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The Expansion of CD25 high IL-10 high FoxP3 high B Regulatory Cells Is in Association with SLE Disease Activity
B regulatory cells (Bregs) belong to a subgroup of activated B cells tasked with maintaining self-tolerance and preventing autoimmunity. While sharing similar regulatory mechanisms such as IL-10 dependency, they also defer in exhibiting their suppressive effects by expressing Fas-Ligand, TGF-beta, a...
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Published in: | Journal of immunology research 2015, Vol.2015, p.254245-6 |
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creator | Vadasz, Zahava Peri, Regina Eiza, Nasren Slobodin, Gleb Balbir-Gurman, Alexandra Toubi, Elias |
description | B regulatory cells (Bregs) belong to a subgroup of activated B cells tasked with maintaining self-tolerance and preventing autoimmunity. While sharing similar regulatory mechanisms such as IL-10 dependency, they also defer in exhibiting their suppressive effects by expressing Fas-Ligand, TGF-beta, and PDL-1. In this study we show, for the first time, the expansion of CD25(high)FoxP3(high) Bregs in systemic lupus erythematosus (SLE) patients compared to healthy individuals (18.5 ± 3.052% versus 11.0 ± 1.654%, p < 0.001, resp.). This expansion was also shown to correlate with SLE disease activity (r = 0.75). In addition, CD25(high)FoxP3(high) Bregs were also IL-10(high) expressing and further expanded when stimulated with semaphorin 3A. In sum we show that CD25(high)FoxP3(high) are an additional subtype of Bregs, involved in regulating SLE disease activity. Being IL-10 expressing, we may assume that they are one of the sources of increased serum IL-10 in SLE patients. Further studies are required in order to assess the relation between high serum IL-10 and CD25(high)FoxP3(high) Breg cells. |
doi_str_mv | 10.1155/2015/254245 |
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While sharing similar regulatory mechanisms such as IL-10 dependency, they also defer in exhibiting their suppressive effects by expressing Fas-Ligand, TGF-beta, and PDL-1. In this study we show, for the first time, the expansion of CD25(high)FoxP3(high) Bregs in systemic lupus erythematosus (SLE) patients compared to healthy individuals (18.5 ± 3.052% versus 11.0 ± 1.654%, p < 0.001, resp.). This expansion was also shown to correlate with SLE disease activity (r = 0.75). In addition, CD25(high)FoxP3(high) Bregs were also IL-10(high) expressing and further expanded when stimulated with semaphorin 3A. In sum we show that CD25(high)FoxP3(high) are an additional subtype of Bregs, involved in regulating SLE disease activity. Being IL-10 expressing, we may assume that they are one of the sources of increased serum IL-10 in SLE patients. Further studies are required in order to assess the relation between high serum IL-10 and CD25(high)FoxP3(high) Breg cells.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antigens, CD19 - metabolism</subject><subject>B-Lymphocyte Subsets - immunology</subject><subject>B-Lymphocyte Subsets - metabolism</subject><subject>B-Lymphocytes, Regulatory - immunology</subject><subject>B-Lymphocytes, Regulatory - metabolism</subject><subject>Biomarkers</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Forkhead Transcription Factors - metabolism</subject><subject>Humans</subject><subject>Immunophenotyping</subject><subject>Interleukin-10 - metabolism</subject><subject>Interleukin-2 Receptor alpha Subunit - metabolism</subject><subject>Lupus Erythematosus, Systemic - diagnosis</subject><subject>Lupus Erythematosus, Systemic - immunology</subject><subject>Lupus Erythematosus, Systemic - metabolism</subject><subject>Lymphocyte Activation - immunology</subject><subject>Lymphocyte Count</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Semaphorin-3A - metabolism</subject><subject>Severity of Illness Index</subject><subject>Young Adult</subject><issn>2314-8861</issn><issn>2314-7156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNo9kEFLwzAYhoMobsydvEuOglTzJU2bHme36aCg6DyXNE3XSNfMptXt39vR6eX93sPDy8eD0DWQewDOHyiBPrhPfX6GxpSB74XAg_NTFyKAEZo690kIAQrMp3CJRjTgxBccxsiuS40X-52snbE1tgWO55Tj0mxKvEo8IENd2v0rG-ojftObrpKtbQ441lXl8MphU-OZc1YZ2R53fkxb4vdkgefGaek0nqnWfJv2cIUuClk5PT3dCfpYLtbxs5e8PK3iWeKp_kfwGI-UFjkXOcmpoEWRcR2FRRFRrojyQwKSQS4lFSJXYR4Q3UeRqYyFQinI2ATdDru7xn512rXp1jjVfytrbTuXQkjDKOI0YD16N6Cqsc41ukh3jdnK5pACSY-S06PkdJDc0zen4S7b6vyf_VPKfgFpxHQI</recordid><startdate>2015</startdate><enddate>2015</enddate><creator>Vadasz, Zahava</creator><creator>Peri, Regina</creator><creator>Eiza, Nasren</creator><creator>Slobodin, Gleb</creator><creator>Balbir-Gurman, Alexandra</creator><creator>Toubi, Elias</creator><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>7X8</scope></search><sort><creationdate>2015</creationdate><title>The