Serum transfer of collagen-induced arthritis in mice
Immunization of DBA/1 mice with native chick type II collagen resulted in development of polyarthritis 4-5 wk later. Sera of these mice contained high levels of anticollagen antibodies, and immunoglobulin concentrates of their sera transferred arthritis to unimmunized recipients. Histopathologically...
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Veröffentlicht in: | The Journal of experimental medicine 1983-08, Vol.158 (2), p.378-392 |
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description | Immunization of DBA/1 mice with native chick type II collagen resulted in development of polyarthritis 4-5 wk later. Sera of these mice contained high levels of anticollagen antibodies, and immunoglobulin concentrates of their sera transferred arthritis to unimmunized recipients. Histopathologically, this passively transferred arthritis resembled the early disease of immunized donors. Immunofluorescence studies demonstrated the deposition of IgG and C3 on the articular surface but not in synovial tissue of arthritic joints. Transferred, isotopically labeled anticollagen antibodies rapidly localized to the limbs and to other cartilage-containing tissues. When transfer concentrate was administered to arthritis-resistant strains, they also developed arthritis. Indeed, immunoglobulin concentrates from rats with collagen-induced arthritis transferred arthritis to naive mice. The amount of concentrate required for transfer to B10.D2 resistant mice was reduced by immunizing them with collagen 4 wk before transfer. Although susceptibility to arthritis from immunization is H-2 linked, these studies clearly demonstrate that passive transfer of arthritis depends upon injection of specific antibody and not on other host factors. |
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M ; DIXON, F. J</creator><creatorcontrib>STUART, J. M ; DIXON, F. J</creatorcontrib><description>Immunization of DBA/1 mice with native chick type II collagen resulted in development of polyarthritis 4-5 wk later. Sera of these mice contained high levels of anticollagen antibodies, and immunoglobulin concentrates of their sera transferred arthritis to unimmunized recipients. Histopathologically, this passively transferred arthritis resembled the early disease of immunized donors. Immunofluorescence studies demonstrated the deposition of IgG and C3 on the articular surface but not in synovial tissue of arthritic joints. Transferred, isotopically labeled anticollagen antibodies rapidly localized to the limbs and to other cartilage-containing tissues. When transfer concentrate was administered to arthritis-resistant strains, they also developed arthritis. Indeed, immunoglobulin concentrates from rats with collagen-induced arthritis transferred arthritis to naive mice. The amount of concentrate required for transfer to B10.D2 resistant mice was reduced by immunizing them with collagen 4 wk before transfer. Although susceptibility to arthritis from immunization is H-2 linked, these studies clearly demonstrate that passive transfer of arthritis depends upon injection of specific antibody and not on other host factors.</description><identifier>ISSN: 0022-1007</identifier><identifier>EISSN: 1540-9538</identifier><identifier>DOI: 10.1084/jem.158.2.378</identifier><identifier>PMID: 6886622</identifier><identifier>CODEN: JEMEAV</identifier><language>eng</language><publisher>New York, NY: Rockefeller University Press</publisher><subject>Animals ; Arthritis - immunology ; Arthritis, Experimental - genetics ; Arthritis, Experimental - immunology ; Arthritis, Experimental - pathology ; Autoantibodies - analysis ; Biological and medical sciences ; Collagen - immunology ; Diseases of the osteoarticular system ; Female ; H-2 Antigens - genetics ; Immune Sera - administration & dosage ; Immunity, Innate ; Immunization, Passive ; Immunoglobulin G - analysis ; Inflammatory joint diseases ; Male ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Inbred DBA ; Rats ; Rats, Inbred WF ; Species Specificity ; Time Factors</subject><ispartof>The Journal of experimental medicine, 1983-08, Vol.158 (2), p.378-392</ispartof><rights>1984 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-8922f6bf0c37b42d5cf9601b8ffc5d2119a0a9df2675d64abade2213c8f1b2c13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9415943$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6886622$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>STUART, J. M</creatorcontrib><creatorcontrib>DIXON, F. J</creatorcontrib><title>Serum transfer of collagen-induced arthritis in mice</title><title>The Journal of experimental medicine</title><addtitle>J Exp Med</addtitle><description>Immunization of DBA/1 mice with native chick type II collagen resulted in development of polyarthritis 4-5 wk later. Sera of these mice contained high levels of anticollagen antibodies, and immunoglobulin concentrates of their sera transferred arthritis to unimmunized recipients. Histopathologically, this passively transferred arthritis resembled the early disease of immunized donors. Immunofluorescence studies demonstrated the deposition of IgG and C3 on the articular surface but not in synovial tissue of arthritic joints. Transferred, isotopically labeled anticollagen antibodies rapidly localized to the limbs and to other cartilage-containing tissues. When transfer concentrate was administered to arthritis-resistant strains, they also developed arthritis. Indeed, immunoglobulin concentrates from rats with collagen-induced arthritis transferred arthritis to naive mice. The amount of concentrate required for transfer to B10.D2 resistant mice was reduced by immunizing them with collagen 4 wk before transfer. Although susceptibility to arthritis from immunization is H-2 linked, these studies clearly demonstrate that passive transfer of arthritis depends upon injection of specific antibody and not on other host factors.