Cellular Immunity in COVID-19 Convalescents with PCR-Confirmed Infection but with Undetectable SARS-CoV-2-Specific IgG

Emerg Infect Dis. 2021 Jan;27(1). doi: 10.3201/2701.203772. Epub 2020 Oct 15.

Abstract

We investigated immune responses against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) among a group of convalescent, potential blood donors in Germany who had PCR-confirmed SARS-CoV-2 infection. Sixty days after onset of symptoms, 13/78 (17%) study participants had borderline or negative results to an ELISA detecting IgG against the S1 protein of SARS-CoV-2. We analyzed participants with PCR-confirmed infection who had strong antibody responses (ratio >3) as positive controls and participants without symptoms of SARS-CoV-2 infection and without household contact with infected patients as negative controls. Using interferon-γ ELISpot, we observed that 78% of PCR-positive volunteers with undetectable antibodies showed T cell immunity against SARS-CoV-2. We observed a similar frequency (80%) of T-cell immunity in convalescent donors with strong antibody responses but did not detect immunity in negative controls. We concluded that, in convalescent patients with undetectable SARS-CoV-2 IgG, immunity may be mediated through T cells.

Keywords: B cells; COVID-19; ELISpot; PCR-confirmed infection; SARS; SARS-CoV-2; T cells; cellular immunity; convalescent plasma; coronavirus disease; respiratory infections; seronegativity; severe acute respiratory syndrome; severe acute respiratory syndrome coronavirus 2; viruses; zoonoses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antibodies, Viral / blood
  • Antibody Specificity*
  • Blood Donors
  • COVID-19 / immunology*
  • COVID-19 / virology
  • Enzyme-Linked Immunospot Assay / methods
  • Female
  • Humans
  • Immunity, Cellular / physiology*
  • Immunoglobulin G / blood*
  • Interferon-gamma
  • Male
  • Middle Aged
  • Polymerase Chain Reaction
  • SARS-CoV-2*
  • T-Lymphocytes / physiology*

Substances

  • Antibodies, Viral
  • Immunoglobulin G
  • Interferon-gamma