Neutralization of staphylococcal exotoxins in vitro by human-origin intravenous immunoglobulin
Abstract Human-origin intravenous immunoglobulin (IVIG) collected from healthy individuals was tested for its neutralizing activity against the hemolysin, toxic shock syndrome toxin-1 (TSST-1), and enterotoxins, produced by laboratory strains of methicillin-resistant Staphylococcus aureus (MRSA). Th...
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Veröffentlicht in: | Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy 2007-12, Vol.13 (6), p.368-372 |
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creator | Yanagisawa, Chie Hanaki, Hideaki Natae, Taiji Sunakawa, Keisuke |
description | Abstract Human-origin intravenous immunoglobulin (IVIG) collected from healthy individuals was tested for its neutralizing activity against the hemolysin, toxic shock syndrome toxin-1 (TSST-1), and enterotoxins, produced by laboratory strains of methicillin-resistant Staphylococcus aureus (MRSA). The hemolytic activity of the culture supernatant against sheep red blood cells was reduced from 100% to 5.5% relative hemolysis in the presence of 0.156 mg protein/ml of IVIG. The maximum dilution endpoint of the culture supernatant for TSST-1-mediated latex aggregation was 32-fold. This level of TSST-1 activity was reduced to eightfold dilution by 0.78 mg protein/ml of IVIG, and the latex aggregation activity of undiluted TSST-1 in the culture supernatant was inhibited by 1.56 mg protein/ml of IVIG. Similarly, the enterotoxin A-mediated latex aggregation titer appeared to be a 320-fold dilution. This toxin activity was reduced to an 80-fold dilution and below a tenfold dilution by 0.049 through 0.78 and 1.56 mg protein/ml, respectively, of IVIG. These results show that IVIG has powerful neutralizing activity against hemolysin, TSST-1, and enterotoxin A. Therefore, IVIG may be useful for passive immunization therapy in patients suffering from diseases caused by MRSA exotoxins. |
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The hemolytic activity of the culture supernatant against sheep red blood cells was reduced from 100% to 5.5% relative hemolysis in the presence of 0.156 mg protein/ml of IVIG. The maximum dilution endpoint of the culture supernatant for TSST-1-mediated latex aggregation was 32-fold. This level of TSST-1 activity was reduced to eightfold dilution by 0.78 mg protein/ml of IVIG, and the latex aggregation activity of undiluted TSST-1 in the culture supernatant was inhibited by 1.56 mg protein/ml of IVIG. Similarly, the enterotoxin A-mediated latex aggregation titer appeared to be a 320-fold dilution. This toxin activity was reduced to an 80-fold dilution and below a tenfold dilution by 0.049 through 0.78 and 1.56 mg protein/ml, respectively, of IVIG. These results show that IVIG has powerful neutralizing activity against hemolysin, TSST-1, and enterotoxin A. 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The hemolytic activity of the culture supernatant against sheep red blood cells was reduced from 100% to 5.5% relative hemolysis in the presence of 0.156 mg protein/ml of IVIG. The maximum dilution endpoint of the culture supernatant for TSST-1-mediated latex aggregation was 32-fold. This level of TSST-1 activity was reduced to eightfold dilution by 0.78 mg protein/ml of IVIG, and the latex aggregation activity of undiluted TSST-1 in the culture supernatant was inhibited by 1.56 mg protein/ml of IVIG. Similarly, the enterotoxin A-mediated latex aggregation titer appeared to be a 320-fold dilution. This toxin activity was reduced to an 80-fold dilution and below a tenfold dilution by 0.049 through 0.78 and 1.56 mg protein/ml, respectively, of IVIG. These results show that IVIG has powerful neutralizing activity against hemolysin, TSST-1, and enterotoxin A. Therefore, IVIG may be useful for passive immunization therapy in patients suffering from diseases caused by MRSA exotoxins.</description><subject>Bacterial Toxins - genetics</subject><subject>Bacterial Toxins - immunology</subject><subject>Enterotoxins - genetics</subject><subject>Enterotoxins - immunology</subject><subject>Exotoxins - immunology</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Hemolysin Proteins - genetics</subject><subject>Hemolysin Proteins - immunology</subject><subject>Humans</subject><subject>Immunoglobulins, Intravenous - immunology</subject><subject>Latex Fixation Tests</subject><subject>Methicillin Resistance</subject><subject>Staphylococcal Infections - immunology</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - drug effects</subject><subject>Staphylococcus aureus - genetics</subject><subject>Staphylococcus aureus - immunology</subject><subject>Superantigens - genetics</subject><subject>Superantigens - immunology</subject><issn>1341-321X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkT9PwzAQxT2AaCl8ABaUiS3gs2MnWZBQxT-pggGQmLAc12ldErvYSdXy6XHUSkx3Or17uvc7hC4AXwPG-U0ADIynsU0xY5DyIzQGmkFKCXyO0GkIK4whZ0VxgkZQ4JLhIhujrxfdd1425ld2xtnE1Uno5Hq5a5xySskm0VvXua2xITE22ZjOu6TaJcu-lTZ13izi1NhosdHW9VHUtr11i8ZVfWPsGTquZRP0-aFO0MfD_fv0KZ29Pj5P72apyqDsUqhoSUqo60oXqswAKJcSeDWfE1UBJRnHpCQ0ozXkmmcVrSXnRBGWFUpzhukEXe1919799Dp0ojVB6aaRVserBIlhKWNlFMJeqLwLwetarL1ppd8JwGIAKfYgxdAOIAWPO5cH875q9fx_40AxCm73Ah0jboz2QsXsJtL71jsdVq73NqYXIAIRWLwNfxnegvMcF0By-gdkiIdB</recordid><startdate>200712</startdate><enddate>200712</enddate><creator>Yanagisawa, Chie</creator><creator>Hanaki, Hideaki</creator><creator>Natae, Taiji</creator><creator>Sunakawa, Keisuke</creator><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>C1K</scope></search><sort><creationdate>200712</creationdate><title>Neutralization of staphylococcal exotoxins in vitro by human-origin intravenous immunoglobulin</title><author>Yanagisawa, Chie ; Hanaki, Hideaki ; Natae, Taiji ; Sunakawa, Keisuke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-1b39291ffbe8c941136aa16bdd2cb132460292343f17e64b3fa662c2548ce6503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Bacterial Toxins - genetics</topic><topic>Bacterial Toxins - immunology</topic><topic>Enterotoxins - genetics</topic><topic>Enterotoxins - immunology</topic><topic>Exotoxins - immunology</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Hemolysin Proteins - genetics</topic><topic>Hemolysin Proteins - immunology</topic><topic>Humans</topic><topic>Immunoglobulins, Intravenous - immunology</topic><topic>Latex Fixation Tests</topic><topic>Methicillin Resistance</topic><topic>Staphylococcal Infections - immunology</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - drug effects</topic><topic>Staphylococcus aureus - genetics</topic><topic>Staphylococcus aureus - immunology</topic><topic>Superantigens - genetics</topic><topic>Superantigens - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yanagisawa, Chie</creatorcontrib><creatorcontrib>Hanaki, Hideaki</creatorcontrib><creatorcontrib>Natae, Taiji</creatorcontrib><creatorcontrib>Sunakawa, Keisuke</creatorcontrib><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>Environmental Sciences and Pollution Management</collection><jtitle>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yanagisawa, Chie</au><au>Hanaki, Hideaki</au><au>Natae, Taiji</au><au>Sunakawa, Keisuke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neutralization of staphylococcal exotoxins in vitro by human-origin intravenous immunoglobulin</atitle><jtitle>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</jtitle><addtitle>J Infect Chemother</addtitle><date>2007-12</date><risdate>2007</risdate><volume>13</volume><issue>6</issue><spage>368</spage><epage>372</epage><pages>368-372</pages><issn>1341-321X</issn><abstract>Abstract Human-origin intravenous immunoglobulin (IVIG) collected from healthy individuals was tested for its neutralizing activity against the hemolysin, toxic shock syndrome toxin-1 (TSST-1), and enterotoxins, produced by laboratory strains of methicillin-resistant Staphylococcus aureus (MRSA). The hemolytic activity of the culture supernatant against sheep red blood cells was reduced from 100% to 5.5% relative hemolysis in the presence of 0.156 mg protein/ml of IVIG. The maximum dilution endpoint of the culture supernatant for TSST-1-mediated latex aggregation was 32-fold. This level of TSST-1 activity was reduced to eightfold dilution by 0.78 mg protein/ml of IVIG, and the latex aggregation activity of undiluted TSST-1 in the culture supernatant was inhibited by 1.56 mg protein/ml of IVIG. Similarly, the enterotoxin A-mediated latex aggregation titer appeared to be a 320-fold dilution. This toxin activity was reduced to an 80-fold dilution and below a tenfold dilution by 0.049 through 0.78 and 1.56 mg protein/ml, respectively, of IVIG. These results show that IVIG has powerful neutralizing activity against hemolysin, TSST-1, and enterotoxin A. Therefore, IVIG may be useful for passive immunization therapy in patients suffering from diseases caused by MRSA exotoxins.</abstract><cop>Netherlands</cop><pmid>18095084</pmid><doi>10.1007/s10156-007-0551-6</doi><tpages>5</tpages></addata></record> |
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subjects | Bacterial Toxins - genetics Bacterial Toxins - immunology Enterotoxins - genetics Enterotoxins - immunology Exotoxins - immunology Hematology, Oncology and Palliative Medicine Hemolysin Proteins - genetics Hemolysin Proteins - immunology Humans Immunoglobulins, Intravenous - immunology Latex Fixation Tests Methicillin Resistance Staphylococcal Infections - immunology Staphylococcus aureus Staphylococcus aureus - drug effects Staphylococcus aureus - genetics Staphylococcus aureus - immunology Superantigens - genetics Superantigens - immunology |
title | Neutralization of staphylococcal exotoxins in vitro by human-origin intravenous immunoglobulin |
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