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The Early Humoral Response in Human Granulocytic Ehrlichiosis
The early antibody response in patients with human granulocytic ehrlichiosis (HGE) and in mice infected with the HGE agent was characterized by using sera to probe lysates of HL-60 cells infected with HGE organisms. Sera were obtained from 18 patients with HGE, mostly within the first 6 weeks of cli...
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Published in: | The Journal of infectious diseases 1997-09, Vol.176 (3), p.687-692 |
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container_title | The Journal of infectious diseases |
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creator | IJdo, Jacob W. Zhang, Yan Hodzic, Emir Magnarelli, Louis A. Wilson, Mark L. Telford, Sam R. Barthold, Stephen W. Fikrig, Erol |
description | The early antibody response in patients with human granulocytic ehrlichiosis (HGE) and in mice infected with the HGE agent was characterized by using sera to probe lysates of HL-60 cells infected with HGE organisms. Sera were obtained from 18 patients with HGE, mostly within the first 6 weeks of clinical infection, and from mice infected with the HGE agent for up to 3 weeks. A 44-kDa antigen was reactive with IgG in all 18 patients, and IgG to 40-, 65-, and 80-kDa antigens was present in 6, 8, and 7 patients, respectively. In addition, IgM to 40-, 44-, 65-, and 80-kDa antigens was found in 9, 5, 4, and 4 subjects. Immunoglobulins to antigens ranging between 95 and 125 kDa were detected less frequently. HGE agent-infected C3H/HeJ mice had an antibody response similar to that in humans. Thus, the 40- and 44-kDa proteins of the HGE agent elicit early strong antibody responses during infection. Characterization of the antigens recognized by antibodies during HGE should aid in diagnosis and understanding of the disease. |
doi_str_mv | 10.1086/514091 |
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Sera were obtained from 18 patients with HGE, mostly within the first 6 weeks of clinical infection, and from mice infected with the HGE agent for up to 3 weeks. A 44-kDa antigen was reactive with IgG in all 18 patients, and IgG to 40-, 65-, and 80-kDa antigens was present in 6, 8, and 7 patients, respectively. In addition, IgM to 40-, 44-, 65-, and 80-kDa antigens was found in 9, 5, 4, and 4 subjects. Immunoglobulins to antigens ranging between 95 and 125 kDa were detected less frequently. HGE agent-infected C3H/HeJ mice had an antibody response similar to that in humans. Thus, the 40- and 44-kDa proteins of the HGE agent elicit early strong antibody responses during infection. Characterization of the antigens recognized by antibodies during HGE should aid in diagnosis and understanding of the disease.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1086/514091</identifier><identifier>PMID: 9291316</identifier><identifier>CODEN: JIDIAQ</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>Anaplasma phagocytophilum ; Animals ; Antibodies ; Antibodies, Bacterial - blood ; Antigens ; Bacterial diseases ; Biological and medical sciences ; Blood ; Ehrlichia ; Ehrlichia chaffeensis - immunology ; Ehrlichiosis ; Ehrlichiosis - blood ; Ehrlichiosis - immunology ; Granulocytes ; Hematopoietic stem cells ; HL-60 Cells ; Human bacterial diseases ; Humans ; Immunoglobulin G - blood ; Immunoglobulin M - blood ; Infections ; Infectious diseases ; Major Articles ; Medical sciences ; Mice ; Mice, Inbred C3H ; Reactivity ; Rickettsial diseases ; Tropical bacterial diseases</subject><ispartof>The Journal of infectious diseases, 1997-09, Vol.176 (3), p.687-692</ispartof><rights>Copyright 1997 The University of Chicago</rights><rights>1997 INIST-CNRS</rights><rights>Copyright University of Chicago, acting through its Press Sep 1997</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-93827423752842a7afc83b7393ae7dbd639468d8b72e83d424ddae3af86938133</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2824451$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9291316$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>IJdo, Jacob W.</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Hodzic, Emir</creatorcontrib><creatorcontrib>Magnarelli, Louis A.</creatorcontrib><creatorcontrib>Wilson, Mark L.</creatorcontrib><creatorcontrib>Telford, Sam R.</creatorcontrib><creatorcontrib>Barthold, Stephen W.</creatorcontrib><creatorcontrib>Fikrig, Erol</creatorcontrib><title>The Early Humoral Response in Human Granulocytic Ehrlichiosis</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>The early antibody response in patients with human granulocytic ehrlichiosis (HGE) and in mice infected with the HGE agent was characterized by using sera to probe lysates of HL-60 cells infected with HGE organisms. Sera were obtained from 18 patients with HGE, mostly within the first 6 weeks of clinical infection, and from mice infected with the HGE agent for up to 3 weeks. A 44-kDa antigen was reactive with IgG in all 18 patients, and IgG to 40-, 65-, and 80-kDa antigens was present in 6, 8, and 7 patients, respectively. In addition, IgM to 40-, 44-, 65-, and 80-kDa antigens was found in 9, 5, 4, and 4 subjects. Immunoglobulins to antigens ranging between 95 and 125 kDa were detected less frequently. HGE agent-infected C3H/HeJ mice had an antibody response similar to that in humans. Thus, the 40- and 44-kDa proteins of the HGE agent elicit early strong antibody responses during infection. Characterization of the antigens recognized by antibodies during HGE should aid in diagnosis and understanding of the disease.