ABSTRACT
The affinity of T-cell receptor (TCR) determines the efficacy of TCR-based immunotherapy. By using human leucocyte antigen (HLA)-A*02 transgenic mice, a TCR was generated previously specific for human tumour testis antigen peptide MAGE-A3112-120 (KVAELVHFL) HLA-A*02 complex. We developed an approach to humanize the murine TCR by replacing the mouse framework with sequences of folding optimized human TCR variable domains for retaining binding affinity. The resultant humanized TCR exhibited higher affinity and conferred better anti-tumour activity than its parent murine MAGE-A3 TCR (SRm1). In addition, the affinity of humanized TCR was enhanced further to achieve improved T-cell activation. Our studies demonstrated that the human TCR variable domain frameworks could provide support for complementarity-determining regions from a murine TCR, and retain the original binding activity. It could be used as a generic approach of TCR humanization.
Subject(s)
HLA-A2 Antigen/immunology , Immunotherapy , Lung Neoplasms/immunology , Lung Neoplasms/therapy , Receptors, Antigen, T-Cell/immunology , Animals , Cell Survival , Cells, Cultured , HLA-A2 Antigen/genetics , HLA-A2 Antigen/isolation & purification , Humans , Lung Neoplasms/pathology , Mice , Mice, Transgenic , Receptors, Antigen, T-Cell/genetics , Receptors, Antigen, T-Cell/isolation & purificationABSTRACT
The new HLA-A*02:06:01:02 allele differs from HLA-A*02:06:01 by a CâG substitution in Intron 1.
Subject(s)
Genes, MHC Class II , HLA-A2 Antigen/isolation & purification , Alleles , Base Sequence , HLA-A2 Antigen/genetics , Histocompatibility Testing , Humans , Molecular Sequence Data , Real-Time Polymerase Chain Reaction , Sequence Alignment , Sequence Analysis, DNA , Sequence Homology, Nucleic AcidABSTRACT
One nucleotide substitution at residue 410 of HLA-A*02:07:01 results in a new allele, HLA-A*02:575.
Subject(s)
Asian People/genetics , Genes, MHC Class II , HLA-A2 Antigen/isolation & purification , Amino Acid Sequence , Base Sequence , HLA-A2 Antigen/genetics , Humans , Molecular Sequence Data , Sequence Alignment , Sequence Homology , TaiwanABSTRACT
T cell recognition of minor histocompatibility Ags (MiHA) plays an important role in the graft-versus-tumor effect of allogeneic stem cell transplantation. Selective infusion of T cells reactive for hematopoiesis-restricted MiHA presented in the context of HLA class I or II molecules may help to separate the graft-versus-tumor effects from graft-versus-host disease effects after allogeneic stem cell transplantation. Over the years, increasing numbers of MiHA have been identified by forward immunology approaches, and the relevance of these MiHA has been illustrated by correlation with clinical outcome. As the tissue distribution of MiHA affects the clinical outcome of T cell responses against these Ags, it would be beneficial to identify additional predefined MiHA that are exclusively expressed on hematopoietic cells. Therefore, several reverse immunology approaches have been explored for the prediction of MiHA. Thus far, these approaches frequently resulted in the identification of T cells directed against epitopes that are not naturally processed and presented. In this study we established a method for the identification of biologically relevant MiHA, implementing mass spectrometry-based HLA-peptidomics into a reverse immunology approach. For this purpose, HLA class I binding peptides were eluted from transformed B cells, analyzed by mass spectrometry, and matched with a database dedicated to identifying polymorphic peptides. This process resulted in a set of 40 MiHA candidates that were evaluated in multiple selection steps. The identification of LB-NISCH-1A demonstrated the technical feasibility of our approach. On the basis of these results, we present an approach that can be of value for the efficient identification of MiHA or other T cell epitopes.
