The SARS-CoV-2 pandemic poses the greatest global public health challenge in a century. Neutralizing antibody is a correlate of protection and data on kinetics of virus neutralizing antibody responses are needed. We tested 293 sera from an observational cohort of 195 reverse transcription polymerase chain reaction (RT-PCR) confirmed SARS-CoV-2 infections collected from 0 to 209 days after onset of symptoms. Of 115 sera collected ≥61 days after onset of illness tested using plaque reduction neutralization (PRNT) assays, 99.1% remained seropositive for both 90% (PRNT90) and 50% (PRNT50) neutralization endpoints. We estimate that it takes at least 372, 416 and 133 days for PRNT50 titres to drop to the detection limit of a titre of 1:10 for severe, mild and asymptomatic patients, respectively. At day 90 after onset of symptoms (or initial RT-PCR detection in asymptomatic infections), it took 69, 87 and 31 days for PRNT50 antibody titres to decrease by half (T1/2) in severe, mild and asymptomatic infections, respectively. Patients with severe disease had higher peak PRNT90 and PRNT50 antibody titres than patients with mild or asymptomatic infections. Age did not appear to compromise antibody responses, even after accounting for severity. We conclude that SARS-CoV-2 infection elicits robust neutralizing antibody titres in most individuals.
Virus neutralizing antibody is likely to be a key correlate of protection for COVID-191 and data on kinetics of virus neutralizing antibody responses are needed2. Development of population immunity, achieved through natural infection, or preferably through vaccination is essential for combating the COVID-19 pandemic. Antibody and T cell responses are the main arms of the adaptive immune response. The mechanisms of protective immunity and the duration of such protection against COVID-19 remain to be elucidated. In other respiratory infections such as influenza, antibody responses are known to protect against infection and T cell responses modulate the severity of disease3. Correlates of protection provided by antibody are well established for influenza, and approximately 50% of those with serum haemagglutination inhibition antibody titers of 1:40 were protected from infection, the proportion protected increasing progressively with higher antibody titers4,5,6. Patients with SARS developed both neutralizing antibody as well as T cell immunity, with neutralizing antibody and T cell responses being detectable for around 3 years and >17 years post-infection, respectively7,8. Since SARS-CoV-1 is no longer circulating in humans, there is no direct evidence of protection from reinfection, if any, provided by antibody or T cell responses. In experimental animal models, the spike protein was necessary and sufficient to elicit neutralizing antibody and protection from challenge with SARS-CoV-1. Other virus structural proteins N, M, and E were not able to mediate protection in the absence of S protein9.
In experimental animal models of SARS-CoV-2 infection in Golden Syrian hamsters and in non-human primates, prior infection as well as transfer of immune serum protected animals from disease though it did not provide sterilizing immunity10,11. Rhesus macaques immunized with SARS-CoV-2 spike were protected from challenge and protection correlated with neutralizing antibody levels12. Evidence of protection against reinfection of humans with SARS-CoV-2 is limited. Pre-existing SARS-CoV-2 neutralizing antibody was protective from reinfection in an outbreak of SARS-CoV-2 on a fishing vessel1. It is noted however, that the association of protection with neutralizing antibody may not necessarily be causal13 as other forms of immunity (e.g., T cell immunity, non-neutralizing antibody) may contribute to protection. Neutralizing monoclonal antibodies protect rhesus macaques and mice from disease after experimental challenge14. The therapeutic use of convalescent plasma has been given Emergency Use Authorization by the U.S. Food and Drug Administration15. Taken together, these observations suggest that neutralizing antibody is a key correlate of protection against SARS-CoV-2 infection, although it may not be the only correlate of protection against SARS-CoV-2.
