Loading…
The role of a nuclear protein, histone H1, on signalling pathways for the maturation of dendritic cells
Summary We have demonstrated previously that liver allograft tolerance is associated with the immunosuppressive activity of anti‐histone H1 autoreactive antibodies induced in the serum of liver transplantation. Furthermore, we and others have shown that nuclear proteins such as histone H1 and high m...
Saved in:
Published in: | Clinical and experimental immunology 2008-06, Vol.152 (3), p.576-584 |
---|---|
Main Authors: | , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c5332-e7939f76e82975f88fcec6b6dcfe0200a9d806b9e5474d7113cd8eab0ebc24ba3 |
---|---|
cites | cdi_FETCH-LOGICAL-c5332-e7939f76e82975f88fcec6b6dcfe0200a9d806b9e5474d7113cd8eab0ebc24ba3 |
container_end_page | 584 |
container_issue | 3 |
container_start_page | 576 |
container_title | Clinical and experimental immunology |
container_volume | 152 |
creator | Hsu, L. W. Chen, C. L. Nakano, T. Lai, C. Y. Chiang, K. C. Lin, Y. C. Kao, Y. H. Chen, S. H. Goto, T. Sung, W. C. Yang, C. H. Cheng, Y. F. Jawan, B. Chiu, K. W. Goto, S. |
description | Summary
We have demonstrated previously that liver allograft tolerance is associated with the immunosuppressive activity of anti‐histone H1 autoreactive antibodies induced in the serum of liver transplantation. Furthermore, we and others have shown that nuclear proteins such as histone H1 and high mobility group box 1 play an important role in maturation of dendritic cells (DCs), although the precise mechanisms are still unknown. In the present study, we focus upon the significance of histone H1 on DCs in terms of the intracellular signalling pathway of DCs. Our immunostaining and immunoblot studies demonstrated that histone H1 was detected in cytoplasm and culture supernatants upon the activation of DCs. Histone H1 blockage by anti‐histone H1 antibody down‐regulated the intracellular activation of mitogen‐activated protein kinases (MAPKs) (p38) and IκBα of DCs, and inhibited DC activity in the proliferation of CD4+ T cells. On the other hand, the addition of histone H1 without endotoxin stimulation up‐regulated major histocompatibility complex class II, the CD80 and CD86 surface markers of DCs and the activation of MAPKs (p38 and extracellular‐regulated kinase 1/2) and IκBα. These results suggest that the translocation of histone H1 from nuclei to cytoplasm and the release of their own histone H1 are necessary for the maturation of DCs and the activation for T lymphocytes. |
doi_str_mv | 10.1111/j.1365-2249.2008.03652.x |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2453206</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20438552</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5332-e7939f76e82975f88fcec6b6dcfe0200a9d806b9e5474d7113cd8eab0ebc24ba3</originalsourceid><addsrcrecordid>eNqNkU1vGyEQhlHUKnHS_oWKS3vKblnYDzi0UmUlTaRIuSRnxLKzNhYGF9gm_vdla8ttb50LM5pnXmb0IoQrUlY5Pm_KirVNQWktSkoIL0kuafl6hhanxhu0IISIQlSkvkCXMW5y2bYtPUcXFa9Zw0mzQKunNeDgLWA_YoXdpC2ogHfBJzDuGq9NTN4BvquusXc4mpVT1hq3wjuV1i9qH_HoA05ZZavSFFQyGctaA7ghmGQ01mBtfIfejspGeH98r9Dz7c3T8q54ePx-v_z2UOiGMVpAJ5gYuxY4FV0zcj5q0G3fDnoEki9VYuCk7QU0dVcPXVUxPXBQPYFe07pX7Ap9Pejupn4LgwaXgrJyF8xWhb30ysh_O86s5cr_lLRuGCVtFvh0FAj-xwQxya2J8wnKgZ-ipKRmvGloBvkB1MHHGGA8fVIRObskN3I2Q85myNkl-dsl-ZpHP_y95J_Boy0Z-HgEVNTKjkE5beKJo4TVgoqZ-3LgXoyF_X8vIJc393PGfgGwZK-u</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20438552</pqid></control><display><type>article</type><title>The role of a nuclear protein, histone H1, on signalling pathways for the maturation of dendritic cells</title><source>PubMed Central (Open Access)</source><creator>Hsu, L. W. ; Chen, C. L. ; Nakano, T. ; Lai, C. Y. ; Chiang, K. C. ; Lin, Y. C. ; Kao, Y. H. ; Chen, S. H. ; Goto, T. ; Sung, W. C. ; Yang, C. H. ; Cheng, Y. F. ; Jawan, B. ; Chiu, K. W. ; Goto, S.