Subject(s)
Epitopes, T-Lymphocyte/metabolism , Histocompatibility Antigens Class I/metabolism , Peptides/metabolism , Proteomics , B-Lymphocyte Subsets/immunology , B-Lymphocyte Subsets/metabolism , Cell Line, Transformed , Cells, Cultured , Coculture Techniques , HLA-A2 Antigen/isolation & purification , HLA-A2 Antigen/metabolism , Humans , Minor Histocompatibility Antigens/isolation & purification , Minor Histocompatibility Antigens/metabolism , Protein Binding/immunology , T-Lymphocyte Subsets/immunology , T-Lymphocyte Subsets/metabolismABSTRACT
Major histocompatibility (MHC) class I tetramers are used in the quantitative analysis of epitope peptide-specific CD8+ T-cells. An MHC class I tetramer was composed of 4 MHC class I complexes and a fluorescently labeled streptavidin (SA) molecule. Each MHC class I complex consists of an MHC heavy chain, a beta(2)-microglobulin (beta(2)m) molecule and a synthetic epitope peptide. In most previous studies, an MHC class I complex was formed in the refolding buffer with an expressed MHC heavy chain molecule and beta(2)m, respectively. This procedure inevitably resulted in the disadvantages of forming unwanted multimers and self-refolding products, and the purification of each kind of monomer was time-consuming. In the present study, the genes of a human/murine chimeric MHC heavy chain (HLA-A2 alpha1, HLA-A2 alpha2 and MHC-H2D alpha3) and beta(2)m were tandem-cloned into plasmid pET17b and expressed as a fusion protein. The recombinant fusion protein was refolded with each of the three HLA-A2 restricted peptides (HBc18-27 FLPSDFFPSI, HBx52-60 HLSLRGLPV, and HBx92-100 VLHKRTLGL) and thus three chimeric MHC class I complexes were obtained. Biotinylation was performed, and its level of efficiency was observed via a band-shift assay in non-reducing polyacrylamide gel electrophoresis (PAGE). Such chimeric MHC class I tetramers showed a sensitive binding activity in monitoring HLA/A2 restrictive cytotoxic T lymphocytes (CTLs) in immunized HLA/A*0201 transgenic mice.
Subject(s)
Histocompatibility Antigens Class I/isolation & purification , Recombinant Fusion Proteins/isolation & purification , beta 2-Microglobulin/isolation & purification , Animals , Biotinylation , CD8 Antigens/immunology , Cloning, Molecular , Escherichia coli , Female , HLA-A Antigens/genetics , HLA-A2 Antigen/genetics , HLA-A2 Antigen/immunology , HLA-A2 Antigen/isolation & purification , Histocompatibility Antigens Class I/genetics , Histocompatibility Antigens Class I/immunology , Humans , In Vitro Techniques , Mice , Mice, Transgenic , Plasmids , Protein Folding , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/immunology , T-Lymphocytes, Cytotoxic/immunology , beta 2-Microglobulin/genetics , beta 2-Microglobulin/immunologyABSTRACT
Tetramer analysis is a novel technique in immunological research that has dramatically changed our knowledge of the immune response to pathogens, tumors and autoimmune disease. Through the formation of major histocompatibility complex (MHC)-peptide tetrameric complexes, it can provide accurate counts of antigen-specific T-cells and it allows their phenotypical and functional analysis. The tetramer is composed of the human leukocyte antigen (HLA) heavy chain, beta-2 microglobulin (beta-2m), the nominal peptide, and streptavidin. The HLA heavy chain and the beta-2m are expressed in Escherichia coli. But up to now, all laboratories have been expressing these two proteins by using isopropyl beta-d-thiogalactopyranoside IPTG. IPTG is very expensive, and it is tedious and laborious to induce expression protein. So it is difficult to scale up to express the objective protein. To address this problem, extracellular fractions of HLA-A0201 and beta-2m (absent signal peptide) genes were cloned from peripheral blood mononuclear cells (PBMCs) by RT-PCR. DNA coding for a Gly-Ser linker and a BSP (15-amino acid substrate peptide for BirA-dependent biotinylation) was added to the COOH-terminus of the extracellular fraction of HLA-A0201 by PCR, using an HLA-A0201 as the template. Then the HLA-A0201-BSP and beta-2m genes were cloned into pBV220 vector and expressed, respectively. The expressed proteins were purified and detected by ELISA and Western blot analyses. High-efficient expressions of HLA-A0201-BSP and beta-2m proteins lay a good foundation for further expression and purification in prokaryotic system and constructing MHC class I-peptide tetramer complexes to study the function of CTLs.