Many studies have reported antibody responses in COVID-19 patients using ELISA or other binding assays, but there are fewer reports using virus neutralization tests. Patients with COVID-19 infection develop detectable SARS-CoV-2 neutralizing antibody responses with some having detectable antibody at the end of the 1st week of illness, and almost all having neutralizing antibody after 4 weeks of illness16,17,18,19,20,21. The magnitude of the antibody responses and the proportion of patients developing antibody responses have varied. Severely ill patients are reported to have higher peak neutralizing antibody titers17,19,20. The methods used for detecting neutralizing antibody has also varied. These include the use of pseudoparticle neutralization (ppNT), microneutralization, fluorescent focus reduction assays, microneutralization assays, and plaque reduction neutralization tests (PRNT). Pseudoparticle neutralization tests are convenient and do not require bio-safety level 3 containment, but it is not clear how closely different types of virus pseudoparticles expressing SARS-CoV-2 spike protein mimics authentic virus, or how results from one pseudoparticle assay compares with another. Even with neutralization of live virus, microneutralization tests were found to be less sensitive than plaque reduction neutralization assays, which are regarded as the “gold-standard” for neutralizing antibody testing16. The major outstanding question is the duration of these neutralizing antibody responses. There are reports of rapid waning of antibody with some reports claiming that a third of patients have lost pseudoparticle neutralizing antibody by around 1–2 months after onset of illness22. If true, such findings have major implications for the duration of protective immunity from reinfection, and the likely success of vaccination in prevention from reinfection and disease. It is therefore essential that the duration of neutralizing antibody responses are assessed using live virus neutralization assays.
In this work, we used 293 sera from 195 individuals with RT-PCR confirmed SARS-CoV-2 infection, 70 of them providing multiple sequential sera, to assess the kinetics of PRNT50 and PRNT90 antibody titers. The spike protein receptor binding domain (RBD) is the most immune-dominant neutralizing epitope eliciting virus neutralization23. Therefore, for comparison, we have also analysed the duration of positivity of ELISA antibody responses to the virus spike RBD in a subset of 231 sera from 150 individuals. We show that SARS-CoV-2 infection elicits robust neutralizing antibody titers in most individuals that last beyond 6 months.
The RT-PCR confirmed SARS-CoV-infected patients ranged in age from 3 months to 80 years, 118 being males and 77 female (Supplementary Table 1). Thirteen patients had severe illness requiring >3 l of supplemental oxygen/minute, 151 were mild-moderate in severity (symptomatic but not requiring >3 l of supplemental oxygen per minute) and 31 were asymptomatic throughout the infection. Clotted blood was collected for serology. As expected, most of the severely ill patients were aged ≥60 years of age (Supplementary Table 2).
Two hundred and ninety three sera from 195 patients were tested in PRNT assays and the highest serum dilution reducing plaque numbers by 90% (PRNT90) and 50% (PRNT50) were determined. Of 234 sera collected from individuals 15–209 days after onset of illness, 98.7% and 99.6% were positive by PRNT90 and PRNT50 antibody tests, respectively (Supplementary Table 3). Of sera collected ≥61 days after onset of illness, 99.1% were positive in PRNT90 and PRNT50 antibody tests. The individual data-points for PRNT90 (Fig. 1) and PRNT50 (Fig. 2) for each serum are shown for the cohort as a whole, and stratified into those with severe disease, mild disease, or asymptomatic infections. Patients with severe disease had higher peak PRNT90 and PRNT50 antibody titers but took longer (around day 90) to reach peak antibody titers than the mild (around day 60) and asymptomatic (around day 30) infections. To obtain a conservative estimate of the duration of antibody responses, we fitted a Weibull curve to the existing data, and we estimate that it takes 292, 295, and 90 days for PRNT90 titers to drop to the detection limit of 1:10 in severe, mild and asymptomatic patients respectively. Similarly, it takes 372, 416, and 133 days for PRNT50 titers to drop to the detection limit of a titre of 1:10 for severe, mild and asymptomatic patients, respectively. At day 90 after onset of symptoms (or initial detection in asymptomatic infections), PRNT50 antibody titers declined by half (T1/2) by 69, 87, and 31 days in severe, mild, and asymptomatic infections was, respectively. Corresponding T1/2 for PRNT90 antibody for severe and mild infections was 58 and 95 days, respectively, the T1/2 for asymptomatic infections beyond day 90 being too low to quantitate.
