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Identification of bacterial antigens in circulating immune complexes of infective endocarditis
The presence of circulating immune complexes (IC) in patients with infective endocarditis has been well documented but the contributions of host and bacterial components to these IC have not been defined. To study this question, IC were isolated from serum of a patient with Streptococcus faecalis en...
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Published in: | The Journal of clinical investigation 1982-08, Vol.70 (2), p.271-280 |
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container_title | The Journal of clinical investigation |
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creator | Inman, R D Redecha, P B Knechtle, S J Schned, E S van de Rijn, I Christian, C L |
description | The presence of circulating immune complexes (IC) in patients with infective endocarditis has been well documented but the contributions of host and bacterial components to these IC have not been defined. To study this question, IC were isolated from serum of a patient with Streptococcus faecalis endocarditis by differential polyethylene glycol precipitation and competitive binding to staphylococcal protein A. A rabbit antiserum raised against the purified IC had reactivity by crossed immunoelectrophoresis primarily with an antigen derived from the cytoplasm of the infective organism. The antigen was a protein with a 12,000-dalton molecular mass. In situ radiolabeling of the IC bound to the protein A demonstrated a component of the same molecular mass as the bacterial antigen recognized by the antiserum. The patient serum had multiple antibody specificities reactive with bacterial antigens, including the antigen recognized by the rabbit anti-IC antiserum. These techniques for isolation and characterization of circulating IC may have value in the study of IC diseases in which the inciting antigens are not known. |
doi_str_mv | 10.1172/JCI110614 |
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To study this question, IC were isolated from serum of a patient with Streptococcus faecalis endocarditis by differential polyethylene glycol precipitation and competitive binding to staphylococcal protein A. A rabbit antiserum raised against the purified IC had reactivity by crossed immunoelectrophoresis primarily with an antigen derived from the cytoplasm of the infective organism. The antigen was a protein with a 12,000-dalton molecular mass. In situ radiolabeling of the IC bound to the protein A demonstrated a component of the same molecular mass as the bacterial antigen recognized by the antiserum. The patient serum had multiple antibody specificities reactive with bacterial antigens, including the antigen recognized by the rabbit anti-IC antiserum. These techniques for isolation and characterization of circulating IC may have value in the study of IC diseases in which the inciting antigens are not known.</description><identifier>ISSN: 0021-9738</identifier><identifier>DOI: 10.1172/JCI110614</identifier><identifier>PMID: 6808025</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Antigen-Antibody Complex - analysis ; Antigens, Bacterial - analysis ; Electrophoresis, Polyacrylamide Gel ; Endocarditis, Bacterial - immunology ; Enterococcus faecalis ; Humans ; Immunoelectrophoresis, Two-Dimensional ; Molecular Weight ; Rabbits ; Staphylococcal Protein A - metabolism ; Streptococcal Infections - immunology</subject><ispartof>The Journal of clinical investigation, 1982-08, Vol.70 (2), p.271-280</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-cbcb3e5959385140030b494c3fffc46acac53b89c1e6bca3738ef599af864ddf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC371233/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC371233/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6808025$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Inman, R D</creatorcontrib><creatorcontrib>Redecha, P B</creatorcontrib><creatorcontrib>Knechtle, S J</creatorcontrib><creatorcontrib>Schned, E S</creatorcontrib><creatorcontrib>van de Rijn, I</creatorcontrib><creatorcontrib>Christian, C L</creatorcontrib><title>Identification of bacterial antigens in circulating immune complexes of infective endocarditis</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>The presence of circulating immune complexes (IC) in patients with infective endocarditis has been well documented but the contributions of host and bacterial components to these IC have not been defined. To study this question, IC were isolated from serum of a patient with Streptococcus faecalis endocarditis by differential polyethylene glycol precipitation and competitive binding to staphylococcal protein A. A rabbit antiserum raised against the purified IC had reactivity by crossed immunoelectrophoresis primarily with an antigen derived from the cytoplasm of the infective organism. The antigen was a protein with a 12,000-dalton molecular mass. In situ radiolabeling of the IC bound to the protein A demonstrated a component of the same molecular mass as the bacterial antigen recognized by the antiserum. The patient serum had multiple antibody specificities reactive with bacterial antigens, including the antigen recognized by the rabbit anti-IC antiserum. These techniques for isolation and characterization of circulating IC may have value in the study of IC diseases in which the inciting antigens are not known.