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Subpopulations of regulatory T cells in rheumatoid arthritis, systemic lupus erythematosus, and Behcet's disease
Recently, subpopulations of regulatory T (Treg) cells, resting Treg (rTreg) and activated Treg (aTreg), have been discovered. The authors investigated the relationship between the change of Treg, aTreg and rTreg and autoimmune diseases. Treg cells and those subpopulations were analyzed by using the...
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Published in: | Journal of Korean medical science 2012, 27(9), 168, pp.1009-1013 |
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description | Recently, subpopulations of regulatory T (Treg) cells, resting Treg (rTreg) and activated Treg (aTreg), have been discovered. The authors investigated the relationship between the change of Treg, aTreg and rTreg and autoimmune diseases. Treg cells and those subpopulations were analyzed by using the human regulatory T cell staining kit and CD45RA surface marker for 42 rheumatoid arthritis (RA), 13 systemic lupus sclerosis (SLE), 7 Behcet's disease (BD), and 22 healthy controls. The proportion of Treg cells was significantly lower in RA (3.8% ± 1.0%) (P < 0.001) and BD (3.3% ± 0.5%) (P < 0.01) compared to healthy controls (5.0% ± 1.3%). The proportion of aTreg cells was also significantly lower in RA (0.4% ± 0.2%) (P = 0.008) and BD (0.3% ± 0.1%) (P = 0.013) compared to healthy controls (0.6% ± 0.3%). The rTreg cells showed no significant differences. The ratio of aTreg to rTreg was lower in RA patients (0.4% ± 0.2%) than that in healthy controls (0.7% ± 0.4%) (P = 0.002). This study suggests that the decrement of aTreg not rTreg cells contributes the decrement of total Treg cells in peripheral blood of RA and BD autoimmune diseases. Detailed analysis of Treg subpopulations would be more informative than total Treg cells in investigating mechanism of autoimmune disease. |
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The authors investigated the relationship between the change of Treg, aTreg and rTreg and autoimmune diseases. Treg cells and those subpopulations were analyzed by using the human regulatory T cell staining kit and CD45RA surface marker for 42 rheumatoid arthritis (RA), 13 systemic lupus sclerosis (SLE), 7 Behcet's disease (BD), and 22 healthy controls. The proportion of Treg cells was significantly lower in RA (3.8% ± 1.0%) (P < 0.001) and BD (3.3% ± 0.5%) (P < 0.01) compared to healthy controls (5.0% ± 1.3%). The proportion of aTreg cells was also significantly lower in RA (0.4% ± 0.2%) (P = 0.008) and BD (0.3% ± 0.1%) (P = 0.013) compared to healthy controls (0.6% ± 0.3%). The rTreg cells showed no significant differences. The ratio of aTreg to rTreg was lower in RA patients (0.4% ± 0.2%) than that in healthy controls (0.7% ± 0.4%) (P = 0.002). This study suggests that the decrement of aTreg not rTreg cells contributes the decrement of total Treg cells in peripheral blood of RA and BD autoimmune diseases. Detailed analysis of Treg subpopulations would be more informative than total Treg cells in investigating mechanism of autoimmune disease.</description><identifier>ISSN: 1011-8934</identifier><identifier>EISSN: 1598-6357</identifier><identifier>DOI: 10.3346/jkms.2012.27.9.1009</identifier><identifier>PMID: 22969245</identifier><language>eng</language><publisher>Korea (South): The Korean Academy of Medical Sciences</publisher><subject>Adult ; Aged ; Arthritis, Rheumatoid - immunology ; Arthritis, Rheumatoid - metabolism ; Behcet Syndrome - immunology ; Behcet Syndrome - metabolism ; CD4 Antigens - metabolism ; Female ; Forkhead Transcription Factors - metabolism ; Humans ; Interleukin-2 Receptor alpha Subunit - metabolism ; Leukocyte Common Antigens - metabolism ; Leukocyte Count ; Lupus Erythematosus, Systemic - immunology ; Lupus Erythematosus, Systemic - metabolism ; Male ; Middle Aged ; Original ; T-Lymphocytes, Regulatory - cytology ; T-Lymphocytes, Regulatory - immunology ; T-Lymphocytes, Regulatory - metabolism ; 의학일반</subject><ispartof>Journal of Korean Medical Science, 2012, 27(9), 168, pp.1009-1013</ispartof><rights>2012 The Korean Academy of Medical Sciences. