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Citrullinated glucose-regulated protein 78 is a candidate target for melanoma immunotherapy
Post translational modification of proteins plays a significant role in immune recognition. In particular the modification of arginine to citrulline which is mediated by PAD enzymes is increased during cellular stress (autophagy) which permits the presentation of modified epitopes upon MHC class II...
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Published in: | Frontiers in immunology 2022-12, Vol.13, p.1066185-1066185 |
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creator | Brentville, Victoria Anne Symonds, Peter Chua, JiaXin Skinner, Anne Daniels, Ian Cook, Katherine Wendy Koncarevic, Sasa Martinez-Pinna, Roxana Shah, Sabaria Choudhury, Ruhul Hasan Vaghela, Poonam Weston, Daisy Al-Omari, Abdullah Davis, James Durrant, Lindy G |
description | Post translational modification of proteins plays a significant role in immune recognition. In particular the modification of arginine to citrulline which is mediated by PAD enzymes is increased during cellular stress (autophagy) which permits the presentation of modified epitopes upon MHC class II molecules for recognition by CD4 T cells. Citrullination also occurs in tumour cells as a result of continuous environmental stresses and increased autophagy. We have shown in animal models the efficient stimulation of citrullinated epitope specific CD4 T cells resulting in dramatic elimination/regression of tumours. The ER chaperone glucose-regulated protein 78 (GRP78) is known to also be required for stress-induced autophagy and is directly linked to autophagosome formation. GRP78 is known to be highly expressed by many tumour types. In this study we investigate the potential of targeting citrullinated GRP78 for cancer therapy.
A citrullinated GRP78 specific antibody was used to assess citrullinated GRP78 expression in murine and human tumour cells by flow cytometry. Five peptides were selected and used to vaccinate HLA transgenic mice and immune responses were characterised by ex vivo cytokine ELISpot assay. T cell repertoire in humans was assessed through proliferation assays and cytokine ELISpot assay. Citrullinated peptide was identified in murine B16 melanoma by mass spectrometry and the peptide vaccine was assessed for tumour therapy in a mouse melanoma model.
We show the identification CD4 T cell responses to one citrullinated GRP78 epitope that are restricted through HLA DP*0401 and HLA-DR*0101 alleles. This peptide is detected by mass spectrometry in B16 melanoma grown in vivo and citrulline specific CD4 responses to two peptides spanning this epitope mediate efficient therapy of established B16 melanoma tumours in HHDII/DP4 (p |
doi_str_mv | 10.3389/fimmu.2022.1066185 |
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A citrullinated GRP78 specific antibody was used to assess citrullinated GRP78 expression in murine and human tumour cells by flow cytometry. Five peptides were selected and used to vaccinate HLA transgenic mice and immune responses were characterised by ex vivo cytokine ELISpot assay. T cell repertoire in humans was assessed through proliferation assays and cytokine ELISpot assay. Citrullinated peptide was identified in murine B16 melanoma by mass spectrometry and the peptide vaccine was assessed for tumour therapy in a mouse melanoma model.
We show the identification CD4 T cell responses to one citrullinated GRP78 epitope that are restricted through HLA DP*0401 and HLA-DR*0101 alleles. This peptide is detected by mass spectrometry in B16 melanoma grown in vivo and citrulline specific CD4 responses to two peptides spanning this epitope mediate efficient therapy of established B16 melanoma tumours in HHDII/DP4 (p<0.0001) transgenic mouse model. Finally, we demonstrate the existence of a repertoire of responses to the citrullinated GRP78 peptide in healthy individuals (p=0.0023) with 13/17 (76%) individuals showing a response to this peptide.
