK-SIAT1 cells [32] with a Lentiviral vector encoding a cDNA expressing RBD amino acids 340-538 (NITNLCPFGEVFNATRFASVYAWNRKRI SNCVADYSVLYNSASFSTFKCYGVSPTKLNDLCFTNVYADSFVIRGDEVRQIAPGQTGKI ADYNYKLPDDFTGCVIAWNSNNLDSKVGGNYNYLYRLFRKSNLKPFERDISTEIYQAG STPCNGVEGFNCYFPLQSYGFQPTNGVGYQPYRVVVLSFELLHAPATVCGPKK) fused via a short linker to the transmembrane domain of haemagglutinin H7 (A/Hong Kong/125/ 2017) (EPI977395) at the C-terminus for surface expression. MDCK-NTD cells were produced by stably transfecting parental MDCK-SIAT1 cells [32] with cDNA expressing the SARS-CoV-2 NTD amino acids (VNLTTRTQLPPAYTNSFTRGVYYPDKVFRSSVLHSTQDLFLPFFSN VTWFHAIHVSGTNGTKRFDNPVLPFNDGVYFASTEKSNIIRGWIFGTTLDSKTQSLLIVN NATNVVIKVCEFQFCNDPFLGVYYHKNNKSWMESEFRVYSSANNCTFEYVSQPFLMDL EGKQGNFKNLREFVFKNIDGYFKIYSKHTPINLVRDLPQGFSALEPLVDLPIGINITRFQTL LALHRSYLTPGDSSSGWTAGAAAYYVGYLQPRTFLLKYNENGTITDAVDCALDPLSET KCTLKS) fused to the transmembrane domain of haemagglutinin H7 (A/Hong Kong/125/ 2017) (EPI977395) at the C-terminus for surface expression. MDCK-Spike, MDCK-RBD and MDCK-NTD cells were then FACS sorted for highly expressing cells using the CR3022 or FD 7C antibody. MDCK-Spike or MDCK-RBD or MDCK-NTD cells were prepared and resuspended. Cells were probed with purified MAbs in 3% BSA. Bound primary antibodies were detected with FITC-conjugated anti-IgG secondary. The binding activities were analysed by BD FACSCanto II flow cytometer (BD Biosciences, USA).

Under biosafety level 3 (BSL-3) conditions, Vero E6 cells were infected with 100 TCID 50 (median tissue culture infectious dose) SARS-CoV-2 (hCoV-19/Taiwan/CGMH-CGU-01/ 2020, EPI_ISL_411915). Infected cells were placed on coverslips and, and fixed with acetone at room temperature for 10 minutes. After blocking with 1% BSA at room temperature for 1 hour and washing, fixed cells were incubated with MAb-containing cell culture supernatant. The anti-influenza human monoclonal antibody BS 1A, anti-SARS spike glycoprotein MAb CR3022 and convalescent serum were used as antibody controls for each experiment. Following incubation and wash, cells were stained with FITC-conjugated anti-human IgG secondary antibody and Evans blue dye as counterstain. Antibody-bound infected cells demonstrated an apple-green fluorescence against a background of red fluorescing material stained by the Evans Blue counterstain. Images were acquired with original magnification 40x, scale bar 20 μm.

Confluent monolayers of Vero E6 cells in 96-well plates were incubated with~14 plaque forming units (PFU) of SARS CoV-2 (hCoV-19/England/02/2020, EPI_ISL_407073) and antibodies in a 2-fold dilution series (triplicates) for 3 hours at room temperature. Inoculum was then removed, and cells were overlaid with plaque assay overlay. Cells were incubated at 37˚C, 5% CO 2 for 24 hours prior to fixation with 4% paraformaldehyde at 4˚C for 30 minutes. Fixed cells were then permeabilised with 0.2% Triton-X-100 and stained with a horseradish peroxidase conjugated-antibody against virus protein for 1 hour at room temperature. TMB substrate was then added to visualise virus plaques as described previously for influenza virus [68] . Convalescent serum from COVID-19 patients was used as a control.

