Reduced virus specific T helper cell induction by autologous dendritic cells in patients with chronic hepatitis B-restoration by exogenous interleukin-12

التفاصيل البيبلوغرافية
العنوان: Reduced virus specific T helper cell induction by autologous dendritic cells in patients with chronic hepatitis B-restoration by exogenous interleukin-12
المؤلفون: S. Herzog-Hauff, Peter R. Galle, Helga Bernhard, Stefan Rose-John, W. O. Böcher, Hanns F. Löhr, Sabine Pingel
المصدر: Web of Science
مصطلحات موضوعية: Recombinant Fusion Proteins, T cell, Immunology, Antigen presentation, Biology, Hepatitis B, Chronic, Immune system, Antigen, Clinical Studies, Tetanus Toxoid, medicine, Humans, Immunology and Allergy, Cells, Cultured, Antigen Presentation, Lymphokines, Stem Cell Factor, Hepatitis B Surface Antigens, Interleukin-6, Granulocyte-Macrophage Colony-Stimulating Factor, Cell Differentiation, Convalescence, Dendritic Cells, T-Lymphocytes, Helper-Inducer, T helper cell, Dendritic cell, Hepatitis B, medicine.disease, Hepatitis B Core Antigens, Interleukin-12, Virology, Coculture Techniques, medicine.anatomical_structure, Interleukin 12
الوصف: SUMMARYInsufficient stimulatory capacities of autologous dendritic cells (DC) may contribute in part to impaired T cell stimulation and therefore viral persistence in patients with chronic hepatitis B virus (HBV) infection. In order to characterize the antigen presenting functions of DC from chronic HBV carriers and controls antigen specific T cell responses were analysed. CD34+ peripheral blood progenitor cells were differentiated to immature DC in the presence of GM-CSF, IL-6/IL-6R fusion protein and stem cell factor. Proliferative CD4+ T cell responses and specific cytokine release were analysed in co-cultures of DC pulsed with HBV surface and core antigens or tetanus toxoid and autologous CD4+ T cells. Cultured under identical conditions DC from chronic HBV carriers, individuals with acute resolved hepatitis B and healthy controls expressed similar phenotypical markers but chronic HBV carriers showed less frequent and weaker HBV antigen specific proliferative T helper cell responses and secreted less interferon-γ while responses to the tetanus toxoid control antigen was not affected. Preincubation with recombinant IL-12 enhanced the HBV specific immune reactivities in chronic HBV patients and controls. In conclusion, the weak antiviral immune responses observed in chronic hepatitis B may result in part from insufficient T cell stimulating capacities of DC. Immunostimulation by IL-12 restored the HBV antigen specific T cell responses and could have some therapeutical benefit to overcome viral persistence.
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e46eaed0b814ebb1b71d5b8b115af760
https://publons.com/wos-op/publon/7105301/
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....e46eaed0b814ebb1b71d5b8b115af760
قاعدة البيانات: OpenAIRE