We propose that citrullinated GRP78 is a candidate tumour antigen and vaccination against citrullinated GRP78 may provide a promising tumour therapy approach.</description><identifier>ISSN: 1664-3224</identifier><identifier>EISSN: 1664-3224</identifier><identifier>DOI: 10.3389/fimmu.2022.1066185</identifier><identifier>PMID: 36544781</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>Animals ; cancer ; citrullination ; Citrulline - metabolism ; Cytokines ; Endoplasmic Reticulum Chaperone BiP ; Epitopes ; GRP78 ; Humans ; Immunology ; Immunotherapy ; Melanoma, Experimental - therapy ; Membrane Proteins ; MHC-II ; Mice ; Peptides ; post-translation modifications</subject><ispartof>Frontiers in immunology, 2022-12, Vol.13, p.1066185-1066185</ispartof><rights>Copyright © 2022 Brentville, Symonds, Chua, Skinner, Daniels, Cook, Koncarevic, Martinez-Pinna, Shah, Choudhury, Vaghela, Weston, Al-Omari, Davis and Durrant.</rights><rights>Copyright © 2022 Brentville, Symonds, Chua, Skinner, Daniels, Cook, Koncarevic, Martinez-Pinna, Shah, Choudhury, Vaghela, Weston, Al-Omari, Davis and Durrant 2022 Brentville, Symonds, Chua, Skinner, Daniels, Cook, Koncarevic, Martinez-Pinna, Shah, Choudhury, Vaghela, Weston, Al-Omari, Davis and Durrant</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-cca960e14e58a97f4e7dd40d190ce76ae224175c9c3d442afdc2dd27ceb7de6d3</citedby><cites>FETCH-LOGICAL-c468t-cca960e14e58a97f4e7dd40d190ce76ae224175c9c3d442afdc2dd27ceb7de6d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9760948/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9760948/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36544781$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brentville, Victoria Anne</creatorcontrib><creatorcontrib>Symonds, Peter</creatorcontrib><creatorcontrib>Chua, JiaXin</creatorcontrib><creatorcontrib>Skinner, Anne</creatorcontrib><creatorcontrib>Daniels, Ian</creatorcontrib><creatorcontrib>Cook, Katherine Wendy</creatorcontrib><creatorcontrib>Koncarevic, Sasa</creatorcontrib><creatorcontrib>Martinez-Pinna, Roxana</creatorcontrib><creatorcontrib>Shah, Sabaria</creatorcontrib><creatorcontrib>Choudhury, Ruhul Hasan</creatorcontrib><creatorcontrib>Vaghela, Poonam</creatorcontrib><creatorcontrib>Weston, Daisy</creatorcontrib><creatorcontrib>Al-Omari, Abdullah</creatorcontrib><creatorcontrib>Davis, James</creatorcontrib><creatorcontrib>Durrant, Lindy G</creatorcontrib><title>Citrullinated glucose-regulated protein 78 is a candidate target for melanoma immunotherapy</title><title>Frontiers in immunology</title><addtitle>Front Immunol</addtitle><description>Post translational modification of proteins plays a significant role in immune recognition. In particular the modification of arginine to citrulline which is mediated by PAD enzymes is increased during cellular stress (autophagy) which permits the presentation of modified epitopes upon MHC class II molecules for recognition by CD4 T cells. Citrullination also occurs in tumour cells as a result of continuous environmental stresses and increased autophagy. We have shown in animal models the efficient stimulation of citrullinated epitope specific CD4 T cells resulting in dramatic elimination/regression of tumours. The ER chaperone glucose-regulated protein 78 (GRP78) is known to also be required for stress-induced autophagy and is directly linked to autophagosome formation. GRP78 is known to be highly expressed by many tumour types. In this study we investigate the potential of targeting citrullinated GRP78 for cancer therapy.
A citrullinated GRP78 specific antibody was used to assess citrullinated GRP78 expression in murine and human tumour cells by flow cytometry. Five peptides were selected and used to vaccinate HLA transgenic mice and immune responses were characterised by ex vivo cytokine ELISpot assay. T cell repertoire in humans was assessed through proliferation assays and cytokine ELISpot assay. Citrullinated peptide was identified in murine B16 melanoma by mass spectrometry and the peptide vaccine was assessed for tumour therapy in a mouse melanoma model.
We show the identification CD4 T cell responses to one citrullinated GRP78 epitope that are restricted through HLA DP*0401 and HLA-DR*0101 alleles. This peptide is detected by mass spectrometry in B16 melanoma grown in vivo and citrulline specific CD4 responses to two peptides spanning this epitope mediate efficient therapy of established B16 melanoma tumours in HHDII/DP4 (p<0.0001) transgenic mouse model. Finally, we demonstrate the existence of a repertoire of responses to the citrullinated GRP78 peptide in healthy individuals (p=0.0023) with 13/17 (76%) individuals showing a response to this peptide.