In brief, this rapid, high-throughput assay determines the concentration of antibody that produces a 50% reduction in infectious focus-forming units of authentic SARS-CoV-2 in Vero cells, as follows. Triplicate serial dilutions of antibody are pre-incubated with a fixed dose of SARS-CoV-2 (Australia/VIC01/2020, GenBank MT007544) [69] in triplicate before incubation with Vero cells. A carboxymethyl cellulose-containing overlay is used to prevent satellite focus formation. Twenty hours post-infection, the monolayers are fixed with paraformaldehyde and stained for N antigen using MAb EY 2A. After development with a peroxidase-conjugated antibody and substrate, foci are enumerated by enzyme-linked immune absorbent spot reader. Data are analysed using four-parameter logistic regression (Hill equation) in GraphPad Prism 8.3.

Neutralisation activity of MAb-containing supernatant was measured using SARS-CoV-2 (hCoV-19/Taiwan/CGMH-CGU-01/2020, EPI_ISL_411915) infected Vero E6 cells. Briefly, Vero E6 cells were pre-seeded in a 96 well plate at a concentration of 10 4 cells per well. The following day, MAb-containing supernatants were mixed with equal volumes of 100 TCID 50 virus preparation and incubated at 37˚C for 1 hour, then mixtures were added to seeded Vero E6 cells and incubated at 37˚C for 5 days. Cell, virus and virus back-titration controls were setup for each experiment. At day 5 the culture supernatant was harvested from each well, and virus RNA was extracted and quantified by real-time RT-PCR targeting the E gene of SARS--CoV-2 as previously described. The cycle threshold values of real-time RT-PCR were used as indicators of the copy number of SARS-CoV-2 RNA in samples with lower cycle threshold values corresponding to higher virus copy numbers.

Vero E6 cells in Dulbecco's Modified Eagle's Medium containing 10% FBS were added into 96-well plates and incubated at 37˚C with 5% CO 2 overnight to reach confluence. After washing with virus growth medium (VGM: Dulbecco's Modified Eagle's Medium containing 2% FBS), two-fold serially diluted MAbs in VGM starting at 100 μg/ml were added to each duplicated well. The plates were immediately transferred to a BSL-3 laboratory and 100 TCID 50 SARS-CoV-2 (hCoV-19/Taiwan/4/2020, EPI_ISL_411927) in VGM was added. The plates were further incubated at 37˚C with 5% CO 2 for three days and the cytopathic morphology of the cells was recorded using an ImageXpress Nano Automated Cellular Imaging System.

Competitive binding assays were performed as described previously [25] with slight modifications for epitope mapping of the anti-RBD MAbs. Briefly, 0.5 μg/ml of RBD-VLP were coated on NUNC plates (50 μl per well) overnight at 4˚C, washed and blocked with 300 μl of 5% (w/v) dried skimmed milk in PBS for 1 hour at room temperature prior to the assays. Antibody was biotinylated using EZ-Link Sulfo-NHS-LC-biotin (21237; Life Technologies) and then mixed with competing MAb (in at least 10-fold excess) and transferred to the blocked NUNC plates for 1 hour. A second layer Streptavidin-HRP (S911, Life Technologies) diluted 1:1,600 in PBS/ 0.1% BSA (37525; Thermo Fisher Scientific) was then added and incubated for another 1 hour. Plates were then washed, and signal was developed by adding POD substrate (11484281001, Roche) for 5 minutes before stopping the reaction with 1 M H 2 SO 4 . Absorbance (OD 450 ) was measured using a Clariostar plate reader (BMG, Labtech). Mean and 95% confidence interval of 4 replicate measurements were calculated. Competition was measured as: (X-minimum binding/(maximum binding-minimum binding), where X is the binding of the biotinylated MAb in the presence of competing MAb. Minimum binding is the self-blocking of the biotinylated MAb or background binding. Maximum binding is binding of biotinylated MAb in the presence of non-competing MAb (anti-influenza N1 neuraminidase MAb).