</creator><creatorcontrib>Hsu, L. W. ; Chen, C. L. ; Nakano, T. ; Lai, C. Y. ; Chiang, K. C. ; Lin, Y. C. ; Kao, Y. H. ; Chen, S. H. ; Goto, T. ; Sung, W. C. ; Yang, C. H. ; Cheng, Y. F. ; Jawan, B. ; Chiu, K. W. ; Goto, S.</creatorcontrib><description>Summary
We have demonstrated previously that liver allograft tolerance is associated with the immunosuppressive activity of anti‐histone H1 autoreactive antibodies induced in the serum of liver transplantation. Furthermore, we and others have shown that nuclear proteins such as histone H1 and high mobility group box 1 play an important role in maturation of dendritic cells (DCs), although the precise mechanisms are still unknown. In the present study, we focus upon the significance of histone H1 on DCs in terms of the intracellular signalling pathway of DCs. Our immunostaining and immunoblot studies demonstrated that histone H1 was detected in cytoplasm and culture supernatants upon the activation of DCs. Histone H1 blockage by anti‐histone H1 antibody down‐regulated the intracellular activation of mitogen‐activated protein kinases (MAPKs) (p38) and IκBα of DCs, and inhibited DC activity in the proliferation of CD4+ T cells. On the other hand, the addition of histone H1 without endotoxin stimulation up‐regulated major histocompatibility complex class II, the CD80 and CD86 surface markers of DCs and the activation of MAPKs (p38 and extracellular‐regulated kinase 1/2) and IκBα. These results suggest that the translocation of histone H1 from nuclei to cytoplasm and the release of their own histone H1 are necessary for the maturation of DCs and the activation for T lymphocytes.</description><identifier>ISSN: 0009-9104</identifier><identifier>EISSN: 1365-2249</identifier><identifier>DOI: 10.1111/j.1365-2249.2008.03652.x</identifier><identifier>PMID: 18435805</identifier><identifier>CODEN: CEXIAL</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Analytical, structural and metabolic biochemistry ; Animals ; antigen‐presenting cells ; Basic Immunology ; Biological and medical sciences ; Bone Marrow Cells - metabolism ; CD4-Positive T-Lymphocytes - immunology ; Cell Differentiation - drug effects ; Cell Differentiation - physiology ; Cell Proliferation ; Cells, Cultured ; Coculture Techniques ; Cytosol - metabolism ; dendritic cells (myeloid, plasmacytoid, monocyte‐derived) ; Dendritic Cells - cytology ; Dendritic Cells - metabolism ; Extracellular Matrix - metabolism ; flow cytometry/FACS ; Fundamental and applied biological sciences. Psychology ; Histones - immunology ; Histones - metabolism ; Histones - pharmacology ; Histones - physiology ; I-kappa B Kinase - physiology ; immune regulation ; Lymphocyte Activation - immunology ; Male ; Molecular biophysics ; p38 Mitogen-Activated Protein Kinases - physiology ; proliferation ; Rats ; Signal Transduction - physiology ; Translocation, Genetic</subject><ispartof>Clinical and experimental immunology, 2008-06, Vol.152 (3), p.576-584</ispartof><rights>2008 The Author(s). Journal compilation © 2008 British Society for Immunology</rights><rights>2008 INIST-CNRS</rights><rights>2008 The Author(s) Journal Compilation © 2008 British Society for Immunology 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5332-e7939f76e82975f88fcec6b6dcfe0200a9d806b9e5474d7113cd8eab0ebc24ba3</citedby><cites>FETCH-LOGICAL-c5332-e7939f76e82975f88fcec6b6dcfe0200a9d806b9e5474d7113cd8eab0ebc24ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2453206/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2453206/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20349295$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18435805$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hsu, L. W.