The survival of B cells is compromised in kidney disease

Nat Commun. 2024 Dec 30;15(1):10842. doi: 10.1038/s41467-024-55187-w.

Abstract

Antibody-mediated protection against pathogens is crucial to a healthy life. However, the recent SARS-CoV-2 pandemic has shown that pre-existing comorbid conditions including kidney disease account for compromised humoral immunity to infections. Individuals with kidney disease are not only susceptible to infections but also exhibit poor vaccine-induced antibody response. Using multiple mouse models of kidney disease, we demonstrate that renal dysfunction inhibits germinal center (GC) response against T-dependent antigens. GC B cells exhibit increased apoptosis in kidney disease. Uremic toxin hippuric acid drives loss of mitochondrial membrane potential, leading to increased apoptosis of GC B cells in a G-protein-coupled receptor 109A dependent manner. Finally, GC B cells and antibody titer are diminished in mice with kidney disease following influenza virus infection, a major cause of mortality in individuals with renal disorders. These results provide a mechanistic understanding of how renal dysfunction suppresses humoral immunity in patients with kidney disease.

MeSH terms

  • Animals
  • Apoptosis* / immunology
  • B-Lymphocytes* / immunology
  • COVID-19* / complications
  • COVID-19* / immunology
  • Cell Survival
  • Disease Models, Animal
  • Female
  • Germinal Center / immunology
  • Humans
  • Immunity, Humoral*
  • Kidney Diseases* / immunology
  • Kidney Diseases* / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Orthomyxoviridae Infections / immunology
  • SARS-CoV-2 / immunology