</description><subject>Anaplasma phagocytophilum</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Antibodies, Bacterial - blood</subject><subject>Antigens</subject><subject>Bacterial diseases</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Ehrlichia</subject><subject>Ehrlichia chaffeensis - immunology</subject><subject>Ehrlichiosis</subject><subject>Ehrlichiosis - blood</subject><subject>Ehrlichiosis - immunology</subject><subject>Granulocytes</subject><subject>Hematopoietic stem cells</subject><subject>HL-60 Cells</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulin M - blood</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Major Articles</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Reactivity</subject><subject>Rickettsial diseases</subject><subject>Tropical bacterial diseases</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkE1r2zAch0XZ6LKu_QYFM8pu7iT9Zb0ceighbfoCg-HB6EUoskyUOlYq2bB8-6kkpKOXnQR6Hv1AD0JnBF8SLPn3ijCsyBGakApEyTmBD2iCMaUlkUp9Qp9TWmGMGXBxjI4VVQQIn6CreumKmYndtpiP6xBNV_x0aRP65Arfv96ZvriNph-7YLeDt8VsGTtvlz4kn76gj63pkjvdnyfo182sns7Lxx-3d9Prx9KyCoZSgaSCURAVlYwaYVorYSFAgXGiWTQcFOOykQtBnYSGUdY0xoFpJc9PCcAJ-rbb3cTwMro06LVP1nWd6V0YkxaK5jXO_ysSTrACzrL49Z24CmPs8yc0paAIyaXe1mwMKUXX6k30axO3mmD9Wl3vqmfxfL82LtauOWj7zJlf7LlJ1nRt7ml9OmhUUsaqf2ZWaQjxgAETLIDJzMsd92lwfw7cxGfNRa6r57-fdH2vHm5qWusH-Audx54q</recordid><startdate>19970901</startdate><enddate>19970901</enddate><creator>IJdo, Jacob W.</creator><creator>Zhang, Yan</creator><creator>Hodzic, Emir</creator><creator>Magnarelli, Louis A.</creator><creator>Wilson, Mark L.</creator><creator>Telford, Sam R.</creator><creator>Barthold, Stephen W.</creator><creator>Fikrig, Erol</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><general>Oxford University Press</general><scope>BSCLL</scope><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>K9.</scope><scope>NAPCQ</scope><scope>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>19970901</creationdate><title>The Early Humoral Response in Human Granulocytic Ehrlichiosis</title><author>IJdo, Jacob W. ; Zhang, Yan ; Hodzic, Emir ; Magnarelli, Louis A. ; Wilson, Mark L. ; Telford, Sam R. ; Barthold, Stephen W. ; Fikrig, Erol</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-93827423752842a7afc83b7393ae7dbd639468d8b72e83d424ddae3af86938133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Anaplasma phagocytophilum</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Antibodies, Bacterial - blood</topic><topic>Antigens</topic><topic>Bacterial diseases</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Ehrlichia</topic><topic>Ehrlichia chaffeensis - immunology</topic><topic>Ehrlichiosis</topic><topic>Ehrlichiosis - blood</topic><topic>Ehrlichiosis - immunology</topic><topic>Granulocytes</topic><topic>Hematopoietic stem cells</topic><topic>HL-60 Cells</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Immunoglobulin G - blood</topic><topic>Immunoglobulin M - blood</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Major Articles</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Reactivity</topic><topic>Rickettsial diseases</topic><topic>Tropical bacterial diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>IJdo, Jacob W.</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Hodzic, Emir</creatorcontrib><creatorcontrib>Magnarelli, Louis A.</creatorcontrib><creatorcontrib>Wilson, Mark L.</creatorcontrib><creatorcontrib>Telford, Sam R.</creatorcontrib><creatorcontrib>Barthold, Stephen W.</creatorcontrib><creatorcontrib>Fikrig, Erol</creatorcontrib><collection>Istex</collection><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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>IJdo, Jacob W.</au><au>Zhang, Yan</au><au>Hodzic, Emir</au><au>Magnarelli, Louis A.</au><au>Wilson, Mark L.</au><au>Telford, Sam R.</au><au>Barthold, Stephen W.</au><au>Fikrig, Erol</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Early Humoral Response in Human Granulocytic Ehrlichiosis</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>1997-09-01</date><risdate>1997</risdate><volume>176</volume><issue>3</issue><spage>687</spage><epage>692</epage><pages>687-692</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>The early antibody response in patients with human granulocytic ehrlichiosis (HGE) and in mice infected with the HGE agent was characterized by using sera to probe lysates of HL-60 cells infected with HGE organisms. Sera were obtained from 18 patients with HGE, mostly within the first 6 weeks of clinical infection, and from mice infected with the HGE agent for up to 3 weeks. A 44-kDa antigen was reactive with IgG in all 18 patients, and IgG to 40-, 65-, and 80-kDa antigens was present in 6, 8, and 7 patients, respectively. In addition, IgM to 40-, 44-, 65-, and 80-kDa antigens was found in 9, 5, 4, and 4 subjects. Immunoglobulins to antigens ranging between 95 and 125 kDa were detected less frequently. HGE agent-infected C3H/HeJ mice had an antibody response similar to that in humans. Thus, the 40- and 44-kDa proteins of the HGE agent elicit early strong antibody responses during infection. Characterization of the antigens recognized by antibodies during HGE should aid in diagnosis and understanding of the disease.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>9291316</pmid><doi>10.1086/514091</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anaplasma phagocytophilum Animals Antibodies Antibodies, Bacterial - blood Antigens Bacterial diseases Biological and medical sciences Blood Ehrlichia Ehrlichia chaffeensis - immunology Ehrlichiosis Ehrlichiosis - blood Ehrlichiosis - immunology Granulocytes Hematopoietic stem cells HL-60 Cells Human bacterial diseases Humans Immunoglobulin G - blood Immunoglobulin M - blood Infections Infectious diseases Major Articles Medical sciences Mice Mice, Inbred C3H Reactivity Rickettsial diseases Tropical bacterial diseases |
title | The Early Humoral Response in Human Granulocytic Ehrlichiosis |
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