Expansion of CD25 high IL-10 high FoxP3 high B Regulatory Cells Is in Association with SLE Disease Activity</title><author>Vadasz, Zahava ; Peri, Regina ; Eiza, Nasren ; Slobodin, Gleb ; Balbir-Gurman, Alexandra ; Toubi, Elias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1341-359ce8d58d0d282ffb5e97ff925c0c4701a31daa288dc7d60e7d6fbcb378cc1b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antigens, CD19 - metabolism</topic><topic>B-Lymphocyte Subsets - immunology</topic><topic>B-Lymphocyte Subsets - metabolism</topic><topic>B-Lymphocytes, Regulatory - immunology</topic><topic>B-Lymphocytes, Regulatory - metabolism</topic><topic>Biomarkers</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Forkhead Transcription Factors - metabolism</topic><topic>Humans</topic><topic>Immunophenotyping</topic><topic>Interleukin-10 - metabolism</topic><topic>Interleukin-2 Receptor alpha Subunit - metabolism</topic><topic>Lupus Erythematosus, Systemic - diagnosis</topic><topic>Lupus Erythematosus, Systemic - immunology</topic><topic>Lupus Erythematosus, Systemic - metabolism</topic><topic>Lymphocyte Activation - immunology</topic><topic>Lymphocyte Count</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Semaphorin-3A - metabolism</topic><topic>Severity of Illness Index</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vadasz, Zahava</creatorcontrib><creatorcontrib>Peri, Regina</creatorcontrib><creatorcontrib>Eiza, Nasren</creatorcontrib><creatorcontrib>Slobodin, Gleb</creatorcontrib><creatorcontrib>Balbir-Gurman, Alexandra</creatorcontrib><creatorcontrib>Toubi, Elias</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of immunology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vadasz, Zahava</au><au>Peri, Regina</au><au>Eiza, Nasren</au><au>Slobodin, Gleb</au><au>Balbir-Gurman, Alexandra</au><au>Toubi, Elias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Expansion of CD25 high IL-10 high FoxP3 high B Regulatory Cells Is in Association with SLE Disease Activity</atitle><jtitle>Journal of immunology research</jtitle><addtitle>J Immunol Res</addtitle><date>2015</date><risdate>2015</risdate><volume>2015</volume><spage>254245</spage><epage>6</epage><pages>254245-6</pages><issn>2314-8861</issn><eissn>2314-7156</eissn><abstract>B regulatory cells (Bregs) belong to a subgroup of activated B cells tasked with maintaining self-tolerance and preventing autoimmunity. While sharing similar regulatory mechanisms such as IL-10 dependency, they also defer in exhibiting their suppressive effects by expressing Fas-Ligand, TGF-beta, and PDL-1. In this study we show, for the first time, the expansion of CD25(high)FoxP3(high) Bregs in systemic lupus erythematosus (SLE) patients compared to healthy individuals (18.5 ± 3.052% versus 11.0 ± 1.654%, p < 0.001, resp.). This expansion was also shown to correlate with SLE disease activity (r = 0.75). In addition, CD25(high)FoxP3(high) Bregs were also IL-10(high) expressing and further expanded when stimulated with semaphorin 3A. In sum we show that CD25(high)FoxP3(high) are an additional subtype of Bregs, involved in regulating SLE disease activity. Being IL-10 expressing, we may assume that they are one of the sources of increased serum IL-10 in SLE patients. 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subjects | Adolescent Adult Antigens, CD19 - metabolism B-Lymphocyte Subsets - immunology B-Lymphocyte Subsets - metabolism B-Lymphocytes, Regulatory - immunology B-Lymphocytes, Regulatory - metabolism Biomarkers Female Flow Cytometry Forkhead Transcription Factors - metabolism Humans Immunophenotyping Interleukin-10 - metabolism Interleukin-2 Receptor alpha Subunit - metabolism Lupus Erythematosus, Systemic - diagnosis Lupus Erythematosus, Systemic - immunology Lupus Erythematosus, Systemic - metabolism Lymphocyte Activation - immunology Lymphocyte Count Male Middle Aged Semaphorin-3A - metabolism Severity of Illness Index Young Adult |
title | The Expansion of CD25 high IL-10 high FoxP3 high B Regulatory Cells Is in Association with SLE Disease Activity |
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