Cao, Thinh-Phat, Shahine, Adam, Cox, Liam R., Besra, Gurdyal S., Moody, D. Branch and Rossjohn, Jamie ![]() ![]() |
Preview |
PDF
- Published Version
Available under License Creative Commons Attribution. Download (3MB) | Preview |
Abstract
The CD1 family of antigen-presenting molecules adopt a Major Histocompatibility Complex class I (MHC-I) fold. Whereas MHC molecules present peptides, the CD1 family has evolved to bind self- and foreign-lipids. The CD1 family of antigen-presenting molecules comprises four members, CD1a, CD1b, CD1c, CD1d, that differ in their architecture around the lipid-binding cleft, thereby enabling diverse lipids to be accommodated. These CD1-lipid complexes are recognised by T cell receptors (TCRs) expressed on T cells, either through dual recognition of CD1 and lipid or in a new model whereby the TCR directly contacts CD1, thereby triggering an immune response. Chemical syntheses of lipid antigens, and analogues thereof, have been crucial in understanding the underlying specificity of T cell-mediated lipid immunity. This review will focus on our current understanding of how TCRs interact with CD1-lipid complexes, highlighting how it can be fundamentally different from TCR-MHC-peptide co-recognition.
Item Type: | Article |
---|---|
Date Type: | Publication |
Status: | Published |
Schools: | Medicine |
Additional Information: | License information from Publisher: LICENSE 1: URL: http://creativecommons.org/licenses/by/4.0/, Start Date: 2024-06-26 |
Publisher: | Elsevier |
ISSN: | 0021-9258 |
Date of First Compliant Deposit: | 2 July 2024 |
Date of Acceptance: | 24 June 2024 |
Last Modified: | 05 Aug 2024 14:05 |
URI: | https://orca.cardiff.ac.uk/id/eprint/170230 |
Actions (repository staff only)
![]() |
Edit Item |