An efficient single‐cell based method for linking human T cell phenotype to T cell receptor sequence and specificity
Ilka Wahl, Sandro Hoffmann, Rebecca Hundsdorfer, Julia Puchan, Stephen L. Hoffman, Peter G. Kremsner, Benjamin Mordmüller, Christian E. Busse, Hedda Wardemann
Abstract
Abstract Single‐cell antigen‐receptor gene amplification and sequencing platforms have been used to characterize T cell receptor (TCR) repertoires but typically fail to generate paired full‐length gene products for direct expression cloning and do not enable linking this data to cell phenotype information. To overcome these limitations, we established a high‐throughput platform for the quantitative and qualitative analysis of human TCR repertoires that provides insights into the clonal and functional composition of human CD4 + and CD8 + αβ T cells at the molecular and cellular level. The strategy is a powerful tool to qualitatively assess differences between antigen receptors of phenotypically defined αβ T cell subsets, e.g. in immune responses to cancer, vaccination, or infection, and in autoimmune diseases.