T-cell-receptor-like antibodies – generation, function and applications

Author(s):  
Rony Dahan ◽  
Yoram Reiter

Tumour and virus-infected cells are recognised by CD8+ cytotoxic T cells that, in response, are activated to eliminate these cells. In order to be activated, the clonotypic T-cell receptor (TCR) needs to encounter a specific peptide antigen presented by the membrane surface major histocompatibility complex (MHC) molecule. Cells that have undergone malignant transformation or viral infection present peptides derived from tumour-associated antigens or viral proteins on their MHC class I molecules. Therefore, disease-specific MHC–peptide complexes are desirable targets for immunotherapeutic approaches. One such approach transforms the unique fine specificity but low intrinsic affinity of TCRs to MHC–peptide complexes into high-affinity soluble antibody molecules endowed with a TCR-like specificity towards tumour or viral epitopes. These antibodies, termed TCR-like antibodies, are being developed as a new class of immunotherapeutics that can target tumour and virus-infected cells and mediate their specific killing. In addition to their therapeutic capabilities, TCR-like antibodies are being developed as diagnostic reagents for cancer and infectious diseases, and serve as valuable research tools for studying MHC class I antigen presentation.

1994 ◽  
Vol 180 (3) ◽  
pp. 1097-1106 ◽  
Author(s):  
O Lantz ◽  
A Bendelac

The mouse thymus contains a mature T cell subset that is distinguishable from the mainstream thymocytes by several characteristics. It is restricted in its usage of T cell receptor (TCR) V beta genes to V beta 8, V beta 7, and V beta 2. Its surface phenotype is that of activated/memory cells. It carries the natural killer NK1.1 surface marker. Furthermore, though it consists entirely of CD4+ and CD4-8- cells, its selection in the thymus depends solely upon major histocompatibility complex (MHC) class I expression by cells of hematopoietic origin. Forced persistence of CD8, in fact, imparts negative selection. Here, we have studied the TCR repertoire of this subset and found that, whereas the beta chain V-D-J junctions are quite variable, a single invariant alpha chain V alpha 14-J281 is used by a majority of the TCRs. This surprisingly restricted usage of the V alpha 14-J281 alpha chain is dependent on MHC class I expression, but independent of the MHC haplotype. In humans, a similar unusual population including CD4-8- cells can also be found that uses a strikingly homologous, invariant alpha chain V alpha 24-JQ. Thus, this unique V alpha-J alpha combination has been conserved in both species, conferring specificity to some shared nonpolymorphic MHC class I/peptide self-ligand(s). This implies that the T cell subset that it defines has a specialized and important role, perhaps related to its unique ability to secrete a large set of lymphokines including interleukin 4, upon primary stimulation in vitro and in vivo.


Nature ◽  
10.1038/42529 ◽  
1997 ◽  
Vol 387 (6633) ◽  
pp. 634-634
Author(s):  
K. Christopher Garcia ◽  
Christopher A. Scott ◽  
Anders Brunmark ◽  
Francis R. Carbone ◽  
Per A. Peterson ◽  
...  

Nature ◽  
1996 ◽  
Vol 384 (6609) ◽  
pp. 577-581 ◽  
Author(s):  
K. Christopher Garcia ◽  
Christopher A. Scott ◽  
Anders Brunmark ◽  
Francis R. Carbone ◽  
Per A. Peterson ◽  
...  

1997 ◽  
Vol 56 ◽  
pp. 347
Author(s):  
N. Torres-Nagel ◽  
B. Mehling ◽  
A. Deutschländer ◽  
E. Joly ◽  
T. Hermann ◽  
...  

Immunity ◽  
2002 ◽  
Vol 16 (3) ◽  
pp. 345-354 ◽  
Author(s):  
Jean-Baptiste Reiser ◽  
Claude Grégoire ◽  
Claudine Darnault ◽  
Thomas Mosser ◽  
Annick Guimezanes ◽  
...  

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