Two assays were used to determine the blocking of binding of ACE2 to RBD by MAbs. RBD was anchored on the plate in the first assay whereas ACE2 was anchored for the second assay.

In the first ACE2 blocking assay, RBD-VLP (Spycatcher-mi3 VLP-particles conjugated with Spytagged-RBD recombinant protein) [19] was coated on ELISA plates as described for the competitive binding assay. Recombinant ACE2-Fc (18-615) protein expressed in Expi293F (Life Technologies) cells was chemically biotinylated using EZ-link Sulfo-NHS-Biotin (A39256; Life Technologies) and buffer exchanged to PBS using a Zebaspin desalting column (Thermo Fischer). MAbs were titrated in duplicate or triplicate as half-log serial dilution, 8-point series starting at 1 μM in 30 μl volume with PBS/0.1% BSA buffer. 30 μl of biotinylated ACE2-Fc at approx. 0.2 nM (40 ng/ml) was added to the antibodies. 50 μl of the mixture was transferred to the PBS-washed RBD-VLP coated plates and incubated for 1 hour at room temperature. Secondary Streptavidin-HRP antibody (S911, Life Technologies) diluted to 1:1600 was then added to the PBS-washed plates and incubated for 1 h at room temperature. Plates were then washed four times with PBS and signal was developed by adding POD substrate (11484281001, Roche) for 5 minutes before stopping with 1 M H 2 SO 4 . OD450 was measured using a Clariostar plate reader (BMG, Labtech). The control antibody (a non-blocking antiinfluenza N1 MAb) or ACE2-Fc without antibody used to obtain the maximum signal and wells with PBS/BSA buffer only were used to determine the minimum signal. Graphs were plotted as % binding of biotinylated ACE2 to RBD. Binding % = {(X-Min)/(Max-Min)} � 100 where X = measurement of the antibody, Min = buffer only, Max = biotinylated ACE2-Fc alone. 50% inhibitory concentrations of the antibodies against ACE2 were determined using non-linear regression curve fit using GraphPad Prism 8.

The second ACE2 blocking assay was performed as described previously [17, 18] . Briefly, MDCK-SIAT1 cells were stably transfected to overexpress codon-optimised human ACE2 cDNA (NM_021804.1) using lentiviral vector and FACS sorted (MDCK-ACE2). Cells (3 x 10 4 per well) were seeded on a flat-bottomed 96-well plate the day before the assay. RBD-6H (340-538; NITN.GPKK) was chemically biotinylated using EZ-link Sulfo-NHS-Biotin (A39256; Life Technologies). Serial half-log dilutions (starting at 1 μM) of antibodies and controls were performed in a U-bottomed 96 well plate in 30 μl volume. 30 μl of biotinylated RBD (25 nM) were mixed and 50 μl of the mixture was then transferred to the MDCK-ACE2 cells. After 1 hour a second layer Streptavidin-HRP antibody (S911, Life Technologies) diluted 1:1,600 in PBS/ 0.1% BSA (37525; Thermo Fisher Scientific) was added and incubated for another 1 hour. Plates were then washed four times with PBS and signal was developed by adding POD substrate (11484281001, Roche) before stopping with 1 M H 2 SO 4 after 5 minutes. OD450 was measured using a Clariostar plate reader (BMG, Labtech). The control antibody (a non-blocking anti-influenza N1 antibody) was used to obtain maximum signal and PBS only wells were used to determine background. Graphs were plotted as % binding of biotinylated RBD to ACE2. The 50% inhibitory concentration of the blocking antibody was determined as described above.