Subject(s)
HLA-A2 Antigen/genetics , beta 2-Microglobulin/genetics , beta 2-Microglobulin/isolation & purification , Base Sequence , Cloning, Molecular , DNA Primers , Electrophoresis, Polyacrylamide Gel , Escherichia coli/genetics , HLA-A2 Antigen/isolation & purification , Recombinant Proteins/genetics , Recombinant Proteins/isolation & purificationABSTRACT
HLA-A2-restricted T cells show peptide-specific activity against cytomegalovirus and leukaemia cells. We retrospectively analysed the influence of donor cytomegalovirus serostatus on the outcome of 103 consecutive patients who had leukaemia and who received bone-marrow transplants from HLA-identical sibling donors. We found that donor cytomegalovirus seropositivity significantly improved overall survival (p=0.02) as a result of lower relapse incidence (p=0.035) in HLA-A2-positive but not HLA-A2-negative recipients. In HLA-A2-positive recipients donor cytomegalovirus seropositivity was associated with chronic graft-versus-host disease (GVHD), but even in patients without chronic GVHD donor cytomegalovirus seropositivity significantly improved survival (p=0.0483). These preliminary data provide evidence that at least in HLA-A2-positive recipients, transplantation of bone marrow from cytomegalovirus positive, HLA-identical sibling donors seems to be associated with substantial graft-versus-leukaemia activity, and suggests a cross-reactivity of cytomegalovirus-specific donor-derived cytotoxic T cells with HLA-A2-restricted recipient minor histocompatibility antigens.
Subject(s)
Bone Marrow Transplantation , Cytomegalovirus/immunology , Leukemia/therapy , Nuclear Family , Adolescent , Adult , Child , Child, Preschool , Combined Modality Therapy , Female , HLA-A2 Antigen/isolation & purification , Humans , Infant , Leukemia/mortality , Male , Retrospective Studies , Survival AnalysisABSTRACT
In this paper we report the identification of a new HLA-A*02 allele in two members of an Afghan family. This novel allele, designed as A*02202, differs from A*02201 by a silent substitution at codon 66 (AAC-->AAT) in the alpha1 domain. A*02202 appears to be the result of a novel mutation (Note).
Subject(s)
Alleles , HLA-A2 Antigen/genetics , HLA-A2 Antigen/isolation & purification , Sequence Analysis, DNA , Base Sequence , Female , Genetic Markers/immunology , Humans , Male , Molecular Sequence Data , Point Mutation , Polymerase Chain Reaction , Thalassemia/geneticsABSTRACT
Prolonged treatment of human platelets with the adenylate cyclase-stimulating prostacyclin analog iloprost leads to reduction in cAMP formation. Previous studies have demonstrated that this may be ascribed to modification of both receptor and Gsalpha function rather than of the catalytic component of adenylate cyclase [Mollner, S., Deppisch, H. & Pfeuffer, T. (1992) Eur. J. Biochem. 210, 539-544]. Iloprost-induced desensitization was accompanied by the formation of a Gsalpha-containing 90-kDa product in membranes treated with the bifunctional cross-linker 1,6-bismaleimidohexane. The cAMP-inducing prostanoid PGD2, which does not promote desensitization, did not cause formation of the 90-kDa species either. The long-term effect of the common G-protein activator [AlF4]- on human platelet adenylate cyclase was shown in many respects to be comparable with that of iloprost. However, [AlF4]- treatment also failed to induce the 90-kDa species, showing that different mechanisms of desensitization were operating. Treatment of the cross-linked 90-kDa complex with PNGase F demonstrated the glycoprotein nature of the Gsalpha-associated component. The 90-kDa cross-linked product was purified by consecutive immunoaffinity chromatography and preparative PAGE to apparent homogeneity. Analysis of the purified protein by MS suggested that, besides Gsalpha, the heavy chain of MHC I (HLA-A2) was part of the complex. This was confirmed by coprecipitation of Gsalpha by the monoclonal anti-(MHC I) antibody W6/32.
Subject(s)
Adenylyl Cyclases/metabolism , Blood Platelets/drug effects , GTP-Binding Protein alpha Subunits, Gs/metabolism , HLA-A2 Antigen/metabolism , Iloprost/pharmacology , Chromatography, Affinity , Cross-Linking Reagents , Epoprostenol/analogs & derivatives , GTP-Binding Protein alpha Subunits, Gs/isolation & purification , HLA-A2 Antigen/isolation & purification , Humans , Platelet Aggregation/physiology , Platelet Aggregation Inhibitors/pharmacology , Precipitin TestsABSTRACT
The HLA-Cw3 heavy chain has been expressed at high level as insoluble protein aggregates in E. coli. The protein aggregates dissolved in strong denaturant solution were efficiently reconstituted by removal of denaturant in the presence of an HLA-Cw3 binding peptide (FAM) and beta 2m. The reconstituted HLA-Cw3/FAM protein binds specifically to a p58 natural killer cell inhibitory receptor, a natural ligand. The HLA-A2 molecule has also been reconstituted in complex with either of a peptide from myelin associated glycoprotein (MAG) or a peptide from the GAG protein of human immunodeficiency virus. The HLA-A2/MAG protein crystallized under the identical conditions as HLA-A2 purified from human lymphoblastoid cells. The reconstitution method has yielded an abundant supply of HLA molecules complexed with single antigenic peptides, and may be of general utility in reconstituting any class I MHC molecules. However, the HLA molecules could not be reconstituted either without a peptide or with an irrelevant peptide. Using this property, the reconstitution method could be used to determine whether a peptide is restricted/bound to certain class I MHC molecule.
