Loading…
Spontaneous diabetes in BB rats: evidence for a T cell dependent immune response defect
Approximately 50% of BB rats develop insulinopenic hyperglycaemia and ketosis spontaneously in association with insulitis. Amelioration of the syndrome by immunosuppression suggests a cell mediated immune pathogenesis. Analysis of the cell-mediated immune profile of overtly diabetic and normoglycaem...
Saved in:
Published in: | Diabetologia 1982-10, Vol.23 (4), p.359-364 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c318t-bfeb039cc0a3bf56b97d503c3d706d94e9789d5eaf6c3d3bf4561261f9875ce03 |
---|---|
cites | |
container_end_page | 364 |
container_issue | 4 |
container_start_page | 359 |
container_title | Diabetologia |
container_volume | 23 |
creator | Bellgrau, D Naji, A Silvers, W K Markmann, J F Barker, C F |
description | Approximately 50% of BB rats develop insulinopenic hyperglycaemia and ketosis spontaneously in association with insulitis. Amelioration of the syndrome by immunosuppression suggests a cell mediated immune pathogenesis. Analysis of the cell-mediated immune profile of overtly diabetic and normoglycaemic diabetes prone BB rats indicates that they are lymphocytopenic relative to non-diabetes prone BB rats and that the T cell pool is particularly affected. Furthermore, lymphocytes from diabetic and diabetes prone BB rats, while producing normal responses to the T cell mitogen concanavalin A, do not respond when mixed in vitro with major histocompatibility complex incompatible lymphocytes. This anergy is not restored either by enriching the responding cell population for T cells or by adding exogenous T cell growth promoting factor. Thus BB rats have a numerical and regulatory deficit of their T cells which could be related to their propensity for diabetes. |
doi_str_mv | 10.1007/BF00253745 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_74286860</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>74286860</sourcerecordid><originalsourceid>FETCH-LOGICAL-c318t-bfeb039cc0a3bf56b97d503c3d706d94e9789d5eaf6c3d3bf4561261f9875ce03</originalsourceid><addsrcrecordid>eNpFkE1LAzEQhoMotVYv3oWcPAirk80mu-vNFqtCwYMVvS3ZZAIr3Q-TbMF_b0qLngbeeXiZeQi5ZHDLAPK7-RIgFTzPxBGZsoynCWRpcUymACxNWCE_T8mZ918AwEUmJ2QiUyYZz6bk423ou6A67EdPTaNqDOhp09H5nDoV_D3FbWOw00ht76iia6pxs6EGB-xiHmjTtmOH1KGPTR7jxqIO5-TEqo3Hi8Ockffl43rxnKxen14WD6tEc1aEpLZYAy-1BsVrK2Rd5kYA19zkIE2ZYZkXpRGorIxZRDIhWSqZLYtcaAQ-I9f73sH13yP6ULWN3124f6nKowhZyB14swe16713aKvBNa1yPxWDamex-rcY4atD61i3aP7Qgzb-C4libCc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>74286860</pqid></control><display><type>article</type><title>Spontaneous diabetes in BB rats: evidence for a T cell dependent immune response defect</title><source>Springer LINK Archives</source><creator>Bellgrau, D ; Naji, A ; Silvers, W K ; Markmann, J F ; Barker, C F</creator><creatorcontrib>Bellgrau, D ; Naji, A ; Silvers, W K ; Markmann, J F ; Barker, C F</creatorcontrib><description>Approximately 50% of BB rats develop insulinopenic hyperglycaemia and ketosis spontaneously in association with insulitis. Amelioration of the syndrome by immunosuppression suggests a cell mediated immune pathogenesis. Analysis of the cell-mediated immune profile of overtly diabetic and normoglycaemic diabetes prone BB rats indicates that they are lymphocytopenic relative to non-diabetes prone BB rats and that the T cell pool is particularly affected. Furthermore, lymphocytes from diabetic and diabetes prone BB rats, while producing normal responses to the T cell mitogen concanavalin A, do not respond when mixed in vitro with major histocompatibility complex incompatible lymphocytes. This anergy is not restored either by enriching the responding cell population for T cells or by adding exogenous T cell growth promoting factor. Thus BB rats have a numerical and regulatory deficit of their T cells which could be related to their propensity for diabetes.