| Literature DB >> 17321896 |
Caroline Zentz1, Martina Wiesner, Stephen Man, Bernhard Frankenberger, Barbara Wollenberg, Peter Hillemanns, Reinhard Zeidler, Wolfgang Hammerschmidt, Andreas Moosmann.
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 10(6) 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.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17321896 DOI: 10.1016/j.humimm.2006.12.004
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850