Inhibition of antibody response to Pseudomonas exotoxin and an immunotoxin containing Pseudomonas exotoxin by 15-deoxyspergualin in mice
Immunotoxins are potent cell-killing agents that may be useful in the treatment of cancer. The early production of neutralizing antibodies to immunotoxins is one of the major limiting factors for their use in humans. 15-Deoxyspergualin (DSG), a derivative of spergualin, which is a metabolite of Baci...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 1990-12, Vol.50 (24), p.7750-7753 |
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description | Immunotoxins are potent cell-killing agents that may be useful in the treatment of cancer. The early production of neutralizing antibodies to immunotoxins is one of the major limiting factors for their use in humans. 15-Deoxyspergualin (DSG), a derivative of spergualin, which is a metabolite of Bacillus laterosporus, has been found to have immunosuppressive activity in rodents, dogs, and primates. We examined the suppressive activity of DSG on the antibody response to Pseudomonas exotoxin in mice by enzyme-linked immunosorbent assay. Male BDF1 mice were immunized with a single dose of a nontoxic mutant of Pseudomonas exotoxin (40 micrograms) and then treated with i.p. injections of DSF at a dose of 10 mg/kg for 3 days. Although antibodies to Pseudomonas exotoxin were observed within 7 days in the control group, there was complete suppression of antibody production in the DSG-treated group. Immunosuppression has also been observed in animals immunized with multiple doses (10 mg x 7 d) of Pseudomonas exotoxin and treated with DSG at a dose of 5 mg/kg for 21 days. Similar immunosuppression was observed in mice given multiple doses of the immunotoxin, anti-Tac-LysPE40. We conclude that the immunosuppressive activity of DSG may be useful in increasing the duration of immunotoxin treatment. |
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H ; FITZGERALD, D. J ; TEPPER, M ; SCHACTER, B ; SPITALNY, G ; PASTAN, I</creator><creatorcontrib>PAI, L. H ; FITZGERALD, D. J ; TEPPER, M ; SCHACTER, B ; SPITALNY, G ; PASTAN, I</creatorcontrib><description>Immunotoxins are potent cell-killing agents that may be useful in the treatment of cancer. The early production of neutralizing antibodies to immunotoxins is one of the major limiting factors for their use in humans. 15-Deoxyspergualin (DSG), a derivative of spergualin, which is a metabolite of Bacillus laterosporus, has been found to have immunosuppressive activity in rodents, dogs, and primates. We examined the suppressive activity of DSG on the antibody response to Pseudomonas exotoxin in mice by enzyme-linked immunosorbent assay. Male BDF1 mice were immunized with a single dose of a nontoxic mutant of Pseudomonas exotoxin (40 micrograms) and then treated with i.p. injections of DSF at a dose of 10 mg/kg for 3 days. Although antibodies to Pseudomonas exotoxin were observed within 7 days in the control group, there was complete suppression of antibody production in the DSG-treated group. Immunosuppression has also been observed in animals immunized with multiple doses (10 mg x 7 d) of Pseudomonas exotoxin and treated with DSG at a dose of 5 mg/kg for 21 days. Similar immunosuppression was observed in mice given multiple doses of the immunotoxin, anti-Tac-LysPE40. We conclude that the immunosuppressive activity of DSG may be useful in increasing the duration of immunotoxin treatment.