Dynamics of CD4+CD25+ T Cells in Spleens and Mesenteric Lymph Nodes of Mice Infected with Schistosoma japonicum

CD4+CD25+ T cells play a major role in modulating immune response, but few reports have been published about schistosomiasis. Here, we investigated the changes in CD4+CD25+ T cell populations in spleens and mesenteric lymph nodes of mice infected with Schistosoma japonicum. The proportions of CD4+CD...

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Veröffentlicht in:Acta biochimica et biophysica Sinica 2006-05, Vol.38 (5), p.299-304
Hauptverfasser: CAI, Xiao‐Ping, ZHANG, Hui, ZHANG, Yong‐Chen, WANG, Yong, SU, Chuan, JI, Min‐Jun, WU, Hai‐Wei, ZHU, Xiang, ZHANG, Zhao‐Song, WU, Guan‐Ling
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container_title Acta biochimica et biophysica Sinica
container_volume 38
creator CAI, Xiao‐Ping
ZHANG, Hui
ZHANG, Yong‐Chen
WANG, Yong
SU, Chuan
JI, Min‐Jun
WU, Hai‐Wei
ZHU, Xiang
ZHANG, Zhao‐Song
WU, Guan‐Ling
description CD4+CD25+ T cells play a major role in modulating immune response, but few reports have been published about schistosomiasis. Here, we investigated the changes in CD4+CD25+ T cell populations in spleens and mesenteric lymph nodes of mice infected with Schistosoma japonicum. The proportions of CD4+CD25+ T cells in total CD4+ T cells were analyzed by flow cytometry. CD25 and Foxp3 expression was measured by real‐time quantitative polymerase chain reaction. The suppressive activities of CD4+CD25+ T cells were detected by in vitro proliferation of splenocytes. Evidence showed that the percentage of CD4+CD25+ T cells was the same as controls 3 weeks post‐infection. At the acute stage of infection, the percentage decreased significantly. However, at the chronic stage of infection, it rebounded to normal levels or even higher. The expression of the CD25 and Foxp3 showed gradual increase along with the infection progress. In vitro experiment also showed the strong suppressive effect of CD4+CD25+ T cells, isolated during the chronic stage, on proliferation of the CD25− splenocytes. This is the first time that the dynamics of CD4+CD25+ T cell populations was demonstrated in mice infected with schistosomiasis. In conclusion, our data indicated that CD4+CD25+ cells might be involved in the immune modulation during S. japonicum infection, which enhances current knowledge of the mechanisms of the immuno‐downregulation and re‐infection in schistosomiasis. Edited by
Yin‐Chang ZHU
doi_str_mv 10.1111/j.1745-7270.2006.00168.x
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ZHANG, Hui ; ZHANG, Yong‐Chen ; WANG, Yong ; SU, Chuan ; JI, Min‐Jun ; WU, Hai‐Wei ; ZHU, Xiang ; ZHANG, Zhao‐Song ; WU, Guan‐Ling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2978-47a6ea2e5eb69f41d50d8c251cd6f5e68ab206623fcfa9ccb70140b360cc8bbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>CD4 Antigens - immunology</topic><topic>CD4+CD25+ T cell</topic><topic>Cells, Cultured</topic><topic>chronic infection</topic><topic>Female</topic><topic>Foxp3</topic><topic>Immunologic Factors - immunology</topic><topic>Lymph Nodes - immunology</topic><topic>Lymph Nodes - pathology</topic><topic>Mesentery - immunology</topic><topic>Mesentery - pathology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Receptors, Interleukin-2 - immunology</topic><topic>Schistosoma japonicum</topic><topic>Schistosomiasis japonica - immunology</topic><topic>Schistosomiasis japonica - pathology</topic><topic>Spleen - immunology</topic><topic>Spleen - pathology</topic><topic>T-Lymphocytes - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CAI, Xiao‐Ping</creatorcontrib><creatorcontrib>ZHANG, Hui</creatorcontrib><creatorcontrib>ZHANG, Yong‐Chen</creatorcontrib><creatorcontrib>WANG, Yong</creatorcontrib><creatorcontrib>SU, Chuan</creatorcontrib><creatorcontrib>JI, Min‐Jun</creatorcontrib><creatorcontrib>WU, Hai‐Wei</creatorcontrib><creatorcontrib>ZHU, Xiang</creatorcontrib><creatorcontrib>ZHANG, Zhao‐Song</creatorcontrib><creatorcontrib>WU, Guan‐Ling</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>Acta biochimica et biophysica Sinica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CAI, Xiao‐Ping</au><au>ZHANG, Hui</au><au>ZHANG, Yong‐Chen</au><au>WANG, Yong</au><au>SU, Chuan</au><au>JI, Min‐Jun</au><au>WU, Hai‐Wei</au><au>ZHU, Xiang</au><au>ZHANG, Zhao‐Song</au><au>WU, Guan‐Ling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamics of CD4+CD25+ T Cells in Spleens and Mesenteric Lymph Nodes of Mice Infected with Schistosoma japonicum</atitle><jtitle>Acta biochimica et biophysica Sinica</jtitle><addtitle>Acta Biochim Biophys Sin (Shanghai)</addtitle><date>2006-05</date><risdate>2006</risdate><volume>38</volume><issue>5</issue><spage>299</spage><epage>304</epage><pages>299-304</pages><issn>1672-9145</issn><eissn>1745-7270</eissn><abstract>CD4+CD25+ T cells play a major role in modulating immune response, but few reports have been published about schistosomiasis. Here, we investigated the changes in CD4+CD25+ T cell populations in spleens and mesenteric lymph nodes of mice infected with Schistosoma japonicum. The proportions of CD4+CD25+ T cells in total CD4+ T cells were analyzed by flow cytometry. CD25 and Foxp3 expression was measured by real‐time quantitative polymerase chain reaction. The suppressive activities of CD4+CD25+ T cells were detected by in vitro proliferation of splenocytes. Evidence showed that the percentage of CD4+CD25+ T cells was the same as controls 3 weeks post‐infection. At the acute stage of infection, the percentage decreased significantly. However, at the chronic stage of infection, it rebounded to normal levels or even higher. The expression of the CD25 and Foxp3 showed gradual increase along with the infection progress. In vitro experiment also showed the strong suppressive effect of CD4+CD25+ T cells, isolated during the chronic stage, on proliferation of the CD25− splenocytes. This is the first time that the dynamics of CD4+CD25+ T cell populations was demonstrated in mice infected with schistosomiasis. In conclusion, our data indicated that CD4+CD25+ cells might be involved in the immune modulation during S. japonicum infection, which enhances current knowledge of the mechanisms of the immuno‐downregulation and re‐infection in schistosomiasis. Edited by
Yin‐Chang ZHU</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Publishing Asia</pub><pmid>16680369</pmid><doi>10.1111/j.1745-7270.2006.00168.x</doi><tpages>6</tpages></addata></record>
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subjects Animals
CD4 Antigens - immunology
CD4+CD25+ T cell
Cells, Cultured
chronic infection
Female
Foxp3
Immunologic Factors - immunology
Lymph Nodes - immunology
Lymph Nodes - pathology
Mesentery - immunology
Mesentery - pathology
Mice
Mice, Inbred BALB C
Receptors, Interleukin-2 - immunology
Schistosoma japonicum
Schistosomiasis japonica - immunology
Schistosomiasis japonica - pathology
Spleen - immunology
Spleen - pathology
T-Lymphocytes - immunology
title Dynamics of CD4+CD25+ T Cells in Spleens and Mesenteric Lymph Nodes of Mice Infected with Schistosoma japonicum
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