Changes of CD4+CD25+FOXP3+ and CD8+CD28− regulatory T cells in non-small cell lung cancer patients undergoing surgery
Little is known about the regulatory T cells (Tregs) in the peripheral blood after surgery of non-small cell lung cancer (NSCLC) patients. In this study, we investigated whether CD4+CD25+FOXP3+ and CD8+CD28− regulatory T cells are decreased in the peripheral blood of NSCLC patients undergoing surger...
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description | Little is known about the regulatory T cells (Tregs) in the peripheral blood after surgery of non-small cell lung cancer (NSCLC) patients. In this study, we investigated whether CD4+CD25+FOXP3+ and CD8+CD28− regulatory T cells are decreased in the peripheral blood of NSCLC patients undergoing surgery. The study group (n=49) comprised NSCLC, and the control group (n=24) consisted of age- and sex-matched nonmalignant diseases. The prevalence of CD4+CD25+FOXP3+ and CD8+CD28− Tregs was analyzed using flow cytometry. The study group showed significantly higher percentage of CD4+CD25+FOXP3+ and CD8+CD28− Tregs than control. The percentage of CD4+CD25+FOXP3+ and CD8+CD28− Tregs increased with tumor stage. One way ANOVA test shows the significant differences between all subgroups. LSD test shows that there was a statistical significance between each of the two subgroups except stage II in CD4+CD25+FOXP3+ Tregs and control vs. each stage, stage I vs. stage III, and stage IV in CD8+CD28− Tregs. There is no significant difference among stages II, III, and IV in CD8+CD28− Tregs. No differences were found between squamous carcinoma and adenocarcinoma. These levels were dropped significantly after operation. Furthermore postoperative Treg percentage in the early stages (stage I and stage II) was not statistically different from that of controls. Postoperative Treg percentage in advanced stage (III+IV) remained above the values shown by controls. Our findings indicate that the percentage of CD4+CD25+FOXP3+ and CD8+CD28− Tregs correlated with the pathological stage in NSCLC and tumor burden.
•CD4+CD25+FOXP3+ and CD8+CD28− tregs were Significantly higher in NSCLC than Controls.•CD4+CD25+FOXP3+ and CD8+CD28− tregs increased with tumor stage and dropped significantly after operation.•Postoperative tregs in early stage was in the same level of controls while in advanced stage was higher than controls. |
doi_str_mv | 10.1016/j.intimp.2013.12.004 |
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•CD4+CD25+FOXP3+ and CD8+CD28− tregs were Significantly higher in NSCLC than Controls.•CD4+CD25+FOXP3+ and CD8+CD28− tregs increased with tumor stage and dropped significantly after operation.•Postoperative tregs in early stage was in the same level of controls while in advanced stage was higher than controls.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2013.12.004</identifier><identifier>PMID: 24345703</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Aged ; Carcinoma, Non-Small-Cell Lung - immunology ; Carcinoma, Non-Small-Cell Lung - pathology ; Carcinoma, Non-Small-Cell Lung - surgery ; CD28 Antigens - immunology ; CD4 Antigens - immunology ; CD4+CD25+FOXP3 ; CD8 Antigens - immunology ; CD8+CD28 ; Female ; Humans ; Interleukin-2 Receptor alpha Subunit - immunology ; Lung Neoplasms - immunology ; Lung Neoplasms - pathology ; Lung Neoplasms - surgery ; Male ; Middle Aged ; Neoplasm Staging ; NSCLC ; Surgery ; T-Lymphocytes, Regulatory - immunology ; Treg</subject><ispartof>International immunopharmacology, 2014-02, Vol.18 (2), p.255-261</ispartof><rights>2013 Elsevier B.V.</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-c1225e90fce91e2b130c04e58f3abcd1a9942b88e5ac69e94137e31f9d1fc8b23</citedby><cites>FETCH-LOGICAL-c395t-c1225e90fce91e2b130c04e58f3abcd1a9942b88e5ac69e94137e31f9d1fc8b23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.intimp.2013.12.