Deficient Positive Selection of CD4 T Cells in Mice Displaying Altered Repertoires of MHC Class II–Bound Self-Peptides
The role of self-peptides in positive selection of CD4 + T cells has been controversial. We show that some self-peptides are presented by the MHC class II molecule I-A b in mice lacking Ii or H-2M but not in mice expressing a transgene-encoded peptide fused to I-A b. In experiments using specific an...
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Veröffentlicht in: | Immunity (Cambridge, Mass.) Mass.), 1997-08, Vol.7 (2), p.197-208 |
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creator | Grubin, Catherine E Kovats, Susan deRoos, Paul Rudensky, Alexander Y |
description | The role of self-peptides in positive selection of CD4
+ T cells has been controversial. We show that some self-peptides are presented by the MHC class II molecule I-A
b in mice lacking Ii or H-2M but not in mice expressing a transgene-encoded peptide fused to I-A
b. In experiments using specific antibodies to block selection, these low-abundance self-peptides were implicated in the positive selection of some CD4
+ T cells in H-2M
−/− mice. However, all three mutant backgrounds failed to positively select two class II–restricted transgenic T cell receptors. Our findings suggest that minor components of the self-peptide repertoire can contribute to positive selection of a significant number of CD4
+ T cells. In addition, the data suggest that T cell receptor repertoires selected in wild-type mice and in mice displaying limited spectra of self-peptides are distinct. |
doi_str_mv | 10.1016/S1074-7613(00)80523-3 |
format | Article |
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b. In experiments using specific antibodies to block selection, these low-abundance self-peptides were implicated in the positive selection of some CD4
+ T cells in H-2M
−/− mice. However, all three mutant backgrounds failed to positively select two class II–restricted transgenic T cell receptors. Our findings suggest that minor components of the self-peptide repertoire can contribute to positive selection of a significant number of CD4
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+ T cells has been controversial. We show that some self-peptides are presented by the MHC class II molecule I-A
b in mice lacking Ii or H-2M but not in mice expressing a transgene-encoded peptide fused to I-A
b. In experiments using specific antibodies to block selection, these low-abundance self-peptides were implicated in the positive selection of some CD4
+ T cells in H-2M
−/− mice. However, all three mutant backgrounds failed to positively select two class II–restricted transgenic T cell receptors. Our findings suggest that minor components of the self-peptide repertoire can contribute to positive selection of a significant number of CD4
+ T cells. In addition, the data suggest that T cell receptor repertoires selected in wild-type mice and in mice displaying limited spectra of self-peptides are distinct.</description><subject>Animals</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - metabolism</subject><subject>Epithelium - immunology</subject><subject>Epithelium - metabolism</subject><subject>Female</subject><subject>H-2 Antigens - genetics</subject><subject>H-2 Antigens - metabolism</subject><subject>Histocompatibility Antigens Class II - genetics</subject><subject>Histocompatibility Antigens Class II - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred A</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Mice, Transgenic</subject><subject>Peptides - genetics</subject><subject>Peptides - immunology</subject><subject>Peptides - metabolism</subject><subject>Receptors, Antigen, T-Cell, alpha-beta - genetics</subject><subject>Thymus Gland - immunology</subject><subject>Thymus Gland - metabolism</subject><subject>Transgenes - immunology</subject><issn>1074-7613</issn><issn>1097-4180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQxi0EKqXwCJV8QnAI-M_YiU-ozQJdqRUVLWcr64yRUTYOtreiN96BN-RJSLorrj15rPm-Gc33I-SUs3eccf3-hrMaqlpz-Yaxtw1TQlbyCTnmzNQV8IY9XeqD5Dl5kfMPxjgow47IkRGNAqaOya8V-uACjoVexxxKuEN6gwO6EuJIo6ftCugtbXEYMg0jvQoO6Srkaejuw_idng0FE_b0K06YSgwJ8-K6umhpO3Q50_X67-8_53E39stcX13jVEKP-SV55rsh46vDe0K-ffp4215Ul18-r9uzy8qBbErllRZaNT3bcACUTbcB0UuPxnttECToBnC-i8P8Yc7oWigvGiM76b3wIE_I6_3cKcWfO8zFbkN28zndiHGXbW2Eqg2oR4Vcc64BxCxUe6FLMeeE3k4pbLt0bzmzCxr7gMYuuVvG7AMaK2ff6WHBbrPF_r_rwGLuf9j3cY7jLmCyeQHjsJ9TdcX2MTyy4R8UEZzo</recordid><startdate>19970801</startdate><enddate>19970801</enddate><creator>Grubin, Catherine