scholarly journals Hagfish Leukocytes Express a Paired Receptor Family with a Variable Domain Resembling Those of Antigen Receptors

2005 ◽  
Vol 174 (5) ◽  
pp. 2885-2891 ◽  
Author(s):  
Takashi Suzuki ◽  
Tadasu Shin-I ◽  
Asao Fujiyama ◽  
Yuji Kohara ◽  
Masanori Kasahara
2014 ◽  
Vol 10 (9) ◽  
pp. e1003852 ◽  
Author(s):  
James Dunbar ◽  
Bernhard Knapp ◽  
Angelika Fuchs ◽  
Jiye Shi ◽  
Charlotte M. Deane

ESMO Open ◽  
2020 ◽  
Vol 4 (Suppl 3) ◽  
pp. e000733 ◽  
Author(s):  
Iñaki Etxeberria ◽  
Javier Glez-Vaz ◽  
Álvaro Teijeira ◽  
Ignacio Melero

CD137 (4-1BB) is a surface glycoprotein that belongs to the tumour necrosis factor receptor family (TNFRSF9). Its expression is induced on activation on a number of leucocyte types. Interestingly, for cancer immunotherapy, CD137 becomes expressed on primed T and natural killer (NK) cells, which on ligation provides powerful costimulatory signals. Perturbation of CD137 by CD137L or agonist monoclonal antibodies on activated CD8 T cells protects such antigen-specific cytotoxic T lymphocytes from apoptosis, enhances effector functionalities and favours persistence and memory differentiation. As a consequence, agonist antibodies exert potent antitumour effects in mouse models and the CD137 signalling domain is critical in chimeric antigen receptors (CAR) of CAR T cells approved to be used in the clinic. New formats of CD137 agonist moieties are being clinically developed, seeking potent costimulation targeted to the tumour microenvironment to avoid liver inflammation side effects, that have thus far limited and delayed clinical development.


2009 ◽  
Vol 62 (1) ◽  
pp. 15-22 ◽  
Author(s):  
Munir Akkaya ◽  
A. Neil Barclay

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Julyun Oh ◽  
Dora Toledo Warshaviak ◽  
Mikayel Mkrtichyan ◽  
Melanie Lisette Munguia ◽  
Abby Lin ◽  
...  

AbstractCell therapy using T cell receptors (TCRs) and chimeric antigen receptors (CARs) represents a new wave of immunotherapies garnering considerable attention and investment. Further progress in this area of medicine depends in part on improving the functional capabilities of the engineered components, while maintaining the overall size of recombinant constructs to ensure their compatibility with existing gene delivery vehicles. We describe a single-variable-domain TCR (svd TCR) that utilizes only the variable domain of the β chain (Vβ). This Vβ module not only works in TCR and CAR formats, but also can be used to create single-chain bispecific CARs and TCRs. Comparison of individual ligand-binding Vβ domains in different formats suggests that the lone Vβ sequence controls the sensitivity and a major part of the specificity of the CAR or TCR construct, regardless of signaling format, in Jurkat and primary T cells.


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