Weaponizing T-cell receptors through molecular engineering.

J Biol Chem

From the Department of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21218; Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland 21218. Electronic address:

Published: April 2019

AI Article Synopsis

  • T-cell receptors (TCRs) are essential for recognizing pathogens and initiating immune responses, making them promising targets for immunotherapy development.
  • Research by Wagner and colleagues has led to new methods for generating high-affinity TCR variants that effectively activate T cells.
  • This research also includes the creation of soluble TCR fusion proteins targeting specific peptides, which can be useful in fighting cytomegalovirus (CMV) infections and advancing engineered TCR-based treatments.

Article Abstract

T-cell receptors (TCRs) recognize pathogens to ignite immune responses, making them attractive scaffolds for development as immunotherapeutics. However, manipulation of TCRs has been impeded by difficulties in their engineering and expression. Wagner and colleagues now establish new platforms to generate high-affinity TCR variants that potently activate T cells, and they also create soluble TCR fusion proteins that specifically recognize cognate peptides. This work provides specific tools to combat cytomegalovirus (CMV) infection and helps illuminate a general path to actuation of engineered TCR-based therapeutics.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6463730PMC
http://dx.doi.org/10.1074/jbc.H119.008479DOI Listing

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