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Identification of a Novel UTY-Encoded Minor Histocompatibility Antigen
Minor histocompatibility antigens (mHags) encoded by the Y‐chromosome (H‐Y‐mHags) are known to play a pivotal role in allogeneic haematopoietic cell transplantation (HCT) involving female donors and male recipients. We present a new H‐Y‐mHag, YYNAFHWAI (UTY139–147), encoded by the UTY gene and prese...
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Published in: | Scandinavian journal of immunology 2012-08, Vol.76 (2), p.141-150 |
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creator | Mortensen, B. K. Rasmussen, A. H. Larsen, M. E. Larsen, M. V. Lund, O. Braendstrup, P. Harndahl, M. Rasmussen, M. Buus, S. Stryhn, A. Vindeløv, L. |
description | Minor histocompatibility antigens (mHags) encoded by the Y‐chromosome (H‐Y‐mHags) are known to play a pivotal role in allogeneic haematopoietic cell transplantation (HCT) involving female donors and male recipients. We present a new H‐Y‐mHag, YYNAFHWAI (UTY139–147), encoded by the UTY gene and presented by HLA‐A*24:02. Briefly, short peptide stretches encompassing multiple putative H‐Y‐mHags were designed using a bioinformatics predictor of peptide‐HLA binding, NetMHCpan. These peptides were used to screen for peptide‐specific HLA‐restricted T cell responses in peripheral blood mononuclear cells obtained post‐HCT from male recipients of female donor grafts. In one of these recipients, a CD8+ T cell response was observed against a peptide stretch encoded by the UTY gene. Another bioinformatics tool, HLArestrictor, was used to identify the optimal peptide and HLA‐restriction element. Using peptide/HLA tetramers, the specificity of the CD8+ T cell response was successfully validated as being HLA‐A*24:02‐restricted and directed against the male UTY139–147 peptide. Functional analysis of these T cells demonstrated male UTY139–147 peptide‐specific cytokine secretion (IFNγ, TNFα and MIP‐1β) and cytotoxic degranulation (CD107a). In contrast, no responses were seen when the T cells were stimulated with patient tumour cells alone. CD8+ T cells specific for this new H‐Y‐mHag were found in three of five HLA‐A*24:02‐positive male recipients of female donor HCT grafts available for this study. |
doi_str_mv | 10.1111/j.1365-3083.2012.02708.x |
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K. ; Rasmussen, A. H. ; Larsen, M. E. ; Larsen, M. V. ; Lund, O. ; Braendstrup, P. ; Harndahl, M. ; Rasmussen, M. ; Buus, S. ; Stryhn, A. ; Vindeløv, L.</creator><creatorcontrib>Mortensen, B. K. ; Rasmussen, A. H. ; Larsen, M. E. ; Larsen, M. V. ; Lund, O. ; Braendstrup, P. ; Harndahl, M. ; Rasmussen, M. ; Buus, S. ; Stryhn, A. ; Vindeløv, L.</creatorcontrib><description>Minor histocompatibility antigens (mHags) encoded by the Y‐chromosome (H‐Y‐mHags) are known to play a pivotal role in allogeneic haematopoietic cell transplantation (HCT) involving female donors and male recipients. We present a new H‐Y‐mHag, YYNAFHWAI (UTY139–147), encoded by the UTY gene and presented by HLA‐A*24:02. Briefly, short peptide stretches encompassing multiple putative H‐Y‐mHags were designed using a bioinformatics predictor of peptide‐HLA binding, NetMHCpan. These peptides were used to screen for peptide‐specific HLA‐restricted T cell responses in peripheral blood mononuclear cells obtained post‐HCT from male recipients of female donor grafts. In one of these recipients, a CD8+ T cell response was observed against a peptide stretch encoded by the UTY gene. Another bioinformatics tool, HLArestrictor, was used to identify the optimal peptide and HLA‐restriction element. Using peptide/HLA tetramers, the specificity of the CD8+ T cell response was successfully validated as being HLA‐A*24:02‐restricted and directed against the male UTY139–147 peptide. Functional analysis of these T cells demonstrated male UTY139–147 peptide‐specific cytokine secretion (IFNγ, TNFα and MIP‐1β) and cytotoxic degranulation (CD107a). In contrast, no responses were seen when the T cells were stimulated with patient tumour cells alone. CD8+ T cells specific for this new H‐Y‐mHag were found in three of five HLA‐A*24:02‐positive male recipients of female donor HCT grafts available for this study.</description><identifier>ISSN: 0300-9475</identifier><identifier>EISSN: 1365-3083</identifier><identifier>DOI: 10.1111/j.1365-3083.2012.02708.x</identifier><identifier>PMID: 22536994</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Amino Acid Sequence ; Blood Cells - transplantation ; CD8-Positive T-Lymphocytes - immunology ; Epitopes - immunology ; Female ; HLA-A24 Antigen - immunology ; Humans ; Male ; Minor Histocompatibility Antigens - immunology ; Nuclear Proteins - chemistry ; Nuclear Proteins - immunology ; Transplantation, Homologous</subject><ispartof>Scandinavian journal of immunology, 2012-08, Vol.76 (2), p.141-150</ispartof><rights>2012 The Authors. Scandinavian Journal of Immunology © 2012 Blackwell Publishing Ltd</rights><rights>2012 The Authors. 