Activated B Cells Mediate Efficient Expansion of Rare Antigen-Specific T Cells

Caroline Zentz, Martina Wiesner, Stephen Man, Bernhard Frankenberger, Barbara Wollenberg, Peter Hillemanns, Reinhard Zeidler, Wolfgang Hammerschmidt, Andreas Moosmann*

*Korrespondierende/r Autor/-in für diese Arbeit
14 Zitate (Scopus)

Abstract

Potent professional antigen-presenting cells (APC) are essential tools to activate and expand antigen-specific T cells in vitro for use in adoptive immunotherapy. CD40-activated B cells can be easily generated and propagated from human donors and have been successfully used to generate antigen-specific T-cell cultures. Here we show that CD40-activated B cells strongly and specifically expand rare populations of antigen-specific CD8 T cells, with frequencies of less than 1 in 20,000 CD8 T cells in peripheral blood. We focused on T cells recognizing an epitope from the human papillomavirus 16 (HPV-16) E7 protein. In 6 of 6 healthy donors, epitope-specific CD8+ T cells were found to be "rare" by this criterion, as shown by staining with human leukocyte antigen (HLA)/peptide multimers. Using peptide-loaded CD40-activated B cells, epitope-specific T cells could be selectively expanded in all donors up to 106 fold, and the resulting T-cell cultures contained up to 88% specific T cells. These results strongly encourage the use of CD40-stimulated B cells as APCs in immunotherapy.

OriginalspracheEnglisch
ZeitschriftHuman Immunology
Jahrgang68
Ausgabenummer2
Seiten (von - bis)75-85
Seitenumfang11
ISSN0198-8859
DOIs
PublikationsstatusVeröffentlicht - 02.2007

Fördermittel

We thank Chris Boswell and Julian Hickling (Cambridge, UK) for kindly providing vaccinia viruses (SR16 and Wyeth), and Gabriele Hollweck, Adam Slusarski and Sabine Eichenlaub (Munich, Germany) for assistance with TCR clonotyping. This study was supported by the Deutsche Forschungsgemeinschaft (SFB455) and H.W. & J. Hector-Stiftung.

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