No Improvement of Hepatitis B Vaccination Response in Patients Dialysed with a Polymethylmethacrylate Membrane Compared to High-Flux Polysulfone: Results of the HEPADIAL Study.


Journal

Blood purification
ISSN: 1421-9735
Titre abrégé: Blood Purif
Pays: Switzerland
ID NLM: 8402040

Informations de publication

Date de publication:
2020
Historique:
received: 14 06 2019
accepted: 10 10 2019
pubmed: 14 11 2019
medline: 1 5 2021
entrez: 14 11 2019
Statut: ppublish

Résumé

An altered immune response and decreased vaccine response are observed in patients with chronic renal failure. A preliminary study of 15 non-immunised patients, despite appropriate previous hepatitis B vaccination, showed a 60% seroconversion rate after 3 months of dialysis with a polymethylmethacrylate (PMMA) membrane. This response was associated with circulating soluble CD40 (CD40s) decrease, a natural inhibitor of the humoral immune response. The aim of the study is to confirm these results in a randomised study. We conducted a multicentre randomised intention-to-treat superiority clinical trial comparing polysulfone and a PMMA membrane in 2 parallel patient groups. The primary end point was the vaccine response rate, as defined by an anti-HBs antibodies titre of >10 IU/L, 1 month after the last vaccination with a double dose of Engerix B20®, performed at weeks 12, 16, 20, and 36. Twenty-five patients were randomised and included in an intention-to-treat analysis. They were dialysed on polysulfone (n = 11) or PMMA (n = 14) for 40 weeks. Fifty percent of the PMMA patients versus 54.5% of the polysulfone patients achieved seroconversion (p = 1.00). The median anti-HBs antibody titre in responders at week 40 was 496 (92-750) versus 395 (43-572) UI/mL for PMMA and polysulfone, respectively (p = 0.46). The median CD40s titre at week 12 was 306 (193-448) versus 491 (281-515) pg/mL (p = 0.21). The CD40s median variation between week 0 and week 12 was 5 (-105 to 90) versus 64 (-63 to 123) pg/mL (p = 0.55). The CD40s level at week 12 in non-responders was slightly inferior to that of the responders: median 193 (168-331) versus 413 (281-512) pg/mL (p = 0.08). We did not observe a better vaccine response with the PMMA membrane compared to high-flux polysulfone. The PMMA membrane did not decrease the CD40s more than the polysulfone membrane probably because the titre was previously low in the 2 groups.

Sections du résumé

BACKGROUND
An altered immune response and decreased vaccine response are observed in patients with chronic renal failure. A preliminary study of 15 non-immunised patients, despite appropriate previous hepatitis B vaccination, showed a 60% seroconversion rate after 3 months of dialysis with a polymethylmethacrylate (PMMA) membrane. This response was associated with circulating soluble CD40 (CD40s) decrease, a natural inhibitor of the humoral immune response. The aim of the study is to confirm these results in a randomised study.
METHODS
We conducted a multicentre randomised intention-to-treat superiority clinical trial comparing polysulfone and a PMMA membrane in 2 parallel patient groups. The primary end point was the vaccine response rate, as defined by an anti-HBs antibodies titre of >10 IU/L, 1 month after the last vaccination with a double dose of Engerix B20®, performed at weeks 12, 16, 20, and 36.
RESULTS
Twenty-five patients were randomised and included in an intention-to-treat analysis. They were dialysed on polysulfone (n = 11) or PMMA (n = 14) for 40 weeks. Fifty percent of the PMMA patients versus 54.5% of the polysulfone patients achieved seroconversion (p = 1.00). The median anti-HBs antibody titre in responders at week 40 was 496 (92-750) versus 395 (43-572) UI/mL for PMMA and polysulfone, respectively (p = 0.46). The median CD40s titre at week 12 was 306 (193-448) versus 491 (281-515) pg/mL (p = 0.21). The CD40s median variation between week 0 and week 12 was 5 (-105 to 90) versus 64 (-63 to 123) pg/mL (p = 0.55). The CD40s level at week 12 in non-responders was slightly inferior to that of the responders: median 193 (168-331) versus 413 (281-512) pg/mL (p = 0.08).
CONCLUSION
We did not observe a better vaccine response with the PMMA membrane compared to high-flux polysulfone. The PMMA membrane did not decrease the CD40s more than the polysulfone membrane probably because the titre was previously low in the 2 groups.

Identifiants

pubmed: 31722332
pii: 000504035
doi: 10.1159/000504035
doi:

Substances chimiques

CD40 Antigens 0
Hepatitis B Antibodies 0
Hepatitis B Vaccines 0
Membranes, Artificial 0
Polymers 0
Sulfones 0
polysulfone P 1700 25135-51-7
Polymethyl Methacrylate 9011-14-7

Banques de données

ClinicalTrials.gov
['NCT01066559']

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

265-271

Informations de copyright

© 2019 S. Karger AG, Basel.

Auteurs

Valérie de Précigout (V)

Department of Nephrology-Transplantation-Dialysis-Apheresis, Bordeaux University Hospital, Bordeaux, France, valerie.deprecigout@chu-bordeaux.fr.

Christine Germain (C)

Clinical Epidemiology Unit, Bordeaux University Hospital, Bordeaux, France.

Antoine Benard (A)

Clinical Epidemiology Unit, Bordeaux University Hospital, Bordeaux, France.

Adeline Lacraz (A)

Department of Nephrology-Haemodialysis, Hospital of the Basque Coast, Bayonne, France.

Philippe Chauveau (P)

AURAD Aquitaine, Gradignan, France.

Carole Deprele (C)

Department of Nephrology-Dialysis, Hospital of North Ardèche, Annonay, France.

Bruno Seigneuric (B)

Department of Nephrology and Organ Transplantation, Toulouse University Hospital, Toulouse, France.

Antoine Pommereau (A)

CTMR, Bordeaux, France.

Cécile Courivaud (C)

Department of Nephrology, Besançon University Hospital, Besançon, France.

Marine Douillet (M)

Department of Nephrology-Transplantation-Dialysis-Apheresis, Bordeaux University Hospital, Bordeaux, France.

Benjamin Taton (B)

Department of Nephrology-Transplantation-Dialysis-Apheresis, Bordeaux University Hospital, Bordeaux, France.

Christian Combe (C)

Department of Nephrology-Transplantation-Dialysis-Apheresis, Bordeaux University Hospital, Bordeaux, France.

Cécile Contin-Bordes (C)

Department of Immunology and Immunogenetics, Bordeaux University Hospital, Bordeaux, France.
CNRS-UMR5164 ImmunoConcEpT, Bordeaux University Hospital, Bordeaux, France.

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Classifications MeSH