Using a generalized additive mixed model which accounted for longitudinal changes in antibody titers and corticosteroid use, mild cases aged >60 years had mean antibody responses 0.40 (95% CI −0.19 to 0.99) and 0.38 (95% CI −0.16 to 0.92) log2 higher for PRNT90 and PRNT50 titers respectively, and 0.34 (95% CI 0.17–0.51) higher for ELISA OD values, compared to younger age groups. Among the severe cases, the differences were not statistically significant, being −1.01 (95% CI −2.32 to 0.30) and −0.38 (95% CI −1.23 to 0.47) log2 difference for PRNT90 and PRNT50 titers, respectively, and 0.06 (95% CI −0.24 to 0.36) difference for ELISA OD values, compared to younger age groups. Most patients with severe disease were treated with corticosteroids. There was apparently no significant independent effect of corticosteroid use on peak antibody titers, although statistical power was suboptimal. We had serial longitudinal sera available from a subset of 70 patients. The numbers of longitudinal sera from the asymptomatic infections were too limited for accurate curve fitting. The longitudinal data from 61 patients (149 sera) with severe and mild disease are shown in Fig. 3 with a Weibull curve fitted to the data. As with the aggregate data, we see that patients with severe disease had higher peak PRNT90 and PRNT50 titers, peaking later than mild infections. From the fitted curve, we estimate that it takes 282 and 297 days for PRNT90 titers to drop to 1:10 for severe and mild patients, respectively. Similarly, it takes 365 and 435 days for PRNT50 titers to drop to 1:10 for severe and mild patients.
Data on spike RBD IgG ELISA were available on 231 sera collected from 150 patients (Fig. 4). Of 209 sera collected from day 15 to 209 after onset of illness, all were positive in the RBD ELISA assay (Supplementary Table 3). Individual ELISA optical density (OD) readings are not quantitative in a manner comparable with PRNT titers, with loss of linearity when OD readings go above 2.0. Extrapolation of the Weibull curve fitted to the aggregate data of severe, mild, and asymptomatic individuals suggests that it takes 448, 337, and 105 days, respectively, for ELISA OD450 values to drop to the negative cut-off value (Fig. 4). Longitudinal data from 134 sera from 54 patients with severe or mild disease are shown (Fig. 3) and it is estimated that the RBD ELISA will be negative by approximately 495 and 416 days in severe and mild patients, respectively. The number of longitudinal sera from the asymptomatic individuals were too few to give reliable estimates.
The correlation of PRNT90 and PRNT50 antibody titers with ELISA OD450 is shown in (Supplementary Fig. 1). There is saturation of OD450 readings once the OD goes above 2.0, leading to a loss of linearity at higher antibody titers.
The kinetics and duration of neutralizing antibody responses of individuals with SARS-CoV-2 infection is required for understanding a key correlate of protection from reinfection and disease. Plaque reduction neutralization tests are the “gold-standard” for assessing neutralizing antibody titers with 50% reduction of plaque numbers (PRNT50) being an established end-point for assessing the serum neutralizing titre. We have determined both the 50% (PRNT50) as well as the more stringent 90% (PRNT90) plaque reduction endpoints to assess neutralizing antibody titers. We found that almost all individuals in our cohort sampled from day 15 to day 209 days after onset of illness had detectable PRNT90 and PRNT50 antibody. Importantly, 99.1% of 115 sera collected ≥61 days after onset of illness remained antibody positive in both PRNT90 and PRNT50 assays. We fitted a Weibull curve to the data to allow us to compare the antibody peak and waning kinetics of those with severe, mild, and asymptomatic infections. As previously reported, patients with severe illness had higher peak titers of PRNT90 and PRNT50 antibody than did those with mild illness or those with asymptomatic infection17,19,20. It is noteworthy that individuals with asymptomatic infection also developed PRNT antibody titers apparently comparable with those with mild illness, but the small numbers of sera tested led to wider confidence bounds. To test the hypothesis that older adults may have lower antibody responses, we investigated the effect of older age on antibody responses, adjusting for disease severity and duration of illness. To our surprise, we found that those aged >60 years had significantly higher mean ELISA antibody responses compared to younger age groups with this difference not reaching statistical significance for the PRNT90 and PRNT50 antibody titers. Thus, it does not appear that age compromises antibody immune responses to natural infection.