</description><subject>Animals</subject><subject>Antigen-Antibody Complex - analysis</subject><subject>Antigens, Bacterial - analysis</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Endocarditis, Bacterial - immunology</subject><subject>Enterococcus faecalis</subject><subject>Humans</subject><subject>Immunoelectrophoresis, Two-Dimensional</subject><subject>Molecular Weight</subject><subject>Rabbits</subject><subject>Staphylococcal Protein A - metabolism</subject><subject>Streptococcal Infections - immunology</subject><issn>0021-9738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><recordid>eNqFkT1PwzAQhj2A-CgM_ACkTEgMBbu203hgQBUfRUgssGI5l3MxSuxiJxX8e1xRVTAxnXT3vHfv6SXkhNELxqaTy4fZnDFaMrFDDiidsLGa8mqfHKb0TikTQoo9sldWtKITeUBe5w363lkHpnfBF8EWtYEeozNtYfJkgT4VzhfgIgxthvyicF03eCwgdMsWPzGtVc5bhN6tsEDfBDCxcb1LR2TXmjbh8aaOyMvtzfPsfvz4dDefXT-OQVDaj6GGmqNUUvFKstzitBZKALfWgigNGJC8rhQwLGswPH-EViplbFWKprF8RK5-9i6HusMG8k_RtHoZXWfilw7G6b8T7970Iqw0n7IJ51l_ttHH8DFg6nXnEmDbGo9hSHoqWD6qqn9BJqUolRAZPP8BIYaUItqtGUb1Oii9DSqzp7_db8lNSvwbb_WTGQ</recordid><startdate>19820801</startdate><enddate>19820801</enddate><creator>Inman, R D</creator><creator>Redecha, P B</creator><creator>Knechtle, S J</creator><creator>Schned, E S</creator><creator>van de Rijn, I</creator><creator>Christian, C L</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>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19820801</creationdate><title>Identification of bacterial antigens in circulating immune complexes of infective endocarditis</title><author>Inman, R D ; Redecha, P B ; Knechtle, S J ; Schned, E S ; van de Rijn, I ; Christian, C L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-cbcb3e5959385140030b494c3fffc46acac53b89c1e6bca3738ef599af864ddf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Animals</topic><topic>Antigen-Antibody Complex - analysis</topic><topic>Antigens, Bacterial - analysis</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Endocarditis, Bacterial - immunology</topic><topic>Enterococcus faecalis</topic><topic>Humans</topic><topic>Immunoelectrophoresis, Two-Dimensional</topic><topic>Molecular Weight</topic><topic>Rabbits</topic><topic>Staphylococcal Protein A - metabolism</topic><topic>Streptococcal Infections - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Inman, R D</creatorcontrib><creatorcontrib>Redecha, P B</creatorcontrib><creatorcontrib>Knechtle, S J</creatorcontrib><creatorcontrib>Schned, E S</creatorcontrib><creatorcontrib>van de Rijn, I</creatorcontrib><creatorcontrib>Christian, C L</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>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Inman, R D</au><au>Redecha, P B</au><au>Knechtle, S J</au><au>Schned, E S</au><au>van de Rijn, I</au><au>Christian, C L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of bacterial antigens in circulating immune complexes of infective endocarditis</atitle><jtitle>The Journal of clinical investigation</jtitle><addtitle>J Clin Invest</addtitle><date>1982-08-01</date><risdate>1982</risdate><volume>70</volume><issue>2</issue><spage>271</spage><epage>280</epage><pages>271-280</pages><issn>0021-9738</issn><abstract>The presence of circulating immune complexes (IC) in patients with infective endocarditis has been well documented but the contributions of host and bacterial components to these IC have not been defined. To study this question, IC were isolated from serum of a patient with Streptococcus faecalis endocarditis by differential polyethylene glycol precipitation and competitive binding to staphylococcal protein A. A rabbit antiserum raised against the purified IC had reactivity by crossed immunoelectrophoresis primarily with an antigen derived from the cytoplasm of the infective organism. The antigen was a protein with a 12,000-dalton molecular mass. In situ radiolabeling of the IC bound to the protein A demonstrated a component of the same molecular mass as the bacterial antigen recognized by the antiserum. The patient serum had multiple antibody specificities reactive with bacterial antigens, including the antigen recognized by the rabbit anti-IC antiserum. These techniques for isolation and characterization of circulating IC may have value in the study of IC diseases in which the inciting antigens are not known.</abstract><cop>United States</cop><pmid>6808025</pmid><doi>10.1172/JCI110614</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigen-Antibody Complex - analysis Antigens, Bacterial - analysis Electrophoresis, Polyacrylamide Gel Endocarditis, Bacterial - immunology Enterococcus faecalis Humans Immunoelectrophoresis, Two-Dimensional Molecular Weight Rabbits Staphylococcal Protein A - metabolism Streptococcal Infections - immunology |
title | Identification of bacterial antigens in circulating immune complexes of infective endocarditis |
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