The two-tailed Mann-Whitney test was performed to compare differences between two independent groups. The 50% effective concentration (EC50) was determined using linear regression analysis. A p value of less than 0.05 was considered significant. Graphs were presented by Microsoft Excel and GraphPad Prism software. This cell membrane-bound full-length spike carries trimer-stabilizing proline mutations (986KV987 to 986PP987) and substitutions at the S1-S2 furin cleavage site (682RRAR685 to 682GSAG685), which indicates that the spike would display the prefusion conformation. MDCK-H3 cells were stained in the control experiment. Anti-influenza H3 MAb BS-1A was included as an antibody control. Each experiment was repeated twice (n = 2). The binding percentage was presented as mean ± standard error of the mean. The CDR3 length (number of amino acids) and MAb gene mutation numbers are presented as mean ± standard error of the mean (< 0.5 μg/ml, n = 5 versus > 0.5 μg/ml, n = 5). The twotailed Mann-Whitney test was performed to compare the CDR3 length and mutation numbers between two groups. � P < 0.05; ns, non-significant; BC 50 , 50% binding concentration. (TIF)

Neutralisation assays were performed on the indicated antibodies according to the fluorescent focus-forming units microneutralisation method (see methods). Data were normalized to control (no antibody) values of foci, and the grey region comprises ± 1 standard deviation the mean control values. Individual points are displayed ± 1 standard deviation of technical, and curves are shown only where the data for a particular antibody fitted the standard doseresponse (Hill) equation (n = 3). Partial: MAb neutralises at least~40% viruses at 100 nM (highest concentration tested). EC 50 

Contributions Conceptualization

Funding acquisition

Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine

Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine

Deployment of convalescent plasma for the prevention and treatment of COVID-19

Effect of Convalescent Plasma Therapy on Time to Clinical Improvement in Patients With Severe and Life-threatening COVID-19: A Randomized Clinical Trial

Early High-Titer Plasma Therapy to Prevent Severe Covid-19 in Older Adults

Use of convalescent plasma therapy in SARS patients in Hong Kong

Structure, Function, and Antigenicity of the SARS-CoV-2 Spike Glycoprotein

Breadth of concomitant immune responses prior to patient recovery: a case report of non-severe COVID-19

Neutralizing antibodies in patients with severe acute respiratory syndrome-associated coronavirus infection

Antibody responses to SARS-CoV-2 in patients with COVID-19

Serology characteristics of SARS-CoV-2 infection since exposure and post symptom onset

An Outbreak of Human Coronavirus OC43 Infection and Serological Cross-reactivity with SARS Coronavirus

Viral epitope profiling of COVID-19 patients reveals cross-reactivity and correlates of severity

Serologic crossreactivity of SARS-CoV-2 with endemic and seasonal Betacoronaviruses

Cross-neutralization of influenza A viruses mediated by a single antibody loop

Structural insights on the role of antibodies in HIV-1 vaccine and therapy

Neutralizing nanobodies bind SARS-CoV-2 spike RBD and block interaction with ACE2

Structural basis for the neutralization of SARS-CoV-2 by an antibody from a convalescent patient

Engineering a Rugged Nanoscaffold To Enhance Plug-and-Display Vaccination

SARS-CoV-2 neutralizing antibody structures inform therapeutic strategies

Human monoclonal antibody combination against SARS coronavirus: synergy and coverage of escape mutants

Neutralization of SARS-CoV-2 by Destruction of the Prefusion Spike

A highly conserved cryptic epitope in the receptor binding domains of SARS-CoV-2 and SARS-CoV

Structural Basis for Potent Neutralization of Betacoronaviruses by Single-Domain Camelid Antibodies

Therapeutic Monoclonal Antibodies for Ebola Virus Infection Derived from Vaccinated Humans

Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody

Protective humoral immunity in SARS-CoV-2 infected pediatric patients

Competence and competition: the challenge of becoming a long-lived plasma cell

Factors Affecting Early Antibody Secreting Cell Maturation Into Long-Lived Plasma Cells

Germinal centres: role in B-cell physiology and malignancy

Origin and Function of Circulating Plasmablasts during Acute Viral Infections

Structure-function analysis of neutralizing antibodies to H7N9 influenza from naturally infected humans

Recovery in tracheal organ cultures of novel viruses from patients with respiratory disease