In typical antibody responses, titers peak at around 30–40 days after onset of illness followed by a biexponential waning of antibody titers. There is a period of rapid waning associated with the contraction by apoptosis of the initial pool of antigen specific B cells as the infection has subsided. This is followed by a slower wane of antibody titers, thereafter with the antibody levels being maintained by antigen specific long-lived plasma cells in the bone marrow24,25. Our data do not allow us to capture this second phase of the slower antibody waning kinetics for which we need more data in later time periods (beyond day 200) after onset of disease. Therefore our estimates of antibody waning, influenced heavily by the early phase rapid of waning, are likely to be overly conservative.
Antibody reactive to the receptor binding domain of SARS-CoV-1 remained detectable for at least 3 years follow-up with 95% of the convalescent patients being seropositive at 3 years of post-infection7,26. The data on neutralizing antibody responses for MERS-CoV has similarities and differences with what is observed here for SARS-CoV-2. While most patients with severe MERS developed strong antibody responses that were long-lasted, a proportion of those with mild infection had very weak or no antibody responses27,28. Seasonal human coronaviruses 229E, OC43, HKU1, and NL63 generally cause mild upper respiratory disease and reinfections with the same are common, with median of approximately 30 months between them, although reinfection can occur at intervals as short as 6 months apart associated with rapid antibody waning29. Experimental challenge of human volunteers with 229E has demonstrated antibody waning but detectable antibody at the end of one year although such antibody did not prevent experimentally rechallenged volunteers from developing symptomatic reinfection30.
Limitations of our study are that we have few sera beyond 200 days after onset of symptoms to define the late antibody waning kinetics. We also have relatively fewer numbers of asymptomatic infections (n = 31) compared to those with mild disease (n = 151). Thus, our findings on asymptomatic infections need to be interpreted with caution. Since the focus of our study was the kinetics of neutralizing antibody, we did not carry out titrations to define the end-points in our spike RBD ELISA IgG antibody assays; our data being OD values at a single serum dilution (1/100).
In summary, our findings of neutralizing antibody responses in SARS-CoV-2 infections are comparable to what is observed with SARS and other some other viral infections. It is likely that neutralizing antibody will be maintained over the first year after mild or severe disease with higher antibody titers and longer duration of detectable antibody in those with severe disease. It is important to note that even once neutralizing antibody levels have dropped below the detectable threshold, that immune memory will lead to rapid anamnestic antibody responses following re-exposure to the virus, and these are likely to be protective against severe disease. It is also noted that antibody may not confer sterilizing immunity but may prevent from reinfection leading to severe disease. A recent case of asymptomatic SARS-CoV-2 reinfection in a person, who failed to develop neutralizing antibody following his first infection is relevant in this regard31,32. Investigation of further cases of reinfection in regard to immune responses and onward transmission will be revealing.