</description><identifier>ISSN: 0012-186X</identifier><identifier>EISSN: 1432-0428</identifier><identifier>DOI: 10.1007/BF00253745</identifier><identifier>PMID: 6216134</identifier><language>eng</language><publisher>Germany</publisher><subject>Animals ; Concanavalin A ; Diabetes Mellitus, Experimental - immunology ; Interleukin-2 ; Leukocyte Count ; Lymphocyte Activation ; Lymphocyte Culture Test, Mixed ; Lymphocytes ; Rats ; T-Lymphocytes - immunology</subject><ispartof>Diabetologia, 1982-10, Vol.23 (4), p.359-364</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c318t-bfeb039cc0a3bf56b97d503c3d706d94e9789d5eaf6c3d3bf4561261f9875ce03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6216134$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bellgrau, D</creatorcontrib><creatorcontrib>Naji, A</creatorcontrib><creatorcontrib>Silvers, W K</creatorcontrib><creatorcontrib>Markmann, J F</creatorcontrib><creatorcontrib>Barker, C F</creatorcontrib><title>Spontaneous diabetes in BB rats: evidence for a T cell dependent immune response defect</title><title>Diabetologia</title><addtitle>Diabetologia</addtitle><description>Approximately 50% of BB rats develop insulinopenic hyperglycaemia and ketosis spontaneously in association with insulitis. Amelioration of the syndrome by immunosuppression suggests a cell mediated immune pathogenesis. Analysis of the cell-mediated immune profile of overtly diabetic and normoglycaemic diabetes prone BB rats indicates that they are lymphocytopenic relative to non-diabetes prone BB rats and that the T cell pool is particularly affected. Furthermore, lymphocytes from diabetic and diabetes prone BB rats, while producing normal responses to the T cell mitogen concanavalin A, do not respond when mixed in vitro with major histocompatibility complex incompatible lymphocytes. This anergy is not restored either by enriching the responding cell population for T cells or by adding exogenous T cell growth promoting factor. Thus BB rats have a numerical and regulatory deficit of their T cells which could be related to their propensity for diabetes.</description><subject>Animals</subject><subject>Concanavalin A</subject><subject>Diabetes Mellitus, Experimental - immunology</subject><subject>Interleukin-2</subject><subject>Leukocyte Count</subject><subject>Lymphocyte Activation</subject><subject>Lymphocyte Culture Test, Mixed</subject><subject>Lymphocytes</subject><subject>Rats</subject><subject>T-Lymphocytes - immunology</subject><issn>0012-186X</issn><issn>1432-0428</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LAzEQhoMotVYv3oWcPAirk80mu-vNFqtCwYMVvS3ZZAIr3Q-TbMF_b0qLngbeeXiZeQi5ZHDLAPK7-RIgFTzPxBGZsoynCWRpcUymACxNWCE_T8mZ918AwEUmJ2QiUyYZz6bk423ou6A67EdPTaNqDOhp09H5nDoV_D3FbWOw00ht76iia6pxs6EGB-xiHmjTtmOH1KGPTR7jxqIO5-TEqo3Hi8Ockffl43rxnKxen14WD6tEc1aEpLZYAy-1BsVrK2Rd5kYA19zkIE2ZYZkXpRGorIxZRDIhWSqZLYtcaAQ-I9f73sH13yP6ULWN3124f6nKowhZyB14swe16713aKvBNa1yPxWDamex-rcY4atD61i3aP7Qgzb-C4libCc</recordid><startdate>198210</startdate><enddate>198210</enddate><creator>Bellgrau, D</creator><creator>Naji, A</creator><creator>Silvers, W K</creator><creator>Markmann, J F</creator><creator>Barker, C F</creator><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>198210</creationdate><title>Spontaneous diabetes in BB rats: evidence for a T cell dependent immune response defect</title><author>Bellgrau, D ; Naji, A ; Silvers, W K ; Markmann, J F ; Barker, C F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c318t-bfeb039cc0a3bf56b97d503c3d706d94e9789d5eaf6c3d3bf4561261f9875ce03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Animals</topic><topic>Concanavalin A</topic><topic>Diabetes Mellitus, Experimental - immunology</topic><topic>Interleukin-2</topic><topic>Leukocyte Count</topic><topic>Lymphocyte Activation</topic><topic>Lymphocyte Culture Test, Mixed</topic><topic>Lymphocytes</topic><topic>Rats</topic><topic>T-Lymphocytes - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bellgrau, D</creatorcontrib><creatorcontrib>Naji, A</creatorcontrib><creatorcontrib>Silvers, W K</creatorcontrib><creatorcontrib>Markmann, J F</creatorcontrib><creatorcontrib>Barker, C F</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><jtitle>Diabetologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bellgrau, D</au><au>Naji, A</au><au>Silvers, W K</au><au>Markmann, J F</au><au>Barker, C F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spontaneous diabetes in BB rats: evidence for a T cell dependent immune response defect</atitle><jtitle>Diabetologia</jtitle><addtitle>Diabetologia</addtitle><date>1982-10</date><risdate>1982</risdate><volume>23</volume><issue>4</issue><spage>359</spage><epage>364</epage><pages>359-364</pages><issn>0012-186X</issn><eissn>1432-0428</eissn><abstract>Approximately 50% of BB rats develop insulinopenic hyperglycaemia and ketosis spontaneously in association with insulitis. Amelioration of the syndrome by immunosuppression suggests a cell mediated immune pathogenesis. Analysis of the cell-mediated immune profile of overtly diabetic and normoglycaemic diabetes prone BB rats indicates that they are lymphocytopenic relative to non-diabetes prone BB rats and that the T cell pool is particularly affected. Furthermore, lymphocytes from diabetic and diabetes prone BB rats, while producing normal responses to the T cell mitogen concanavalin A, do not respond when mixed in vitro with major histocompatibility complex incompatible lymphocytes. This anergy is not restored either by enriching the responding cell population for T cells or by adding exogenous T cell growth promoting factor. Thus BB rats have a numerical and regulatory deficit of their T cells which could be related to their propensity for diabetes.</abstract><cop>Germany</cop><pmid>6216134</pmid><doi>10.1007/BF00253745</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0012-186X |
ispartof | Diabetologia, 1982-10, Vol.23 (4), p.359-364 |
issn | 0012-186X 1432-0428 |
language | eng |
recordid | cdi_proquest_miscellaneous_74286860 |
source | Springer LINK Archives |
subjects | Animals Concanavalin A Diabetes Mellitus, Experimental - immunology Interleukin-2 Leukocyte Count Lymphocyte Activation Lymphocyte Culture Test, Mixed Lymphocytes Rats T-Lymphocytes - immunology |
title | Spontaneous diabetes in BB rats: evidence for a T cell dependent immune response defect |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T19%3A56%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Spontaneous%20diabetes%20in%20BB%20rats:%20evidence%20for%20a%20T%20cell%20dependent%20immune%20response%20defect&rft.jtitle=Diabetologia&rft.au=Bellgrau,%20D&rft.date=1982-10&rft.volume=23&rft.issue=4&rft.spage=359&rft.epage=364&rft.pages=359-364&rft.issn=0012-186X&rft.eissn=1432-0428&rft_id=info:doi/10.1007/BF00253745&rft_dat=%3Cproquest_cross%3E74286860%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c318t-bfeb039cc0a3bf56b97d503c3d706d94e9789d5eaf6c3d3bf4561261f9875ce03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=74286860&rft_id=info:pmid/6216134&rfr_iscdi=true |