T cell response against SARS-CoV-2 persists after one year in patients surviving severe COVID-19

EBioMedicine. 2022 Apr:78:103967. doi: 10.1016/j.ebiom.2022.103967. Epub 2022 Mar 27.

Abstract

Background: In critically ill COVID-19 patients, the initial response to SARS-CoV-2 infection is characterized by major immune dysfunctions. The capacity of these severe patients to mount a robust and persistent SARS-CoV-2 specific T cell response despite the presence of severe immune alterations during the ICU stay is unknown.

Methods: Critically ill COVID-19 patients were sampled five times during the ICU stay and 9 and 13 months afterwards. Immune monitoring included counts of lymphocyte subpopulations, HLA-DR expression on monocytes, plasma IL-6 and IL-10 concentrations, anti-SARS-CoV-2 IgG levels and T cell proliferation in response to three SARS-CoV-2 antigens.

Findings: Despite the presence of major lymphopenia and decreased monocyte HLA-DR expression during the ICU stay, convalescent critically ill COVID-19 patients consistently generated adaptive and humoral immune responses against SARS-CoV-2 maintained for more than one year after hospital discharge. Patients with long hospital stays presented with stronger anti-SARS-CoV-2 specific T cell response but no difference in anti-SARS-CoV2 IgG levels.

Interpretation: Convalescent critically ill COVID-19 patients consistently generated a memory immune response against SARS-CoV-2 maintained for more than one year after hospital discharge. In recovered individuals, the intensity of SARS-CoV-2 specific T cell response was dependent on length of hospital stay.

Funding: This observational study was supported by funds from the Hospices Civils de Lyon, Fondation HCL, Claude Bernard Lyon 1 University and Région Auvergne Rhône-Alpes and by partial funding by REACTing (Research and ACTion targeting emerging infectious diseases) INSERM, France and a donation from Fondation AnBer (http://fondationanber.fr/).

Keywords: Critically ill patients; HLA-DR; Immune memory; SARS-CoV-2; Sepsis; T lymphocyte.

Publication types

  • Observational Study

MeSH terms

  • Antibodies, Viral / blood
  • COVID-19* / immunology
  • Critical Illness
  • HLA-DR Antigens
  • Humans
  • Immunoglobulin G / blood
  • Immunologic Memory*
  • SARS-CoV-2
  • T-Lymphocytes* / immunology

Substances

  • Antibodies, Viral
  • HLA-DR Antigens
  • Immunoglobulin G