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 2253218</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>ADP Ribose Transferases ; Animals ; Antibody Formation - drug effects ; Bacterial Toxins ; Biological and medical sciences ; Cell Line ; Enzyme-Linked Immunosorbent Assay ; Exotoxins - immunology ; Exotoxins - toxicity ; Guanidines - pharmacology ; Humans ; Immunoglobulin G - biosynthesis ; Immunoglobulin M - biosynthesis ; Immunomodulators ; Immunosuppressive Agents - pharmacology ; Immunotoxins - toxicity ; Male ; Medical sciences ; Mice ; Mice, Inbred Strains ; Neutralization Tests ; Pharmacology. Drug treatments ; Pseudomonas ; Pseudomonas aeruginosa Exotoxin A ; Recombinant Proteins - toxicity ; Virulence Factors</subject><ispartof>Cancer research (Chicago, Ill.), 1990-12, Vol.50 (24), p.7750-7753</ispartof><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19481315$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2253218$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PAI, L. H</creatorcontrib><creatorcontrib>FITZGERALD, D. J</creatorcontrib><creatorcontrib>TEPPER, M</creatorcontrib><creatorcontrib>SCHACTER, B</creatorcontrib><creatorcontrib>SPITALNY, G</creatorcontrib><creatorcontrib>PASTAN, I</creatorcontrib><title>Inhibition of antibody response to Pseudomonas exotoxin and an immunotoxin containing Pseudomonas exotoxin by 15-deoxyspergualin in mice</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Immunotoxins are potent cell-killing agents that may be useful in the treatment of cancer. The early production of neutralizing antibodies to immunotoxins is one of the major limiting factors for their use in humans. 15-Deoxyspergualin (DSG), a derivative of spergualin, which is a metabolite of Bacillus laterosporus, has been found to have immunosuppressive activity in rodents, dogs, and primates. We examined the suppressive activity of DSG on the antibody response to Pseudomonas exotoxin in mice by enzyme-linked immunosorbent assay. Male BDF1 mice were immunized with a single dose of a nontoxic mutant of Pseudomonas exotoxin (40 micrograms) and then treated with i.p. injections of DSF at a dose of 10 mg/kg for 3 days. Although antibodies to Pseudomonas exotoxin were observed within 7 days in the control group, there was complete suppression of antibody production in the DSG-treated group. Immunosuppression has also been observed in animals immunized with multiple doses (10 mg x 7 d) of Pseudomonas exotoxin and treated with DSG at a dose of 5 mg/kg for 21 days. Similar immunosuppression was observed in mice given multiple doses of the immunotoxin, anti-Tac-LysPE40. We conclude that the immunosuppressive activity of DSG may be useful in increasing the duration of immunotoxin treatment.</description><subject>ADP Ribose Transferases</subject><subject>Animals</subject><subject>Antibody Formation - drug effects</subject><subject>Bacterial Toxins</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Exotoxins - immunology</subject><subject>Exotoxins - toxicity</subject><subject>Guanidines - pharmacology</subject><subject>Humans</subject><subject>Immunoglobulin G - biosynthesis</subject><subject>Immunoglobulin M - biosynthesis</subject><subject>Immunomodulators</subject><subject>Immunosuppressive Agents - pharmacology</subject><subject>Immunotoxins - toxicity</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Neutralization Tests</subject><subject>Pharmacology. Drug treatments</subject><subject>Pseudomonas</subject><subject>Pseudomonas aeruginosa Exotoxin A</subject><subject>Recombinant Proteins - toxicity</subject><subject>Virulence Factors</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptUEtLxDAQDqKsdfUnCLl4LDSvNj3K4mNhQQ96XvLcjbRJaVJo_4E_24DFkzDDMN9jYL4LUCBGeNlQyi5BUVUVLxlt8DW4ifErrwxVbAM2GDOCES_A996fnXTJBQ-DhcInJ4Ne4GjiEHw0MAX4Hs2kQx-8iNDMIYXZ-azUuaHr-8mvkAo-CeedP_1vkQtErNQmzEsczHiaRJfRXL1T5hZcWdFFc7fOLfh8fvrYvZaHt5f97vFQnnFTpZIrS2hFrGjrpmW8xkxJqi3P7zS6xVwg1jKSeURqg1ulKEaWSq4VVkI1hmzB_e_dYZK90cdhdL0Yl-OaSOYfVl5EJTo7Cq9c_JOhlnJEcsY_DqpuNg</recordid><startdate>19901215</startdate><enddate>19901215</enddate><creator>PAI, L. H</creator><creator>FITZGERALD, D. J</creator><creator>TEPPER, M</creator><creator>SCHACTER, B</creator><creator>SPITALNY, G</creator><creator>PASTAN, I</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>19901215</creationdate><title>Inhibition of antibody response to Pseudomonas exotoxin and an immunotoxin containing Pseudomonas exotoxin by 15-deoxyspergualin in mice</title><author>PAI, L. H ; FITZGERALD, D. J ; TEPPER, M ; SCHACTER, B ; SPITALNY, G ; PASTAN, I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h270t-8cf3403fa967958625cb4df85327d928a159533fa136e29cc421f4b8dc2cac7e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>ADP Ribose Transferases</topic><topic>Animals</topic><topic>Antibody Formation - drug effects</topic><topic>Bacterial Toxins</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Exotoxins - immunology</topic><topic>Exotoxins - toxicity</topic><topic>Guanidines - pharmacology</topic><topic>Humans</topic><topic>Immunoglobulin G - biosynthesis</topic><topic>Immunoglobulin M - biosynthesis</topic><topic>Immunomodulators</topic><topic>Immunosuppressive Agents - pharmacology</topic><topic>Immunotoxins - toxicity</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Neutralization Tests</topic><topic>Pharmacology. Drug treatments</topic><topic>Pseudomonas</topic><topic>Pseudomonas aeruginosa Exotoxin A</topic><topic>Recombinant Proteins - toxicity</topic><topic>Virulence Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PAI, L. H</creatorcontrib><creatorcontrib>FITZGERALD, D. J</creatorcontrib><creatorcontrib>TEPPER, M</creatorcontrib><creatorcontrib>SCHACTER, B</creatorcontrib><creatorcontrib>SPITALNY, G</creatorcontrib><creatorcontrib>PASTAN, I</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PAI, L. H</au><au>FITZGERALD, D. J</au><au>TEPPER, M</au><au>SCHACTER, B</au><au>SPITALNY, G</au><au>PASTAN, I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of antibody response to Pseudomonas exotoxin and an immunotoxin containing Pseudomonas exotoxin by 15-deoxyspergualin in mice</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1990-12-15</date><risdate>1990</risdate><volume>50</volume><issue>24</issue><spage>7750</spage><epage>7753</epage><pages>7750-7753</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Immunotoxins are potent cell-killing agents that may be useful in the treatment of cancer. The early production of neutralizing antibodies to immunotoxins is one of the major limiting factors for their use in humans. 15-Deoxyspergualin (DSG), a derivative of spergualin, which is a metabolite of Bacillus laterosporus, has been found to have immunosuppressive activity in rodents, dogs, and primates. We examined the suppressive activity of DSG on the antibody response to Pseudomonas exotoxin in mice by enzyme-linked immunosorbent assay. Male BDF1 mice were immunized with a single dose of a nontoxic mutant of Pseudomonas exotoxin (40 micrograms) and then treated with i.p. injections of DSF at a dose of 10 mg/kg for 3 days. Although antibodies to Pseudomonas exotoxin were observed within 7 days in the control group, there was complete suppression of antibody production in the DSG-treated group. Immunosuppression has also been observed in animals immunized with multiple doses (10 mg x 7 d) of Pseudomonas exotoxin and treated with DSG at a dose of 5 mg/kg for 21 days. Similar immunosuppression was observed in mice given multiple doses of the immunotoxin, anti-Tac-LysPE40. We conclude that the immunosuppressive activity of DSG may be useful in increasing the duration of immunotoxin treatment.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>2253218</pmid><tpages>4</tpages></addata></record> |
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source | MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals |
subjects | ADP Ribose Transferases Animals Antibody Formation - drug effects Bacterial Toxins Biological and medical sciences Cell Line Enzyme-Linked Immunosorbent Assay Exotoxins - immunology Exotoxins - toxicity Guanidines - pharmacology Humans Immunoglobulin G - biosynthesis Immunoglobulin M - biosynthesis Immunomodulators Immunosuppressive Agents - pharmacology Immunotoxins - toxicity Male Medical sciences Mice Mice, Inbred Strains Neutralization Tests Pharmacology. Drug treatments Pseudomonas Pseudomonas aeruginosa Exotoxin A Recombinant Proteins - toxicity Virulence Factors |
title | Inhibition of antibody response to Pseudomonas exotoxin and an immunotoxin containing Pseudomonas exotoxin by 15-deoxyspergualin in mice |
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