| Literature DB >> 21376640 |
Thierry Mallevaey1, Andrew J Clarke, James P Scott-Browne, Mary H Young, Laila C Roisman, Daniel G Pellicci, Onisha Patel, Julian P Vivian, Jennifer L Matsuda, James McCluskey, Dale I Godfrey, Philippa Marrack, Jamie Rossjohn, Laurent Gapin.
Abstract
The antigen receptor for natural killer T cells (NKT TCR) binds CD1d-restricted microbial and self-lipid antigens, although the molecular basis of self-CD1d recognition is unclear. Here, we have characterized NKT TCR recognition of CD1d molecules loaded with natural self-antigens (Ags) and report the 2.3 Å resolution structure of an autoreactive NKT TCR-phosphatidylinositol-CD1d complex. NKT TCR recognition of self- and foreign antigens was underpinned by a similar mode of germline-encoded recognition of CD1d. However, NKT TCR autoreactivity is mediated by unique sequences within the non-germline-encoded CDR3β loop encoding for a hydrophobic motif that promotes self-association with CD1d. Accordingly, NKT cell autoreactivity may arise from the inherent affinity of the interaction between CD1d and the NKT TCR, resulting in the recognition of a broad range of CD1d-restricted self-antigens. This demonstrates that multiple self-antigens can be recognized in a similar manner by autoreactive NKT TCRs.Entities:
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Year: 2011 PMID: 21376640 PMCID: PMC3070541 DOI: 10.1016/j.immuni.2011.01.013
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745