Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Mar 19:12:654165.
doi: 10.3389/fimmu.2021.654165. eCollection 2021.

Immunity to SARS-CoV-2: Lessons Learned

Affiliations
Review

Immunity to SARS-CoV-2: Lessons Learned

Jaime Fergie et al. Front Immunol. .

Abstract

In the year since the emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and with understanding of the etiology of the coronavirus disease 2019 (COVID-19) pandemic, it has become clear that most infected individuals achieve some form of immunity against the virus with relatively few reported reinfections. A number of vaccines have already achieved emergency use authorization based on data from large phase 3 field efficacy clinical trials. However, our knowledge about the extent and durability of this immunity, and the breadth of vaccine coverage against SARS-CoV-2 variants is still evolving. In this narrative review, we summarize the latest and rapidly developing understanding of immunity to SARS-CoV-2 infection, including what we have learned about the key antigens of SARS-CoV-2 (i.e., the spike protein and its receptor-binding domain), their importance in vaccine development, the immediate immune response to SARS-CoV-2, breadth of coverage of emerging SARS-CoV-2 variants, contributions of preexisting immunity to related coronaviruses, and duration of immunity. We also discuss lessons from newer approaches, such as systems serology, that provide insights into molecular and cellular immune responses elicited and how they relate to the trajectory of infection, and potentially inform immune correlates of protection. We also briefly examine the limited research literature on immune responses in special populations, such as pregnant women and children.

Keywords: COVID-19; SARS-CoV-2; duration of protection; immunity; receptor-binding domain; spike protein; systems serology; vaccination.

PubMed Disclaimer

Conflict of interest statement

The authors declare that this study received funding from Pfizer Inc. The funder had the following involvement in the study: Editorial/medical writing support. JF is a speaker for Pfizer and a consultant/advisory board member for Pfizer and GlaxoSmithKline. AS is a Pfizer employee and may hold stock or stock options.

Figures

Figure 1
Figure 1
Summary of our current knowledge of immunity to SARS-CoV-2. ADE, antibody-dependent enhancement; COVID-19, coronavirus disease 2019; RBD, receptor-binding domain; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.

Similar articles

Cited by

References

    1. Lu R, Zhao X, Li J, Niu P, Yang B, Wu H, et al. . Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet. (2020) 395:565–74. 10.1016/S0140-6736(20)30251-8 - DOI - PMC - PubMed
    1. World Health Organization . WHO Director-General's opening remarks at the media briefing on COVID-19 – 11 March 2020. (2020). Available online at: https://www.who.int/dg/speeches/detail/who-director-general-s-opening-re... (accessed October 23, 2020).
    1. World Health Organization . Coronavirus Disease (COVID-19) Dashboard. (2021). Available online at: https://covid19.who.int/ (accessed February 15, 2021).
    1. Poland GA, Ovsyannikova IG, Kennedy RB. SARS-CoV-2 immunity: review and applications to phase 3 vaccine candidates. Lancet. (2020) 396:1595–606. 10.1016/S0140-6736(20)32137-1 - DOI - PMC - PubMed
    1. Zumla A, Chan JF, Azhar EI, Hui DS, Yuen KY. Coronaviruses - drug discovery and therapeutic options. Nat Rev Drug Discov. (2016) 15:327–47. 10.1038/nrd.2015.37 - DOI - PMC - PubMed

Publication types

Substances