An observational study was carried out on a cohort of one hundred and ninety five individuals with symptomatic or asymptomatic RT-PCR confirmed SARS-CoV-2 infections from the Princess Margaret, Prince of Wales, Queen Elizabeth and Queen Mary hospitals of the Hospital Authority of Hong Kong consented to participate in this study. Patient recruitment commenced on 21st January 2020 and continued until 31st July 2020. Recruited patients were followed up to 22th September 2020. Written informed consent was obtained and the studies were approved by the institutional review boards of the respective hospitals, viz. Kowloon West Cluster (KW/EX-20-039 (144-27)), Kowloon Central/Kowloon East cluster (KC/KE-20-0154/ER2) and HKU/HA Hong Kong West Cluster (UW 20-273). Clinical management of adult and pediatric patients was decided by the attending clinicians based on the standard of care as recommended by the Central Committee on Infectious Diseases and Emergency Response (CCIDER) of the Hospital Authority of Hong Kong, as revised periodically since February 2020. The antivirals used were interferon, lopinavir/ritonavir (Kaletra) or ribavirin, used individually or in combination.
Plaque reduction neutralization test (PRNT)
Vero E6 cells (ATCC CRL-1586) were maintained in Dulbecco’s Modified Eagle Medium (DMEM) medium supplemented with 10% fetal bovine serum (FBS) and 100 U/ml of penicillin–streptomycin. The assay was performed in duplicate using 24-well tissue culture plates (TPP Techno Plastic Products AG, Trasadingen, Switzerland) in a biosafety level 3 facility. Serial dilutions of each serum sample was incubated with 30–40 plaque-forming units of virus for 1 h at 37 °C. The virus-serum mixtures were added onto pre-formed Vero E6 cell monolayers and incubated for 1 h at 37 °C in 5% CO2 incubator. The cell monolayer was then overlaid with 1% agarose in cell culture medium and incubated for 3 days, at which time the plates were fixed and stained. Antibody titers were defined as the highest serum dilution that resulted in ≥90% (PRNT90) reduction or >50% (PRNT50) in the number of virus plaques. This method has been extensively validated on SARS-CoV-2 infected and control sera previously16.
SARS-CoV-2 spike receptor binding domain ELISA
Ninety-six-well ELISA plates (Nunc MaxiSorp, Thermo Fisher Scientific) were coated overnight with 100 ng per well of the purified recombinant RBD protein in PBS buffer. The plates were then blocked with 100 μl of Chonblock blocking/sample dilution ELISA buffer (Chondrex Inc, Redmon, US) and incubated at room temperature for 2 h. Each serum or plasma sample was tested in duplicate at a dilution of 1:100 in Chonblock blocking/sample dilution ELISA buffer and 100 µl was added to the wells of each plate for 2 h incubation at 37 °C. After extensive washing with PBS containing 0.1% Tween 20, horseradish peroxidase (HRP)-conjugated goat anti-human IgG (1:5000, GE Healthcare) was added for 1 h at 37 °C. The ELISA plates were then washed five times with PBS containing 0.1% Tween 20. Subsequently, 100 μl of HRP substrate (Ncm TMB One; New Cell and Molecular Biotech Co. Ltd, Suzhou, China) was added into each well. After 15 min incubation, the reaction was stopped by adding 50 μl of 2 M H2SO4 solution and analysed on a Sunrise (Tecan, Männedorf, Switzerland) absorbance microplate reader at 450 nm wavelength. Normalized results were obtained by calculating the difference between the OD of the purified recombinant protein-coated well and the PBS-coated well. The method was previously validated and reported16.
We presented PRNT90, PRNT50 log titers, and ELISA OD values by severe, mild, and asymptomatic SARS-CoV-2 infections. Nonlinear mixed effects model with Weibull curves were fitted to the data, to model the initial increase, and decay over time and accounted for the correlation among measurements from the same patients. The 95% confidence intervals were constructed using parametric bootstrap based on the estimated values and variance–covariance matrix of the parameters, with 1000 resamples. Based on the fitted Weibull curve, we extrapolated to the time when PRNT titers reach 1:10 and ELISA reaches the negative cut-off threshold. We also presented a subset of the COVID-19 cases where longitudinal data was available. We tested the potential differences in mean antibody response by age for severe and mild cases respectively, using generalized additive mixed effects model accounting for temporal change in antibody response, and use of corticosteroids, using cubic spline function for the antibody response. We also calculated the spearman correlation between PRNT90/PRNT50 titers and ELISA OD values in those sera when paired data were available.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The source data (individual anonymized patient and linked laboratory data) are provided as a Source Data file available on line. Source data are provided with this paper.
