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MHC multimer-guided and cell culture-independent isolation of functional T cell receptors from single cells facilitates TCR identification for immunotherapy

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Item Type:Article
Title:MHC multimer-guided and cell culture-independent isolation of functional T cell receptors from single cells facilitates TCR identification for immunotherapy
Creators Name:Dössinger, G. and Bunse, M. and Bet, J. and Albrecht, J. and Paszkiewicz, P.J. and Weißbrich, B. and Schiedewitz, I. and Henkel, L. and Schiemann, M. and Neuenhahn, M. and Uckert, W. and Busch, D.H.
Abstract:Adoptive therapy using T cells redirected to target tumor- or infection-associated antigens is a promising strategy that has curative potential and broad applicability. In order to accelerate the screening process for suitable antigen-specific T cell receptors (TCRs), we developed a new approach circumventing conventional in vitro expansion-based strategies. Direct isolation of paired full-length TCR sequences from non-expanded antigen-specific T cells was achieved by the establishment of a highly sensitive PCR-based T cell receptor single cell analysis method (TCR-SCAN). Using MHC multimer-labeled and single cell-sorted HCMV-specific T cells we demonstrate a high efficacy (approximately 25%) and target specificity of TCR-SCAN receptor identification. In combination with MHC-multimer based pre-enrichment steps, we were able to isolate TCRs specific for the oncogenes Her2/neu and WT1 even from very small populations (original precursor frequencies of down to 0.00005% of CD3(+) T cells) without any cell culture step involved. Genetic re-expression of isolated receptors demonstrates their functionality and target specificity. We believe that this new strategy of TCR identification may provide broad access to specific TCRs for therapeutically relevant T cell epitopes.
Keywords:alpha-beta T-Cell Antigen Receptors, Amino Acid Sequence, Cell Culture Techniques, Cytomegalovirus, Epitopes, Gene Transfer Techniques, HEK293 Cells, Histocompatibility Antigens, Immunotherapy, Jurkat Cells, Molecular Sequence Data, Neoplasm Antigens, Polymerase Chain Reaction, Protein Multimerization, Protein Sequence Analysis, Single-Cell Analysis, Species Specificity, T-Cell Antigen Receptors, Transgenes, Animals, Mice
Source:PLoS ONE
ISSN:1932-6203
Publisher:Public Library of Science (U.S.A.)
Volume:8
Number:4
Page Range:e61384
Date:26 April 2013
Official Publication:https://doi.org/10.1371/journal.pone.0061384
PubMed:View item in PubMed

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