Tumor-associated antigens are cytokine inducers and hyporeactivity factors to the immune system
We investigated possible mechanisms leading to the inhibition of the immune system in people with chronic disorders. Tumor cell produce protein released into the circulation, such as tumor associated antigens, may play an important role in processes preceding paralysis of the immune system. To test...
Gespeichert in:
Veröffentlicht in: | Biotherapy (Dordrecht) 1998, Vol.11 (1), p.27-37 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 37 |
---|---|
container_issue | 1 |
container_start_page | 27 |
container_title | Biotherapy (Dordrecht) |
container_volume | 11 |
creator | INGLOT, A. D GELDER, F GEORGIADES, J. A |
description | We investigated possible mechanisms leading to the inhibition of the immune system in people with chronic disorders. Tumor cell produce protein released into the circulation, such as tumor associated antigens, may play an important role in processes preceding paralysis of the immune system. To test this hypothesis the following tumor associated antigens were used: AFP, OFP, CA-125, CA-50 and CA-19-9. Their role was assessed by modulating cytokine production in cord blood lymphocytes and peripheral white blood cells obtained from grown population of patients treated with colostrinin, an cytokine inducer. PHA, LPS and colostrinin were used as positive control in those essays. Each antigen tested individually induced IFN, TNF alpha and IL-6 in dose dependent fashion. None of the tested cytokines were spontaneously released by the cells. Data generated from these experiments indicated that tumor associated antigens are inducing type 1 cytokines in similar fashion as LPS or colostrinin. However, lymphocytes taken from patients undergoing therapy with colostrinin revealed progressive loss capability to produce type 1 cytokines as they did in case of colostrinin. The loss of the capability to respond to antigen may represent phenomenon leading to immune tolerance. |
doi_str_mv | 10.1023/A:1007936706416 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_79925111</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>16429308</sourcerecordid><originalsourceid>FETCH-LOGICAL-p266t-850db45f08fc9ea7cc5dfe2f53cf9bae42e1dfed9598b1e64a2ac5004990a75a3</originalsourceid><addsrcrecordid>eNqFkD1PwzAQhj2ASinMTEgZEFvAdmI7ZqsqvqRKLEViiy7OmRqSOMQOUv49kahYme70Ps_d8BJywegNozy7Xd8xSpXOpKIyZ_KILKnmLOVav52Q0xA-KKVa0WJBFloylctsScrd2PohhRC8cRCxTqCL7h27kMCAiZmi_3QdJq6rR4PDnHZ1sp96PyCY6L5dnBI7b35G0SdxP6ttO84XYQoR2zNybKEJeH6YK_L6cL_bPKXbl8fnzXqb9lzKmBaC1lUuLC2s0QjKGFFb5FZkxuoKMOfI5qDWQhcVQ5kDByMozbWmoARkK3L9-7cf_NeIIZatCwabBjr0YyiV1lwwxv4Vmcy5zmgxi5cHcaxarMt-cC0MU3mobuZXBw7BQGMH6IwLfxrnoshUnv0AjGR9uA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16429308</pqid></control><display><type>article</type><title>Tumor-associated antigens are cytokine inducers and hyporeactivity factors to the immune system</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>INGLOT, A. D ; GELDER, F ; GEORGIADES, J. A</creator><creatorcontrib>INGLOT, A. D ; GELDER, F ; GEORGIADES, J. A</creatorcontrib><description>We investigated possible mechanisms leading to the inhibition of the immune system in people with chronic disorders. Tumor cell produce protein released into the circulation, such as tumor associated antigens, may play an important role in processes preceding paralysis of the immune system. To test this hypothesis the following tumor associated antigens were used: AFP, OFP, CA-125, CA-50 and CA-19-9. Their role was assessed by modulating cytokine production in cord blood lymphocytes and peripheral white blood cells obtained from grown population of patients treated with colostrinin, an cytokine inducer. PHA, LPS and colostrinin were used as positive control in those essays. Each antigen tested individually induced IFN, TNF alpha and IL-6 in dose dependent fashion. None of the tested cytokines were spontaneously released by the cells. Data generated from these experiments indicated that tumor associated antigens are inducing type 1 cytokines in similar fashion as LPS or colostrinin. However, lymphocytes taken from patients undergoing therapy with colostrinin revealed progressive loss capability to produce type 1 cytokines as they did in case of colostrinin. The loss of the capability to respond to antigen may represent phenomenon leading to immune tolerance.