Modulation of mouse complement receptors 1 and 2 suppresses antibody responses in vivo

A mAb, 7G6, that binds to mouse CR1 and CR2 and down-modulates their expression on splenic B cells in vivo, was used to determine whether a decrease in CR1 and CR2 expression affects antibody responses to different T-dependent and T-independent Ag. Injection of mice with the mAb 7G6 prior to immuniz...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of immunology (1950) 1991-07, Vol.147 (1), p.224-230
Hauptverfasser: Thyphronitis, G, Kinoshita, T, Inoue, K, Schweinle, JE, Tsokos, GC, Metcalf, ES, Finkelman, FD, Balow, JE
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 230
container_issue 1
container_start_page 224
container_title The Journal of immunology (1950)
container_volume 147
creator Thyphronitis, G
Kinoshita, T
Inoue, K
Schweinle, JE
Tsokos, GC
Metcalf, ES
Finkelman, FD
Balow, JE
description A mAb, 7G6, that binds to mouse CR1 and CR2 and down-modulates their expression on splenic B cells in vivo, was used to determine whether a decrease in CR1 and CR2 expression affects antibody responses to different T-dependent and T-independent Ag. Injection of mice with the mAb 7G6 prior to immunization with FITC haptenated Salmonella typhimurium (SH5771), Salmonella montevideo (SH5770), SRBC, or Ficoll dramatically decreased subsequent antibody responses to FITC. Although both IgM and IgG primary antibody responses were affected similarly, the antibody levels were most inhibited during early phases of the response. In contrast, down-modulation of the CR did not affect memory antibody responses, because injection of mice with 7G6 before a second immunization with FITC-SH5771 had no effect on subsequent anti-FITC antibody production. Moreover, polyclonal in vivo activation of the mouse immune system by anti-mouse IgD antibodies was not affected by previous administration of 7G6, because anti-IgD-induced increases in Ia expression and serum IgG1 levels were not affected. Taken together, these observations suggest that CR1 and CR2 may play an important role in enhancing primary antibody responses to many T-dependent and T-independent Ag and may contribute to a host's response to naturally occurring antigens such as bacteria.
doi_str_mv 10.4049/jimmunol.147.1.224
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_80622737</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>80622737</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3484-f67288afab33983fa83469398e75189c21e5dce91656851c1fa3c7e671e60c3a3</originalsourceid><addsrcrecordid>eNqFkE1v3CAQhlHVKt2m_QOVKnGoevOGAQz4WEXph5Qql6RXxOJxQ4SNC3ZW-fcl2m332BNo5pmX4SHkPbCtZLK7eAjjuE4pbkHqLWw5ly_IBtqWNUox9ZJsGOO8Aa30a_KmlAfGmGJcnpEzMNwYzjfk54_Ur9EtIU00DXRMa0Hq0zhHHHFaaEaP85JyoUDd1FNOyzrPGUvBUgtL2KX-qVJlTtNzKUz0MTymt-TV4GLBd8fznNx9ubq9_NZc33z9fvn5uvFCGtkMStc93OB2QnRGDM4Iqbp6Rd2C6TwHbHuPHahWmRY8DE54jUoDKuaFE-fk0yF3zun3imWxYygeY3QT1q9YwxTnWuj_gqBYx1uQFeQH0OdUSsbBzjmMLj9ZYPbZuv1r3VbrFmy1Xoc-HNPX3Yj9aeSgufY_HvuueBeH7CYfyj9MdlK2gp-WvA-_7vchoy2ji7GGgt3v96f3_gB75Jmz</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16092514</pqid></control><display><type>article</type><title>Modulation of mouse complement receptors 1 and 2 suppresses antibody responses in vivo</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Thyphronitis, G ; Kinoshita, T ; Inoue, K ; Schweinle, JE ; Tsokos, GC ; Metcalf, ES ; Finkelman, FD ; Balow, JE</creator><creatorcontrib>Thyphronitis, G ; Kinoshita, T ; Inoue, K ; Schweinle, JE ; Tsokos, GC ; Metcalf, ES ; Finkelman, FD ; Balow, JE</creatorcontrib><description>A mAb, 7G6, that binds to mouse CR1 and CR2 and down-modulates their expression on splenic B cells in vivo, was used to determine whether a decrease in CR1 and CR2 expression affects antibody responses to different T-dependent and T-independent Ag. Injection of mice with the mAb 7G6 prior to immunization with FITC haptenated Salmonella typhimurium (SH5771), Salmonella montevideo (SH5770), SRBC, or Ficoll dramatically decreased subsequent antibody responses to FITC. Although both IgM and IgG primary antibody responses were affected similarly, the antibody levels were most inhibited during early phases of the response. In contrast, down-modulation of the CR did not affect memory antibody responses, because injection of mice with 7G6 before a second immunization with FITC-SH5771 had no effect on subsequent anti-FITC antibody production. Moreover, polyclonal in vivo activation of the mouse immune system by anti-mouse IgD antibodies was not affected by previous administration of 7G6, because anti-IgD-induced increases in Ia expression and serum IgG1 levels were not affected. Taken together, these observations suggest that CR1 and CR2 may play an important role in enhancing primary antibody responses to many T-dependent and T-independent Ag and may contribute to a host's response to naturally occurring antigens such as bacteria.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.147.1.224</identifier><identifier>PMID: 1828822</identifier><identifier>CODEN: JOIMA3</identifier><language>eng</language><publisher>Bethesda, MD: Am Assoc Immnol</publisher><subject>Animals ; Antibody Formation ; Antigens, Differentiation - immunology ; Antigens, Differentiation, B-Lymphocyte - immunology ; Antigens, Differentiation, B-Lymphocyte - physiology ; B-Lymphocytes - immunology ; Biological and medical sciences ; Down-Regulation ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Immunobiology ; Immunoglobulin G - biosynthesis ; Immunoglobulin Isotypes - biosynthesis ; Immunoglobulin M - biosynthesis ; Immunologic Memory ; Lymphocyte Activation ; Mice ; Mice, Inbred Strains ; Modulation of the immune response (stimulation, suppression) ; Receptors, Complement - physiology ; Receptors, Complement 3b ; Receptors, Complement 3d ; Receptors, Fc - immunology ; Receptors, IgE ; Receptors, IgG</subject><ispartof>The Journal of immunology (1950), 1991-07, Vol.147 (1), p.224-230</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3484-f67288afab33983fa83469398e75189c21e5dce91656851c1fa3c7e671e60c3a3</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&amp;idt=4944532$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1828822$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thyphronitis, G</creatorcontrib><creatorcontrib>Kinoshita, T</creatorcontrib><creatorcontrib>Inoue, K</creatorcontrib><creatorcontrib>Schweinle, JE</creatorcontrib><creatorcontrib>Tsokos, GC</creatorcontrib><creatorcontrib>Metcalf, ES</creatorcontrib><creatorcontrib>Finkelman, FD</creatorcontrib><creatorcontrib>Balow, JE</creatorcontrib><title>Modulation of mouse complement receptors 1 and 2 suppresses antibody responses in vivo</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>A mAb, 7G6, that binds to mouse CR1 and CR2 and down-modulates their expression on splenic B cells in vivo, was used to determine whether a decrease in CR1 and CR2 expression affects antibody responses to different T-dependent and T-independent Ag. Injection of mice with the mAb 7G6 prior to immunization with FITC haptenated Salmonella typhimurium (SH5771), Salmonella montevideo (SH5770), SRBC, or Ficoll dramatically decreased subsequent antibody responses to FITC. Although both IgM and IgG primary antibody responses were affected similarly, the antibody levels were most inhibited during early phases of the response. In contrast, down-modulation of the CR did not affect memory antibody responses, because injection of mice with 7G6 before a second immunization with FITC-SH5771 had no effect on subsequent anti-FITC antibody production. Moreover, polyclonal in vivo activation of the mouse immune system by anti-mouse IgD antibodies was not affected by previous administration of 7G6, because anti-IgD-induced increases in Ia expression and serum IgG1 levels were not affected. Taken together, these observations suggest that CR1 and CR2 may play an important role in enhancing primary antibody responses to many T-dependent and T-independent Ag and may contribute to a host's response to naturally occurring antigens such as bacteria.