In vitro studies of the rabbit immune system: II. Functional characterization of rabbit T and B populations separated by adherence to nylon wool or lysis with anti-thymocyte serum and complement
Identifieur interne : 000D76 ( Istex/Corpus ); précédent : 000D75; suivant : 000D77In vitro studies of the rabbit immune system: II. Functional characterization of rabbit T and B populations separated by adherence to nylon wool or lysis with anti-thymocyte serum and complement
Auteurs : Doug Redelman ; Charles B. Scott ; Haynes W. Sheppard Jr. ; Stewart SellSource :
- Cellular Immunology [ 0008-8749 ] ; 1975.
Abstract
Rabbit spleen lymphocytes with functions analogous to murine T and B cells have been separated by treatment with goat anti-rabbit thymocyte serum plus complement (ATS + C) or passage over columns of nylon wool (NW). ATS + C lysis of spleen cells from sheep erythrocyte (SRBC)-immunized rabbits removes 40–60% of the total cells, but 80–100% of the fully differentiated B cells (PFC) are recovered. Conversely, the primed spleen cells which are nonadherent to NW contain ~5–20% of the applied cells but only 0.05–1.0% of the applied PFC. Neither cell population is capable of producing an anti-SRBC PFC response when cultured individually. However, the two cell types complement each other and act synergistically to reconsitute the in vitro anti-SRBC PFC response. Thus, the rabbit spleen contains separable lymphocyte populations with functions equivalent to T and B cells as defined in the murine system.
Url:
DOI: 10.1016/0008-8749(76)90127-1
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Scott</name><affiliation><mods:affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</mods:affiliation></affiliation></author><author><name sortKey="Sheppard Jr, Haynes W" sort="Sheppard Jr, Haynes W" uniqKey="Sheppard Jr H" first="Haynes W." last="Sheppard Jr.">Haynes W. Sheppard Jr.</name><affiliation><mods:affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</mods:affiliation></affiliation></author><author><name sortKey="Sell, Stewart" sort="Sell, Stewart" uniqKey="Sell S" first="Stewart" last="Sell">Stewart Sell</name><affiliation><mods:affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:AD3CD0CACBD434C0B2974ED1D23AA81813E570DB</idno><date when="1976" year="1976">1976</date><idno type="doi">10.1016/0008-8749(76)90127-1</idno><idno type="url">https://api.istex.fr/document/AD3CD0CACBD434C0B2974ED1D23AA81813E570DB/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000D76</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">In vitro studies of the rabbit immune system: II. Functional characterization of rabbit T and B populations separated by adherence to nylon wool or lysis with anti-thymocyte serum and complement</title><author><name sortKey="Redelman, Doug" sort="Redelman, Doug" uniqKey="Redelman D" first="Doug" last="Redelman">Doug Redelman</name><affiliation><mods:affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</mods:affiliation></affiliation></author><author><name sortKey="Scott, Charles B" sort="Scott, Charles B" uniqKey="Scott C" first="Charles B." last="Scott">Charles B. Scott</name><affiliation><mods:affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</mods:affiliation></affiliation></author><author><name sortKey="Sheppard Jr, Haynes W" sort="Sheppard Jr, Haynes W" uniqKey="Sheppard Jr H" first="Haynes W." last="Sheppard Jr.">Haynes W. Sheppard Jr.</name><affiliation><mods:affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</mods:affiliation></affiliation></author><author><name sortKey="Sell, Stewart" sort="Sell, Stewart" uniqKey="Sell S" first="Stewart" last="Sell">Stewart Sell</name><affiliation><mods:affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Cellular Immunology</title><title level="j" type="abbrev">YCIMM</title><idno type="ISSN">0008-8749</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1975">1975</date><biblScope unit="volume">24</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="11">11</biblScope><biblScope unit="page" to="23">23</biblScope></imprint><idno type="ISSN">0008-8749</idno></series><idno type="istex">AD3CD0CACBD434C0B2974ED1D23AA81813E570DB</idno><idno type="DOI">10.1016/0008-8749(76)90127-1</idno><idno type="PII">0008-8749(76)90127-1</idno><idno type="ArticleID">76901271</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0008-8749</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Rabbit spleen lymphocytes with functions analogous to murine T and B cells have been separated by treatment with goat anti-rabbit thymocyte serum plus complement (ATS + C) or passage over columns of nylon wool (NW). ATS + C lysis of spleen cells from sheep erythrocyte (SRBC)-immunized rabbits removes 40–60% of the total cells, but 80–100% of the fully differentiated B cells (PFC) are recovered. Conversely, the primed spleen cells which are nonadherent to NW contain ~5–20% of the applied cells but only 0.05–1.0% of the applied PFC. Neither cell population is capable of producing an anti-SRBC PFC response when cultured individually. However, the two cell types complement each other and act synergistically to reconsitute the in vitro anti-SRBC PFC response. Thus, the rabbit spleen contains separable lymphocyte populations with functions equivalent to T and B cells as defined in the murine system.</div></front></TEI><istex><corpusName>elsevier</corpusName><author><json:item><name>Doug Redelman</name><affiliations><json:string>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</json:string></affiliations></json:item><json:item><name>Charles B. Scott</name><affiliations><json:string>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</json:string></affiliations></json:item><json:item><name>Haynes W. Sheppard, Jr.