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Dominant TCR α-chain clonotypes and interferon-γ are expressed in the pancreas of patients with recent-onset insulin-dependent diabetes mellitus
In order to clarify the nature of T lymphocytes infiltrating the pancreatic islets of patients with insulin-dependent diabetes mellitus (IDDM), we analysed T cell receptor (TCR) gene transcripts expressed in pancreatic biopsy specimens of patients with recent-onset IDDM. We also investigated the exp...
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Published in: | Diabetes research and clinical practice 1996-09, Vol.34 (1), p.37-46 |
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container_title | Diabetes research and clinical practice |
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creator | Yamagata, Kazuya Nakajima, Hiromu Tomita, Koji Itoh, Naoto Miyagawa, Jun-ichiro Hamaguchi, Tomoya Namba, Mitsuyoshi Tamura, Shinji Kawata, Sumio Kono, Norio Kuwajima, Masamichi Noguchi, Tamio Hanafusa, Toshiaki Matsuzawa, Yuji |
description | In order to clarify the nature of T lymphocytes infiltrating the pancreatic islets of patients with insulin-dependent diabetes mellitus (IDDM), we analysed T cell receptor (TCR) gene transcripts expressed in pancreatic biopsy specimens of patients with recent-onset IDDM. We also investigated the expression of cytokines (interferon-γ: IFN-γ; tumour necrosis factor-α: TNF-α; interleukin-4: IL-4; interleukin-6: IL-6) in the same specimens. The TCR Vβ repertoire was not restricted either in the pancreas or the peripheral lymphocytes of IDDM patients. In contrast, the TCR Vα repertoire was restricted in the pancreas, but not in the peripheral blood lymphocytes, of IDDM patients. The sequence analysis of the complementarity-determining region 3 (CDR3) of the TCRα revealed the presence of dominant clonality in α chains of T cells in the patients. IFN-γ mRNA was highly expressed in the pancreas of IDDM patients, while IL-4 mRNA was deficient. A lower level of expression of IL-6 mRNA was detected in the IDDM pancreas than in the control tissue. These results indicate that T cells bearing a distinct TCRα chain are selectively retained and activated within the pancreas of recent-onset IDDM. |
doi_str_mv | 10.1016/S0168-8227(96)01328-9 |
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We also investigated the expression of cytokines (interferon-γ: IFN-γ; tumour necrosis factor-α: TNF-α; interleukin-4: IL-4; interleukin-6: IL-6) in the same specimens. The TCR Vβ repertoire was not restricted either in the pancreas or the peripheral lymphocytes of IDDM patients. In contrast, the TCR Vα repertoire was restricted in the pancreas, but not in the peripheral blood lymphocytes, of IDDM patients. The sequence analysis of the complementarity-determining region 3 (CDR3) of the TCRα revealed the presence of dominant clonality in α chains of T cells in the patients. IFN-γ mRNA was highly expressed in the pancreas of IDDM patients, while IL-4 mRNA was deficient. A lower level of expression of IL-6 mRNA was detected in the IDDM pancreas than in the control tissue. These results indicate that T cells bearing a distinct TCRα chain are selectively retained and activated within the pancreas of recent-onset IDDM.</description><identifier>ISSN: 0168-8227</identifier><identifier>EISSN: 1872-8227</identifier><identifier>DOI: 10.1016/S0168-8227(96)01328-9</identifier><identifier>PMID: 8968689</identifier><identifier>CODEN: DRCPE9</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Adolescent ; Adult ; Amino Acid Sequence ; Associated diseases and complications ; Base Sequence ; Biological and medical sciences ; Consensus Sequence ; Cytokines - biosynthesis ; Diabetes Mellitus, Type 1 - immunology ; Diabetes. Impaired glucose tolerance ; DNA Primers ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Female ; Gene Expression ; Humans ; Insulin-dependent diabetes mellitus ; Interferon-gamma - biosynthesis ; Interferon-gamma - genetics ; Interferon-γ ; Interleukin-4 ; Interleukin-4 - biosynthesis ; Interleukin-6 - biosynthesis ; Lymphocytes - immunology ; Male ; Medical sciences ; Molecular Sequence Data ; Pancreas ; Pancreas - immunology ; Polymerase Chain Reaction ; Receptor-CD3 Complex, Antigen, T-Cell - biosynthesis ; Receptors, Antigen, T-Cell, alpha-beta - biosynthesis ; Receptors, Antigen, T-Cell, alpha-beta - chemistry ; Receptors, Antigen, T-Cell, alpha-beta - genetics ; T cell receptor ; Transcription, Genetic ; Tumor Necrosis Factor-alpha - biosynthesis</subject><ispartof>Diabetes research and clinical practice, 1996-09, Vol.34 (1), p.37-46</ispartof><rights>1996</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-9dd691cc35330a8ef1ab54e18c6e2e6c655c0033c3a14792eef44c19002988ec3</citedby><cites>FETCH-LOGICAL-c389t-9dd691cc35330a8ef1ab54e18c6e2e6c655c0033c3a14792eef44c19002988ec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2512853$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8968689$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamagata, Kazuya</creatorcontrib><creatorcontrib>Nakajima, Hiromu</creatorcontrib><creatorcontrib>Tomita, Koji</creatorcontrib><creatorcontrib>Itoh, Naoto</creatorcontrib><creatorcontrib>Miyagawa, Jun-ichiro</creatorcontrib><creatorcontrib>Hamaguchi, Tomoya</creatorcontrib><creatorcontrib>Namba, Mitsuyoshi</creatorcontrib><creatorcontrib>Tamura, Shinji</creatorcontrib><creatorcontrib>Kawata, Sumio</creatorcontrib><creatorcontrib>Kono, Norio</creatorcontrib><creatorcontrib>Kuwajima, Masamichi</creatorcontrib><creatorcontrib>Noguchi, Tamio</creatorcontrib><creatorcontrib>Hanafusa, Toshiaki</creatorcontrib><creatorcontrib>Matsuzawa, Yuji</creatorcontrib><title>Dominant TCR α-chain clonotypes and interferon-γ are expressed in the pancreas of patients with recent-onset insulin-dependent diabetes mellitus</title><title>Diabetes research and clinical practice</title><addtitle>Diabetes Res Clin Pract</addtitle><description>In order to clarify the nature of T lymphocytes infiltrating the pancreatic islets of patients with insulin-dependent diabetes mellitus (IDDM), we analysed T cell receptor (TCR) gene transcripts expressed in pancreatic biopsy specimens of patients with recent-onset IDDM. We also investigated the expression of cytokines (interferon-γ: IFN-γ; tumour necrosis factor-α: TNF-α; interleukin-4: IL-4; interleukin-6: IL-6) in the same specimens. The TCR Vβ repertoire was not restricted either in the pancreas or the peripheral lymphocytes of IDDM patients. In contrast, the TCR Vα repertoire was restricted in the pancreas, but not in the peripheral blood lymphocytes, of IDDM patients. The sequence analysis of the complementarity-determining region 3 (CDR3) of the TCRα revealed the presence of dominant clonality in α chains of T cells in the patients. IFN-γ mRNA was highly expressed in the pancreas of IDDM patients, while IL-4 mRNA was deficient. A lower level of expression of IL-6 mRNA was detected in the IDDM pancreas than in the control tissue. These results indicate that T cells bearing a distinct TCRα chain are selectively retained and activated within the pancreas of recent-onset IDDM.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Amino Acid Sequence</subject><subject>Associated diseases and complications</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Consensus Sequence</subject><subject>Cytokines - biosynthesis</subject><subject>Diabetes Mellitus, Type 1 - immunology</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>DNA Primers</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Humans</subject><subject>Insulin-dependent diabetes mellitus</subject><subject>Interferon-gamma - biosynthesis</subject><subject>Interferon-gamma - genetics</subject><subject>Interferon-γ</subject><subject>Interleukin-4</subject><subject>Interleukin-4 - biosynthesis</subject><subject>Interleukin-6 - biosynthesis</subject><subject>Lymphocytes - immunology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Molecular