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Status: Bibliographieeintrag

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Verfasst von:Bauer, Yvonne [VerfasserIn]   i
 Jäger, Claudia [VerfasserIn]   i
 Kramer, Michael D. [VerfasserIn]   i
 Wallich, Reinhard [VerfasserIn]   i
Titel:Phenotype and function of antigen-presenting dendritic cells generated from peripheral blood monocytes
Verf.angabe:Y. Bauer, C. Jäger, M.D. Kramer, R. Wallich
Jahr:1999
Umfang:4 S.
Fussnoten:Gesehen am 01.03.2021
Titel Quelle:Enthalten in: Transfusion medicine and hemotherapy
Ort Quelle:Basel : Karger, 2003
Jahr Quelle:1999
Band/Heft Quelle:26(1999), 2, Seite 115-118
ISSN Quelle:1660-3818
Abstract:Background: Dendritic cells (DC) are specialized for the primary activation of helper and cytotoxic T cells and have therefore been denominated ‘professional’ antigen-presenting cells. Their potent antigen-presenting capacity qualifies these cells as a promising tool in vaccination protocols, in particular in the induction of tumor-specific immunity. Functionally active DC can be generated from peripheral blood monocytes in vitro. Consequently, these cells gained interest in the field of transfusion medicine. Material and Methods: Here we describe a simplified protocol for the generation of large numbers of DC from peripheral blood monocytes and their phenotype and function. DC were generated from CD14+ monocytes by culture in the presence of granulocyte-macrophage colony stimulating factor (GM-CSF) and interleukin-4 (IL-4). Results: On day 7 of culture the expression of the surface markers CD1a, CD80 and HLA-DR was upregulated, whereas CD14 and CD64 were almost completely downregulated, compared to day 0. Moreover, the in vitro generated DC were shown to induce antigen-specific proliferation of autologous T cells after pulsing with tetanus toxoid. Conclusion: The presented protocol allows to generate large numbers of DC for immunotherapy and vaccination.
DOI:doi:10.1159/000053474
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://dx.doi.org/10.1159/000053474
 Volltext: https://www.karger.com/Article/FullText/53474
 DOI: https://doi.org/10.1159/000053474
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1750002159
Verknüpfungen:→ Zeitschrift

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