We propose that citrullinated GRP78 is a candidate tumour antigen and vaccination against citrullinated GRP78 may provide a promising tumour therapy approach.</description><subject>Animals</subject><subject>cancer</subject><subject>citrullination</subject><subject>Citrulline - metabolism</subject><subject>Cytokines</subject><subject>Endoplasmic Reticulum Chaperone BiP</subject><subject>Epitopes</subject><subject>GRP78</subject><subject>Humans</subject><subject>Immunology</subject><subject>Immunotherapy</subject><subject>Melanoma, Experimental - therapy</subject><subject>Membrane Proteins</subject><subject>MHC-II</subject><subject>Mice</subject><subject>Peptides</subject><subject>post-translation modifications</subject><issn>1664-3224</issn><issn>1664-3224</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkctu3CAUQK2qVROl-YEuKpbdeMrLgDeVqlEfkSJ10666QHfg2iHCZgq4Uv4-nkejhA3oPg4XTtO8Z3QjhOk_DWGalg2nnG8YVYqZ7lVzyZSSreBcvn52vmiuS7mn65K9EKJ721wI1UmpDbts_mxDzUuMYYaKnoxxcalgm3Fc4jGyz6limIk2JBQCxMHsg19TpEIesZIhZTJhhDlNQA5DzaneYYb9w7vmzQCx4PV5v2p-f_v6a_ujvf35_Wb75bZ1UpnaOge9osgkdgZ6PUjU3kvqWU8dagW4voHpzvVOeCk5DN5x77l2uNMelRdXzc2J6xPc230OE-QHmyDYYyDl0UKuwUW03HjT8R0bzA7lwDSg77RBz0F1vQO9sj6fWPtlN6F3ONcM8QX0ZWYOd3ZM_2yvFe2lWQEfz4Cc_i5Yqp1CcRjXD8K0FMt1p5linKm1lJ9KXU6lZByermHUHiTbo2R7kGzPktemD88HfGr5r1Q8AlgJpwc</recordid><startdate>20221205</startdate><enddate>20221205</enddate><creator>Brentville, Victoria Anne</creator><creator>Symonds, Peter</creator><creator>Chua, JiaXin</creator><creator>Skinner, Anne</creator><creator>Daniels, Ian</creator><creator>Cook, Katherine Wendy</creator><creator>Koncarevic, Sasa</creator><creator>Martinez-Pinna, Roxana</creator><creator>Shah, Sabaria</creator><creator>Choudhury, Ruhul Hasan</creator><creator>Vaghela, Poonam</creator><creator>Weston, Daisy</creator><creator>Al-Omari, Abdullah</creator><creator>Davis, James</creator><creator>Durrant, Lindy G</creator><general>Frontiers Media S.A</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20221205</creationdate><title>Citrullinated glucose-regulated protein 78 is a candidate target for melanoma immunotherapy</title><author>Brentville, Victoria Anne ; Symonds, Peter ; Chua, JiaXin ; Skinner, Anne ; Daniels, Ian ; Cook, Katherine Wendy ; Koncarevic, Sasa ; Martinez-Pinna, Roxana ; Shah, Sabaria ; Choudhury, Ruhul Hasan ; Vaghela, Poonam ; Weston, Daisy ; Al-Omari, Abdullah ; Davis, James ; Durrant, Lindy G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-cca960e14e58a97f4e7dd40d190ce76ae224175c9c3d442afdc2dd27ceb7de6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>cancer</topic><topic>citrullination</topic><topic>Citrulline - metabolism</topic><topic>Cytokines</topic><topic>Endoplasmic Reticulum Chaperone BiP</topic><topic>Epitopes</topic><topic>GRP78</topic><topic>Humans</topic><topic>Immunology</topic><topic>Immunotherapy</topic><topic>Melanoma, Experimental - therapy</topic><topic>Membrane Proteins</topic><topic>MHC-II</topic><topic>Mice</topic><topic>Peptides</topic><topic>post-translation modifications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brentville, Victoria Anne</creatorcontrib><creatorcontrib>Symonds, Peter</creatorcontrib><creatorcontrib>Chua, JiaXin</creatorcontrib><creatorcontrib>Skinner, Anne</creatorcontrib><creatorcontrib>Daniels, Ian</creatorcontrib><creatorcontrib>Cook, Katherine Wendy</creatorcontrib><creatorcontrib>Koncarevic, Sasa</creatorcontrib><creatorcontrib>Martinez-Pinna, Roxana</creatorcontrib><creatorcontrib>Shah, Sabaria</creatorcontrib><creatorcontrib>Choudhury, Ruhul Hasan</creatorcontrib><creatorcontrib>Vaghela, Poonam</creatorcontrib><creatorcontrib>Weston, Daisy</creatorcontrib><creatorcontrib>Al-Omari, Abdullah</creatorcontrib><creatorcontrib>Davis, James</creatorcontrib><creatorcontrib>Durrant, Lindy