Subject(s)
Histocompatibility Antigens Class I/genetics , Peptides/immunology , Crystallization , Escherichia coli , HLA-A2 Antigen/isolation & purification , Histocompatibility Antigens Class I/biosynthesis , Histocompatibility Antigens Class I/isolation & purification , Humans , Recombinant Proteins/biosynthesis , Recombinant Proteins/isolation & purificationABSTRACT
A subtractive analysis of peptides eluted from major histocompatibility complex (MHC) class I human histocompatibility leukocyte antigen (HLA)-A2.1 molecules purified from either human immunodeficiency virus type-1 (HIV-1)-infected or uninfected cells was performed using micro high-performance liquid chromatography and mass spectrometry. Three peptides unique to infected cells were identified and found to derive from a single protein, human vinculin, a structural protein not known to be involved in viral pathogenesis. Molecular and cytofluorometric analyses revealed vinculin mRNA and vinculin protein overexpression in B and T lymphocytes from HIV-1-infected individuals. Vinculin peptide-specific CTL activity was readily elicited from peripheral blood lymphocytes of the majority of HLA-A2.1+, HIV+ patients tested. Our observations suggest that atypical vinculin expression and MHC class I-mediated presentation of vinculin-derived peptides accompany HIV infection of lymphoid cells in vivo, with a resultant induction of antivinculin CTL in a significant portion of HIV+ (HLA-A2.1+) individuals.
Subject(s)
B-Lymphocytes/immunology , HIV Infections/immunology , HIV-1/immunology , HLA-A2 Antigen/immunology , T-Lymphocytes, Cytotoxic/immunology , T-Lymphocytes/immunology , Vinculin/biosynthesis , Amino Acid Sequence , Binding Sites , Chromatography, High Pressure Liquid , Cytotoxicity, Immunologic , Flow Cytometry , HLA-A2 Antigen/isolation & purification , Humans , Major Histocompatibility Complex , Mass Spectrometry , Molecular Sequence Data , Peptides/chemical synthesis , Peptides/chemistry , Peptides/immunology , Reference Values , Vinculin/immunology , Vinculin/isolation & purification , Viral Proteins/chemistry , Viral Proteins/immunologySubject(s)
B-Lymphocytes/immunology , HLA-A2 Antigen/classification , Indians, South American/genetics , Alleles , Amino Acid Sequence , Base Sequence , Cell Line , DNA , HLA-A2 Antigen/genetics , HLA-A2 Antigen/isolation & purification , Histocompatibility Testing , Humans , Molecular Sequence DataABSTRACT
Peptides and other bioactive materials can be purified from complex biological sources by reverse-phase high-performance liquid chromatography (RP-HPLC), provided the mixture is suitably prepared before injection onto an HPLC system. Ultrafiltration offers a convenient and rapid sample preparation technique with numerous advantages over alternative methods such as conventional gel filtration chromatography. We demonstrate the use of ultrafiltration as an HPLC sample preparation step in the purification of peptides bound to class I major histocompatibility complex (MHC-I) membrane proteins. When ultrafiltration was performed with a Centricon-10 ultrafiltration device, peptides were efficiently separated from the alpha (45 kDa) and beta 2m (12 kDa) chains of MHC-I proteins and could be subjected to HPLC without further treatment. Furthermore, even samples as crude as whole cell lysates or supernatants could be prepared for HPLC in a single ultrafiltration step, affording a remarkably straightforward route to the purification of biologically important peptides.
