Patients receiving hemodialysis do not lose SARS-CoV-2 antibodies more rapidly than non-renal controls: a prospective cohort study

Ren Fail. 2022 Dec;44(1):392-398. doi: 10.1080/0886022X.2022.2042310.

Abstract

Background: Patients with end-stage kidney disease receiving maintenance hemodialysis (HD) are at increased risk for mortality after infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) compared with the general population. However, it is currently unknown whether the long-term SARS-CoV-2 humoral and cellular immune responses in patients receiving HD are comparable to individuals with normal kidney function.

Method: The prospective cohort study included 24 patients treated with maintenance HD and 27 non-renal controls with confirmed history of coronavirus disease (COVID-19). In all participants the levels of specific IgG were quantified at three timepoints: 10, 18, and 26 weeks from disease onset. In a subgroup of patients, specific T-cell responses were evaluated.

Results: The seropositivity rate declined in controls over time and was 85% and 70.4% at weeks 18 and 26, respectively. All HD patients remained seropositive over the study period. Seropositivity rate at week 26 was greater among patients receiving HD: RR = 1.4 [95%CI: 1.17-1.94] (reciprocal of RR = 0.7 [95% CI: 0.52-0.86]), p = 0.0064. In both groups, IgG levels decreased from week 10 to week 26, but antibodies vanished more rapidly in controls than in HD group (ANOVA p = 0.0012). The magnitude of T-cell response was significantly lower in controls than in HD patients at weeks 10 (p = 0.019) and 26 (p = 0.0098) after COVID-19 diagnosis, but not at week 18.

Conclusion: Compared with non-renal adults, patients receiving HD maintain significant long-term humoral and cellular immune responses following natural COVID-19.

Keywords: COVID-19; SARS-CoV-2; antibody; cellular immunity; hemodialysis.

Publication types

  • Video-Audio Media

MeSH terms

  • Adult
  • Antibodies, Viral / blood*
  • COVID-19 / immunology*
  • Case-Control Studies
  • Humans
  • Immunity, Cellular
  • Immunity, Humoral
  • Immunoglobulin G / blood*
  • Kidney Failure, Chronic / immunology*
  • Kidney Failure, Chronic / therapy*
  • Middle Aged
  • Prospective Studies
  • Renal Dialysis*
  • Risk Factors
  • SARS-CoV-2
  • T-Lymphocytes / immunology

Substances

  • Antibodies, Viral
  • Immunoglobulin G

Grants and funding

The study was entirely funded by the Saint Petersburg State University Hospital.