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Relative Ability of Distinct Isotypes of Human Major Histocompatibility Complex Class II Molecules in Binding Staphylococcal Enterotoxin A
Relative ability of distinct isotypes of human major histocompatibility complex class II molecules to bind staphylococcal enterotoxin A (SEA) was investigated. SEA-binding was observed in L cells transfected with DR2 and DQw1 genes. By contrast, it was not detected in L cells transfected with DPw4 a...
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Published in: | MICROBIOLOGY and IMMUNOLOGY 1991, Vol.35(8), pp.661-673 |
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cites | cdi_FETCH-LOGICAL-c6898-5e8a11a7259fdc168a66a36f25e3bb2e98fa9bed5d8c67835cd8d608a1ea295b3 |
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container_title | MICROBIOLOGY and IMMUNOLOGY |
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creator | Saito, Shinji Imanishi, Ken'ichi Araake, Minako Yan, Xiao Jie Igarashi, Hideo Uchiyama, Takehiko |
description | Relative ability of distinct isotypes of human major histocompatibility complex class II molecules to bind staphylococcal enterotoxin A (SEA) was investigated. SEA-binding was observed in L cells transfected with DR2 and DQw1 genes. By contrast, it was not detected in L cells transfected with DPw4 and DP (Cp63) genes. All the transfectants supported SEA-induced IL-2 production by human T cells. Levels of the accessory activity were low in the DPw4 and DP (Cp63) transfectants compared with the DR2 and DQw1 transfectants. In view of the observation that all the transfectants express well the transfected gene products on their surface, the results indicate that DR and DQ molecules bind SEA with high affinity, while DP molecules bind it with fairly low affinity. |
doi_str_mv | 10.1111/j.1348-0421.1991.tb01598.x |
format | article |
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SEA-binding was observed in L cells transfected with DR2 and DQw1 genes. By contrast, it was not detected in L cells transfected with DPw4 and DP (Cp63) genes. All the transfectants supported SEA-induced IL-2 production by human T cells. Levels of the accessory activity were low in the DPw4 and DP (Cp63) transfectants compared with the DR2 and DQw1 transfectants. In view of the observation that all the transfectants express well the transfected gene products on their surface, the results indicate that DR and DQ molecules bind SEA with high affinity, while DP molecules bind it with fairly low affinity.</description><identifier>ISSN: 0385-5600</identifier><identifier>EISSN: 1348-0421</identifier><identifier>DOI: 10.1111/j.1348-0421.1991.tb01598.x</identifier><identifier>PMID: 1753884</identifier><identifier>CODEN: MIIMDV</identifier><language>eng</language><publisher>Tokyo: Blackwell Publishing Ltd</publisher><subject>Animals ; Antigens ; B-Lymphocytes - chemistry ; Binding Sites, Antibody - analysis ; Binding Sites, Antibody - immunology ; Biological and medical sciences ; Enterotoxins - analysis ; Enterotoxins - immunology ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Histocompatibility antigens (hla, h-2 and other systems) ; HLA-DQ Antigens - genetics ; HLA-DQ Antigens - immunology ; HLA-DR Antigens - genetics ; HLA-DR Antigens - immunology ; L Cells (Cell Line) ; Mice ; Molecular immunology ; T-Lymphocytes - chemistry ; Transfection</subject><ispartof>MICROBIOLOGY and IMMUNOLOGY, 1991, Vol.35(8), pp.661-673</ispartof><rights>Center for Academic Publications Japan</rights><rights>owned by Center for Academic Publications Japan (Publisher)</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6898-5e8a11a7259fdc168a66a36f25e3bb2e98fa9bed5d8c67835cd8d608a1ea295b3</citedby><cites>FETCH-LOGICAL-c6898-5e8a11a7259fdc168a66a36f25e3bb2e98fa9bed5d8c67835cd8d608a1ea295b3</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=5090850$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1753884$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saito, Shinji</creatorcontrib><creatorcontrib>Imanishi, Ken'ichi</creatorcontrib><creatorcontrib>Araake, Minako</creatorcontrib><creatorcontrib>Yan, Xiao Jie</creatorcontrib><creatorcontrib>Igarashi, Hideo</creatorcontrib><creatorcontrib>Uchiyama, Takehiko</creatorcontrib><title>Relative Ability of Distinct Isotypes of Human Major Histocompatibility Complex Class II Molecules in Binding Staphylococcal Enterotoxin A</title><title>MICROBIOLOGY and IMMUNOLOGY</title><addtitle>Microbiology and Immunology</addtitle><description>Relative ability of distinct isotypes of human major histocompatibility complex class II molecules to bind staphylococcal enterotoxin A (SEA) was investigated. SEA-binding was observed in L cells transfected with DR2 and DQw1 genes. By contrast, it was not detected in L cells transfected with DPw4 and DP (Cp63) genes. All the transfectants supported SEA-induced IL-2 production by human T cells. Levels of the accessory activity were low in the DPw4 and DP (Cp63) transfectants compared with the DR2 and DQw1 transfectants. In view of the observation that all the transfectants express well the transfected gene products on their surface, the results indicate that DR and DQ molecules bind SEA with high affinity, while DP molecules bind it with fairly low affinity.</description><subject>Animals</subject><subject>Antigens</subject><subject>B-Lymphocytes - chemistry</subject><subject>Binding Sites, Antibody - analysis</subject><subject>Binding Sites, Antibody - immunology</subject><subject>Biological and medical sciences</subject><subject>Enterotoxins - analysis</subject><subject>Enterotoxins - immunology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Histocompatibility antigens (hla, h-2 and other systems)</subject><subject>HLA-DQ Antigens - genetics</subject><subject>HLA-DQ Antigens - immunology</subject><subject>HLA-DR Antigens - genetics</subject><subject>HLA-DR Antigens - immunology</subject><subject>L Cells (Cell Line)</subject><subject>Mice</subject><subject>Molecular immunology</subject><subject>T-Lymphocytes - chemistry</subject><subject>Transfection</subject><issn>0385-5600</issn><issn>1348-0421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNqVks2O0zAUhSMEGsrAIyBZCCE2KXYcOzYrSinTSu0gBhASG8txbmbccZMSu9C-Ak-NQ6rCCoQX_rvfObZ8nCRPCB6T2F6sx4TmIsV5RsZESjIOJSZMivH-TjI6le4mI0wFSxnH-H7ywPs1xlmRifwsOSMFo0Lko-THFTgd7DdAk9I6Gw6ordEb64NtTEAL34bDFny_Od9tdINWet12aB6B1rSbbZQeZdO4crBHU6e9R4sFWrUOzM5FsW3Qa9tUtrlGH4Le3hxc1BqjHZo1Abo2tPuITB4m92rtPDw6jufJp7ezj9N5unx3sZhOlqnhQoqUgdCE6CJjsq4M4UJzrimvMwa0LDOQotayhIpVwvBCUGYqUXEcRaAzyUp6njwbfLdd-3UHPqiN9Qac0w20O6-iM8dFzv8JEk4lwYxE8PnfwVxmnGaF7NGXA2q61vsOarXt7EZ3B0Ww6sNVa9UnqPoEVR-uOoar9lH8-HjOrtxA9Vs6pBnrT4917ePz1p1ujPUnjGGJBcMRezVg362Dw39cQK0Wq1_TaDEbLNY-6Gs4eeguWONAxa9SWSKLQlGmxNBxTk51c6M7BU30SQef-KFg_4fNreIFLZj6fHmhLrG44nj5Rb2nPwEgIOr5</recordid><startdate>19910101</startdate><enddate>19910101</enddate><creator>Saito, Shinji</creator><creator>Imanishi, Ken'ichi</creator><creator>Araake, Minako</creator><creator>Yan, Xiao Jie</creator><creator>Igarashi, Hideo</creator><creator>Uchiyama, Takehiko</creator><general>Blackwell Publishing Ltd</general><general>Center For Academic Publications Japan</general><general>Center for Academic Publications Japan</general><scope>BSCLL</scope><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>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19910101</creationdate><title>Relative Ability of Distinct Isotypes of Human Major Histocompatibility Complex Class II Molecules in Binding Staphylococcal Enterotoxin A</title><author>Saito, Shinji ; Imanishi, Ken'ichi ; Araake, Minako ; Yan, Xiao Jie ; Igarashi, Hideo ; Uchiyama, Takehiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6898-5e8a11a7259fdc168a66a36f25e3bb2e98fa9bed5d8c67835cd8d608a1ea295b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animals</topic><topic>Antigens</topic><topic>B-Lymphocytes - chemistry</topic><topic>Binding Sites, Antibody - analysis</topic><topic>Binding Sites, Antibody - immunology</topic><topic>Biological and medical sciences</topic><topic>Enterotoxins - analysis</topic><topic>Enterotoxins - immunology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Histocompatibility antigens (hla, h-2 and other systems)</topic><topic>HLA-DQ Antigens - genetics</topic><topic>HLA-DQ Antigens - immunology</topic><topic>HLA-DR Antigens - genetics</topic><topic>HLA-DR Antigens - immunology</topic><topic>L Cells (Cell Line)</topic><topic>Mice</topic><topic>Molecular immunology</topic><topic>T-Lymphocytes - chemistry</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saito, Shinji</creatorcontrib><creatorcontrib>Imanishi, Ken'ichi</creatorcontrib><creatorcontrib>Araake, Minako</creatorcontrib><creatorcontrib>Yan, Xiao Jie</creatorcontrib><creatorcontrib>Igarashi, Hideo</creatorcontrib><creatorcontrib>Uchiyama, Takehiko</creatorcontrib><collection>Istex</collection><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>MICROBIOLOGY and IMMUNOLOGY</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saito, Shinji</au><au>Imanishi, Ken'ichi</au><au>Araake, Minako</au><au>Yan, Xiao Jie</au><au>Igarashi, Hideo</au><au>Uchiyama, Takehiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relative Ability of Distinct Isotypes of Human Major Histocompatibility Complex Class II Molecules in Binding Staphylococcal Enterotoxin A</atitle><jtitle>MICROBIOLOGY and IMMUNOLOGY</jtitle><addtitle>Microbiology and Immunology</addtitle><date>1991-01-01</date><risdate>1991</risdate><volume>35</volume><issue>8</issue><spage>661</spage><epage>673</epage><pages>661-673</pages><issn>0385-5600</issn><eissn>1348-0421</eissn><coden>MIIMDV</coden><abstract>Relative ability of distinct isotypes of human major histocompatibility complex class II molecules to bind staphylococcal enterotoxin A (SEA) was investigated. SEA-binding was observed in L cells transfected with DR2 and DQw1 genes. By contrast, it was not detected in L cells transfected with DPw4 and DP (Cp63) genes. All the transfectants supported SEA-induced IL-2 production by human T cells. Levels of the accessory activity were low in the DPw4 and DP (Cp63) transfectants compared with the DR2 and DQw1 transfectants. In view of the observation that all the transfectants express well the transfected gene products on their surface, the results indicate that DR and DQ molecules bind SEA with high affinity, while DP molecules bind it with fairly low affinity.</abstract><cop>Tokyo</cop><pub>Blackwell Publishing Ltd</pub><pmid>1753884</pmid><doi>10.1111/j.1348-0421.1991.tb01598.x</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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ispartof | MICROBIOLOGY and IMMUNOLOGY, 1991, Vol.35(8), pp.661-673 |
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subjects | Animals Antigens B-Lymphocytes - chemistry Binding Sites, Antibody - analysis Binding Sites, Antibody - immunology Biological and medical sciences Enterotoxins - analysis Enterotoxins - immunology Fundamental and applied biological sciences. Psychology Fundamental immunology Histocompatibility antigens (hla, h-2 and other systems) HLA-DQ Antigens - genetics HLA-DQ Antigens - immunology HLA-DR Antigens - genetics HLA-DR Antigens - immunology L Cells (Cell Line) Mice Molecular immunology T-Lymphocytes - chemistry Transfection |
title | Relative Ability of Distinct Isotypes of Human Major Histocompatibility Complex Class II Molecules in Binding Staphylococcal Enterotoxin A |
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