PDC-E3BP is not a dominant T-cell autoantigen in primary biliary cirrhosis
: Background: Autoantibody responses reactive with the E2 and E3BP components of pyruvate dehydrogenase complex (PDC), which characterise primary biliary cirrhosis (PBC) crossreact, precluding the identification, from serological studies, of the antigen to which the principal breakdown of tolerance...
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Veröffentlicht in: | Liver international 2006-05, Vol.26 (4), p.406-413 |
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description | : Background: Autoantibody responses reactive with the E2 and E3BP components of pyruvate dehydrogenase complex (PDC), which characterise primary biliary cirrhosis (PBC) crossreact, precluding the identification, from serological studies, of the antigen to which the principal breakdown of tolerance occurs. Although autoreactive T‐cell responses to PDC‐E2 have been well characterised it is, at present, unclear whether T‐cell tolerance breakdown also occurs to PDC‐E3BP. The aims of this study were to characterise autoreactive T‐cell responses to PDC‐E3BP in PBC and potential factors regulating their expression.
Methods: Peripheral blood T‐cell proliferative responses to purified recombinant human PDC‐E2 and PDC‐E3BP at a range of concentrations were characterised in PBC patients and control subjects.
Results: T‐cell proliferative responses to both E2 and E3BP were absent from control subjects (median peak stimulation index (SI) to PDC‐E2 1.2 [range 0.3–1.9], 0/10 positive (SI>2.32), median peak SI to PDC‐E3BP 1.1 [0.7–2.1]], 0/10 positive). Significant responses to PDC‐E2 were seen in the majority of patients (median peak SI 11.4 [0.4–24.4], 17/20 (85%) positive) but to PDC‐E3BP in only a minority (median peak SI 1–9 [0.6–9.95], 8/20 (40%) positive). Where responses to PDC‐E3BP were seen they were universally secondary to responses to PDC‐E2.
Conclusions: Despite the presence of antibodies reactive with PDC‐E3BP in the majority of PBC patients this self‐protein is not a dominant T‐cell autoantigen in PBC. |
doi_str_mv | 10.1111/j.1478-3231.2006.01253.x |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67894060</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67894060</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4053-d4ca639a9652cc6a89f0761767cde76b52c08f7b2d8b6b7a6235ade14baba1573</originalsourceid><addsrcrecordid>eNqNkEtTgzAUhTOOjq3Vv-Bk5Q7MAxJYuLC01mqndpyqy0yAoKk8KoGx_feCMHVrNvfe5JybMx8AECMbN-d6Y2OHexYlFNsEIWYjTFxq747A8PBwfOgJHYAzYzYIYd938SkYYMaIzxw6BA-rSWBN6XgFtYF5UUEJ4yLTucwruLYilaZQ1lXRjPpd5VDncFvqTJZ7GOpUtzXSZflRGG3OwUkiU6Mu-joCL3fTdXBvLZ5m8-B2YUUOcqkVO5Fk1Jc-c0kUMen5CeIMc8ajWHEWNrfIS3hIYi9kIZeMUFfGCjuhDCV2OR2Bq27vtiy-amUqkWnTJpW5KmojGPd8BzHUCL1OGJWFMaVKRJ9dYCRajmIjWkSixSVajuKXo9g11sv-jzrMVPxn7ME1gptO8K1Ttf_3YrGYv7Zd47c6vzaV2h38svxs8lPuirflTHh88hzMHpdiTH8Arx2PMQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67894060</pqid></control><display><type>article</type><title>PDC-E3BP is not a dominant T-cell autoantigen in primary biliary cirrhosis</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>McHugh, Anna ; Robe, Amanda J. ; Palmer, Jeremy M. ; Jones, David E. J.</creator><creatorcontrib>McHugh, Anna ; Robe, Amanda J. ; Palmer, Jeremy M. ; Jones, David E. J.</creatorcontrib><description>: Background: Autoantibody responses reactive with the E2 and E3BP components of pyruvate dehydrogenase complex (PDC), which characterise primary biliary cirrhosis (PBC) crossreact, precluding the identification, from serological studies, of the antigen to which the principal breakdown of tolerance occurs. Although autoreactive T‐cell responses to PDC‐E2 have been well characterised it is, at present, unclear whether T‐cell tolerance breakdown also occurs to PDC‐E3BP. The aims of this study were to characterise autoreactive T‐cell responses to PDC‐E3BP in PBC and potential factors regulating their expression.