</description><identifier>ISSN: 0921-299X</identifier><identifier>DOI: 10.1023/A:1007936706416</identifier><identifier>PMID: 9617463</identifier><language>eng</language><publisher>Dordrecht: Kluwer</publisher><subject>Aged ; Aged, 80 and over ; Antigens, Tumor-Associated, Carbohydrate - immunology ; Antigens, Tumor-Associated, Carbohydrate - pharmacology ; Biological and medical sciences ; CA-19-9 Antigen - pharmacology ; Child ; Cytokines - biosynthesis ; Fetal Blood - drug effects ; Fetal Blood - immunology ; Fetal Blood - metabolism ; Humans ; Immunomodulators ; Immunosuppressive Agents - immunology ; Immunosuppressive Agents - pharmacology ; Infant, Newborn ; Leukocytes - drug effects ; Leukocytes - immunology ; Leukocytes - metabolism ; Lymphocyte Activation - drug effects ; Lymphocyte Activation - immunology ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments</subject><ispartof>Biotherapy (Dordrecht), 1998, Vol.11 (1), p.27-37</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4009,27902,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2258374$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9617463$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>INGLOT, A. D</creatorcontrib><creatorcontrib>GELDER, F</creatorcontrib><creatorcontrib>GEORGIADES, J. A</creatorcontrib><title>Tumor-associated antigens are cytokine inducers and hyporeactivity factors to the immune system</title><title>Biotherapy (Dordrecht)</title><addtitle>Biotherapy</addtitle><description>We investigated possible mechanisms leading to the inhibition of the immune system in people with chronic disorders. Tumor cell produce protein released into the circulation, such as tumor associated antigens, may play an important role in processes preceding paralysis of the immune system. To test this hypothesis the following tumor associated antigens were used: AFP, OFP, CA-125, CA-50 and CA-19-9. Their role was assessed by modulating cytokine production in cord blood lymphocytes and peripheral white blood cells obtained from grown population of patients treated with colostrinin, an cytokine inducer. PHA, LPS and colostrinin were used as positive control in those essays. Each antigen tested individually induced IFN, TNF alpha and IL-6 in dose dependent fashion. None of the tested cytokines were spontaneously released by the cells. Data generated from these experiments indicated that tumor associated antigens are inducing type 1 cytokines in similar fashion as LPS or colostrinin. However, lymphocytes taken from patients undergoing therapy with colostrinin revealed progressive loss capability to produce type 1 cytokines as they did in case of colostrinin. The loss of the capability to respond to antigen may represent phenomenon leading to immune tolerance.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antigens, Tumor-Associated, Carbohydrate - immunology</subject><subject>Antigens, Tumor-Associated, Carbohydrate - pharmacology</subject><subject>Biological and medical sciences</subject><subject>CA-19-9 Antigen - pharmacology</subject><subject>Child</subject><subject>Cytokines - biosynthesis</subject><subject>Fetal Blood - drug effects</subject><subject>Fetal Blood - immunology</subject><subject>Fetal Blood - metabolism</subject><subject>Humans</subject><subject>Immunomodulators</subject><subject>Immunosuppressive Agents - immunology</subject><subject>Immunosuppressive Agents - pharmacology</subject><subject>Infant, Newborn</subject><subject>Leukocytes - drug effects</subject><subject>Leukocytes - immunology</subject><subject>Leukocytes - metabolism</subject><subject>Lymphocyte Activation - drug effects</subject><subject>Lymphocyte Activation - immunology</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><issn>0921-299X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQhj2ASinMTEgZEFvAdmI7ZqsqvqRKLEViiy7OmRqSOMQOUv49kahYme70Ps_d8BJywegNozy7Xd8xSpXOpKIyZ_KILKnmLOVav52Q0xA-KKVa0WJBFloylctsScrd2PohhRC8cRCxTqCL7h27kMCAiZmi_3QdJq6rR4PDnHZ1sp96PyCY6L5dnBI7b35G0SdxP6ttO84XYQoR2zNybKEJeH6YK_L6cL_bPKXbl8fnzXqb9lzKmBaC1lUuLC2s0QjKGFFb5FZkxuoKMOfI5qDWQhcVQ5kDByMozbWmoARkK3L9-7cf_NeIIZatCwabBjr0YyiV1lwwxv4Vmcy5zmgxi5cHcaxarMt-cC0MU3mobuZXBw7BQGMH6IwLfxrnoshUnv0AjGR9uA</recordid><startdate>1998</startdate><enddate>1998</enddate><creator>INGLOT, A. D</creator><creator>GELDER, F</creator><creator>GEORGIADES, J. A</creator><general>Kluwer</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>1998</creationdate><title>Tumor-associated antigens are cytokine inducers and hyporeactivity factors to the immune system</title><author>INGLOT, A. D ; GELDER, F ; GEORGIADES, J. A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p266t-850db45f08fc9ea7cc5dfe2f53cf9bae42e1dfed9598b1e64a2ac5004990a75a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antigens, Tumor-Associated, Carbohydrate - immunology</topic><topic>Antigens, Tumor-Associated, Carbohydrate - pharmacology</topic><topic>Biological and medical sciences</topic><topic>CA-19-9 Antigen - pharmacology</topic><topic>Child</topic><topic>Cytokines - biosynthesis</topic><topic>Fetal Blood - drug effects</topic><topic>Fetal Blood - immunology</topic><topic>Fetal Blood - metabolism</topic><topic>Humans</topic><topic>Immunomodulators</topic><topic>Immunosuppressive Agents - immunology</topic><topic>Immunosuppressive Agents - pharmacology</topic><topic>Infant, Newborn</topic><topic>Leukocytes - drug effects</topic><topic>Leukocytes - immunology</topic><topic>Leukocytes - metabolism</topic><topic>Lymphocyte Activation - drug effects</topic><topic>Lymphocyte Activation - immunology</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>INGLOT, A. D</creatorcontrib><creatorcontrib>GELDER, F</creatorcontrib><creatorcontrib>GEORGIADES, J. A</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotherapy (Dordrecht)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>INGLOT, A. D</au><au>GELDER, F</au><au>GEORGIADES, J. A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumor-associated antigens are cytokine inducers and hyporeactivity factors to the immune system</atitle><jtitle>Biotherapy (Dordrecht)</jtitle><addtitle>Biotherapy</addtitle><date>1998</date><risdate>1998</risdate><volume>11</volume><issue>1</issue><spage>27</spage><epage>37</epage><pages>27-37</pages><issn>0921-299X</issn><abstract>We investigated possible mechanisms leading to the inhibition of the immune system in people with chronic disorders. Tumor cell produce protein released into the circulation, such as tumor associated antigens, may play an important role in processes preceding paralysis of the immune system. To test this hypothesis the following tumor associated antigens were used: AFP, OFP, CA-125, CA-50 and CA-19-9. Their role was assessed by modulating cytokine production in cord blood lymphocytes and peripheral white blood cells obtained from grown population of patients treated with colostrinin, an cytokine inducer. PHA, LPS and colostrinin were used as positive control in those essays. Each antigen tested individually induced IFN, TNF alpha and IL-6 in dose dependent fashion. None of the tested cytokines were spontaneously released by the cells. Data generated from these experiments indicated that tumor associated antigens are inducing type 1 cytokines in similar fashion as LPS or colostrinin. However, lymphocytes taken from patients undergoing therapy with colostrinin revealed progressive loss capability to produce type 1 cytokines as they did in case of colostrinin. The loss of the capability to respond to antigen may represent phenomenon leading to immune tolerance.</abstract><cop>Dordrecht</cop><pub>Kluwer</pub><pmid>9617463</pmid><doi>10.1023/A:1007936706416</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0921-299X |
ispartof | Biotherapy (Dordrecht), 1998, Vol.11 (1), p.27-37 |
issn | 0921-299X |
language | eng |
recordid | cdi_proquest_miscellaneous_79925111 |
source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | Aged Aged, 80 and over Antigens, Tumor-Associated, Carbohydrate - immunology Antigens, Tumor-Associated, Carbohydrate - pharmacology Biological and medical sciences CA-19-9 Antigen - pharmacology Child Cytokines - biosynthesis Fetal Blood - drug effects Fetal Blood - immunology Fetal Blood - metabolism Humans Immunomodulators Immunosuppressive Agents - immunology Immunosuppressive Agents - pharmacology Infant, Newborn Leukocytes - drug effects Leukocytes - immunology Leukocytes - metabolism Lymphocyte Activation - drug effects Lymphocyte Activation - immunology Medical sciences Middle Aged Pharmacology. Drug treatments |
title | Tumor-associated antigens are cytokine inducers and hyporeactivity factors to the immune system |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T09%3A16%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Tumor-associated%20antigens%20are%20cytokine%20inducers%20and%20hyporeactivity%20factors%20to%20the%20immune%20system&rft.jtitle=Biotherapy%20(Dordrecht)&rft.au=INGLOT,%20A.%20D&rft.date=1998&rft.volume=11&rft.issue=1&rft.spage=27&rft.epage=37&rft.pages=27-37&rft.issn=0921-299X&rft_id=info:doi/10.1023/A:1007936706416&rft_dat=%3Cproquest_pubme%3E16429308%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16429308&rft_id=info:pmid/9617463&rfr_iscdi=true |