Interaction of HLA-B27 homodimers with KIR3DL1 and KIR3DL2, unlike HLA-B27 heterotrimers, is independent of the sequence of bound peptide.

Journal article

HLA-B27 can form beta-2 microglobulin (beta2m)-associated heterotrimers (HLA-B27) and beta2m-free homodimers (B27(2)). Here, we study the role of complexed peptide in the interaction of these forms of B27 with the killer cell immunoglobulin (Ig)-like receptors KIR3DL1 and KIR3DL2 and with Ig-like transcripts LILRB1 and LILRB2. HLA-B27 tetramers complexed with three of five different naturally processed self peptides and three of seven pathogen-derived epitopes bound to KIR3DL1-expressing transfectants and NK cells. Heterotrimeric complexes containing peptides with charged amino acids at position 8 did not bind to KIR3DL1; however, studies with analogue peptides demonstrated that these are not the only peptide residues involved in binding. KIR3DL1 ligation by HLA-B27 inhibited NK cell IFN-gamma production in a peptide-dependent fashion. B27 but not HLA-A2, B7 or B57 heavy chains formed homodimers in the presence of peptide epitopes. B27(2) bound to KIR3DL1, KIR3DL2 and LILRB2 but not LILRB1. KIR3DL2 ligation by B27(2) inhibited NK and T cell IFN-gamma production. By contrast with HLA heterotrimers, B27(2) binding to KIR did not depend on the sequence of the bound peptide. Differences in KIR binding to classical HLA and B27(2) could be involved in the pathogenesis of spondyloarthritis.

Authors: Kollnberger, S; Chan, A; Sun, M; Chen, L; Wright, C

• Publication status: Published
• Journal: European journal of immunology
• Volume: 37
• Issue: 5
• Pages: 1313-1322
• Publication date: 2007-05-01
• DOI: 10.1002/eji.200635997
• EISSN: 1521-4141
• ISSN: 0014-2980
• Language: English
• Keywords: Molecular Sequence Data; Peptides; Lymphocyte Activation; Dimerization; Killer Cells, Natural; Receptors, KIR3DL2; Antigen Presentation; Epitopes; HLA-B27 Antigen; Spondylarthritis; T-Lymphocytes; Amino Acid Sequence; Humans; Electrophoresis, Polyacrylamide Gel; Flow Cytometry; Transfection; Receptors, Immunologic; Receptors, KIR3DL1; Blotting, Western; Receptors, KIR