Antibody response to mRNA SARS-CoV-2 vaccines in haemodialysis patients

Author:

Paal Michael1,Arend Florian M1,Lau Tobias2,Hasmann Sandra3,Soreth-Rieke Daniela4,Sorodoc-Otto Johanna5,Beuthien Wilke5,Krappe Julia3,Toepfer Marcell6,Gersdorff Gero von7,Thaller Norbert4,Rau Simon2,Northoff Bernd1ORCID,Teupser Daniel1,Bruegel Mathias1,Fischereder Michael3,Schönermarck Ulf3

Affiliation:

1. Institute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany

2. Dialysezentrum Bad Tölz und Wolfratshausen, Bad Tölz, Germany

3. Department of Medicine IV, University Hospital, LMU Munich, Munich, Germany

4. KfH-Nierenzentrum Miesbach, Miesbach, Germany

5. KfH-Nierenzentrum Germering, Germering, Germany

6. Dialysezentrum Garmisch-Partenkirchen-Murnau-Weilheim, Murnau am Staffelsee, Germany

7. Programm “Qualität in der Nephrologie” (QiN), KfH—Kuratorium für Dialyse und Nierentransplantation, Neu-Isenburg, Germany

Abstract

Abstract Background Some studies have shown an attenuated immune response in haemodialysis patients after vaccination. The present study examines the humoral response after mRNA vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a large population of haemodialysis patients from different outpatient dialysis centres. Methods We retrospectively assessed antibodies against SARS-CoV-2 spike protein and nucleocapsid protein (chemiluminescence immunoassays, Roche diagnostics) 3–6 weeks after the second mRNA vaccine dose in 179 maintenance haemodialysis and 70 non-dialysis patients (control cohort). Differences in anti-SARS-CoV-2 spike protein titers were statistically analysed with respect to patient-relevant factors, including age, gender, previous coronavirus disease 2019 (COVID-19) infection, systemic immunosuppressive therapy and time on dialysis. Results We found a favourable, but profoundly lower SARS-CoV-2 spike protein antibody response in comparison with a non-dialysis cohort (median 253.5 versus 1756 U/mL, P < 0.001). In multivariate analysis, previous COVID-19 infection (P < 0.001) and female gender were associated with a significantly higher vaccine response (P = 0.006) in haemodialysis patients, while there was a significant inverse correlation with increasing patient age and systemic immunosuppression (P < 0.001). There was no statistically significant correlation between the antibody titer and time on dialysis. Immune response in haemodialysis patients with a previous COVID-19 infection led to substantially higher antibody titers that were equal to those of vaccinated non-dialysis individuals with previous infection. Conclusion We strongly argue in favour of regular antibody testing after COVID-19 vaccination in haemodialysis patients. Further studies should elucidate the utility of booster vaccinations to foster a stronger and persistent antibody response.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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