Abstract
The two main T cell lineages, αβ and γδ T cells, play a central role in immunity. Unlike αβ T cells that recognize antigens bound to the Major Histocompatibility Complex (MHC) or MHC class I-like antigen-presenting molecules, the ligands for γδ T cell receptors (TCRs) are much more diverse. However, it is now clear that γδ TCRs can also recognize MHC class I-like molecules, including CD1b, CD1c, CD1d and the MHC class I-related protein 1 (MR1). Yet, our understanding at the molecular level of γδ T cell immunity to CD1 and MR1 is still very limited. Here, we discuss new molecular paradigms underpinning γδ TCRs recognition of antigens, antigen-presenting molecules or both. The recent discovery of recognition of MR1 by a γδ TCR at a position located underneath the antigen display platform reinforces the view that γδ TCRs can approach their ligands from many directions, unlike αβ TCRs that bind MHC, CD1 and MR1 targets in an aligned, end to end fashion.
| Original language | English |
|---|---|
| Pages (from-to) | 95-100 |
| Number of pages | 6 |
| Journal | Molecular Immunology |
| Volume | 133 |
| Early online date | 23 Feb 2021 |
| DOIs | |
| Publication status | Published - May 2021 |
Bibliographical note
Funding Information:IVR was supported by National Institutes of Health (NIH) grant R01 AI049313 , and NIH Tuberculosis Research Unit Network , Grant U19 AI111224 . JLN is supported by an Australian Research Council Future Fellowship ( FT160100074 ).
Publisher Copyright:
© 2021 Elsevier Ltd
Keywords
- CD1 glycoproteins
- MHC-like molecules
- MR1 molecule
- γδ T cells