Subject(s)
Chromatography, High Pressure Liquid/methods , Peptides/isolation & purification , Ultrafiltration/methods , Biotechnology , Evaluation Studies as Topic , HLA-A2 Antigen/isolation & purification , HLA-B7 Antigen/isolation & purification , Humans , beta 2-Microglobulin/isolation & purificationABSTRACT
The human class I histocompatibility antigen HLA-A2 has been assembled from subunits expressed separately in E. coli. A peptide that is known to be recognized by human cytotoxic T lymphocytes (CTLs) in association with HLA-A2 is a necessary component of the reconstitution mixture. The N-terminal extracellular fragment of the HLA-A2 heavy chain is initially synthesised as an insoluble aggregate. The aggregate is solubilized in denaturant, mixed with the influenza nucleoprotein 85-94 decapeptide (NP peptide), and diluted into a solution containing human beta 2-microglobulin (beta 2 m) isolated from the E. coli periplasm. The HLA-A2 heavy chain becomes soluble in physiological solutions if both beta 2m and the NP peptide are present. The reconstituted HLA-A2 complex is recognised by a monoclonal antibody that is specific for the native HLA-A2/beta 2m heterodimer, and is also recognised by a monoclonal antibody that recognises beta 2m. When other peptides known from CTL studies to associate with HLA-A2 are used, a significantly lower yield of reconstituted complex is obtained. The isoelectric point of the reconstituted complex depends on which peptide is used, confirming that the peptide is a component of the reconstituted complex.
Subject(s)
Escherichia coli/genetics , HLA-A2 Antigen , Oligopeptides , Recombinant Proteins , Viral Proteins , beta 2-Microglobulin , Amino Acid Sequence , Cloning, Molecular , Electrophoresis, Polyacrylamide Gel , HLA-A2 Antigen/isolation & purification , Humans , Molecular Sequence Data , Mutagenesis, Site-Directed , Plasmids , TransfectionABSTRACT
The heavy chain of class I molecules of the major histocompatibility complex forms the binding site for antigenic peptides. We describe the binding of a synthetic peptide to the purified heavy chain of the human major histocompatibility complex molecule HLA-A2. The peptide binding capacity is found to be markedly increased if the protein is first partly denatured by reduction of its disulfide bonds in detergent and subsequently renatured by reoxidation. In the presence of certain detergents, the heavy chain binds peptides even when the protein is partly unfolded.
Subject(s)
HLA-A2 Antigen/immunology , Amino Acid Sequence , Electrophoresis, Polyacrylamide Gel , Fluorescent Dyes , HLA-A2 Antigen/isolation & purification , Histocompatibility Antigens Class I/immunology , Humans , Macromolecular Substances , Molecular Sequence Data , Orthomyxoviridae , Peptides/chemical synthesis , Protein Binding , Viral Matrix Proteins/chemical synthesisABSTRACT
Two human alloantisera, previously described as possibly detecting new beta 2-microglobulin associated proteins, selectively expressed on HLA-A2 and HLA-A1 phytohaemagglutinin (PHA)-activated lymphocytes, immunoprecipitated only molecules with the same isoelectric point as HLA-A1 and A2 products. This result suggests that the selected alloantisera do not react with the products of an HLA class I locus different from ABC but probably recognize a new epitope arising on HLA-A molecules upon conformational changes consequent to cell activation.
Subject(s)
HLA Antigens/isolation & purification , Antilymphocyte Serum , Epitopes , HLA-A1 Antigen/isolation & purification , HLA-A2 Antigen/isolation & purification , Humans , Isoantibodies , Isoelectric Focusing , Lymphocyte Activation , Precipitin TestsABSTRACT
Recent findings suggest that peptide fragments of newly synthesized proteins may associate intracellularly with nascent chains of class I histocompatibility antigens (termed MHC-I proteins because they are encoded by genes of the major histocompatibility complex) and that these peptide adducts may be required for the folding or stability and perhaps even the transport of these proteins to the cell surface. To determine whether these proteins can be reconstituted from their separated subunits into ostensibly native molecules in the absence of added peptides, we denatured a purified human MHC-I protein (HLA-A2) with 4 M NaSCN, separated its heavy (alpha) and light (beta 2-microglobulin) chains by gel filtration, and then mixed them in the presence of a 3-fold molar excess of beta 2-microglobulin and absence of added peptides. The reconstituted protein, recovered in 10% yield, was indistinguishable from native A2 in its reactivity with a monoclonal antibody (BB7.7) and its ability to specifically activate A2-specific CD8+ T cells. Inasmuch as the reconstituted A2 contained no detectable peptide adducts (we estimate less than 1 per 100 on a molar basis, assuming peptides of 2-5 kDa), the results suggest that peptide-free A2 can be recognized by CD8+ T cells and that peptide adducts are not essential for the MHC-I protein to maintain an ostensibly native structure.