Sequence Data</subject><subject>Pancreas</subject><subject>Pancreas - immunology</subject><subject>Polymerase Chain Reaction</subject><subject>Receptor-CD3 Complex, Antigen, T-Cell - biosynthesis</subject><subject>Receptors, Antigen, T-Cell, alpha-beta - biosynthesis</subject><subject>Receptors, Antigen, T-Cell, alpha-beta - chemistry</subject><subject>Receptors, Antigen, T-Cell, alpha-beta - genetics</subject><subject>T cell receptor</subject><subject>Transcription, Genetic</subject><subject>Tumor Necrosis Factor-alpha - biosynthesis</subject><issn>0168-8227</issn><issn>1872-8227</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNqFkUtuFDEQhi1EFIaBI0TyAqGw6GC3uz32CkXDU4qEBGFtedzVGqNuu3G5IbkGN0HcI2fC89Bs2fhR_1-u8leEXHB2xRmXr7-WRVWqrleXWr5iXNSq0o_IgqtVvQ8_JouT5Ql5ividMSZF056Tc6WlkkovyO-3cfTBhkxv11_ow5_Kba0P1A0xxHw_AVIbOupDhtRDiqF6-EttAgp3UwJE2Gk0b4FONrgEFmnsyzl7CBnpL5-3NIErlyoGhFzcOA8-VB1MELoSp523G8il0AjD4POMz8hZbweE58d9Sb69f3e7_ljdfP7waX19UzmhdK5010nNnROtEMwq6LndtA1w5STUIJ1sW8eYEE5Y3qx0DdA3jeOasVorBU4sycvDu1OKP2bAbEaPrjRhA8QZzUpJrpVuirE9GF2KiAl6MyU_2nRvODO7WZj9LMwOtNHS7GdhdMm7OBaYNyN0p6wj_KK_OOoWnR36VBB6PNnqlteqfG5J3hxsUGD89JAMuoLXQecL2my66P_TyD9IE6o5</recordid><startdate>19960901</startdate><enddate>19960901</enddate><creator>Yamagata, Kazuya</creator><creator>Nakajima, Hiromu</creator><creator>Tomita, Koji</creator><creator>Itoh, Naoto</creator><creator>Miyagawa, Jun-ichiro</creator><creator>Hamaguchi, Tomoya</creator><creator>Namba, Mitsuyoshi</creator><creator>Tamura, Shinji</creator><creator>Kawata, Sumio</creator><creator>Kono, Norio</creator><creator>Kuwajima, Masamichi</creator><creator>Noguchi, Tamio</creator><creator>Hanafusa, Toshiaki</creator><creator>Matsuzawa, Yuji</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Science</general><scope>IQODW</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>19960901</creationdate><title>Dominant TCR α-chain clonotypes and interferon-γ are expressed in the pancreas of patients with recent-onset insulin-dependent diabetes mellitus</title><author>Yamagata, Kazuya ; Nakajima, Hiromu ; Tomita, Koji ; Itoh, Naoto ; Miyagawa, Jun-ichiro ; Hamaguchi, Tomoya ; Namba, Mitsuyoshi ; Tamura, Shinji ; Kawata, Sumio ; Kono, Norio ; Kuwajima, Masamichi ; Noguchi, Tamio ; Hanafusa, Toshiaki ; Matsuzawa, Yuji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-9dd691cc35330a8ef1ab54e18c6e2e6c655c0033c3a14792eef44c19002988ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Amino Acid Sequence</topic><topic>Associated diseases and complications</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Consensus Sequence</topic><topic>Cytokines - biosynthesis</topic><topic>Diabetes Mellitus, Type 1 - immunology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>DNA Primers</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Humans</topic><topic>Insulin-dependent diabetes mellitus</topic><topic>Interferon-gamma - biosynthesis</topic><topic>Interferon-gamma - genetics</topic><topic>Interferon-γ</topic><topic>Interleukin-4</topic><topic>Interleukin-4 - biosynthesis</topic><topic>Interleukin-6 - biosynthesis</topic><topic>Lymphocytes - immunology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Molecular Sequence Data</topic><topic>Pancreas</topic><topic>Pancreas - immunology</topic><topic>Polymerase Chain Reaction</topic><topic>Receptor-CD3 Complex, Antigen, T-Cell - biosynthesis</topic><topic>Receptors, Antigen, T-Cell, alpha-beta - biosynthesis</topic><topic>Receptors, Antigen, T-Cell, alpha-beta - chemistry</topic><topic>Receptors, Antigen, T-Cell, alpha-beta - genetics</topic><topic>T cell receptor</topic><topic>Transcription, Genetic</topic><topic>Tumor Necrosis Factor-alpha - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamagata, Kazuya</creatorcontrib><creatorcontrib>Nakajima, Hiromu</creatorcontrib><creatorcontrib>Tomita, Koji</creatorcontrib><creatorcontrib>Itoh, Naoto</creatorcontrib><creatorcontrib>Miyagawa, Jun-ichiro</creatorcontrib><creatorcontrib>Hamaguchi, Tomoya</creatorcontrib><creatorcontrib>Namba, Mitsuyoshi</creatorcontrib><creatorcontrib>Tamura, Shinji</creatorcontrib><creatorcontrib>Kawata, Sumio</creatorcontrib><creatorcontrib>Kono, Norio</creatorcontrib><creatorcontrib>Kuwajima, Masamichi</creatorcontrib><creatorcontrib>Noguchi, Tamio</creatorcontrib><creatorcontrib>Hanafusa, Toshiaki</creatorcontrib><creatorcontrib>Matsuzawa, Yuji</creatorcontrib><collection>Pascal-Francis</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>Diabetes research and clinical practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamagata, Kazuya</au><au>Nakajima, Hiromu</au><au>Tomita, Koji</au><au>Itoh, Naoto</au><au>Miyagawa, Jun-ichiro</au><au>Hamaguchi, Tomoya</au><au>Namba, Mitsuyoshi</au><au>Tamura, Shinji</au><au>Kawata, Sumio</au><au>Kono, Norio</au><au>Kuwajima, Masamichi</au><au>Noguchi, Tamio</au><au>Hanafusa, Toshiaki</au><au>Matsuzawa, Yuji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dominant TCR α-chain clonotypes and interferon-γ are expressed in the pancreas of patients with recent-onset insulin-dependent diabetes mellitus</atitle><jtitle>Diabetes research and clinical practice</jtitle><addtitle>Diabetes Res Clin Pract</addtitle><date>1996-09-01</date><risdate>1996</risdate><volume>34</volume><issue>1</issue><spage>37</spage><epage>46</epage><pages>37-46</pages><issn>0168-8227</issn><eissn>1872-8227</eissn><coden>DRCPE9</coden><abstract>In order to clarify the nature of T lymphocytes infiltrating the pancreatic islets of patients with insulin-dependent diabetes mellitus (IDDM), we analysed T cell receptor (TCR) gene transcripts expressed in pancreatic biopsy specimens of patients with recent-onset IDDM. We also investigated the expression of cytokines (interferon-γ: IFN-γ; tumour necrosis factor-α: TNF-α; interleukin-4: IL-4; interleukin-6: IL-6) in the same specimens. The TCR Vβ repertoire was not restricted either in the pancreas or the peripheral lymphocytes of IDDM patients. In contrast, the TCR Vα repertoire was restricted in the pancreas, but not in the peripheral blood lymphocytes, of IDDM patients. The sequence analysis of the complementarity-determining region 3 (CDR3) of the TCRα revealed the presence of dominant clonality in α chains of T cells in the patients. IFN-γ mRNA was highly expressed in the pancreas of IDDM patients, while IL-4 mRNA was deficient. A lower level of expression of IL-6 mRNA was detected in the IDDM pancreas than in the control tissue. These results indicate that T cells bearing a distinct TCRα chain are selectively retained and activated within the pancreas of recent-onset IDDM.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>8968689</pmid><doi>10.1016/S0168-8227(96)01328-9</doi><tpages>10</tpages></addata></record> |
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subjects | Adolescent Adult Amino Acid Sequence Associated diseases and complications Base Sequence Biological and medical sciences Consensus Sequence Cytokines - biosynthesis Diabetes Mellitus, Type 1 - immunology Diabetes. Impaired glucose tolerance DNA Primers Endocrine pancreas. Apud cells (diseases) Endocrinopathies Female Gene Expression Humans Insulin-dependent diabetes mellitus Interferon-gamma - biosynthesis Interferon-gamma - genetics Interferon-γ Interleukin-4 Interleukin-4 - biosynthesis Interleukin-6 - biosynthesis Lymphocytes - immunology Male Medical sciences Molecular Sequence Data Pancreas Pancreas - immunology Polymerase Chain Reaction Receptor-CD3 Complex, Antigen, T-Cell - biosynthesis Receptors, Antigen, T-Cell, alpha-beta - biosynthesis Receptors, Antigen, T-Cell, alpha-beta - chemistry Receptors, Antigen, T-Cell, alpha-beta - genetics T cell receptor Transcription, Genetic Tumor Necrosis Factor-alpha - biosynthesis |
title | Dominant TCR α-chain clonotypes and interferon-γ are expressed in the pancreas of patients with recent-onset insulin-dependent diabetes mellitus |
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