TCR Bias and Affinity Define Two Compartments of the CD1b- Glycolipid-Specific T Cell Repertoire

I. van Rhijn, N. Gherardin, A. Kasmar, W. de Jager, D.G. Pellicci, L. Kostenko, L.L. Tan, M. Bhati, S. Gras, D.I. Godfrey, J. Rossjohn, D.B. Moody

    Research output: Contribution to journalArticleAcademicpeer-review

    Abstract

    Current views emphasize TCR diversity as a key feature that differentiates the group 1 (CD1a, CD1b, CD1c) and group 2 (CD1d)
    CD1 systems. Whereas TCR sequence motifs define CD1d-reactive NKT cells, the available data do not allow a TCR-based organization
    of the group 1 CD1 repertoire. The observed TCR diversity might result from donor-to-donor differences in TCR repertoire,
    as seen for MHC-restricted T cells. Alternatively, diversity might result from differing CD1 isoforms, Ags, and methods used
    to identify TCRs. Using CD1b tetramers to isolate clones recognizing the same glycolipid, we identified a previously unknown pattern
    of V gene usage (TRAV17, TRBV4-1) among unrelated human subjects. These TCRs are distinct from those present on
    NKT cells and germline-encoded mycolyl lipid–reactive T cells. Instead, they resemble the TCR of LDN5, one of the first known
    CD1b-reactive clones that was previously thought to illustrate the diversity of the TCR repertoire. Interdonor TCR conservation
    was observed in vitro and ex vivo, identifying LDN5-like T cells as a distinct T cell type. These data support TCR-based
    organization of the CD1b repertoire, which consists of at least two compartments that differ in TCR sequence motifs, affinity,
    and coreceptor expression.
    Original languageEnglish
    Pages (from-to)4054-4060
    Number of pages7
    JournalJournal of Immunology
    Volume192
    DOIs
    Publication statusPublished - 2014

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