Failure of IL-1 receptor antagonist and monoclonal anti-IL-1 receptor antibody to inhibit antigen-specific immune responses in vivo
rIL-1R antagonist (rIL-1ra) and 35F5, a neutralizing mAb, have been shown to inhibit the ability of IL-1 alpha and IL-1 beta to bind to type I but not type II murine receptors. Additionally, IL-1ra and 35F5 inhibit a variety of inflammatory responses in vitro and in vivo. In the present report we ha...
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Veröffentlicht in: | The Journal of immunology (1950) 1992-02, Vol.148 (3), p.766-771 |
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creator | Faherty, DA Claudy, V Plocinski, JM Kaffka, K Kilian, P Thompson, RC Benjamin, WR |
description | rIL-1R antagonist (rIL-1ra) and 35F5, a neutralizing mAb, have been shown to inhibit the ability of IL-1 alpha and IL-1 beta to bind to type I but not type II murine receptors. Additionally, IL-1ra and 35F5 inhibit a variety of inflammatory responses in vitro and in vivo. In the present report we have evaluated the activity of human IL-1ra and 35F5 in murine Ag-specific cell-mediated and humoral immune response models. Administration of IL-1ra, either twice daily or as a continuous infusion, did not inhibit the cytolytic T lymphocyte response to allogeneic splenocytes. The CTL response was also not inhibited by daily administration of 35F5. The delayed type hypersensitivity response to oxazolone was similarly refractory to administration of IL-1ra and 35F5. In the humoral immune response models, neither the splenic plaque response to SRBC nor the IgG or IgM response to TNP-keyhole limpet hemocyanin was inhibited by treatment with IL-1ra or 35F5. These data suggest that signaling through the type I IL-1R is not required for these Ag-specific immune responses. |
doi_str_mv | 10.4049/jimmunol.148.3.766 |
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Additionally, IL-1ra and 35F5 inhibit a variety of inflammatory responses in vitro and in vivo. In the present report we have evaluated the activity of human IL-1ra and 35F5 in murine Ag-specific cell-mediated and humoral immune response models. Administration of IL-1ra, either twice daily or as a continuous infusion, did not inhibit the cytolytic T lymphocyte response to allogeneic splenocytes. The CTL response was also not inhibited by daily administration of 35F5. The delayed type hypersensitivity response to oxazolone was similarly refractory to administration of IL-1ra and 35F5. In the humoral immune response models, neither the splenic plaque response to SRBC nor the IgG or IgM response to TNP-keyhole limpet hemocyanin was inhibited by treatment with IL-1ra or 35F5. These data suggest that signaling through the type I IL-1R is not required for these Ag-specific immune responses.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.148.3.766</identifier><identifier>PMID: 1530956</identifier><identifier>CODEN: JOIMA3</identifier><language>eng</language><publisher>Bethesda, MD: Am Assoc Immnol</publisher><subject>Analysis of the immune response. Humoral and cellular immunity ; Animals ; Antibodies, Monoclonal ; Antibody Formation - drug effects ; Antigens - immunology ; Biological and medical sciences ; Cells, Cultured ; Cytotoxicity, Immunologic - drug effects ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Immunobiology ; In Vitro Techniques ; Interleukin 1 Receptor Antagonist Protein ; Interleukin-1 - pharmacology ; Interleukin-6 - biosynthesis ; Lymphokines, interleukins ( function, expression) ; Mice ; Mice, Inbred C57BL ; Proteins - pharmacology ; Receptors, Immunologic - physiology ; Receptors, Interleukin-1 ; Regulatory factors and their cellular receptors ; Sialoglycoproteins ; T-Lymphocytes, Cytotoxic - immunology</subject><ispartof>The Journal of immunology (1950), 1992-02, Vol.148 (3), p.766-771</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4146-97cb6f0d474dd4de3fcd426564deaa08fdda332184f9a4bc6e43e23eb19516453</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5109917$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1530956$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Faherty, DA</creatorcontrib><creatorcontrib>Claudy, V</creatorcontrib><creatorcontrib>Plocinski, JM</creatorcontrib><creatorcontrib>Kaffka, K</creatorcontrib><creatorcontrib>Kilian, P</creatorcontrib><creatorcontrib>Thompson, RC</creatorcontrib><creatorcontrib>Benjamin, WR</creatorcontrib><title>Failure of IL-1 receptor antagonist and monoclonal anti-IL-1 receptor antibody to inhibit antigen-specific immune responses in vivo</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>rIL-1R antagonist (rIL-1ra) and 35F5, a neutralizing mAb, have been shown to inhibit the ability of IL-1 alpha and IL-1 beta to bind to type I but not type II murine receptors. Additionally, IL-1ra and 35F5 inhibit a variety of inflammatory responses in vitro and in vivo. In the present report we have evaluated the activity of human IL-1ra and 35F5 in murine Ag-specific cell-mediated and humoral immune response models. Administration of IL-1ra, either twice daily or as a continuous infusion, did not inhibit the cytolytic T lymphocyte response to allogeneic splenocytes. The CTL response was also not inhibited by daily administration of 35F5. The delayed type hypersensitivity response to oxazolone was similarly refractory to administration of IL-1ra and 35F5. In the humoral immune response models, neither the splenic plaque response to SRBC nor the IgG or IgM response to TNP-keyhole limpet hemocyanin was inhibited by treatment with IL-1ra or 35F5. These data suggest that signaling through the type I IL-1R is not required for these Ag-specific immune responses.</description><subject>Analysis of the immune response. Humoral and cellular immunity</subject><subject>Animals</subject><subject>Antibodies, Monoclonal</subject><subject>Antibody Formation - drug effects</subject><subject>Antigens - immunology</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>Cytotoxicity, Immunologic - drug effects</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Immunobiology</subject><subject>In Vitro Techniques</subject><subject>Interleukin 1 Receptor Antagonist Protein</subject><subject>Interleukin-1 - pharmacology</subject><subject>Interleukin-6 - biosynthesis</subject><subject>Lymphokines, interleukins ( function, expression)</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Proteins - pharmacology</subject><subject>Receptors, Immunologic - physiology</subject><subject>Receptors, Interleukin-1</subject><subject>Regulatory factors and their cellular receptors</subject><subject>Sialoglycoproteins</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUGPFCEQhYnRrOPoHzAx4WC89QgNTQ9Hs3F1k0m86JnQUMywoaGF7p3s2T8uuzM6Bw-eqPC-96qSh9BbSjaccPnxzo_jElPYUL7dsE0vxDO0ol1HGiGIeI5WhLRtQ3vRv0SvSrkjhAjS8it0RTtGZCdW6NeN9mHJgJPDt7uG4gwGpjllrOOs9yn6MtfR4jHFZEKKOjwqvvkH9kOyD3hO2MeDH_z89LeH2JQJjHfe4KdroZrKlGKBUkl87-_Ta_TC6VDgzfldox83n79ff212377cXn_aNYZTLhrZm0E4YnnPreUWmDOWt6ITddaabJ21mrGWbrmTmg9GAGfQMhio7KjgHVujD6fcKaefC5RZjb4YCEFHSEtRfdtvKZPivyAVlDBZ2TVqT6DJqZQMTk3Zjzo_KErUY0XqT0WqVqSYqhVV07tz-jKMYC-WUydVf3_WdTE6uKyj8eUv1lEiJe0vRx78_nD0GVQZdQg1lKrj8XjZ9xs95qri</recordid><startdate>19920201</startdate><enddate>19920201</enddate><creator>Faherty, DA</creator><creator>Claudy, V</creator><creator>Plocinski, JM</creator><creator>Kaffka, K</creator><creator>Kilian, P</creator><creator>Thompson, RC</creator><creator>Benjamin, WR</creator><general>Am Assoc Immnol</general><general>American Association of Immunologists</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19920201</creationdate><title>Failure of IL-1 receptor antagonist and monoclonal anti-IL-1 receptor antibody to inhibit antigen-specific immune responses in vivo</title><author>Faherty, DA ; Claudy, V ; Plocinski, JM ; Kaffka, K ; Kilian, P ; Thompson, RC ; Benjamin, WR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4146-97cb6f0d474dd4de3fcd426564deaa08fdda332184f9a4bc6e43e23eb19516453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Analysis