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BRIEF RESEARCH REPORT article

Front. Public Health

Sec. Infectious Diseases: Epidemiology and Prevention

Volume 13 - 2025 | doi: 10.3389/fpubh.2025.1523733

This article is part of the Research Topic Chronic Hepatitis B Management: Current Status and Future Directions View all 14 articles

"Immunogenicity and Predictive Factors of Hepatitis B Vaccination with Fendrix® in Chronic Kidney Disease Patients"

Provisionally accepted
Cristina Hernan-Garcia Cristina Hernan-Garcia 1,2Daniel Leonardo Sanchez-Carmona Daniel Leonardo Sanchez-Carmona 1*Lucia Czestochowa Mateo-Otero Lucia Czestochowa Mateo-Otero 3Virginia Fernández-Espinilla Virginia Fernández-Espinilla 1,2Paula Andrea Rodríguez Ducuara Paula Andrea Rodríguez Ducuara 1Jose Javier Castrodeza-Sanz Jose Javier Castrodeza-Sanz 1,2Camino Prada-García Camino Prada-García 2,4
  • 1 Hospital Clínico Universitario de Valladolid, Valladolid, Spain
  • 2 University of Valladolid, Valladolid, Spain
  • 3 Hospital Universitario Río Hortega, Valladolid, Spain
  • 4 Complejo Asistencial Universitario de León (CHLeon), Leon, Spain

The final, formatted version of the article will be published soon.

    Hepatitis B virus (HBV) infection and chronic kidney disease (CKD) pose major global health challenges. CKD patients face a heightened risk of HBV infection, worsening their prognosis. This study evaluated the immune response to hepatitis B vaccination in CKD patients, the persistence of antibodies, and factors influencing vaccine efficacy.A retrospective study was conducted on 173 CKD patients (2014173 CKD patients ( -2019) ) receiving routine vaccination at the Hospital Clínico Universitario de Valladolid, Spain. (ZIP Code:47003) Patients were immunized with Fendrix® on a 0-1-2-6-month schedule, and verbal informed consent was obtained. A protective response was defined as Anti-HBs >10 IU/L, and a robust response as >100 IU/L. Overall, 90.8% achieved a protective response. Age was not a significant predictor (p=0.137) between non-responders and protective or robust responders. 32.95% of patients died during follow-up. A robust response at the end of vaccination cycle was associated with higher antibody titers at 12 months (p=0.002) but not at 24 (p=0.550) or 36 months (p=0.739). Kaplan-Meier analysis estimated median antibody duration as 26.5 months (Anti-HBs>10IU/L) and 25.4 months (Anti-HBs>100IU/L). A delay in vaccination compared to the recommended schedule was observed (one-sample Wilcoxon test, p < 0.001).Fendrix® effectively induces protective immunity in CKD patients, but a robust early response does not ensure long-term persistence. The decline in antibody levels suggests the need for booster doses and periodic antibody monitoring to optimize long-term protection. Suboptimal vaccination adherence may reflect the inherent complexities of real-world clinical practice.

    Keywords: Chronic Kidney Disease, Hepatitis B Vaccine (HBV), Vaccination, Dialysis, Observational

    Received: 06 Nov 2024; Accepted: 10 Mar 2025.

    Copyright: © 2025 Hernan-Garcia, Sanchez-Carmona, Mateo-Otero, Fernández-Espinilla, Rodríguez Ducuara, Castrodeza-Sanz and Prada-García. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Daniel Leonardo Sanchez-Carmona, Hospital Clínico Universitario de Valladolid, Valladolid, Spain

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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