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24345703$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Cheng</creatorcontrib><creatorcontrib>Chen, Dongdong</creatorcontrib><creatorcontrib>Zhang, Yongkui</creatorcontrib><creatorcontrib>Chen, Zhijun</creatorcontrib><creatorcontrib>Zhu, Wangyu</creatorcontrib><creatorcontrib>Zhang, Binjie</creatorcontrib><creatorcontrib>Wang, Zhaoye</creatorcontrib><creatorcontrib>Le, Hanbo</creatorcontrib><title>Changes of CD4+CD25+FOXP3+ and CD8+CD28− regulatory T cells in non-small cell lung cancer patients undergoing surgery</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>Little is known about the regulatory T cells (Tregs) in the peripheral blood after surgery of non-small cell lung cancer (NSCLC) patients. In this study, we investigated whether CD4+CD25+FOXP3+ and CD8+CD28− regulatory T cells are decreased in the peripheral blood of NSCLC patients undergoing surgery. The study group (n=49) comprised NSCLC, and the control group (n=24) consisted of age- and sex-matched nonmalignant diseases. The prevalence of CD4+CD25+FOXP3+ and CD8+CD28− Tregs was analyzed using flow cytometry. The study group showed significantly higher percentage of CD4+CD25+FOXP3+ and CD8+CD28− Tregs than control. The percentage of CD4+CD25+FOXP3+ and CD8+CD28− Tregs increased with tumor stage. One way ANOVA test shows the significant differences between all subgroups. LSD test shows that there was a statistical significance between each of the two subgroups except stage II in CD4+CD25+FOXP3+ Tregs and control vs. each stage, stage I vs. stage III, and stage IV in CD8+CD28− Tregs. There is no significant difference among stages II, III, and IV in CD8+CD28− Tregs. No differences were found between squamous carcinoma and adenocarcinoma. These levels were dropped significantly after operation. Furthermore postoperative Treg percentage in the early stages (stage I and stage II) was not statistically different from that of controls. Postoperative Treg percentage in advanced stage (III+IV) remained above the values shown by controls. Our findings indicate that the percentage of CD4+CD25+FOXP3+ and CD8+CD28− Tregs correlated with the pathological stage in NSCLC and tumor burden.
•CD4+CD25+FOXP3+ and CD8+CD28− tregs were Significantly higher in NSCLC than Controls.•CD4+CD25+FOXP3+ and CD8+CD28− tregs increased with tumor stage and dropped significantly after operation.•Postoperative tregs in early stage was in the same level of controls while in advanced stage was higher than controls.</description><subject>Aged</subject><subject>Carcinoma, Non-Small-Cell Lung - immunology</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Carcinoma, Non-Small-Cell Lung - surgery</subject><subject>CD28 Antigens - immunology</subject><subject>CD4 Antigens - immunology</subject><subject>CD4+CD25+FOXP3</subject><subject>CD8 Antigens - immunology</subject><subject>CD8+CD28</subject><subject>Female</subject><subject>Humans</subject><subject>Interleukin-2 Receptor alpha Subunit - immunology</subject><subject>Lung Neoplasms - immunology</subject><subject>Lung Neoplasms - pathology</subject><subject>Lung Neoplasms - surgery</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>NSCLC</subject><subject>Surgery</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><subject>Treg</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQhyMEoqXwBgj5iLRK6vGfJL4goZQCUqVyKBI3y3EmwavEWeykaN-AM4_Ik9TLtj3CydbP33hG82XZa6AFUCjPt4Xzi5t2BaPAC2AFpeJJdgp1VedQUfk03WVZ5bIq1Un2IsYtpSkX8Dw7YYILWVF-mv1svhs_YCRzT5oLsWkumNxcXn_7wjfE-C5l9SGr__z6TQIO62iWOezJDbE4jpE4T_zs8ziZcfwbkXH1A7HGWwxkZxaHfolk9R2GYXbpKa5hwLB_mT3rzRjx1f15ln29_HDTfMqvrj9-bt5f5ZYrueQWGJOoaG9RAbIWOLVUoKx7blrbgVFKsLauURpbKlQCeIUcetVBb-uW8bPs7fHfXZh_rBgXPbl4GNR4nNeoQUJZScpl9X9UKFbWUiqeUHFEbZhjDNjrXXCTCXsNVB_s6K0-2tEHOxqYTnZS2Zv7Dms7YfdY9KAjAe-OAKaV3DoMOtq0QYudC2gX3c3u3x3uAH6CoUg</recordid><startdate>201402</startdate><enddate>201402</enddate><creator>Chen, Cheng</creator><creator>Chen, Dongdong</creator><creator>Zhang, Yongkui</creator><creator>Chen, Zhijun</creator><creator>Zhu, Wangyu</creator><creator>Zhang, Binjie</creator><creator>Wang, Zhaoye</creator><creator>Le, Hanbo</creator><general>Elsevier B.V</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>7T5</scope><scope>H94</scope></search><sort><creationdate>201402</creationdate><title>Changes of CD4+CD25+FOXP3+ and CD8+CD28− regulatory T cells in non-small cell lung cancer patients undergoing surgery</title><author>Chen, Cheng ; Chen, Dongdong ; Zhang, Yongkui ; Chen, Zhijun ; Zhu, Wangyu ; Zhang, Binjie ; Wang, Zhaoye ; Le, Hanbo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-c1225e90fce91e2b130c04e58f3abcd1a9942b88e5ac69e94137e31f9d1fc8b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Carcinoma, Non-Small-Cell Lung - immunology</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Carcinoma, Non-Small-Cell