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
. 2024 Feb;22(2):75-88.
doi: 10.1038/s41579-023-01001-1. Epub 2023 Dec 19.

Clinical course and management of COVID-19 in the era of widespread population immunity

Affiliations
Review

Clinical course and management of COVID-19 in the era of widespread population immunity

Eric A Meyerowitz et al. Nat Rev Microbiol. 2024 Feb.

Abstract

The clinical implications of COVID-19 have changed since SARS-CoV-2 first emerged in humans. The current high levels of population immunity, due to prior infection and/or vaccination, have been associated with a vastly decreased overall risk of severe disease. Some people, particularly those with immunocompromising conditions, remain at risk for severe outcomes. Through the course of the pandemic, variants with somewhat different symptom profiles from the original SARS-CoV-2 virus have emerged. The management of COVID-19 has also changed since 2020, with the increasing availability of evidence-based treatments in two main classes: antivirals and immunomodulators. Selecting the appropriate treatment(s) for patients with COVID-19 requires a deep understanding of the evidence and an awareness of the limitations of applying data that have been largely based on immune-naive populations to patients today who most likely have vaccine-derived and/or infection-derived immunity. In this Review, we provide a summary of the clinical manifestations and approaches to caring for adult patients with COVID-19 in the era of vaccine availability and the dominance of the Omicron subvariants, with a focus on the management of COVID-19 in different patient groups, including immunocompromised, pregnant, vaccinated and unvaccinated patients.

PubMed Disclaimer

References

    1. Lewnard, J. A. et al. Clinical outcomes associated with SARS-CoV-2 Omicron (B.1.1.529) variant and BA.1/BA.1.1 or BA.2 subvariant infection in southern California. Nat. Med. 28, 1933–1943 (2022). - PubMed - PMC - DOI
    1. Nyberg, T. et al. Comparative analysis of the risks of hospitalisation and death associated with SARS-CoV-2 Omicron (B.1.1.529) and Delta (B.1.617.2) variants in England: a cohort study. Lancet 399, 1303–1312 (2022). - PubMed - PMC - DOI
    1. Esper, F. P. et al. Alpha to Omicron: disease severity and clinical outcomes of major SARS-CoV-2 variants. J. Infect. Dis. 227, 344–352 (2023). - PubMed - DOI
    1. Abu-Raddad, L. J., Chemaitelly, H. & Bertollini, R.; National Study Group for COVID-19 Epidemiology. Severity of SARS-CoV-2 reinfections as compared with primary infections. N. Engl. J. Med. 385, 2487–2489 (2021). - PubMed - DOI
    1. Britton, A. et al. Effectiveness of COVID-19 mRNA vaccines against COVID-19-associated hospitalizations among immunocompromised adults during SARS-CoV-2 Omicron predominance—VISION network, 10 states, December 2021–August 2022. MMWR Morb. Mortal. Wkly. Rep. 71, 1335–1342 (2022). - PubMed - PMC - DOI

LinkOut - more resources