</description><subject>Animals</subject><subject>Antibody Formation</subject><subject>Antigens, Differentiation - immunology</subject><subject>Antigens, Differentiation, B-Lymphocyte - immunology</subject><subject>Antigens, Differentiation, B-Lymphocyte - physiology</subject><subject>B-Lymphocytes - immunology</subject><subject>Biological and medical sciences</subject><subject>Down-Regulation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Immunobiology</subject><subject>Immunoglobulin G - biosynthesis</subject><subject>Immunoglobulin Isotypes - biosynthesis</subject><subject>Immunoglobulin M - biosynthesis</subject><subject>Immunologic Memory</subject><subject>Lymphocyte Activation</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Modulation of the immune response (stimulation, suppression)</subject><subject>Receptors, Complement - physiology</subject><subject>Receptors, Complement 3b</subject><subject>Receptors, Complement 3d</subject><subject>Receptors, Fc - immunology</subject><subject>Receptors, IgE</subject><subject>Receptors, IgG</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1v3CAQhlHVKt2m_QOVKnGoevOGAQz4WEXph5Qql6RXxOJxQ4SNC3ZW-fcl2m332BNo5pmX4SHkPbCtZLK7eAjjuE4pbkHqLWw5ly_IBtqWNUox9ZJsGOO8Aa30a_KmlAfGmGJcnpEzMNwYzjfk54_Ur9EtIU00DXRMa0Hq0zhHHHFaaEaP85JyoUDd1FNOyzrPGUvBUgtL2KX-qVJlTtNzKUz0MTymt-TV4GLBd8fznNx9ubq9_NZc33z9fvn5uvFCGtkMStc93OB2QnRGDM4Iqbp6Rd2C6TwHbHuPHahWmRY8DE54jUoDKuaFE-fk0yF3zun3imWxYygeY3QT1q9YwxTnWuj_gqBYx1uQFeQH0OdUSsbBzjmMLj9ZYPbZuv1r3VbrFmy1Xoc-HNPX3Yj9aeSgufY_HvuueBeH7CYfyj9MdlK2gp-WvA-_7vchoy2ji7GGgt3v96f3_gB75Jmz</recordid><startdate>19910701</startdate><enddate>19910701</enddate><creator>Thyphronitis, G</creator><creator>Kinoshita, T</creator><creator>Inoue, K</creator><creator>Schweinle, JE</creator><creator>Tsokos, GC</creator><creator>Metcalf, ES</creator><creator>Finkelman, FD</creator><creator>Balow, JE</creator><general>Am Assoc Immnol</general><general>American Association of Immunologists</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></search><sort><creationdate>19910701</creationdate><title>Modulation of mouse complement receptors 1 and 2 suppresses antibody responses in vivo</title><author>Thyphronitis, G ; Kinoshita, T ; Inoue, K ; Schweinle, JE ; Tsokos, GC ; Metcalf, ES ; Finkelman, FD ; Balow, JE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3484-f67288afab33983fa83469398e75189c21e5dce91656851c1fa3c7e671e60c3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animals</topic><topic>Antibody Formation</topic><topic>Antigens, Differentiation - immunology</topic><topic>Antigens, Differentiation, B-Lymphocyte - immunology</topic><topic>Antigens, Differentiation, B-Lymphocyte - physiology</topic><topic>B-Lymphocytes - immunology</topic><topic>Biological and medical sciences</topic><topic>Down-Regulation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Immunobiology</topic><topic>Immunoglobulin G - biosynthesis</topic><topic>Immunoglobulin Isotypes - biosynthesis</topic><topic>Immunoglobulin M - biosynthesis</topic><topic>Immunologic Memory</topic><topic>Lymphocyte Activation</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Modulation of the immune response (stimulation, suppression)</topic><topic>Receptors, Complement - physiology</topic><topic>Receptors, Complement 3b</topic><topic>Receptors, Complement 3d</topic><topic>Receptors, Fc - immunology</topic><topic>Receptors, IgE</topic><topic>Receptors, IgG</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thyphronitis, G</creatorcontrib><creatorcontrib>Kinoshita, T</creatorcontrib><creatorcontrib>Inoue, K</creatorcontrib><creatorcontrib>Schweinle, JE</creatorcontrib><creatorcontrib>Tsokos, GC</creatorcontrib><creatorcontrib>Metcalf, ES</creatorcontrib><creatorcontrib>Finkelman, FD</creatorcontrib><creatorcontrib>Balow, JE</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><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thyphronitis, G</au><au>Kinoshita, T</au><au>Inoue, K</au><au>Schweinle, JE</au><au>Tsokos, GC</au><au>Metcalf, ES</au><au>Finkelman, FD</au><au>Balow, JE</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation of mouse complement receptors 1 and 2 suppresses antibody responses in vivo</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1991-07-01</date><risdate>1991</risdate><volume>147</volume><issue>1</issue><spage>224</spage><epage>230</epage><pages>224-230</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><coden>JOIMA3</coden><abstract>A mAb, 7G6, that binds to mouse CR1 and CR2 and down-modulates their expression on splenic B cells in vivo, was used to determine whether a decrease in CR1 and CR2 expression affects antibody responses to different T-dependent and T-independent Ag. Injection of mice with the mAb 7G6 prior to immunization with FITC haptenated Salmonella typhimurium (SH5771), Salmonella montevideo (SH5770), SRBC, or Ficoll dramatically decreased subsequent antibody responses to FITC. Although both IgM and IgG primary antibody responses were affected similarly, the antibody levels were most inhibited during early phases of the response. In contrast, down-modulation of the CR did not affect memory antibody responses, because injection of mice with 7G6 before a second immunization with FITC-SH5771 had no effect on subsequent anti-FITC antibody production. Moreover, polyclonal in vivo activation of the mouse immune system by anti-mouse IgD antibodies was not affected by previous administration of 7G6, because anti-IgD-induced increases in Ia expression and serum IgG1 levels were not affected. Taken together, these observations suggest that CR1 and CR2 may play an important role in enhancing primary antibody responses to many T-dependent and T-independent Ag and may contribute to a host's response to naturally occurring antigens such as bacteria.</abstract><cop>Bethesda, MD</cop><pub>Am Assoc Immnol</pub><pmid>1828822</pmid><doi>10.4049/jimmunol.147.1.224</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-1767
ispartof The Journal of immunology (1950), 1991-07, Vol.147 (1), p.224-230
issn 0022-1767
1550-6606
language eng
recordid cdi_proquest_miscellaneous_80622737
source MEDLINE; Alma/SFX Local Collection
subjects Animals
Antibody Formation
Antigens, Differentiation - immunology
Antigens, Differentiation, B-Lymphocyte - immunology
Antigens, Differentiation, B-Lymphocyte - physiology
B-Lymphocytes - immunology
Biological and medical sciences
Down-Regulation
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Immunobiology
Immunoglobulin G - biosynthesis
Immunoglobulin Isotypes - biosynthesis
Immunoglobulin M - biosynthesis
Immunologic Memory
Lymphocyte Activation
Mice
Mice, Inbred Strains
Modulation of the immune response (stimulation, suppression)
Receptors, Complement - physiology
Receptors, Complement 3b
Receptors, Complement 3d
Receptors, Fc - immunology
Receptors, IgE
Receptors, IgG
title Modulation of mouse complement receptors 1 and 2 suppresses antibody responses in vivo
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T00%3A01%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Modulation%20of%20mouse%20complement%20receptors%201%20and%202%20suppresses%20antibody%20responses%20in%20vivo&rft.jtitle=The%20Journal%20of%20immunology%20(1950)&rft.au=Thyphronitis,%20G&rft.date=1991-07-01&rft.volume=147&rft.issue=1&rft.spage=224&rft.epage=230&rft.pages=224-230&rft.issn=0022-1767&rft.eissn=1550-6606&rft.coden=JOIMA3&rft_id=info:doi/10.4049/jimmunol.147.1.224&rft_dat=%3Cproquest_cross%3E80622737%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16092514&rft_id=info:pmid/1828822&rfr_iscdi=true