Epidemiology of Seasonal Coronaviruses: Establishing the Context for the Emergence of Coronavirus Disease

Human Coronavirus OC43 Associated with Fatal Encephalitis

Development of a nucleocapsid-based human coronavirus immunoassay and estimates of individuals exposed to coronavirus in a U.S. metropolitan population

The dominance of human coronavirus OC43 and NL63 infections in infants

The human immune response to Dengue virus is dominated by highly cross-reactive antibodies endowed with neutralizing and enhancing activity

Zika virus activates de novo and cross-reactive memory B cell responses in dengue-experienced donors

Broadly cross-reactive antibodies dominate the human B cell response against 2009 pandemic H1N1 influenza virus infection

Receptor-binding domain of severe acute respiratory syndrome coronavirus spike protein contains multiple conformation-dependent epitopes that induce highly potent neutralizing antibodies

Convergent antibody responses to SARS-CoV-2 in convalescent individuals

Potent Neutralizing Antibodies against SARS-CoV-2 Identified by High-Throughput Single-Cell Sequencing of Convalescent Patients' B Cells

Potent neutralizing antibodies against multiple epitopes on SARS-CoV-2 spike

A noncompeting pair of human neutralizing antibodies block COVID-19 virus binding to its receptor ACE2

Potent neutralizing antibodies from COVID-19 patients define multiple targets of vulnerability

Studies in humanized mice and convalescent humans yield a SARS-CoV-2 antibody cocktail

Isolation of potent SARS-CoV-2 neutralizing antibodies and protection from disease in a small animal model

Human neutralizing antibodies elicited by SARS-CoV-2 infection

A human monoclonal antibody blocking SARS-CoV-2 infection

Human monoclonal antibodies block the binding of SARS-CoV-2 spike protein to angiotensin converting enzyme 2 receptor

Receptor-binding domain as a target for developing SARS vaccines

The SARS-CoV-2 receptor-binding domain elicits a potent neutralizing response without antibody-dependent enhancement

A vaccine targeting the RBD of the S protein of SARS-CoV-2 induces protective immunity

Structural basis of receptor recognition by SARS-CoV-2

Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor

Structural and Functional Basis of SARS-CoV-2 Entry by Using Human ACE2

Complete mapping of mutations to the SARS-CoV-2 spike receptor-binding domain that escape antibody recognition

Antibody cocktail to SARS-CoV-2 spike protein prevents rapid mutational escape seen with individual antibodies

A neutralizing human antibody binds to the Nterminal domain of the Spike protein of SARS-CoV-2

Monoclonal antibodies for the S2 subunit of spike of SARS-CoV-1 cross-react with the newly-emerged SARS-CoV-2

Monoclonal antibodies targeting the HR2 domain and the region immediately upstream of the HR2 of the S protein neutralize in vitro infection of severe acute respiratory syndrome coronavirus

Fully human monoclonal antibody directed to proteolytic cleavage site in severe acute respiratory syndrome (SARS) coronavirus S protein neutralizes the virus in a rhesus macaque SARS model

Antibody signature induced by SARS-CoV-2 spike protein immunogens in rabbits

Antibodies to SARS-CoV-2 and their potential for therapeutic passive immunization

Preexisting and de novo humoral immunity to SARS-CoV-2 in humans

S Protein-Reactive IgG and Memory B Cell Production after Human SARS-CoV-2 Infection Includes Broad Reactivity to the S2 Subunit

Optimisation of a micro-neutralisation assay and its application in antigenic characterisation of influenza viruses. Influenza Other Respir Viruses

Isolation and rapid sharing of the 2019 novel coronavirus (SARS-CoV-2) from the first patient diagnosed with COVID-19 in Australia

We acknowledge the BD FACSAria cell sorter service provided by the Core Instrument Center of Chang Gung University. We would like to acknowledge Paul Sopp and Craig Waugh in the flow cytometry facility at the MRC WIMM for providing cell sorting services.