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-b86e6106c6f16a7043cf5fae92880a4eb9ce5b444de21baef3915f283a2cc2693</citedby><cites>FETCH-LOGICAL-c438t-b86e6106c6f16a7043cf5fae92880a4eb9ce5b444de21baef3915f283a2cc2693</cites><orcidid>0000-0002-6475-4886</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429816/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429816/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22969245$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001692142$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Jae-Ryong</creatorcontrib><creatorcontrib>Chae, Jin-Nyeong</creatorcontrib><creatorcontrib>Kim, Sang-Hyon</creatorcontrib><creatorcontrib>Ha, Jung-Sook</creatorcontrib><title>Subpopulations of regulatory T cells in rheumatoid arthritis, systemic lupus erythematosus, and Behcet's disease</title><title>Journal of Korean medical science</title><addtitle>J Korean Med Sci</addtitle><description>Recently, subpopulations of regulatory T (Treg) cells, resting Treg (rTreg) and activated Treg (aTreg), have been discovered. The authors investigated the relationship between the change of Treg, aTreg and rTreg and autoimmune diseases. Treg cells and those subpopulations were analyzed by using the human regulatory T cell staining kit and CD45RA surface marker for 42 rheumatoid arthritis (RA), 13 systemic lupus sclerosis (SLE), 7 Behcet's disease (BD), and 22 healthy controls. The proportion of Treg cells was significantly lower in RA (3.8% ± 1.0%) (P < 0.001) and BD (3.3% ± 0.5%) (P < 0.01) compared to healthy controls (5.0% ± 1.3%). The proportion of aTreg cells was also significantly lower in RA (0.4% ± 0.2%) (P = 0.008) and BD (0.3% ± 0.1%) (P = 0.013) compared to healthy controls (0.6% ± 0.3%). The rTreg cells showed no significant differences. The ratio of aTreg to rTreg was lower in RA patients (0.4% ± 0.2%) than that in healthy controls (0.7% ± 0.4%) (P = 0.002). This study suggests that the decrement of aTreg not rTreg cells contributes the decrement of total Treg cells in peripheral blood of RA and BD autoimmune diseases. Detailed analysis of Treg subpopulations would be more informative than total Treg cells in investigating mechanism of autoimmune disease.</description><subject>Adult</subject><subject>Aged</subject><subject>Arthritis, Rheumatoid - immunology</subject><subject>Arthritis, Rheumatoid - metabolism</subject><subject>Behcet Syndrome - immunology</subject><subject>Behcet Syndrome - metabolism</subject><subject>CD4 Antigens - metabolism</subject><subject>Female</subject><subject>Forkhead Transcription Factors - metabolism</subject><subject>Humans</subject><subject>Interleukin-2 Receptor alpha Subunit - metabolism</subject><subject>Leukocyte Common Antigens - metabolism</subject><subject>Leukocyte Count</subject><subject>Lupus Erythematosus, Systemic - immunology</subject><subject>Lupus Erythematosus, Systemic - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Original</subject><subject>T-Lymphocytes, Regulatory - cytology</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><subject>T-Lymphocytes, Regulatory - metabolism</subject><subject>의학일반</subject><issn>1011-8934</issn><issn>1598-6357</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpVkctu1TAQhiMEohd4AiTkHSxI8D3xBqmtKFSqhASHteU4k8Y9ueGJkc7bk_RAgdXMeP5_ZuQvy14xWggh9fv7_YAFp4wXvCxMwSg1T7JTpkyVa6HKp2tOGcsrI-RJdoZ4TylXiovn2QnnRhsu1Wk2f0v1PM2pd0uYRiRTSyLcbeUUD2RHPPQ9kjCS2EEa1tfQEBeXLoYl4DuCB1xgCJ70aU5IIB6WDjYZprXrxoZcQudheYOkCQgO4UX2rHU9wsvf8Tz7fv1xd_U5v_3y6ebq4jb3UlRLXlcaNKPa65ZpV1IpfKtaB4ZXFXUSauNB1VLKBjirHbTCMNXySjjuPddGnGdvj3PH2Nq9D3Zy4SHeTXYf7cXX3Y1VpVCsXKUfjtI51QM0HsYlut7OMQwuHh6M_3fG0K1jflohuamY_rtrjtOPBLjYIeD2c26EKaFlVKwQZFluZ4mj1McJMUL7uIZRu2G1G1a7YbW8tMZuWFfX638vfPT84Sh-AeBtoqA</recordid><startdate>20120901</startdate><enddate>20120901</enddate><creator>Kim, Jae-Ryong</creator><creator>Chae, Jin-Nyeong</creator><creator>Kim, Sang-Hyon</creator><creator>Ha, Jung-Sook</creator><general>The Korean Academy of Medical Sciences</general><general>대한의학회</general><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><scope>5PM</scope><scope>ACYCR</scope><orcidid>https://orcid.org/0000-0002-6475-4886</orcidid></search><sort><creationdate>20120901</creationdate><title>Subpopulations of regulatory T cells in rheumatoid arthritis, systemic lupus erythematosus, and