Epitopes described in "The HLA-A*0201-restricted minor histocompatibility antigen HA-1H peptide can also be presented by another HLA-A2 subtype, A*0206."

Article Authors:H Torikai; Y Akatsuka; H Miyauchi; S Terakura; M Onizuka; K Tsujimura; K Miyamura; Y Morishima; Y Kodera; K Kuzushima; T Takahashi
Article Title:The HLA-A*0201-restricted minor histocompatibility antigen HA-1H peptide can also be presented by another HLA-A2 subtype, A*0206.
Reference Detail
Reference ID:1020271
Abstract:HA-1(H) is one of the most attractive minor histocompatibility antigens (mHA) as a target for immunotherapy of hematopoietic malignancies, but HLA-A*0201 and HLA-B60 molecules capable of presenting HA-1(H)-derived peptides are less common in eastern Asian populations when compared with Caucasian populations. Therefore, an attempt was made to search for novel epitopes presented by HLA alleles other than those previously reported by generating CTL lines from patients undergoing HLA-identical, HA-1 disparate hematopoietic stem cell transplantation (hematopoietic SCT) by stimulation with a 29-mer HA-1(H) peptide spanning a central polymorphic histidine (His). Two CTL clones established were found to be restricted by HLA-A*0206, which is the second or third most common HLA-A2 subtype worldwide. Epitope mapping revealed that the clones recognized the same nonameric peptide as A*0201-restricted HA-1(H), VLHDDLLEA. This epitope was unexpected, since it does not contain any preferred anchor motifs for HLA-A*0206. However, an HLA peptide binding assay revealed stronger binding of this peptide to A*0206 than to A*0201. Interestingly, HLA-A*0206-restricted CTL clones could lyse both HLA-A*0206(+) and HLA-A*0201(+) targets (including leukemic blasts) that express HA-1(H) peptide endogenously, whereas an HLA-A*0201-restricted, HA-1(H)-specific CTL clone failed to lyse HLA-A*0206(+) targets. This finding will expand the patient population who can benefit from HA-1(H)-based immunotherapy.
Affiliations:Division of Immunology, Aichi Cancer Center Research Institute, 1-1 Kanokoden, Chikusa-ku, Nagoya 464-8681, Japan.
Reference Type:Literature
PubMed ID:17530010
Journal:Bone Marrow Transplant
Journal Volume:40
Article Pages:165-74
Journal ISSN:0268-3369
Article Chemical List:gov.nih.nlm.ncbi.www.jaxb.impl.NameOfSubstanceImpl@2b068ff4;gov.nih.nlm.ncbi.www.jaxb.impl.NameOfSubstanceImpl@3bd4f23d;gov.nih.nlm.ncbi.www.jaxb.impl.NameOfSubstanceImpl@196ba17b;gov.nih.nlm.ncbi.www.jaxb.impl.NameOfSubstanceImpl@69369f46;gov.nih.nlm.ncbi.www.jaxb.impl.NameOfSubstanceImpl@112e2a1;gov.nih.nlm.ncbi.www.jaxb.impl.NameOfSubstanceImpl@7edcb893;gov.nih.nlm.ncbi.www.jaxb.impl.NameOfSubstanceImpl@4cd9fbf6
Article MeSH List:Amino Acid Sequence; Antigen Presentation; Base Sequence; Cell Line; Cohort Studies; Cytotoxicity, Immunologic; DNA Primers(genetics); Epitope Mapping; Genes, T-Cell Receptor; HLA-A Antigens(genetics; metabolism); HLA-A2 Antigen(genetics; metabolism); Hematopoietic Stem Cell Transplantation; Humans; In Vitro Techniques; Minor Histocompatibility Antigens(genetics; metabolism); Molecular Sequence Data; Oligopeptides(genetics; metabolism); Protein Binding; T-Lymphocytes, Cytotoxic(immunology); Transplantation, Homologous
Curation Last Updated:2015-01-17 23:14:31