Decreased percentage of memory B cells is independently associated with increased susceptibility to infection in patients on maintenance hemodialysis

Int Urol Nephrol. 2018 Nov;50(11):2081-2090. doi: 10.1007/s11255-018-1977-8. Epub 2018 Oct 1.

Abstract

Purpose: Infection is a common complication and cause of death in patients on maintenance hemodialysis (MHD). B lymphocytes, which are an important component of the immune system, play a significant role in defending against pathogen invasion. However, in patients on MHD, the connection between infection and B cell subsets remains largely unknown. Our study aims to clarify the potential role of the distribution of B cell subsets in the infection process in patients on MHD.

Methods: In this cross-sectional study, basic information was collected from 175 patients on MHD from July 2016 to July 2017 at Zhongshan Hospital, Fudan University. The distributions of the B cell subsets in patients with and without infection were analyzed using flow cytometry to determine the role of B lymphocyte subsets in the infection process in patients on MHD.

Results: Among the 175 patients, 45 suffered from infection. The respiratory tract was the most common infection site, accounting for 67.86% of all infections. After adjustment using multivariate logistic regression models, memory B cells [per 1% increase, odds ratio [95% confidence interval (CI)]: 0.949 (0.915, 0.984), P < 0.01], switched memory B cells [per 1% increase, odds ratio (95% CI): 0.939 (0.898, 0.982), P < 0.01], naïve B cells [per 1% increase, odds ratio (95% CI): 1.042 (1.009, 1.075), P < 0.05] and IgG titers [per 1 g/L increase, odds ratio (95% CI): 0.779 (0.630, 0.963), P < 0.05] were independent risk factors for infection in dialysis patients.

Conclusion: A decrease in memory B cells is independently associated with an increased risk of infection in patients on dialysis.

Keywords: B cell subsets; Hemodialysis; Immunoglobulin; Infection; Memory B cells.

MeSH terms

  • Aged
  • B-Lymphocytes*
  • Cross-Sectional Studies
  • Female
  • Humans
  • Incidence
  • Infections / blood
  • Infections / epidemiology*
  • Kidney Failure, Chronic / blood*
  • Kidney Failure, Chronic / complications
  • Kidney Failure, Chronic / therapy*
  • Logistic Models
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Renal Dialysis*
  • Risk Factors