Duration of Effective Antibody Levels After COVID-19
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Duration of Effective Antibody Levels After COVID-19 Andrea T. Cruz, MD, MPH,a Steven L. Zeichner, MD, PhDb After having coronavirus disease levels of nAbs and that these levels 2019 (COVID-19), patients develop a remained high for the duration of humoral immune response thought their 7- to 8-month follow-up period. to protect against reinfection, but In contrast, lower nAb levels and antibody levels can decline over more transient nAb responses were time. Understanding how long seen in school-aged children and antibody levels remain high enough adults. to prevent infection is important in understanding, absent vaccination, These findings are intriguing for whether children may be vulnerable several reasons. First, nAbs persisted to COVID-19 and in modeling how in younger children at high levels for COVID-19 spreads through the several months. This is in contrast to population. the experience with both adults and a Department of Pediatrics, Baylor College of Medicine, with non–SARS-CoV-2 coronavirus Houston, Texas; and bDepartments of Pediatrics and The levels of antibodies capable of infections. In one study, researchers Microbiology, Immunology, and Cancer Biology, School of neutralizing the virus (neutralizing found that after COVID-19, only one- Medicine, University of Virginia, Charlottesville, Virginia antibodies [nAbs]) provide a direct third of adults had detectable nAbs Dr Cruz conceptualized the commentary, drafted the marker of a protective humoral and, even in those patients, nAb initial commentary, and reviewed and revised the immune response. The nAbs can be levels decayed rapidly over a few manuscript; Dr Zeichner critically reviewed and revised the manuscript for important intellectual content; and measured directly by determining months.5 For non–SARS-CoV-2 all authors approved the final manuscript as submitted how well a patient’s serum coronaviruses, nAbs wane within and agree to be accountable for all aspects of the work. inactivates virus when a known several months of infection, resulting Opinions expressed in these commentaries are those of amount of virus is placed on cells in in repetitive infections by many the authors and not necessarily those of the American tissue culture, which is known as a Academy of Pediatrics or its Committees. coronaviruses that cause a significant plaque reduction neutralization test. DOI: https://doi.org/10.1542/peds.2021-052589 fraction of viruses causing common The remarkably safe and effective colds.6 Reasons for the enhanced Accepted for publication Jun 8, 2021 approved COVID-19 vaccines elicit persistence of nAbs in younger Address correspondence to: Andrea T. Cruz, Department of potent antibody responses against Pediatrics, Baylor College of Medicine, 6621 Fannin St, Suite children is unclear. One explanation A2210, Houston, TX 77030. E-mail: acruz@bcm.edu portions of the virus mediating may be that the immune response in PEDIATRICS (ISSN Numbers: Print, 0031-4005; Online, attachment to host cells and viral 1098-4275). adults, who have had repetitive entry, the spike protein and its Copyright © 2021 by the American Academy of Pediatrics receptor-binding domain. The exposure to endemic coronaviruses, may target these previous viruses FINANCIAL DISCLOSURE: The authors have indicated concentration of antibodies a patient they have no financial relationships relevant to this has against spike protein and and may not respond as easily to article to disclose. receptor-binding domain provides a SARS-CoV-2 as the relatively less FUNDING: No external funding. marker of susceptibility to infection experienced (and potentially more POTENTIAL CONFLICT OF INTEREST: Both authors are or reinfection.1–3 flexible) immune response seen in associate editors for Pediatrics. young children. This concept is called COMPANION PAPER: A companion to this article can be In their study in Pediatrics, Bonfante original antigenic sin.7 Although found online at www.pediatrics.org/cgi/doi/10.1542/ peds.2021-052173. et al4 report that preschool-aged original antigenic sin may result in a children with asymptomatic or more robust response to viral strains previously encountered, antibodies To cite: Cruz AT, Zeichner SL. Duration of Effective mildly symptomatic severe acute Antibody Levels After COVID-19. Pediatrics. respiratory syndrome coronavirus 2 made against a newly encountered 2021;148(3):e2021052589 (SARS-CoV-2) infection had high coronavirus in patients who have Downloaded from www.aappublications.org/news by guest on September 15, 2021 PEDIATRICS Volume 148, number 3, September 2021:e2021052589 COMMENTARY