Lung - surgery</topic><topic>CD28 Antigens - immunology</topic><topic>CD4 Antigens - immunology</topic><topic>CD4+CD25+FOXP3</topic><topic>CD8 Antigens - immunology</topic><topic>CD8+CD28</topic><topic>Female</topic><topic>Humans</topic><topic>Interleukin-2 Receptor alpha Subunit - immunology</topic><topic>Lung Neoplasms - immunology</topic><topic>Lung Neoplasms - pathology</topic><topic>Lung Neoplasms - surgery</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Staging</topic><topic>NSCLC</topic><topic>Surgery</topic><topic>T-Lymphocytes, Regulatory - immunology</topic><topic>Treg</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Cheng</creatorcontrib><creatorcontrib>Chen, Dongdong</creatorcontrib><creatorcontrib>Zhang, Yongkui</creatorcontrib><creatorcontrib>Chen, Zhijun</creatorcontrib><creatorcontrib>Zhu, Wangyu</creatorcontrib><creatorcontrib>Zhang, Binjie</creatorcontrib><creatorcontrib>Wang, Zhaoye</creatorcontrib><creatorcontrib>Le, Hanbo</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Cheng</au><au>Chen, Dongdong</au><au>Zhang, Yongkui</au><au>Chen, Zhijun</au><au>Zhu, Wangyu</au><au>Zhang, Binjie</au><au>Wang, Zhaoye</au><au>Le, Hanbo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes of CD4+CD25+FOXP3+ and CD8+CD28− regulatory T cells in non-small cell lung cancer patients undergoing surgery</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2014-02</date><risdate>2014</risdate><volume>18</volume><issue>2</issue><spage>255</spage><epage>261</epage><pages>255-261</pages><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>Little is known about the regulatory T cells (Tregs) in the peripheral blood after surgery of non-small cell lung cancer (NSCLC) patients. In this study, we investigated whether CD4+CD25+FOXP3+ and CD8+CD28− regulatory T cells are decreased in the peripheral blood of NSCLC patients undergoing surgery. The study group (n=49) comprised NSCLC, and the control group (n=24) consisted of age- and sex-matched nonmalignant diseases. The prevalence of CD4+CD25+FOXP3+ and CD8+CD28− Tregs was analyzed using flow cytometry. The study group showed significantly higher percentage of CD4+CD25+FOXP3+ and CD8+CD28− Tregs than control. The percentage of CD4+CD25+FOXP3+ and CD8+CD28− Tregs increased with tumor stage. One way ANOVA test shows the significant differences between all subgroups. LSD test shows that there was a statistical significance between each of the two subgroups except stage II in CD4+CD25+FOXP3+ Tregs and control vs. each stage, stage I vs. stage III, and stage IV in CD8+CD28− Tregs. There is no significant difference among stages II, III, and IV in CD8+CD28− Tregs. No differences were found between squamous carcinoma and adenocarcinoma. These levels were dropped significantly after operation. Furthermore postoperative Treg percentage in the early stages (stage I and stage II) was not statistically different from that of controls. Postoperative Treg percentage in advanced stage (III+IV) remained above the values shown by controls. Our findings indicate that the percentage of CD4+CD25+FOXP3+ and CD8+CD28− Tregs correlated with the pathological stage in NSCLC and tumor burden.
•CD4+CD25+FOXP3+ and CD8+CD28− tregs were Significantly higher in NSCLC than Controls.•CD4+CD25+FOXP3+ and CD8+CD28− tregs increased with tumor stage and dropped significantly after operation.•Postoperative tregs in early stage was in the same level of controls while in advanced stage was higher than controls.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>24345703</pmid><doi>10.1016/j.intimp.2013.12.004</doi><tpages>7</tpages></addata></record> |
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subjects | Aged Carcinoma, Non-Small-Cell Lung - immunology Carcinoma, Non-Small-Cell Lung - pathology Carcinoma, Non-Small-Cell Lung - surgery CD28 Antigens - immunology CD4 Antigens - immunology CD4+CD25+FOXP3 CD8 Antigens - immunology CD8+CD28 Female Humans Interleukin-2 Receptor alpha Subunit - immunology Lung Neoplasms - immunology Lung Neoplasms - pathology Lung Neoplasms - surgery Male Middle Aged Neoplasm Staging NSCLC Surgery T-Lymphocytes, Regulatory - immunology Treg |
title | Changes of CD4+CD25+FOXP3+ and CD8+CD28− regulatory T cells in non-small cell lung cancer patients undergoing surgery |
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