E</creator><creator>Kovats, Susan</creator><creator>deRoos, Paul</creator><creator>Rudensky, Alexander Y</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>19970801</creationdate><title>Deficient Positive Selection of CD4 T Cells in Mice Displaying Altered Repertoires of MHC Class II–Bound Self-Peptides</title><author>Grubin, Catherine E ; Kovats, Susan ; deRoos, Paul ; Rudensky, Alexander Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-f562658d0b144e38ab42d3fe9ff69e434684e00114e430c96725f2893a3ff2f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD4-Positive T-Lymphocytes - metabolism</topic><topic>Epithelium - immunology</topic><topic>Epithelium - metabolism</topic><topic>Female</topic><topic>H-2 Antigens - genetics</topic><topic>H-2 Antigens - metabolism</topic><topic>Histocompatibility Antigens Class II - genetics</topic><topic>Histocompatibility Antigens Class II - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred A</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Mice, Transgenic</topic><topic>Peptides - genetics</topic><topic>Peptides - immunology</topic><topic>Peptides - metabolism</topic><topic>Receptors, Antigen, T-Cell, alpha-beta - genetics</topic><topic>Thymus Gland - immunology</topic><topic>Thymus Gland - metabolism</topic><topic>Transgenes - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grubin, Catherine E</creatorcontrib><creatorcontrib>Kovats, Susan</creatorcontrib><creatorcontrib>deRoos, Paul</creatorcontrib><creatorcontrib>Rudensky, Alexander Y</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Immunity (Cambridge, Mass.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grubin, Catherine E</au><au>Kovats, Susan</au><au>deRoos, Paul</au><au>Rudensky, Alexander Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deficient Positive Selection of CD4 T Cells in Mice Displaying Altered Repertoires of MHC Class II–Bound Self-Peptides</atitle><jtitle>Immunity (Cambridge, Mass.)</jtitle><addtitle>Immunity</addtitle><date>1997-08-01</date><risdate>1997</risdate><volume>7</volume><issue>2</issue><spage>197</spage><epage>208</epage><pages>197-208</pages><issn>1074-7613</issn><eissn>1097-4180</eissn><abstract>The role of self-peptides in positive selection of CD4
+ T cells has been controversial. We show that some self-peptides are presented by the MHC class II molecule I-A
b in mice lacking Ii or H-2M but not in mice expressing a transgene-encoded peptide fused to I-A
b. In experiments using specific antibodies to block selection, these low-abundance self-peptides were implicated in the positive selection of some CD4
+ T cells in H-2M
−/− mice. However, all three mutant backgrounds failed to positively select two class II–restricted transgenic T cell receptors. Our findings suggest that minor components of the self-peptide repertoire can contribute to positive selection of a significant number of CD4
+ T cells. In addition, the data suggest that T cell receptor repertoires selected in wild-type mice and in mice displaying limited spectra of self-peptides are distinct.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>9285405</pmid><doi>10.1016/S1074-7613(00)80523-3</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Cell Press Free Archives; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals CD4-Positive T-Lymphocytes - immunology CD4-Positive T-Lymphocytes - metabolism Epithelium - immunology Epithelium - metabolism Female H-2 Antigens - genetics H-2 Antigens - metabolism Histocompatibility Antigens Class II - genetics Histocompatibility Antigens Class II - metabolism Mice Mice, Inbred A Mice, Inbred BALB C Mice, Inbred C57BL Mice, Knockout Mice, Transgenic Peptides - genetics Peptides - immunology Peptides - metabolism Receptors, Antigen, T-Cell, alpha-beta - genetics Thymus Gland - immunology Thymus Gland - metabolism Transgenes - immunology |
title | Deficient Positive Selection of CD4 T Cells in Mice Displaying Altered Repertoires of MHC Class II–Bound Self-Peptides |
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