</description><subject>Animals</subject><subject>Arthritis - immunology</subject><subject>Arthritis, Experimental - genetics</subject><subject>Arthritis, Experimental - immunology</subject><subject>Arthritis, Experimental - pathology</subject><subject>Autoantibodies - analysis</subject><subject>Biological and medical sciences</subject><subject>Collagen - immunology</subject><subject>Diseases of the osteoarticular system</subject><subject>Female</subject><subject>H-2 Antigens - genetics</subject><subject>Immune Sera - administration & dosage</subject><subject>Immunity, Innate</subject><subject>Immunization, Passive</subject><subject>Immunoglobulin G - analysis</subject><subject>Inflammatory joint diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred DBA</subject><subject>Rats</subject><subject>Rats, Inbred WF</subject><subject>Species Specificity</subject><subject>Time Factors</subject><issn>0022-1007</issn><issn>1540-9538</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTlLBTEUhYMo-lxKS2EKsZtn7s0ymUYQcQPBQq1DJpNoZBZNZgT_vREfD62sbnE-DufyEXIIdAlU8dNX1y9BqCUuWaU2yAIEp2UtmNokC0oRS6C02iG7Kb1SCpwLuU22pVJSIi4If3Bx7ospmiF5F4vRF3bsOvPshjIM7WxdW5g4vcQwhVSEoeiDdftky5suuYPV3SNPV5ePFzfl3f317cX5XWkFVVOpakQvG08tqxqOrbC-lhQa5b0VLQLUhpq69Sgr0UpuGtM6RGBWeWjQAtsjZz-9b3PTu9a6Ie_s9FsMvYmfejRB_02G8KKfxw-NoCrGeC44WRXE8X12adJ9SNbl_wY3zkkrKhFQ0n9BYAo5Vt-Tyh_QxjGl6Px6DVD97UNnHzr70Kizj8wf_X5hTa8E5Px4lZtkTeezBxvSGqs5iJoz9gVKIpPI</recordid><startdate>19830801</startdate><enddate>19830801</enddate><creator>STUART, J. M</creator><creator>DIXON, F. J</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</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><scope>5PM</scope></search><sort><creationdate>19830801</creationdate><title>Serum transfer of collagen-induced arthritis in mice</title><author>STUART, J. M ; DIXON, F. J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-8922f6bf0c37b42d5cf9601b8ffc5d2119a0a9df2675d64abade2213c8f1b2c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Animals</topic><topic>Arthritis - immunology</topic><topic>Arthritis, Experimental - genetics</topic><topic>Arthritis, Experimental - immunology</topic><topic>Arthritis, Experimental - pathology</topic><topic>Autoantibodies - analysis</topic><topic>Biological and medical sciences</topic><topic>Collagen - immunology</topic><topic>Diseases of the osteoarticular system</topic><topic>Female</topic><topic>H-2 Antigens - genetics</topic><topic>Immune Sera - administration & dosage</topic><topic>Immunity, Innate</topic><topic>Immunization, Passive</topic><topic>Immunoglobulin G - analysis</topic><topic>Inflammatory joint diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred DBA</topic><topic>Rats</topic><topic>Rats, Inbred WF</topic><topic>Species Specificity</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>STUART, J. M</creatorcontrib><creatorcontrib>DIXON, F. J</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of experimental medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>STUART, J. M</au><au>DIXON, F. J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum transfer of collagen-induced arthritis in mice</atitle><jtitle>The Journal of experimental medicine</jtitle><addtitle>J Exp Med</addtitle><date>1983-08-01</date><risdate>1983</risdate><volume>158</volume><issue>2</issue><spage>378</spage><epage>392</epage><pages>378-392</pages><issn>0022-1007</issn><eissn>1540-9538</eissn><coden>JEMEAV</coden><abstract>Immunization of DBA/1 mice with native chick type II collagen resulted in development of polyarthritis 4-5 wk later. Sera of these mice contained high levels of anticollagen antibodies, and immunoglobulin concentrates of their sera transferred arthritis to unimmunized recipients. Histopathologically, this passively transferred arthritis resembled the early disease of immunized donors. Immunofluorescence studies demonstrated the deposition of IgG and C3 on the articular surface but not in synovial tissue of arthritic joints. Transferred, isotopically labeled anticollagen antibodies rapidly localized to the limbs and to other cartilage-containing tissues. When transfer concentrate was administered to arthritis-resistant strains, they also developed arthritis. Indeed, immunoglobulin concentrates from rats with collagen-induced arthritis transferred arthritis to naive mice. The amount of concentrate required for transfer to B10.D2 resistant mice was reduced by immunizing them with collagen 4 wk before transfer. Although susceptibility to arthritis from immunization is H-2 linked, these studies clearly demonstrate that passive transfer of arthritis depends upon injection of specific antibody and not on other host factors.</abstract><cop>New York, NY</cop><pub>Rockefeller University Press</pub><pmid>6886622</pmid><doi>10.1084/jem.158.2.378</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Arthritis - immunology Arthritis, Experimental - genetics Arthritis, Experimental - immunology Arthritis, Experimental - pathology Autoantibodies - analysis Biological and medical sciences Collagen - immunology Diseases of the osteoarticular system Female H-2 Antigens - genetics Immune Sera - administration & dosage Immunity, Innate Immunization, Passive Immunoglobulin G - analysis Inflammatory joint diseases Male Medical sciences Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Inbred DBA Rats Rats, Inbred WF Species Specificity Time Factors |
title | Serum transfer of collagen-induced arthritis in mice |
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