had many coronavirus infections that nAb levels are highly patient to control SARS-CoV-2.13 To may bind suboptimally to strains correlated with immunity.10 The fully understand the durability with more antigenic drift. mean nAb levels seen after immune responses of children to vaccination are higher than levels COVID-19 and how these differ The ability to generate an immune seen in convalescent adults.10,11 from those in adults, it will be response in younger children was Levels of nAbs decay with time, so necessary to describe pediatric not contingent on illness severity. In the efficacy of a vaccine will not long-term, cell-mediated immune adults, several studies have shown remain static over time. This may responses in addition to humoral that antibody responses were higher be a reason that boosters will be responses. in more severely ill than in mildly ill necessary, and boosters may also patients.8 Given that up to 50% of be needed to target newer SARS- Although many aspects of what children with SARS-CoV-2 have CoV-2 variants for which existing comprises an effective immune subclinical or mild symptoms,9 the vaccines may provide inadequate response to SARS-CoV-2 require ability to mount an immune additional study, the work of protection. Another reason for response that yields good nAb levels Bonfante et al advances our previously infected individuals to for at least several months is understanding, demonstrating a be vaccinated is that nAbs are only reassuring because vaccines remain more durable (and likely effective) part of the host immune response. unavailable to younger children. response in younger children. Immunoprotection may stem from Even after vaccines are approved for Because children constitute an other arms of the immune system, the youngest children, barriers to important contribution to the some of which may be more vaccine uptake (including vaccine spread of COVID-19 through the durable (eg, memory B-cell or T- hesitancy and logistic barriers to population,13 knowledge of the cell responses). For example, in widespread global distribution) potential susceptibility of children one study, researchers evaluated mean that many children will not to reinfection is important in how immunity to endemic benefit from vaccination in the near modeling COVID-19 epidemiology. future. As such, the data presented coronaviruses may impact host in this study suggest that reinfection response to SARS-CoV-2. They may be a less common occurrence, found that, although there was little evidence of cross-reactive ABBREVIATIONS given the magnitude and durability SARS-CoV-2 serum antibodies, COVID-19: coronavirus disease of the antibody response. preexisting memory B cells were 2019 This does not mean that children activated during SARS-CoV-2 nAb: neutralizing antibody who have already had SARS-CoV-2 infection.12 The study by Bonfante SARS-CoV-2: severe acute should remain unimmunized once et al was focused on the patients’ respiratory vaccines are approved for younger antibody responses to SARS-CoV-2, syndrome children. Recent data from but it is important to remember coronavirus 2 vaccinated individuals and that cellular immunity plays an convalescent adult cohorts indicate important role in the ability of a REFERENCES disease severity in COVID-19 patients: a seasonal human coronaviruses and 1. Dispinseri S, Secchi M, Pirillo MF, et al. retrospective study. Emerg Microbes implications for the SARS-CoV-2 pan- Neutralizing antibody responses to SARS- Infect. 2021;10(1):664–676 demic: a retrospective study in Stock- CoV-2 in symptomatic COVID-19 is persis- 4. Bonfante F, Costenaro P, Cantarutti A, et holm, Sweden, 2009-2020. J Clin Virol. tent and critical for survival. Nat Com- al. Mild SARS-CoV-2 infections and neu- 2021;136:104754 mun. 2021;12(1):2670 tralizing antibody titers. Pediatrics. 