Severe COVID-19 is a T cell immune dysregulatory disorder triggered by SARS-CoV-2

Expert Rev Clin Immunol. 2022 Jun;18(6):557-565. doi: 10.1080/1744666X.2022.2074403. Epub 2022 May 26.

Abstract

Introduction: COVID-19 has had a calamitous impact on the global community. Apart from at least 6 M deaths, hundreds of millions have been infected and a much greater number have been plunged into poverty. Vaccines have been effective but financial and logistical challenges have hampered their rapid global deployment. Vaccine disparities have allowed the emergence of new SARS-CoV-2 variants including delta and omicron, perpetuating the pandemic.

Areas covered: The immunological response to SARS-CoV-2 is now better understood. Many of the clinical manifestations of severe disease are a consequence of immune dysregulation triggered by the virus. This may explain the lack of efficacy of antiviral treatments, such as convalescent plasma infusions, given later in the disease.

Expert opinion: T cells play a crucial role in both the outcome of COVID-19 as well as the protective response to vaccines. Vaccines do not prevent infection but reduce the risk of a chaotic and destructive cellular immune response to the virus. Severe COVID-19 should be considered a virus-induced secondary immune dysregulatory disorder of cellular immunity, with broad host susceptibility. This perspective of COVID-19 will lead to better diagnostic tests, vaccines, and therapeutic strategies in the future.

Keywords: COVID-19; Omicron; SARS-CoV2; Vaccines; immunodeficiency; plasma therapy.

MeSH terms

  • COVID-19 Serotherapy
  • COVID-19* / therapy
  • Humans
  • Immune System Diseases*
  • Immunization, Passive
  • SARS-CoV-2
  • T-Lymphocytes
  • Vaccines*

Substances

  • Vaccines

Supplementary concepts

  • SARS-CoV-2 variants