Addetia, A. et al. Neutralizing antibodies correlate with protection from SARS-CoV-2 in humans during a fishery vessel outbreak with high attack rate. J Clin Microbiol. https://doi.org/10.1128/JCM.02107-20 (2020).
Huang, A. T. et al. A systematic review of antibody mediated immunity to coronaviruses: antibody kinetics, correlates of protection, and association of antibody responses with severity of disease. medRxiv. https://doi.org/10.1101/2020.04.14.20065771 (2020).
Valkenburg, S. A. et al. The hurdles from bench to bedside in the realization and implementation of a universal influenza vaccine. Front. Immunol. 9, 1479 (2018).
Hobson, D., Curry, R. L., Beare, A. S. & Ward-Gardner, A. The role of serum haemagglutination-inhibiting antibody in protection against challenge infection with influenza A2 and B viruses. J. Hyg. 70, 767–777 (1972).
Cowling, B. J. et al. Influenza hemagglutination-inhibition antibody titer as a mediator of vaccine-induced protection for influenza B. Clin. Infect. Dis. 68, 1713–1717 (2019).
Gilbert, P. B. et al. HAI and NAI titer correlates of inactivated and live attenuated influenza vaccine efficacy. BMC Infect. Dis. 19, 453 (2019).
Liu, L. et al. Longitudinal profiles of immunoglobulin G antibodies against severe acute respiratory syndrome coronavirus components and neutralizing activities in recovered patients. Scand. J. Infect. Dis. 43, 515–521 (2011).
Le Bert, N. et al. SARS-CoV-2-specific T cell immunity in cases of COVID-19 and SARS, and uninfected controls. Nature 584, 457–462 (2020).
Buchholz, U. J. et al. Contributions of the structural proteins of severe acute respiratory syndrome coronavirus to protective immunity. Proc. Natl Acad. Sci. USA 101, 9804–9809 (2004).
Chan, J. F. et al. Simulation of the clinical and pathological manifestations of Coronavirus Disease 2019 (COVID-19) in golden Syrian hamster model: implications for disease pathogenesis and transmissibility. Clin. Infect. Dis. https://doi.org/10.1093/cid/ciaa325 (2020).
Chandrashekar, A. et al. SARS-CoV-2 infection protects against rechallenge in rhesus macaques. Science 369, 812–817 (2020).
Yu, J. et al. DNA vaccine protection against SARS-CoV-2 in rhesus macaques. Science 369, 806–811 (2020).
Lim, W. W., Leung, N. H. L., Sullivan, S. G., Tchetgen Tchetgen, E. J. & Cowling, B. J. Distinguishing causation from correlation in the use of correlates of protection to evaluate and develop influenza vaccines. Am. J. Epidemiol. 189, 185–192 (2020).
Zost, S. J. et al. Potently neutralizing and protective human antibodies against SARS-CoV-2. Nature 584, 443–449 (2020).
Food and Drug Administration, USA. FDA issues emergency use authorization for convalescent plasma as potential promising COVID–19 treatment, another achievement in administration’s fight against pandemic. https://www.fda.gov/news-events/press-announcements/fda-issues-emergency-use-authorization-convalescent-plasma-potential-promising-covid-19-treatment. (2020).
Perera, R. A. et al. Serological assays for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), March 2020. Eur. Surveill. 25, 2000421 (2020).
