Investigation of the frequencies of various B cell populations in non-responder healthcare workers in comparison with responders to hepatitis B virus vaccination.


Journal

Transactions of the Royal Society of Tropical Medicine and Hygiene
ISSN: 1878-3503
Titre abrégé: Trans R Soc Trop Med Hyg
Pays: England
ID NLM: 7506129

Informations de publication

Date de publication:
01 Sep 2023
Historique:
received: 18 01 2023
revised: 12 03 2023
accepted: 18 03 2023
medline: 23 10 2023
pubmed: 14 4 2023
entrez: 13 4 2023
Statut: ppublish

Résumé

Hepatitis B is a major global health problem. More than 90% of hepatitis B-vaccinated immunocompetent adults become fully immune. The main purpose of vaccination is immunization. Whether non-responders have a lower percentage of total or antigen-specific memory B cells in comparison with responders is still controversial. We aimed to assess and compare the frequency of various B cell subpopulations in non-responders and responders. Fourteen responders and 14 non-responders of hospital healthcare workers were enrolled in this study. We used flow cytometry to evaluate various CD19+ B cell subpopulations using fluorescent-labeled antibodies against CD19, CD10, CD21, CD27 and IgM and ELISA to evaluate total anti-HBs antibodies. We found no significant differences in the frequency of various B cell subpopulations between the non-responder and responder groups. Furthermore, the frequency of the isotype-switched memory B cell population was significantly higher in the atypical memory B cell subset compared with the classical memory B cell subset in the responder and total groups (p=0.010 and 0.003, respectively). Responders and non-responders to HBsAg vaccine had comparable memory B cell populations. Whether anti-HBs Ab production has a correlation with the level of class switching in B lymphocytes in healthy vaccinated individuals needs further investigation.

Sections du résumé

BACKGROUND BACKGROUND
Hepatitis B is a major global health problem. More than 90% of hepatitis B-vaccinated immunocompetent adults become fully immune. The main purpose of vaccination is immunization. Whether non-responders have a lower percentage of total or antigen-specific memory B cells in comparison with responders is still controversial. We aimed to assess and compare the frequency of various B cell subpopulations in non-responders and responders.
METHODS METHODS
Fourteen responders and 14 non-responders of hospital healthcare workers were enrolled in this study. We used flow cytometry to evaluate various CD19+ B cell subpopulations using fluorescent-labeled antibodies against CD19, CD10, CD21, CD27 and IgM and ELISA to evaluate total anti-HBs antibodies.
RESULTS RESULTS
We found no significant differences in the frequency of various B cell subpopulations between the non-responder and responder groups. Furthermore, the frequency of the isotype-switched memory B cell population was significantly higher in the atypical memory B cell subset compared with the classical memory B cell subset in the responder and total groups (p=0.010 and 0.003, respectively).
CONCLUSIONS CONCLUSIONS
Responders and non-responders to HBsAg vaccine had comparable memory B cell populations. Whether anti-HBs Ab production has a correlation with the level of class switching in B lymphocytes in healthy vaccinated individuals needs further investigation.

Identifiants

pubmed: 37052149
pii: 7116938
doi: 10.1093/trstmh/trad016
doi:

Substances chimiques

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

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

628-636

Subventions

Organisme : Shiraz University of Medical Sciences
ID : 18582

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene.

Auteurs

Sara Karimi (S)

Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.

Fereshteh Mehdipour (F)

Institute for Cancer Research, School of Medicine, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.

Jamal Sarvari (J)

Department of Bacteriology and Virology, School of Medicine, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.
Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.

Mohammad Reza Ataollahi (MR)

Department of Immunology, School of Medicine, Fasa University of Medical Sciences, Fasa 7134845794, Iran.

Amin Ramezani (A)

Institute for Cancer Research, School of Medicine, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.

Seppo Meri (S)

Department of Bacteriology & Immunology and the Translational Immunology Research Program (TRIMM), University of Helsinki, PO Box 21, Helsinki, Finland.

Kurosh Kalantar (K)

Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.
Autoimmune Diseases Research Center, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.

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