Behcet's disease</title><author>Kim, Jae-Ryong ; Chae, Jin-Nyeong ; Kim, Sang-Hyon ; Ha, Jung-Sook</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-b86e6106c6f16a7043cf5fae92880a4eb9ce5b444de21baef3915f283a2cc2693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Arthritis, Rheumatoid - immunology</topic><topic>Arthritis, Rheumatoid - metabolism</topic><topic>Behcet Syndrome - immunology</topic><topic>Behcet Syndrome - metabolism</topic><topic>CD4 Antigens - metabolism</topic><topic>Female</topic><topic>Forkhead Transcription Factors - metabolism</topic><topic>Humans</topic><topic>Interleukin-2 Receptor alpha Subunit - metabolism</topic><topic>Leukocyte Common Antigens - metabolism</topic><topic>Leukocyte Count</topic><topic>Lupus Erythematosus, Systemic - immunology</topic><topic>Lupus Erythematosus, Systemic - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Original</topic><topic>T-Lymphocytes, Regulatory - cytology</topic><topic>T-Lymphocytes, Regulatory - immunology</topic><topic>T-Lymphocytes, Regulatory - metabolism</topic><topic>의학일반</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Jae-Ryong</creatorcontrib><creatorcontrib>Chae, Jin-Nyeong</creatorcontrib><creatorcontrib>Kim, Sang-Hyon</creatorcontrib><creatorcontrib>Ha, Jung-Sook</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><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Journal of Korean medical science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Jae-Ryong</au><au>Chae, Jin-Nyeong</au><au>Kim, Sang-Hyon</au><au>Ha, Jung-Sook</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subpopulations of regulatory T cells in rheumatoid arthritis, systemic lupus erythematosus, and Behcet's disease</atitle><jtitle>Journal of Korean medical science</jtitle><addtitle>J Korean Med Sci</addtitle><date>2012-09-01</date><risdate>2012</risdate><volume>27</volume><issue>9</issue><spage>1009</spage><epage>1013</epage><pages>1009-1013</pages><issn>1011-8934</issn><eissn>1598-6357</eissn><abstract>Recently, subpopulations of regulatory T (Treg) cells, resting Treg (rTreg) and activated Treg (aTreg), have been discovered. The authors investigated the relationship between the change of Treg, aTreg and rTreg and autoimmune diseases. Treg cells and those subpopulations were analyzed by using the human regulatory T cell staining kit and CD45RA surface marker for 42 rheumatoid arthritis (RA), 13 systemic lupus sclerosis (SLE), 7 Behcet's disease (BD), and 22 healthy controls. The proportion of Treg cells was significantly lower in RA (3.8% ± 1.0%) (P < 0.001) and BD (3.3% ± 0.5%) (P < 0.01) compared to healthy controls (5.0% ± 1.3%). The proportion of aTreg cells was also significantly lower in RA (0.4% ± 0.2%) (P = 0.008) and BD (0.3% ± 0.1%) (P = 0.013) compared to healthy controls (0.6% ± 0.3%). The rTreg cells showed no significant differences. The ratio of aTreg to rTreg was lower in RA patients (0.4% ± 0.2%) than that in healthy controls (0.7% ± 0.4%) (P = 0.002). This study suggests that the decrement of aTreg not rTreg cells contributes the decrement of total Treg cells in peripheral blood of RA and BD autoimmune diseases. Detailed analysis of Treg subpopulations would be more informative than total Treg cells in investigating mechanism of autoimmune disease.</abstract><cop>Korea (South)</cop><pub>The Korean Academy of Medical Sciences</pub><pmid>22969245</pmid><doi>10.3346/jkms.2012.27.9.1009</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-6475-4886</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Arthritis, Rheumatoid - immunology Arthritis, Rheumatoid - metabolism Behcet Syndrome - immunology Behcet Syndrome - metabolism CD4 Antigens - metabolism Female Forkhead Transcription Factors - metabolism Humans Interleukin-2 Receptor alpha Subunit - metabolism Leukocyte Common Antigens - metabolism Leukocyte Count Lupus Erythematosus, Systemic - immunology Lupus Erythematosus, Systemic - metabolism Male Middle Aged Original T-Lymphocytes, Regulatory - cytology T-Lymphocytes, Regulatory - immunology T-Lymphocytes, Regulatory - metabolism 의학일반 |
title | Subpopulations of regulatory T cells in rheumatoid arthritis, systemic lupus erythematosus, and Behcet's disease |
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