</name><affiliations><json:string>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</json:string></affiliations></json:item><json:item><name>Stewart Sell</name><affiliations><json:string>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</json:string></affiliations></json:item></author><articleId><json:string>76901271</json:string></articleId><language><json:string>eng</json:string></language><abstract>Rabbit spleen lymphocytes with functions analogous to murine T and B cells have been separated by treatment with goat anti-rabbit thymocyte serum plus complement (ATS + C) or passage over columns of nylon wool (NW). ATS + C lysis of spleen cells from sheep erythrocyte (SRBC)-immunized rabbits removes 40–60% of the total cells, but 80–100% of the fully differentiated B cells (PFC) are recovered. Conversely, the primed spleen cells which are nonadherent to NW contain ~5–20% of the applied cells but only 0.05–1.0% of the applied PFC. Neither cell population is capable of producing an anti-SRBC PFC response when cultured individually. However, the two cell types complement each other and act synergistically to reconsitute the in vitro anti-SRBC PFC response. Thus, the rabbit spleen contains separable lymphocyte populations with functions equivalent to T and B cells as defined in the murine system.</abstract><qualityIndicators><score>5.962</score><pdfVersion>1.3</pdfVersion><pdfPageSize>468 x 720 pts</pdfPageSize><refBibsNative>true</refBibsNative><keywordCount>0</keywordCount><abstractCharCount>906</abstractCharCount><pdfWordCount>4258</pdfWordCount><pdfCharCount>26645</pdfCharCount><pdfPageCount>13</pdfPageCount><abstractWordCount>142</abstractWordCount></qualityIndicators><title>In vitro studies of the rabbit immune system: II. 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Functional characterization of rabbit T and B populations separated by adherence to nylon wool or lysis with anti-thymocyte serum and complement</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>ELSEVIER</publisher><availability><p>ELSEVIER</p></availability><date>1976</date></publicationStmt><notesStmt><note>Supported in part by NIH Grant No. AI-11780 and NIH Training Grant No. AI-00453.</note><note>Portions of these studies were previously reported: Redelman, D., and Scott, C. B., Fed. Proc.34, 986, 1975.</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">In vitro studies of the rabbit immune system: II. Functional characterization of rabbit T and B populations separated by adherence to nylon wool or lysis with anti-thymocyte serum and complement</title><author><persName><forename type="first">Doug</forename><surname>Redelman</surname></persName><note type="biography">Recipient of NIH Postdoctoral Fellowship No. CA-01139.</note><affiliation>Recipient of NIH Postdoctoral Fellowship No. CA-01139.</affiliation><affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</affiliation></author><author><persName><forename type="first">Charles B.</forename><surname>Scott</surname></persName><affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</affiliation></author><author><persName><forename type="first">Haynes W.</forename><surname>Sheppard, Jr.</surname></persName><affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</affiliation></author><author><persName><forename type="first">Stewart</forename><surname>Sell</surname></persName><affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</affiliation></author></analytic><monogr><title level="j">Cellular Immunology</title><title level="j" type="abbrev">YCIMM</title><idno type="pISSN">0008-8749</idno><idno type="PII">S0008-8749(00)X0325-5</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1975"></date><biblScope unit="volume">24</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="11">11</biblScope><biblScope unit="page" to="23">23</biblScope></imprint></monogr><idno type="istex">AD3CD0CACBD434C0B2974ED1D23AA81813E570DB</idno><idno type="DOI">10.1016/0008-8749(76)90127-1</idno><idno type="PII">0008-8749(76)90127-1</idno><idno type="ArticleID">76901271</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1976</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Rabbit spleen lymphocytes with functions analogous to murine T and B cells have been separated by treatment with goat anti-rabbit thymocyte serum plus complement (ATS + C) or passage over columns of nylon wool (NW). ATS + C lysis of spleen cells from sheep erythrocyte (SRBC)-immunized rabbits removes 40–60% of the total cells, but 80–100% of the fully differentiated B cells (PFC) are recovered. Conversely, the primed spleen cells which are nonadherent to NW contain ~5–20% of the applied cells but only 0.05–1.0% of the applied PFC. Neither cell population is capable of producing an anti-SRBC PFC response when cultured individually. However, the two cell types complement each other and act synergistically to reconsitute the in vitro anti-SRBC PFC response. Thus, the rabbit spleen contains separable lymphocyte populations with functions equivalent to T and B cells as defined in the murine system.