Methods: Peripheral blood T‐cell proliferative responses to purified recombinant human PDC‐E2 and PDC‐E3BP at a range of concentrations were characterised in PBC patients and control subjects.
Results: T‐cell proliferative responses to both E2 and E3BP were absent from control subjects (median peak stimulation index (SI) to PDC‐E2 1.2 [range 0.3–1.9], 0/10 positive (SI>2.32), median peak SI to PDC‐E3BP 1.1 [0.7–2.1]], 0/10 positive). Significant responses to PDC‐E2 were seen in the majority of patients (median peak SI 11.4 [0.4–24.4], 17/20 (85%) positive) but to PDC‐E3BP in only a minority (median peak SI 1–9 [0.6–9.95], 8/20 (40%) positive). Where responses to PDC‐E3BP were seen they were universally secondary to responses to PDC‐E2.
Conclusions: Despite the presence of antibodies reactive with PDC‐E3BP in the majority of PBC patients this self‐protein is not a dominant T‐cell autoantigen in PBC.</description><identifier>ISSN: 1478-3223</identifier><identifier>EISSN: 1478-3231</identifier><identifier>DOI: 10.1111/j.1478-3231.2006.01253.x</identifier><identifier>PMID: 16629643</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Autoantigens - blood ; Autoantigens - immunology ; autoimmune disease ; Case-Control Studies ; CD4-Positive T-Lymphocytes - immunology ; CD4-Positive T-Lymphocytes - pathology ; Cross Reactions - immunology ; Dihydrolipoyllysine-Residue Acetyltransferase - immunology ; human study ; Humans ; immune tolerance ; Immune Tolerance - immunology ; liver cirrhosis biliary ; Liver Cirrhosis, Biliary - blood ; Liver Cirrhosis, Biliary - immunology ; Liver Cirrhosis, Biliary - pathology ; Mitochondrial Proteins - immunology ; pyruvate dehydrogenase complex ; Pyruvate Dehydrogenase Complex - immunology ; Receptors, Interleukin-2 - immunology ; regulatory T-cell</subject><ispartof>Liver international, 2006-05, Vol.26 (4), p.406-413</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4053-d4ca639a9652cc6a89f0761767cde76b52c08f7b2d8b6b7a6235ade14baba1573</citedby><cites>FETCH-LOGICAL-c4053-d4ca639a9652cc6a89f0761767cde76b52c08f7b2d8b6b7a6235ade14baba1573</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1478-3231.2006.01253.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1478-3231.2006.01253.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16629643$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McHugh, Anna</creatorcontrib><creatorcontrib>Robe, Amanda J.</creatorcontrib><creatorcontrib>Palmer, Jeremy M.</creatorcontrib><creatorcontrib>Jones, David E. J.</creatorcontrib><title>PDC-E3BP is not a dominant T-cell autoantigen in primary biliary cirrhosis</title><title>Liver international</title><addtitle>Liver Int</addtitle><description>: Background: Autoantibody responses reactive with the E2 and E3BP components of pyruvate dehydrogenase complex (PDC), which characterise primary biliary cirrhosis (PBC) crossreact, precluding the identification, from serological studies, of the antigen to which the principal breakdown of tolerance occurs. Although autoreactive T‐cell responses to PDC‐E2 have been well characterised it is, at present, unclear whether T‐cell tolerance breakdown also occurs to PDC‐E3BP. The aims of this study were to characterise autoreactive T‐cell responses to PDC‐E3BP in PBC and potential factors regulating their expression.
