Severity of SARS-CoV-2 infection is linked to double-negative (CD27- IgD-) B cell subset numbers

Inflamm Res. 2022 Jan;71(1):131-140. doi: 10.1007/s00011-021-01525-3. Epub 2021 Nov 30.

Abstract

Objectives: The role of B cells in COVID-19, beyond the production of specific antibodies against SARS-CoV-2, is still not well understood. Here, we describe the novel landscape of circulating double-negative (DN) CD27- IgD- B cells in COVID-19 patients, representing a group of atypical and neglected subpopulations of this cell lineage.

Methods: Using multiparametric flow cytometry, we determined DN B cell subset amounts from 91 COVID-19 patients, correlated those with cytokines, clinical and laboratory parameters, and segregated them by principal components analysis.

Results: We detected significant increments in the DN2 and DN3 B cell subsets, while we found a relevant decrease in the DN1 B cell subpopulation, according to disease severity and patient outcomes. These DN cell numbers also appeared to correlate with pro- or anti-inflammatory signatures, respectively, and contributed to the segregation of the patients into disease severity groups.

Conclusion: This study provides insights into DN B cell subsets' potential role in immune responses against SARS-CoV-2, particularly linked to the severity of COVID-19.

Keywords: B cell; COVID-19; DN B cell; Inflammation.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • B-Lymphocytes / cytology
  • COVID-19 / blood*
  • COVID-19 / diagnosis
  • COVID-19 / immunology*
  • COVID-19 / virology
  • Cell Lineage
  • Computational Biology
  • Disease Progression
  • Female
  • Humans
  • Immunoglobulin D / blood*
  • Male
  • Middle Aged
  • Principal Component Analysis
  • Prognosis
  • Respiration, Artificial
  • SARS-CoV-2*
  • Severity of Illness Index
  • Tumor Necrosis Factor Receptor Superfamily, Member 7 / blood*
  • Young Adult

Substances

  • Immunoglobulin D
  • Tumor Necrosis Factor Receptor Superfamily, Member 7