Evaluation of the immune response to hepatitis B vaccine in patients on biological therapy: results of the RIER cohort study.


Journal

Clinical rheumatology
ISSN: 1434-9949
Titre abrégé: Clin Rheumatol
Pays: Germany
ID NLM: 8211469

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 05 11 2019
accepted: 10 03 2020
revised: 12 02 2020
pubmed: 6 4 2020
medline: 15 5 2021
entrez: 6 4 2020
Statut: ppublish

Résumé

To evaluate the response to hepatitis B virus (HBV) vaccine in patients on biological therapy. Adults with autoimmune inflammatory diseases on biological therapy such as anti-TNFα, rituximab, tocilizumab, abatacept, or anakinra were included. Hepatitis B surface antibody (anti-HBs) was measured by ELISA before and after vaccination. Seroconversion was considered when an anti-HBs titer > 10 mIU/mL was achieved. The effect of treatment on the immunoprotective state was studied. The response was compared with that obtained in patients on synthetic disease modifying anti-rheumatic drugs (DMARDs) and healthy controls. A total of 187 patients on biologicals, 48 on synthetic DMARDs, and 49 on healthy controls were analyzed. More than 80% of patients on biologics responded to the vaccine but required more boosters and second vaccine series. Patients who achieved seroconversion were younger than those who did not (47.10 ± 12.99 vs. 53.18 ± 10.54 years, p = 0.012). Being on etanercept or golimumab was associated with seroconversion, while being on rituximab was not. Seroconversion was achieved in 93.75% of patients on synthetic DMARDs and 97.96% of healthy controls. The seroconversion rate in the biologics group was lower than in the synthetic DMARD group (p = 0.043) and tended to be lower than in the healthy group (p = 0.056). In patients on biological therapy, a high rate of HBV vaccine response can be achieved when a complete vaccination schedule is administered. Vaccination while not on biological agents reduces the requirement for boosters and revaccination. Key points: • Patients on biological therapy can achieve high rates of immune response to HBV vaccine when complete vaccination schedules are administered. • However, to achieve such a high seroconversion rate, more boosters and second vaccination series are required. • This supports the proposal already made to provide HBV vaccination to all patients with an autoimmune inflammatory disease after the diagnosis is made and not when the use of a biological treatment is under consideration.

Identifiants

pubmed: 32248433
doi: 10.1007/s10067-020-05042-2
pii: 10.1007/s10067-020-05042-2
doi:

Substances chimiques

Hepatitis B Antibodies 0
Hepatitis B Surface Antigens 0
Hepatitis B Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2751-2756

Subventions

Organisme : Sociedad de Reumatología Comunidad de Madrid (SORCOM)/MSD
ID : 20141
Organisme : Pfizer
ID : NA

Références

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Auteurs

Patricia Richi (P)

Rheumatology Unit, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain. patricia.richi@salud.madrid.org.
Faculty of Biomedical and Health Sciences. Department of Medicine, Universidad Europea de Madrid, Madrid, Spain. patricia.richi@salud.madrid.org.

Oriol Alonso (O)

Internal Medicine Service, Hospital Comarcal Sant Jaume de Calella, Calella, Barcelona, Spain.

María Dolores Martín (MD)

Bacteriology Department, BR Salud Laboratories, San Sebastián de los Reyes, Madrid, Spain.

Laura González-Hombrado (L)

Rheumatology Unit, Hospital del Tajo, Aranjuez, Madrid, Spain.

Teresa Navío (T)

Rheumatology Unit, Hospital Universitario Infanta Leonor, Madrid, Spain.

Marina Salido (M)

Rheumatology Unit, Hospital Universitario Infanta Cristina, Parla, Madrid, Spain.

Jesús Llorente (J)

Pharmacy Department, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain.

Cristina Andreu-Vázquez (C)

Faculty of Biomedical and Health Sciences. Department of Medicine, Universidad Europea de Madrid, Madrid, Spain.

Cristina García-Fernández (C)

Preventive Medicine Department, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain.

Ana Jiménez-Diaz (A)

Rheumatology Unit, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain.

Leticia Lojo (L)

Rheumatology Unit, Hospital Universitario Infanta Leonor, Madrid, Spain.

Laura Cebrián (L)

Rheumatology Unit, Hospital Universitario Infanta Leonor, Madrid, Spain.

Israel Thuissard-Vasallo (I)

Faculty of Biomedical and Health Sciences. Department of Medicine, Universidad Europea de Madrid, Madrid, Spain.

María José Martínez de Aramayona (MJ)

Occupational Medicine Department, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain.

Tatiana Cobo (T)

Rheumatology Unit, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain.
Faculty of Biomedical and Health Sciences. Department of Medicine, Universidad Europea de Madrid, Madrid, Spain.

Marta García-Castro (M)

Rheumatology Unit, Hospital del Tajo, Aranjuez, Madrid, Spain.

Patricia Castro (P)

Rheumatology Unit, Hospital Universitario Infanta Cristina, Parla, Madrid, Spain.

Mónica Fernández-Castro (M)

Rheumatology Service, Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, Spain.

Óscar Illera (Ó)

Rheumatology Unit, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain.
Faculty of Biomedical and Health Sciences. Department of Medicine, Universidad Europea de Madrid, Madrid, Spain.

Martina Steiner (M)

Rheumatology Unit, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain.
Faculty of Biomedical and Health Sciences. Department of Medicine, Universidad Europea de Madrid, Madrid, Spain.

Santiago Muñoz-Fernández (S)

Rheumatology Unit, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain.
Faculty of Biomedical and Health Sciences. Department of Medicine, Universidad Europea de Madrid, Madrid, Spain.

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