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V.</creatorcontrib><creatorcontrib>Lund, O.</creatorcontrib><creatorcontrib>Braendstrup, P.</creatorcontrib><creatorcontrib>Harndahl, M.</creatorcontrib><creatorcontrib>Rasmussen, M.</creatorcontrib><creatorcontrib>Buus, S.</creatorcontrib><creatorcontrib>Stryhn, A.</creatorcontrib><creatorcontrib>Vindeløv, L.</creatorcontrib><title>Identification of a Novel UTY-Encoded Minor Histocompatibility Antigen</title><title>Scandinavian journal of immunology</title><addtitle>Scand J Immunol</addtitle><description>Minor histocompatibility antigens (mHags) encoded by the Y‐chromosome (H‐Y‐mHags) are known to play a pivotal role in allogeneic haematopoietic cell transplantation (HCT) involving female donors and male recipients. We present a new H‐Y‐mHag, YYNAFHWAI (UTY139–147), encoded by the UTY gene and presented by HLA‐A*24:02. Briefly, short peptide stretches encompassing multiple putative H‐Y‐mHags were designed using a bioinformatics predictor of peptide‐HLA binding, NetMHCpan. These peptides were used to screen for peptide‐specific HLA‐restricted T cell responses in peripheral blood mononuclear cells obtained post‐HCT from male recipients of female donor grafts. In one of these recipients, a CD8+ T cell response was observed against a peptide stretch encoded by the UTY gene. Another bioinformatics tool, HLArestrictor, was used to identify the optimal peptide and HLA‐restriction element. Using peptide/HLA tetramers, the specificity of the CD8+ T cell response was successfully validated as being HLA‐A*24:02‐restricted and directed against the male UTY139–147 peptide. Functional analysis of these T cells demonstrated male UTY139–147 peptide‐specific cytokine secretion (IFNγ, TNFα and MIP‐1β) and cytotoxic degranulation (CD107a). In contrast, no responses were seen when the T cells were stimulated with patient tumour cells alone. CD8+ T cells specific for this new H‐Y‐mHag were found in three of five HLA‐A*24:02‐positive male recipients of female donor HCT grafts available for this study.</description><subject>Amino Acid Sequence</subject><subject>Blood Cells - transplantation</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Epitopes - immunology</subject><subject>Female</subject><subject>HLA-A24 Antigen - immunology</subject><subject>Humans</subject><subject>Male</subject><subject>Minor Histocompatibility Antigens - immunology</subject><subject>Nuclear Proteins - chemistry</subject><subject>Nuclear Proteins - immunology</subject><subject>Transplantation, Homologous</subject><issn>0300-9475</issn><issn>1365-3083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNkE9v0zAYxi3ExLrBV0CRuHBJeOP_PnCYxv50GuXAJsTJchwbuaRxidOt_fZz6NYDJ3yxJf-e149_CBU1VHVen5ZVTTgrCUhSYahxBViArLav0Oxw8RrNgACUigp2jE5SWgLUBAvyBh1jzAhXis7Q5bx1_Rh8sGYMsS-iL0yxiA-uK-7vfpYXvY2ta4uvoY9DcR3SGG1crTPbhC6Mu-Ish3-5_i068qZL7t3zforuLy_uzq_L229X8_Oz29JSyWRpHW-lMIy1XGGXy4DjynraKC4dEONFQ5URBFosiVWe5cqYemVBNkq2npyij_u56yH-2bg06lVI1nWd6V3cJF1PX5aAKc3oh3_QZdwMfW6na0owBmC8zpTcU3aIKQ3O6_UQVmbY5VF6cq2XelKqJ6V6cq3_utbbHH3__MCmWbn2EHyRm4HPe-AxdG7334P195v5dMr5cp_P2t32kDfDb80FEUz_WFxprLi4WUjQX8gTQ-aZxw</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>Mortensen, B. 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K.</au><au>Rasmussen, A. H.</au><au>Larsen, M. E.</au><au>Larsen, M. V.</au><au>Lund, O.</au><au>Braendstrup, P.</au><au>Harndahl, M.</au><au>Rasmussen, M.</au><au>Buus, S.</au><au>Stryhn, A.</au><au>Vindeløv, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of a Novel UTY-Encoded Minor Histocompatibility Antigen</atitle><jtitle>Scandinavian journal of immunology</jtitle><addtitle>Scand J Immunol</addtitle><date>2012-08</date><risdate>2012</risdate><volume>76</volume><issue>2</issue><spage>141</spage><epage>150</epage><pages>141-150</pages><issn>0300-9475</issn><eissn>1365-3083</eissn><abstract>Minor histocompatibility antigens (mHags) encoded by the Y‐chromosome (H‐Y‐mHags) are known to play a pivotal role in allogeneic haematopoietic cell transplantation (HCT) involving female donors and male recipients. We present a new H‐Y‐mHag, YYNAFHWAI (UTY139–147), encoded by the UTY gene and presented by HLA‐A*24:02. 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In contrast, no responses were seen when the T cells were stimulated with patient tumour cells alone. CD8+ T cells specific for this new H‐Y‐mHag were found in three of five HLA‐A*24:02‐positive male recipients of female donor HCT grafts available for this study.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22536994</pmid><doi>10.1111/j.1365-3083.2012.02708.x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Blood Cells - transplantation CD8-Positive T-Lymphocytes - immunology Epitopes - immunology Female HLA-A24 Antigen - immunology Humans Male Minor Histocompatibility Antigens - immunology Nuclear Proteins - chemistry Nuclear Proteins - immunology Transplantation, Homologous |
title | Identification of a Novel UTY-Encoded Minor Histocompatibility Antigen |
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