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Hepatitis B vaccine responders show higher frequencies of CD8+ effector memory and central memory T cells compared to non-responders.
Vakili, Mahsa Eshkevar; Mashhadi, Niloofar; Ataollahi, Mohammad Reza; Meri, Seppo; Kabelitz, Dieter; Kalantar, Kurosh.
Afiliação
  • Vakili ME; Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Mashhadi N; Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Ataollahi MR; Department of Immunology, School of Medicine, Fasa University of Medical Sciences, Fasa, Iran.
  • Meri S; Department of Bacteriology and Immunology and the Translational Immunology Research Program (TRIMM), Helsinki University Hospital, The University of Helsinki and HUSLAB, Helsinki, Finland.
  • Kabelitz D; Institute of Immunology, Christian-Albrechts University of Kiel and University Hospital Schleswig, Holstein Campus Kiel, Kiel, Germany.
  • Kalantar K; Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Scand J Immunol ; : e13402, 2024 Aug 27.
Article em En | MEDLINE | ID: mdl-39189677
ABSTRACT
Hepatitis B (HB) infection is a major global health problem. There is limited knowledge about HB vaccination-induced immune memory responses. We compared the frequency of CD8+ memory T cell subsets between responders (RSs) and non-responders (NRs) to HB vaccination. Blood samples were collected from RSs and NRs. PBMCs were cultured in the presence of Hepatitis B surface antigens (HBsAg) and PHA for 48 h to restimulate CD8+ memory T cells and T cell memory subsets were detected by flow cytometry using memory cell markers. The frequency of TEM, TCM, and TCM hi was significantly higher in responders compared to non-responders (p = 0.024, 0.022, and 0.047, respectively). Additionally, we report a positive correlation between the frequency of TEM cells in RSs with age and anti-HBsAb level (p = 0.03 and rs = 0.5; p = 0.01 and rs = 0.06). Responders display a higher level of CD8+ T cell-mediated immunity. Therefore, we suggest a possible defect in the formation of immunological CD8+ memory T cells in NRs and it may reduce antibody production compared to the RSs, although more experiments are needed.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article