of the immune response. Humoral and cellular immunity</topic><topic>Animals</topic><topic>Antibodies, Monoclonal</topic><topic>Antibody Formation - drug effects</topic><topic>Antigens - immunology</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Cytotoxicity, Immunologic - drug effects</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Immunobiology</topic><topic>In Vitro Techniques</topic><topic>Interleukin 1 Receptor Antagonist Protein</topic><topic>Interleukin-1 - pharmacology</topic><topic>Interleukin-6 - biosynthesis</topic><topic>Lymphokines, interleukins ( function, expression)</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Proteins - pharmacology</topic><topic>Receptors, Immunologic - physiology</topic><topic>Receptors, Interleukin-1</topic><topic>Regulatory factors and their cellular receptors</topic><topic>Sialoglycoproteins</topic><topic>T-Lymphocytes, Cytotoxic - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Faherty, DA</creatorcontrib><creatorcontrib>Claudy, V</creatorcontrib><creatorcontrib>Plocinski, JM</creatorcontrib><creatorcontrib>Kaffka, K</creatorcontrib><creatorcontrib>Kilian, P</creatorcontrib><creatorcontrib>Thompson, RC</creatorcontrib><creatorcontrib>Benjamin, WR</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Faherty, DA</au><au>Claudy, V</au><au>Plocinski, JM</au><au>Kaffka, K</au><au>Kilian, P</au><au>Thompson, RC</au><au>Benjamin, WR</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Failure of IL-1 receptor antagonist and monoclonal anti-IL-1 receptor antibody to inhibit antigen-specific immune responses in vivo</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1992-02-01</date><risdate>1992</risdate><volume>148</volume><issue>3</issue><spage>766</spage><epage>771</epage><pages>766-771</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><coden>JOIMA3</coden><abstract>rIL-1R antagonist (rIL-1ra) and 35F5, a neutralizing mAb, have been shown to inhibit the ability of IL-1 alpha and IL-1 beta to bind to type I but not type II murine receptors. Additionally, IL-1ra and 35F5 inhibit a variety of inflammatory responses in vitro and in vivo. In the present report we have evaluated the activity of human IL-1ra and 35F5 in murine Ag-specific cell-mediated and humoral immune response models. Administration of IL-1ra, either twice daily or as a continuous infusion, did not inhibit the cytolytic T lymphocyte response to allogeneic splenocytes. The CTL response was also not inhibited by daily administration of 35F5. The delayed type hypersensitivity response to oxazolone was similarly refractory to administration of IL-1ra and 35F5. In the humoral immune response models, neither the splenic plaque response to SRBC nor the IgG or IgM response to TNP-keyhole limpet hemocyanin was inhibited by treatment with IL-1ra or 35F5. These data suggest that signaling through the type I IL-1R is not required for these Ag-specific immune responses.</abstract><cop>Bethesda, MD</cop><pub>Am Assoc Immnol</pub><pmid>1530956</pmid><doi>10.4049/jimmunol.148.3.766</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis of the immune response. Humoral and cellular immunity Animals Antibodies, Monoclonal Antibody Formation - drug effects Antigens - immunology Biological and medical sciences Cells, Cultured Cytotoxicity, Immunologic - drug effects Fundamental and applied biological sciences. Psychology Fundamental immunology Immunobiology In Vitro Techniques Interleukin 1 Receptor Antagonist Protein Interleukin-1 - pharmacology Interleukin-6 - biosynthesis Lymphokines, interleukins ( function, expression) Mice Mice, Inbred C57BL Proteins - pharmacology Receptors, Immunologic - physiology Receptors, Interleukin-1 Regulatory factors and their cellular receptors Sialoglycoproteins T-Lymphocytes, Cytotoxic - immunology |
title | Failure of IL-1 receptor antagonist and monoclonal anti-IL-1 receptor antibody to inhibit antigen-specific immune responses in vivo |
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