Incorporation of cells into an ELISA system enhances antigen-driven lymphokine detection
The ability to measure successfully the levels of Th 1 or Th 2 cytokines during an in vitro antigen-driven, polyclonal T-cell response has proven to be more difficult than expected. Here we describe the development of a highly sensitive cell-based ELISA (celELISA) technique for the detection of muri...
Gespeichert in:
Veröffentlicht in: | Journal of immunological methods 1997-07, Vol.205 (2), p.163-168 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 168 |
---|---|
container_issue | 2 |
container_start_page | 163 |
container_title | Journal of immunological methods |
container_volume | 205 |
creator | Beech, Jonathan T Bainbridge, Tracy Thompson, Stephen J |
description | The ability to measure successfully the levels of Th
1 or Th
2 cytokines during an in vitro antigen-driven, polyclonal T-cell response has proven to be more difficult than expected. Here we describe the development of a highly sensitive cell-based ELISA (celELISA) technique for the detection of murine Th
1 and Th
2 cytokines. The celELISA combines the quantification aspects of the conventional sandwich ELISA with the sensitivity of the ELISPOT assay. The celELISA was particularly useful for the improved detection of IL-2, IL-4, and to a lessor extent, IFN-γ. |
doi_str_mv | 10.1016/S0022-1759(97)00072-0 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79274899</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022175997000720</els_id><sourcerecordid>16037037</sourcerecordid><originalsourceid>FETCH-LOGICAL-c391t-4e10283ac145d769b97f6d48fa5f5605c75839ce0c38f2b974ea54ffbe743fc23</originalsourceid><addsrcrecordid>eNqFkE1LAzEQhoMoWj9-gpCT6GF1srvZbE4ixY9CwYMK3kKanWi0m9RkK_Tfm9riVRjIwPvMDHkIOWVwyYA1V08AZVkwweW5FBcAIMoCdsiItbkREvguGf0hB-QwpY8MMWhgn-zLUtZctiPyOvEmxEWIenDB02Cpwfk8UeeHQLWnt9PJ0w1NqzRgT9G_a28w5WBwb-iLLrpv9HS-6hfv4dN5pB0OaNarjsme1fOEJ9v3iLzc3T6PH4rp4_1kfDMtTCXZUNTIoGwrbVjNO9HImRS26erWam55A9wI3lbSIJiqtWVOa9S8tnaGoq6sKasjcrbZu4jha4lpUL1L6z9oj2GZlJClqFsp_wVZA5XIlUG-AU0MKUW0ahFdr-NKMVBr9epXvVp7VVKoX_UK8tzp9sBy1mP3N7V1nfPrTY5Zx7fDqJJxmH12LmZnqgvunws_CaaTjA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16037037</pqid></control><display><type>article</type><title>Incorporation of cells into an ELISA system enhances antigen-driven lymphokine detection</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Beech, Jonathan T ; Bainbridge, Tracy ; Thompson, Stephen J</creator><creatorcontrib>Beech, Jonathan T ; Bainbridge, Tracy ; Thompson, Stephen J</creatorcontrib><description>The ability to measure successfully the levels of Th
1 or Th
2 cytokines during an in vitro antigen-driven, polyclonal T-cell response has proven to be more difficult than expected. Here we describe the development of a highly sensitive cell-based ELISA (celELISA) technique for the detection of murine Th
1 and Th
2 cytokines. The celELISA combines the quantification aspects of the conventional sandwich ELISA with the sensitivity of the ELISPOT assay. The celELISA was particularly useful for the improved detection of IL-2, IL-4, and to a lessor extent, IFN-γ.</description><identifier>ISSN: 0022-1759</identifier><identifier>EISSN: 1872-7905</identifier><identifier>DOI: 10.1016/S0022-1759(97)00072-0</identifier><identifier>PMID: 9294598</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>AIDS/HIV ; Animals ; Antigens - administration & dosage ; Bacterial Proteins ; Cells, Cultured ; Chaperonin 60 ; Chaperonins - administration & dosage ; Chaperonins - immunology ; Concanavalin A - administration & dosage ; Cytokine ; ELISA ; Enzyme-Linked Immunosorbent Assay - methods ; Enzyme-Linked Immunosorbent Assay - statistics & numerical data ; Evaluation Studies as Topic ; Immunization ; Interferon-gamma - analysis ; Interferon-gamma - biosynthesis ; Interleukin-2 - analysis ; Interleukin-2 - biosynthesis ; Interleukin-4 - analysis ; Interleukin-4 - biosynthesis ; Lymphocyte Activation ; Lymphokines - analysis ; Lymphokines - biosynthesis ; Male ; Mice ; Mice, Inbred CBA ; Sensitivity and Specificity ; Spleen - cytology ; Spleen - immunology ; Th1 