Methods: Peripheral blood T‐cell proliferative responses to purified recombinant human PDC‐E2 and PDC‐E3BP at a range of concentrations were characterised in PBC patients and control subjects.
Results: T‐cell proliferative responses to both E2 and E3BP were absent from control subjects (median peak stimulation index (SI) to PDC‐E2 1.2 [range 0.3–1.9], 0/10 positive (SI>2.32), median peak SI to PDC‐E3BP 1.1 [0.7–2.1]], 0/10 positive). Significant responses to PDC‐E2 were seen in the majority of patients (median peak SI 11.4 [0.4–24.4], 17/20 (85%) positive) but to PDC‐E3BP in only a minority (median peak SI 1–9 [0.6–9.95], 8/20 (40%) positive). Where responses to PDC‐E3BP were seen they were universally secondary to responses to PDC‐E2.
Conclusions: Despite the presence of antibodies reactive with PDC‐E3BP in the majority of PBC patients this self‐protein is not a dominant T‐cell autoantigen in PBC.</description><subject>Autoantigens - blood</subject><subject>Autoantigens - immunology</subject><subject>autoimmune disease</subject><subject>Case-Control Studies</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - pathology</subject><subject>Cross Reactions - immunology</subject><subject>Dihydrolipoyllysine-Residue Acetyltransferase - immunology</subject><subject>human study</subject><subject>Humans</subject><subject>immune tolerance</subject><subject>Immune Tolerance - immunology</subject><subject>liver cirrhosis biliary</subject><subject>Liver Cirrhosis, Biliary - blood</subject><subject>Liver Cirrhosis, Biliary - immunology</subject><subject>Liver Cirrhosis, Biliary - pathology</subject><subject>Mitochondrial Proteins - immunology</subject><subject>pyruvate dehydrogenase complex</subject><subject>Pyruvate Dehydrogenase Complex - immunology</subject><subject>Receptors, Interleukin-2 - immunology</subject><subject>regulatory T-cell</subject><issn>1478-3223</issn><issn>1478-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtTgzAUhTOOjq3Vv-Bk5Q7MAxJYuLC01mqndpyqy0yAoKk8KoGx_feCMHVrNvfe5JybMx8AECMbN-d6Y2OHexYlFNsEIWYjTFxq747A8PBwfOgJHYAzYzYIYd938SkYYMaIzxw6BA-rSWBN6XgFtYF5UUEJ4yLTucwruLYilaZQ1lXRjPpd5VDncFvqTJZ7GOpUtzXSZflRGG3OwUkiU6Mu-joCL3fTdXBvLZ5m8-B2YUUOcqkVO5Fk1Jc-c0kUMen5CeIMc8ajWHEWNrfIS3hIYi9kIZeMUFfGCjuhDCV2OR2Bq27vtiy-amUqkWnTJpW5KmojGPd8BzHUCL1OGJWFMaVKRJ9dYCRajmIjWkSixSVajuKXo9g11sv-jzrMVPxn7ME1gptO8K1Ttf_3YrGYv7Zd47c6vzaV2h38svxs8lPuirflTHh88hzMHpdiTH8Arx2PMQ</recordid><startdate>200605</startdate><enddate>200605</enddate><creator>McHugh, Anna</creator><creator>Robe, Amanda J.</creator><creator>Palmer, Jeremy M.</creator><creator>Jones, David E. J.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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></search><sort><creationdate>200605</creationdate><title>PDC-E3BP is not a dominant T-cell autoantigen in primary biliary cirrhosis</title><author>McHugh, Anna ; Robe, Amanda J. ; Palmer, Jeremy M. ; Jones, David E. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4053-d4ca639a9652cc6a89f0761767cde76b52c08f7b2d8b6b7a6235ade14baba1573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Autoantigens - blood</topic><topic>Autoantigens - immunology</topic><topic>autoimmune disease</topic><topic>Case-Control Studies</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD4-Positive T-Lymphocytes - pathology</topic><topic>Cross Reactions - immunology</topic><topic>Dihydrolipoyllysine-Residue Acetyltransferase - immunology</topic><topic>human study</topic><topic>Humans</topic><topic>immune tolerance</topic><topic>Immune Tolerance - immunology</topic><topic>liver cirrhosis biliary</topic><topic>Liver Cirrhosis, Biliary - blood</topic><topic>Liver Cirrhosis, Biliary - immunology</topic><topic>Liver Cirrhosis, Biliary - pathology</topic><topic>Mitochondrial Proteins - immunology</topic><topic>pyruvate dehydrogenase complex</topic><topic>Pyruvate Dehydrogenase Complex - immunology</topic><topic>Receptors, Interleukin-2 - immunology</topic><topic>regulatory T-cell</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McHugh, Anna</creatorcontrib><creatorcontrib>Robe, Amanda J.