Structural bases for the affinity-driven selection of a public TCR against a dominant human cytomegalovirus epitope

J Immunol. 2009 Jul 1;183(1):430-7. doi: 10.4049/jimmunol.0900556.

Abstract

Protective T cell responses elicited along chronic human CMV (HCMV) infections are sometimes dominated by CD8 T cell clones bearing highly related or identical public TCR in unrelated individuals. To understand the principles that guide emergence of these public T cell responses, we have performed structural, biophysical, and functional analyses of an immunodominant public TCR (RA14) directed against a major HLA-A*0201-restricted HCMV Ag (pp65(495-503)) and selected in vivo from a diverse repertoire after chronic stimulations. Unlike the two immunodominant public TCRs crystallized so far, which focused on one peptide hotspot, the HCMV-specific RA14 TCR interacts with the full array of available peptide residues. The conservation of some peptide-MHC complex-contacting amino acids by lower-affinity TCRs suggests a shared TCR-peptide-MHC complex docking mode and supports an Ag-driven selection of optimal TCRs. Therefore, the emergence of a public TCR of an oligoclonal Ag-specific response after repeated viral stimulations is based on a receptor displaying a high structural complementarity with the entire peptide and focusing on three peptide hotspots. This highlights key parameters underlying the selection of a protective T cell response against HCMV infection, which remains a major health issue in patients undergoing bone marrow transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Clone Cells
  • Crystallography, X-Ray
  • Cytomegalovirus / immunology*
  • Cytomegalovirus Infections / immunology
  • Cytomegalovirus Infections / metabolism
  • Epitopes, T-Lymphocyte / chemistry*
  • Epitopes, T-Lymphocyte / genetics
  • Epitopes, T-Lymphocyte / metabolism
  • HLA-A Antigens / chemistry
  • HLA-A Antigens / genetics
  • HLA-A Antigens / metabolism
  • HLA-A2 Antigen
  • Humans
  • Immunodominant Epitopes / chemistry*
  • Immunodominant Epitopes / genetics
  • Immunodominant Epitopes / metabolism
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / immunology
  • Peptides / chemistry
  • Peptides / genetics
  • Peptides / metabolism
  • Phosphoproteins / chemistry*
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • Protein Binding / immunology
  • Receptors, Antigen, T-Cell / chemistry*
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / metabolism
  • Viral Matrix Proteins / chemistry*
  • Viral Matrix Proteins / genetics
  • Viral Matrix Proteins / metabolism
  • Virus Activation / immunology

Substances

  • Epitopes, T-Lymphocyte
  • HLA-A Antigens
  • HLA-A*02:01 antigen
  • HLA-A2 Antigen
  • Immunodominant Epitopes
  • Peptides
  • Phosphoproteins
  • Receptors, Antigen, T-Cell
  • Viral Matrix Proteins
  • cytomegalovirus matrix protein 65kDa

Associated data

  • PDB/3GSN
  • PDB/3GSO
  • PDB/3GSQ
  • PDB/3GSR
  • PDB/3GSU
  • PDB/3GSV
  • PDB/3GSW
  • PDB/3GSX