Cells - immunology ; Th2 Cells - immunology</subject><ispartof>Journal of immunological methods, 1997-07, Vol.205 (2), p.163-168</ispartof><rights>1997 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-4e10283ac145d769b97f6d48fa5f5605c75839ce0c38f2b974ea54ffbe743fc23</citedby><cites>FETCH-LOGICAL-c391t-4e10283ac145d769b97f6d48fa5f5605c75839ce0c38f2b974ea54ffbe743fc23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0022-1759(97)00072-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9294598$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beech, Jonathan T</creatorcontrib><creatorcontrib>Bainbridge, Tracy</creatorcontrib><creatorcontrib>Thompson, Stephen J</creatorcontrib><title>Incorporation of cells into an ELISA system enhances antigen-driven lymphokine detection</title><title>Journal of immunological methods</title><addtitle>J Immunol Methods</addtitle><description>The ability to measure successfully the levels of Th
1 or Th
2 cytokines during an in vitro antigen-driven, polyclonal T-cell response has proven to be more difficult than expected. Here we describe the development of a highly sensitive cell-based ELISA (celELISA) technique for the detection of murine Th
1 and Th
2 cytokines. The celELISA combines the quantification aspects of the conventional sandwich ELISA with the sensitivity of the ELISPOT assay. The celELISA was particularly useful for the improved detection of IL-2, IL-4, and to a lessor extent, IFN-γ.</description><subject>AIDS/HIV</subject><subject>Animals</subject><subject>Antigens - administration & dosage</subject><subject>Bacterial Proteins</subject><subject>Cells, Cultured</subject><subject>Chaperonin 60</subject><subject>Chaperonins - administration & dosage</subject><subject>Chaperonins - immunology</subject><subject>Concanavalin A - administration & dosage</subject><subject>Cytokine</subject><subject>ELISA</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>Enzyme-Linked Immunosorbent Assay - statistics & numerical data</subject><subject>Evaluation Studies as Topic</subject><subject>Immunization</subject><subject>Interferon-gamma - analysis</subject><subject>Interferon-gamma - biosynthesis</subject><subject>Interleukin-2 - analysis</subject><subject>Interleukin-2 - biosynthesis</subject><subject>Interleukin-4 - analysis</subject><subject>Interleukin-4 - biosynthesis</subject><subject>Lymphocyte Activation</subject><subject>Lymphokines - analysis</subject><subject>Lymphokines - biosynthesis</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred CBA</subject><subject>Sensitivity and Specificity</subject><subject>Spleen - cytology</subject><subject>Spleen - immunology</subject><subject>Th1 Cells - immunology</subject><subject>Th2 Cells - immunology</subject><issn>0022-1759</issn><issn>1872-7905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LAzEQhoMoWj9-gpCT6GF1srvZbE4ixY9CwYMK3kKanWi0m9RkK_Tfm9riVRjIwPvMDHkIOWVwyYA1V08AZVkwweW5FBcAIMoCdsiItbkREvguGf0hB-QwpY8MMWhgn-zLUtZctiPyOvEmxEWIenDB02Cpwfk8UeeHQLWnt9PJ0w1NqzRgT9G_a28w5WBwb-iLLrpv9HS-6hfv4dN5pB0OaNarjsme1fOEJ9v3iLzc3T6PH4rp4_1kfDMtTCXZUNTIoGwrbVjNO9HImRS26erWam55A9wI3lbSIJiqtWVOa9S8tnaGoq6sKasjcrbZu4jha4lpUL1L6z9oj2GZlJClqFsp_wVZA5XIlUG-AU0MKUW0ahFdr-NKMVBr9epXvVp7VVKoX_UK8tzp9sBy1mP3N7V1nfPrTY5Zx7fDqJJxmH12LmZnqgvunws_CaaTjA</recordid><startdate>19970714</startdate><enddate>19970714</enddate><creator>Beech, Jonathan T</creator><creator>Bainbridge, Tracy</creator><creator>Thompson, Stephen J</creator><general>Elsevier B.V</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19970714</creationdate><title>Incorporation of cells into an ELISA system enhances antigen-driven lymphokine detection</title><author>Beech, Jonathan T ; Bainbridge, Tracy ; Thompson, Stephen J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-4e10283ac145d769b97f6d48fa5f5605c75839ce0c38f2b974ea54ffbe743fc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>AIDS/HIV</topic><topic>Animals</topic><topic>Antigens - administration & dosage</topic><topic>Bacterial Proteins</topic><topic>Cells, Cultured</topic><topic>Chaperonin 60</topic><topic>Chaperonins - administration & dosage</topic><topic>Chaperonins - immunology</topic><topic>Concanavalin A - administration & dosage</topic><topic>Cytokine</topic><topic>ELISA</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>Enzyme-Linked Immunosorbent Assay - statistics & numerical data</topic><topic>Evaluation Studies as Topic</topic><topic>Immunization</topic><topic>Interferon-gamma - analysis</topic><topic>Interferon-gamma - biosynthesis</topic><topic>Interleukin-2 - analysis</topic><topic>Interleukin-2 - biosynthesis</topic><topic>Interleukin-4 - analysis</topic><topic>Interleukin-4 - biosynthesis</topic><topic>Lymphocyte Activation</topic><topic>Lymphokines - analysis</topic><topic>Lymphokines - biosynthesis</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred CBA</topic><topic>Sensitivity and Specificity</topic><topic>Spleen - cytology</topic><topic>Spleen - immunology</topic><topic>Th1 Cells - immunology</topic><topic>Th2 Cells - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beech, Jonathan T</creatorcontrib><creatorcontrib>Bainbridge, Tracy</creatorcontrib><creatorcontrib>Thompson, Stephen J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of immunological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beech, Jonathan T</au><au>Bainbridge, Tracy</au><au>Thompson, Stephen J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Incorporation of cells into an ELISA system enhances antigen-driven lymphokine detection</atitle><jtitle>Journal of immunological methods</jtitle><addtitle>J Immunol Methods</addtitle><date>1997-07-14</date><risdate>1997</risdate><volume>205</volume><issue>2</issue><spage>163</spage><epage>168</epage><pages>163-168</pages><issn>0022-1759</issn><eissn>1872-7905</eissn><abstract>The ability to measure successfully the levels of Th
1 or Th
2 cytokines during an in vitro antigen-driven, polyclonal T-cell response has proven to be more difficult than expected. Here we describe the development of a highly sensitive cell-based ELISA (celELISA) technique for the detection of murine Th
1 and Th
2 cytokines. The celELISA combines the quantification aspects of the conventional sandwich ELISA with the sensitivity of the ELISPOT assay. The celELISA was particularly useful for the improved detection of IL-2, IL-4, and to a lessor extent, IFN-γ.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>9294598</pmid><doi>10.1016/S0022-1759(97)00072-0</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-1759 |
ispartof | Journal of immunological methods, 1997-07, Vol.205 (2), p.163-168 |
issn | 0022-1759 1872-7905 |
language | eng |
recordid | cdi_proquest_miscellaneous_79274899 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | AIDS/HIV Animals Antigens - administration & dosage Bacterial Proteins Cells, Cultured Chaperonin 60 Chaperonins - administration & dosage Chaperonins - immunology Concanavalin A - administration & dosage Cytokine ELISA Enzyme-Linked Immunosorbent Assay - methods Enzyme-Linked Immunosorbent Assay - statistics & numerical data Evaluation Studies as Topic Immunization Interferon-gamma - analysis Interferon-gamma - biosynthesis Interleukin-2 - analysis Interleukin-2 - biosynthesis Interleukin-4 - analysis Interleukin-4 - biosynthesis Lymphocyte Activation Lymphokines - analysis Lymphokines - biosynthesis Male Mice Mice, Inbred CBA Sensitivity and Specificity Spleen - cytology Spleen - immunology Th1 Cells - immunology Th2 Cells - immunology |
title | Incorporation of cells into an ELISA system enhances antigen-driven lymphokine detection |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T00%3A58%3A56IST&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=Incorporation%20of%20cells%20into%20an%20ELISA%20system%20enhances%20antigen-driven%20lymphokine%20detection&rft.jtitle=Journal%20of%20immunological%20methods&rft.au=Beech,%20Jonathan%20T&rft.date=1997-07-14&rft.volume=205&rft.issue=2&rft.spage=163&rft.epage=168&rft.pages=163-168&rft.issn=0022-1759&rft.eissn=1872-7905&rft_id=info:doi/10.1016/S0022-1759(97)00072-0&rft_dat=%3Cproquest_cross%3E16037037%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16037037&rft_id=info:pmid/9294598&rft_els_id=S0022175997000720&rfr_iscdi=true |