Deficiency of Tfh Cells and Germinal Center in Deceased COVID-19 Patients

Curr Med Sci. 2020 Aug;40(4):618-624. doi: 10.1007/s11596-020-2225-x. Epub 2020 Aug 29.

Abstract

The COVID-19 pandemic caused by SARS-CoV2 is characterized by a remarkable variation in clinical severity ranging from a mild illness to a fatal multi-organ disease. Understanding the dysregulated human immune responses in the fatal subjects is critical for management of COVID-19 patients and the pandemic. In this study, we examined the immune cell compositions in the lung tissues and hilar lymph nodes using immunohistochemistry on 6 deceased COVID-19 patients and 4 focal organizing pneumonia (FOP) patients who underwent lung surgery and served as controls. We found a dominant presence of macrophages and a general deficiency of T cells and B cells in the lung tissues from deceased COVID-19 patients. In contrast to the FOP patients, Tfh cells and germinal center formation were largely absent in the draining hilar lymph nodes in the deceased COVID-19 patients. This was correlated with reduced IgM and IgG levels compared to convalescent COVID-19 patients. In summary, our data highlight a defect of germinal center structure in deceased COVID-19 patients leading to an impaired humoral immunity. Understanding the mechanisms of this deficiency will be one of the key points for the management of this epidemic.

Keywords: COVID-19; T follicular helper cells; germinal center; immune responses.

Publication types

  • Case Reports

MeSH terms

  • Adaptive Immunity
  • Aged
  • Aged, 80 and over
  • Betacoronavirus*
  • COVID-19
  • Case-Control Studies
  • China / epidemiology
  • Coronavirus Infections / immunology*
  • Coronavirus Infections / mortality
  • Coronavirus Infections / pathology
  • Fatal Outcome
  • Female
  • Germinal Center / immunology*
  • Germinal Center / pathology
  • Humans
  • Lymphopenia / immunology
  • Lymphopenia / mortality
  • Lymphopenia / pathology
  • Macrophages / immunology
  • Macrophages / pathology
  • Male
  • Middle Aged
  • Pandemics
  • Pneumonia, Viral / immunology*
  • Pneumonia, Viral / mortality
  • Pneumonia, Viral / pathology
  • SARS-CoV-2
  • T-Lymphocytes, Helper-Inducer / immunology*
  • T-Lymphocytes, Helper-Inducer / pathology