G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ</collection><jtitle>Frontiers in immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brentville, Victoria Anne</au><au>Symonds, Peter</au><au>Chua, JiaXin</au><au>Skinner, Anne</au><au>Daniels, Ian</au><au>Cook, Katherine Wendy</au><au>Koncarevic, Sasa</au><au>Martinez-Pinna, Roxana</au><au>Shah, Sabaria</au><au>Choudhury, Ruhul Hasan</au><au>Vaghela, Poonam</au><au>Weston, Daisy</au><au>Al-Omari, Abdullah</au><au>Davis, James</au><au>Durrant, Lindy G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Citrullinated glucose-regulated protein 78 is a candidate target for melanoma immunotherapy</atitle><jtitle>Frontiers in immunology</jtitle><addtitle>Front Immunol</addtitle><date>2022-12-05</date><risdate>2022</risdate><volume>13</volume><spage>1066185</spage><epage>1066185</epage><pages>1066185-1066185</pages><issn>1664-3224</issn><eissn>1664-3224</eissn><abstract>Post translational modification of proteins plays a significant role in immune recognition. In particular the modification of arginine to citrulline which is mediated by PAD enzymes is increased during cellular stress (autophagy) which permits the presentation of modified epitopes upon MHC class II molecules for recognition by CD4 T cells. Citrullination also occurs in tumour cells as a result of continuous environmental stresses and increased autophagy. We have shown in animal models the efficient stimulation of citrullinated epitope specific CD4 T cells resulting in dramatic elimination/regression of tumours. The ER chaperone glucose-regulated protein 78 (GRP78) is known to also be required for stress-induced autophagy and is directly linked to autophagosome formation. GRP78 is known to be highly expressed by many tumour types. In this study we investigate the potential of targeting citrullinated GRP78 for cancer therapy.
A citrullinated GRP78 specific antibody was used to assess citrullinated GRP78 expression in murine and human tumour cells by flow cytometry. Five peptides were selected and used to vaccinate HLA transgenic mice and immune responses were characterised by ex vivo cytokine ELISpot assay. T cell repertoire in humans was assessed through proliferation assays and cytokine ELISpot assay. Citrullinated peptide was identified in murine B16 melanoma by mass spectrometry and the peptide vaccine was assessed for tumour therapy in a mouse melanoma model.
We show the identification CD4 T cell responses to one citrullinated GRP78 epitope that are restricted through HLA DP*0401 and HLA-DR*0101 alleles. This peptide is detected by mass spectrometry in B16 melanoma grown in vivo and citrulline specific CD4 responses to two peptides spanning this epitope mediate efficient therapy of established B16 melanoma tumours in HHDII/DP4 (p<0.0001) transgenic mouse model. Finally, we demonstrate the existence of a repertoire of responses to the citrullinated GRP78 peptide in healthy individuals (p=0.0023) with 13/17 (76%) individuals showing a response to this peptide.
We propose that citrullinated GRP78 is a candidate tumour antigen and vaccination against citrullinated GRP78 may provide a promising tumour therapy approach.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>36544781</pmid><doi>10.3389/fimmu.2022.1066185</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals cancer citrullination Citrulline - metabolism Cytokines Endoplasmic Reticulum Chaperone BiP Epitopes GRP78 Humans Immunology Immunotherapy Melanoma, Experimental - therapy Membrane Proteins MHC-II Mice Peptides post-translation modifications |
title | Citrullinated glucose-regulated protein 78 is a candidate target for melanoma immunotherapy |
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