</p></abstract></profileDesc><revisionDesc><change when="1975-10-24">Received</change><change when="1975">Published</change></revisionDesc></teiHeader></istex:fulltextTEI></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier, elements deleted: tail"><istex:xmlDeclaration>version="1.0" encoding="UTF-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="fla" xml:lang="en"><item-info><jid>YCIMM</jid><aid>76901271</aid><ce:pii>0008-8749(76)90127-1</ce:pii><ce:doi>10.1016/0008-8749(76)90127-1</ce:doi><ce:copyright type="unknown" year="1976"></ce:copyright></item-info><head><ce:article-footnote><ce:label>☆</ce:label><ce:note-para>Supported in part by NIH Grant No. AI-11780 and NIH Training Grant No. AI-00453.</ce:note-para></ce:article-footnote><ce:article-footnote><ce:label>☆☆</ce:label><ce:note-para>Portions of these studies were previously reported: Redelman, D., and Scott, C. B., <ce:italic>Fed. Proc.</ce:italic><ce:bold>34</ce:bold>, 986, 1975.</ce:note-para></ce:article-footnote><ce:title><ce:italic>In vitro</ce:italic> studies of the rabbit immune system: II. Functional characterization of rabbit T and B populations separated by adherence to nylon wool or lysis with anti-thymocyte serum and complement</ce:title><ce:author-group><ce:author><ce:given-name>Doug</ce:given-name><ce:surname>Redelman</ce:surname><ce:cross-ref refid="FN1"><ce:sup loc="post">3</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Charles B.</ce:given-name><ce:surname>Scott</ce:surname></ce:author><ce:author><ce:given-name>Haynes W.</ce:given-name><ce:surname>Sheppard</ce:surname><ce:suffix>Jr.</ce:suffix></ce:author><ce:author><ce:given-name>Stewart</ce:given-name><ce:surname>Sell</ce:surname></ce:author><ce:affiliation><ce:textfn>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</ce:textfn></ce:affiliation><ce:footnote id="FN1"><ce:label>3</ce:label><ce:note-para>Recipient of NIH Postdoctoral Fellowship No. CA-01139.</ce:note-para></ce:footnote></ce:author-group><ce:date-received day="24" month="10" year="1975"></ce:date-received><ce:abstract class="author"><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para view="all" id="simple-para.0010">Rabbit spleen lymphocytes with functions analogous to murine T and B cells have been separated by treatment with goat anti-rabbit thymocyte serum plus complement (ATS + C) or passage over columns of nylon wool (NW). ATS + C lysis of spleen cells from sheep erythrocyte (SRBC)-immunized rabbits removes 40–60% of the total cells, but 80–100% of the fully differentiated B cells (PFC) are recovered. Conversely, the primed spleen cells which are nonadherent to NW contain ~5–20% of the applied cells but only 0.05–1.0% of the applied PFC. Neither cell population is capable of producing an anti-SRBC PFC response when cultured individually. However, the two cell types complement each other and act synergistically to reconsitute the <ce:italic>in vitro</ce:italic> anti-SRBC PFC response. Thus, the rabbit spleen contains separable lymphocyte populations with functions equivalent to T and B cells as defined in the murine system.</ce:simple-para></ce:abstract-sec></ce:abstract></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>In vitro studies of the rabbit immune system: II. Functional characterization of rabbit T and B populations separated by adherence to nylon wool or lysis with anti-thymocyte serum and complement</title></titleInfo><titleInfo type="alternative" lang="en" contentType="CDATA"><title>studies of the rabbit immune system: II. Functional characterization of rabbit T and B populations separated by adherence to nylon wool or lysis with anti-thymocyte serum and complement</title></titleInfo><name type="personal"><namePart type="given">Doug</namePart><namePart type="family">Redelman</namePart><affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</affiliation><description>Recipient of NIH Postdoctoral Fellowship No. CA-01139.</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Charles B.</namePart><namePart type="family">Scott</namePart><affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Haynes W.</namePart><namePart type="family">Sheppard, Jr.</namePart><affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Stewart</namePart><namePart type="family">Sell</namePart><affiliation>Department of Pathology, University of California, San Diego, La Jolla, California 92093 U.S.A.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article"></genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1975</dateIssued><dateCaptured encoding="w3cdtf">1975-10-24</dateCaptured><copyrightDate encoding="w3cdtf">1976</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">Rabbit spleen lymphocytes with functions analogous to murine T and B cells have been separated by treatment with goat anti-rabbit thymocyte serum plus complement (ATS + C) or passage over columns of nylon wool (NW). ATS + C lysis of spleen cells from sheep erythrocyte (SRBC)-immunized rabbits removes 40–60% of the total cells, but 80–100% of the fully differentiated B cells (PFC) are recovered. Conversely, the primed spleen cells which are nonadherent to NW contain ~5–20% of the applied cells but only 0.05–1.0% of the applied PFC. Neither cell population is capable of producing an anti-SRBC PFC response when cultured individually. However, the two cell types complement each other and act synergistically to reconsitute the in vitro anti-SRBC PFC response. Thus, the rabbit spleen contains separable lymphocyte populations with functions equivalent to T and B cells as defined in the murine system.</abstract><note>Supported in part by NIH Grant No. AI-11780 and NIH Training Grant No. AI-00453.</note><note>Portions of these studies were previously reported: Redelman, D., and Scott, C. B., Fed. 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