7. Francis T. On the doctrine of original 2. Lucas C, Klein J, Sundaram ME, et al. 2021;148(3):e2021052173 antigenic sin. Proc Am Philos Soc. Delayed production of neutralizing anti- 5. Aziz NA, Corman VM, Echterhoff AKC, et 1960;104(6):572–578 bodies correlates with fatal COVID-19 al. Seroprevalence and correlates of 8. Cervia C, Nilsson J, Zurbuchen Y, et al. [published online ahead of print May 5, SARS-CoV-2 neutralizing antibodies Systemic and mucosal antibody 2021]. Nat Med. doi:10.1038/s41591-021- from a population-based study in responses specific to SARS-CoV-2 during 01355-0 Bonn, Germany. Nat Commun. mild versus severe COVID-19. J Allergy 3. Guo L, Wang Y, Kang L, et al. Cross-reac- 2021;12(1):2117 Clin Immunol. 2021;147(2):545–557.e9 tive antibody against human coronavirus 6. Dyrdak R, Hodcroft EB, Wahlund M, Neher 9. Soriano-Arandes A, Gatell A, Serrano P, et OC43 spike protein correlates with RA, Albert J. Interactions between al. Household SARS-CoV-2 transmission Downloaded from www.aappublications.org/news by guest on September 15, 2021 2 CRUZ and ZEICHNER
and children: a network prospective [published online ahead of print May 17, 12. Song G, He W-T, Callaghan S, et al. Cross- study [published online ahead of print 2021]. Nat Med. doi:10.1038/s41591-021- reactive serum and memory B-cell March 12, 2021]. Clin Infect Dis. 01377-8 responses to spike protein in SARS-CoV-2 doi:10.1093/cid/ciab228 11. Widge AT, Rouphael NG, Jackson LA, et al; and endemic coronavirus infection. Nat 10. Khoury DS, Cromer D, Reylandi A, et al. mRNA-1273 Study Group. Durability of Commun. 2021;12(1):2938 Neutralizing antibody levels are highly responses after SARS-CoV-2 mRNA-1273 13. Sette A, Crotty S. Adaptive immunity to predictive of immune protection from vaccination. N Engl J Med. SARS-CoV-2 and COVID-19. Cell. symptomatic SARS-CoV-2 infection 2021;384(1):80–82 2021;184(4):861–880 PEDIATRICS Volume 148, number 3,Downloaded September from 2021 www.aappublications.org/news by guest on September 15, 2021 3
Duration of Effective Antibody Levels After COVID-19 Andrea T. Cruz and Steven L. Zeichner Pediatrics 2021;148; DOI: 10.1542/peds.2021-052589 originally published online June 22, 2021; Updated Information & including high resolution figures, can be found at: Services http://pediatrics.aappublications.org/content/148/3/e2021052589 References This article cites 10 articles, 1 of which you can access for free at: http://pediatrics.aappublications.org/content/148/3/e2021052589#BI BL Subspecialty Collections This article, along with others on similar topics, appears in the following collection(s): Infectious Disease http://www.aappublications.org/cgi/collection/infectious_diseases_su b Vaccine/Immunization http://www.aappublications.org/cgi/collection/vaccine:immunization _sub Permissions & Licensing Information about reproducing this article in parts (figures, tables) or in its entirety can be found online at: http://www.aappublications.org/site/misc/Permissions.xhtml Reprints Information about ordering reprints can be found online: http://www.aappublications.org/site/misc/reprints.xhtml Downloaded from www.aappublications.org/news by guest on September 15, 2021
Duration of Effective Antibody Levels After COVID-19 Andrea T. Cruz and Steven L. Zeichner Pediatrics 2021;148; DOI: 10.1542/peds.2021-052589 originally published online June 22, 2021; The online version of this article, along with updated information and services, is located on the World Wide Web at: http://pediatrics.aappublications.org/content/148/3/e2021052589 Pediatrics is the official journal of the American Academy of Pediatrics. A monthly publication, it has been published continuously since 1948. Pediatrics is owned, published, and trademarked by the American Academy of Pediatrics, 345 Park Avenue, Itasca, Illinois, 60143. Copyright © 2021 by the American Academy of Pediatrics. All rights reserved. Print ISSN: 1073-0397. Downloaded from www.aappublications.org/news by guest on September 15, 2021
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