</creatorcontrib><creatorcontrib>Palmer, Jeremy M.</creatorcontrib><creatorcontrib>Jones, David E. J.</creatorcontrib><collection>Istex</collection><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><jtitle>Liver international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McHugh, Anna</au><au>Robe, Amanda J.</au><au>Palmer, Jeremy M.</au><au>Jones, David E. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PDC-E3BP is not a dominant T-cell autoantigen in primary biliary cirrhosis</atitle><jtitle>Liver international</jtitle><addtitle>Liver Int</addtitle><date>2006-05</date><risdate>2006</risdate><volume>26</volume><issue>4</issue><spage>406</spage><epage>413</epage><pages>406-413</pages><issn>1478-3223</issn><eissn>1478-3231</eissn><abstract>: Background: Autoantibody responses reactive with the E2 and E3BP components of pyruvate dehydrogenase complex (PDC), which characterise primary biliary cirrhosis (PBC) crossreact, precluding the identification, from serological studies, of the antigen to which the principal breakdown of tolerance occurs. Although autoreactive T‐cell responses to PDC‐E2 have been well characterised it is, at present, unclear whether T‐cell tolerance breakdown also occurs to PDC‐E3BP. The aims of this study were to characterise autoreactive T‐cell responses to PDC‐E3BP in PBC and potential factors regulating their expression.
Methods: Peripheral blood T‐cell proliferative responses to purified recombinant human PDC‐E2 and PDC‐E3BP at a range of concentrations were characterised in PBC patients and control subjects.
Results: T‐cell proliferative responses to both E2 and E3BP were absent from control subjects (median peak stimulation index (SI) to PDC‐E2 1.2 [range 0.3–1.9], 0/10 positive (SI>2.32), median peak SI to PDC‐E3BP 1.1 [0.7–2.1]], 0/10 positive). Significant responses to PDC‐E2 were seen in the majority of patients (median peak SI 11.4 [0.4–24.4], 17/20 (85%) positive) but to PDC‐E3BP in only a minority (median peak SI 1–9 [0.6–9.95], 8/20 (40%) positive). Where responses to PDC‐E3BP were seen they were universally secondary to responses to PDC‐E2.
Conclusions: Despite the presence of antibodies reactive with PDC‐E3BP in the majority of PBC patients this self‐protein is not a dominant T‐cell autoantigen in PBC.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>16629643</pmid><doi>10.1111/j.1478-3231.2006.01253.x</doi><tpages>8</tpages></addata></record> |
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subjects | Autoantigens - blood Autoantigens - immunology autoimmune disease Case-Control Studies CD4-Positive T-Lymphocytes - immunology CD4-Positive T-Lymphocytes - pathology Cross Reactions - immunology Dihydrolipoyllysine-Residue Acetyltransferase - immunology human study Humans immune tolerance Immune Tolerance - immunology liver cirrhosis biliary Liver Cirrhosis, Biliary - blood Liver Cirrhosis, Biliary - immunology Liver Cirrhosis, Biliary - pathology Mitochondrial Proteins - immunology pyruvate dehydrogenase complex Pyruvate Dehydrogenase Complex - immunology Receptors, Interleukin-2 - immunology regulatory T-cell |
title | PDC-E3BP is not a dominant T-cell autoantigen in primary biliary cirrhosis |
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