Wang, Y. et al. Kinetics of viral load and antibody response in relation to COVID-19 severity. J. Clin. Invest. https://doi.org/10.1172/JCI138759 (2020).
Wu, F. et al. Neutralizing antibody responses to SARS-CoV-2 in a COVID-19 recovered 2 patient cohort and their implications. medRxiv. https://doi.org/10.1101/2020.03.30.20047365.
Seow, J. et al. Longitudinal evaluation and decline of antibody responses in 1 SARS-CoV-2 infection. Nature Microbiology 5, 1598–1607 (2020).
Liu, L. et al. High neutralizing antibody titer in intensive care unit patients with COVID-19. Emerg. Microbes Infect. 9, 1664–1670 (2020).
Long, Q. X. et al. Clinical and immunological assessment of asymptomatic SARS-CoV-2 infections. Nat. Med. 26, 1200–1204 (2020).
Robbiani, D. F. et al. Convergent antibody responses to SARS-CoV-2 in convalescent individuals. Nature 584, 437–442 (2020).
Ju, B. et al. Human neutralizing antibodies elicited by SARS-CoV-2 infection. Nature 584, 115–119 (2020).
Fairfax, K. A., Kallies, A., Nutt, S. L. & Tarlinton, D. M. Plasma cell development: from B-cell subsets to long-term survival niches. Semin. Immunol. 20, 49–58 (2008).
Van Twillert, I. et al. Impact of age and vaccination history on long term serological responses after symptomatic B. pertussis infection, a high dimensional data analysis. Sci. Rep. 7, 40328 (2017).
Cao, Z. et al. Potent and persistent antibody responses against the receptor-binding domain of SARS-CoV spike protein in recovered patients. Virol. J. 7, 299 (2010).
Choe, P. G. et al. MERS-CoV antibody responses 1 year after symptom onset, South Korea, 2015. Emerg. Infect. Dis. 23, 1079–1084 (2017).
Zhao, J. et al. Recovery from the Middle East respiratory syndrome is associated with antibody and T-cell responses. Sci. Immunol. 2, eaan5393 (2017).
Edridge, A. W. D. et al. Seasonal coronavirus protective immunity is short-lasting. Nat. Med. https://doi.org/10.1038/s41591-020-1083-1. (2020).
Callow, K. A., Parry, H. F., Sergeant, M. & Tyrrell, D. A. The time course of the immune response to experimental coronavirus infection of man. Epidemiol. Infect. 105, 435–446 (1990).
To, K. K. et al. COVID-19 re-infection by a phylogenetically distinct SARS-coronavirus-2 strain confirmed by whole genome sequencing. Clin Infect Dis. https://doi.org/10.1093/cid/ciaa1275 (2020).
Chan, P. K. S. et al. Serologic responses in healthy adult with SARS-CoV-2 reinfection. Emerg Infect Dis. in press.
The study was supported by the Health and Medical Research Fund—Commissioned Research on the Novel Coronavirus Disease (COVID-19) (reference nos. COVID190126) from the Food and Health Bureau, Hong Kong SAR Government and U.S. National Institutes of Health (Contract No. HHSN272201400006C).
The authors declare no competing interests.
Peer review information Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Lau, E.H.Y., Tsang, O.T.Y., Hui, D.S.C. et al. Neutralizing antibody titres in SARS-CoV-2 infections. Nat Commun 12, 63 (2021). https://doi.org/10.1038/s41467-020-20247-4
This article is cited by
BMC Medicine (2022)
Scientific Reports (2022)
A single intranasal dose of human parainfluenza virus type 3-vectored vaccine induces effective antibody and memory T cell response in the lungs and protects hamsters against SARS-CoV-2
npj Vaccines (2022)
Seroprevalence of SARS-CoV-2 spike IgG antibodies after the second BNT162b2 mRNA vaccine in Japanese kidney transplant recipients
Scientific Reports (2022)
Nature Communications (2022)