</creatorcontrib><creatorcontrib>Chen, C. L.</creatorcontrib><creatorcontrib>Nakano, T.</creatorcontrib><creatorcontrib>Lai, C. Y.</creatorcontrib><creatorcontrib>Chiang, K. C.</creatorcontrib><creatorcontrib>Lin, Y. C.</creatorcontrib><creatorcontrib>Kao, Y. H.</creatorcontrib><creatorcontrib>Chen, S. H.</creatorcontrib><creatorcontrib>Goto, T.</creatorcontrib><creatorcontrib>Sung, W. C.</creatorcontrib><creatorcontrib>Yang, C. H.</creatorcontrib><creatorcontrib>Cheng, Y. F.</creatorcontrib><creatorcontrib>Jawan, B.</creatorcontrib><creatorcontrib>Chiu, K. W.</creatorcontrib><creatorcontrib>Goto, S.</creatorcontrib><title>The role of a nuclear protein, histone H1, on signalling pathways for the maturation of dendritic cells</title><title>Clinical and experimental immunology</title><addtitle>Clin Exp Immunol</addtitle><description>Summary
We have demonstrated previously that liver allograft tolerance is associated with the immunosuppressive activity of anti‐histone H1 autoreactive antibodies induced in the serum of liver transplantation. Furthermore, we and others have shown that nuclear proteins such as histone H1 and high mobility group box 1 play an important role in maturation of dendritic cells (DCs), although the precise mechanisms are still unknown. In the present study, we focus upon the significance of histone H1 on DCs in terms of the intracellular signalling pathway of DCs. Our immunostaining and immunoblot studies demonstrated that histone H1 was detected in cytoplasm and culture supernatants upon the activation of DCs. Histone H1 blockage by anti‐histone H1 antibody down‐regulated the intracellular activation of mitogen‐activated protein kinases (MAPKs) (p38) and IκBα of DCs, and inhibited DC activity in the proliferation of CD4+ T cells. On the other hand, the addition of histone H1 without endotoxin stimulation up‐regulated major histocompatibility complex class II, the CD80 and CD86 surface markers of DCs and the activation of MAPKs (p38 and extracellular‐regulated kinase 1/2) and IκBα. These results suggest that the translocation of histone H1 from nuclei to cytoplasm and the release of their own histone H1 are necessary for the maturation of DCs and the activation for T lymphocytes.</description><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>antigen‐presenting cells</subject><subject>Basic Immunology</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Cells - metabolism</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Coculture Techniques</subject><subject>Cytosol - metabolism</subject><subject>dendritic cells (myeloid, plasmacytoid, monocyte‐derived)</subject><subject>Dendritic Cells - cytology</subject><subject>Dendritic Cells - metabolism</subject><subject>Extracellular Matrix - metabolism</subject><subject>flow cytometry/FACS</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Histones - immunology</subject><subject>Histones - metabolism</subject><subject>Histones - pharmacology</subject><subject>Histones - physiology</subject><subject>I-kappa B Kinase - physiology</subject><subject>immune regulation</subject><subject>Lymphocyte Activation - immunology</subject><subject>Male</subject><subject>Molecular biophysics</subject><subject>p38 Mitogen-Activated Protein Kinases - physiology</subject><subject>proliferation</subject><subject>Rats</subject><subject>Signal Transduction - physiology</subject><subject>Translocation, Genetic</subject><issn>0009-9104</issn><issn>1365-2249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqNkU1vGyEQhlHUKnHS_oWKS3vKblnYDzi0UmUlTaRIuSRnxLKzNhYGF9gm_vdla8ttb50LM5pnXmb0IoQrUlY5Pm_KirVNQWktSkoIL0kuafl6hhanxhu0IISIQlSkvkCXMW5y2bYtPUcXFa9Zw0mzQKunNeDgLWA_YoXdpC2ogHfBJzDuGq9NTN4BvquusXc4mpVT1hq3wjuV1i9qH_HoA05ZZavSFFQyGctaA7ghmGQ01mBtfIfejspGeH98r9Dz7c3T8q54ePx-v_z2UOiGMVpAJ5gYuxY4FV0zcj5q0G3fDnoEki9VYuCk7QU0dVcPXVUxPXBQPYFe07pX7Ap9Pejupn4LgwaXgrJyF8xWhb30ysh_O86s5cr_lLRuGCVtFvh0FAj-xwQxya2J8wnKgZ-ipKRmvGloBvkB1MHHGGA8fVIRObskN3I2Q85myNkl-dsl-ZpHP_y95J_Boy0Z-HgEVNTKjkE5beKJo4TVgoqZ-3LgXoyF_X8vIJc393PGfgGwZK-u</recordid><startdate>200806</startdate><enddate>200806</enddate><creator>Hsu, L. W.</creator><creator>Chen, C. L.</creator><creator>Nakano, T.</creator><creator>Lai, C. Y.</creator><creator>Chiang, K. C.</creator><creator>Lin, Y. C.</creator><creator>Kao, Y. H.</creator><creator>Chen, S. H.</creator><creator>Goto, T.</creator><creator>Sung, W. C.</creator><creator>Yang, C. H.</creator><creator>Cheng, Y. F.</creator><creator>Jawan, B.</creator><creator>Chiu, K. W.</creator><creator>Goto, S.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Blackwell Science Inc</general><scope>IQODW</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>7TM</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>200806</creationdate><title>The role of a nuclear protein, histone H1, on signalling pathways for the maturation of dendritic cells</title><author>Hsu, L. W. ; Chen, C. L. ; Nakano, T. ; Lai, C. Y. ; Chiang, K. C. ; Lin, Y. C. ; Kao, Y. H. ; Chen, S. H. ; Goto, T. ; Sung, W. C. ; Yang, C. H. ; Cheng, Y. F. ; Jawan, B. ; Chiu, K. W. ; Goto, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5332-e7939f76e82975f88fcec6b6dcfe0200a9d806b9e5474d7113cd8eab0ebc24ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>antigen‐presenting cells</topic><topic>Basic Immunology</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Cells - metabolism</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Differentiation - physiology</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Coculture Techniques</topic><topic>Cytosol - metabolism</topic><topic>dendritic cells (myeloid, plasmacytoid, monocyte‐derived)</topic><topic>Dendritic Cells - cytology</topic><topic>Dendritic Cells - metabolism</topic><topic>Extracellular Matrix - metabolism</topic><topic>flow cytometry/FACS</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Histones - immunology</topic><topic>Histones - metabolism</topic><topic>Histones - pharmacology</topic><topic>Histones - physiology</topic><topic>I-kappa B Kinase - physiology</topic><topic>immune regulation</topic><topic>Lymphocyte Activation - immunology</topic><topic>Male</topic><topic>Molecular biophysics</topic><topic>p38 Mitogen-Activated Protein Kinases - physiology</topic><topic>proliferation</topic><topic>Rats</topic><topic>Signal Transduction - physiology</topic><topic>Translocation, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hsu, L. W.</creatorcontrib><creatorcontrib>Chen, C. L.</creatorcontrib><creatorcontrib>Nakano, T.</creatorcontrib><creatorcontrib>Lai, C. Y.</creatorcontrib><creatorcontrib>Chiang, K. C.</creatorcontrib><creatorcontrib>Lin, Y. C.</creatorcontrib><creatorcontrib>Kao, Y. H.</creatorcontrib><creatorcontrib>Chen, S. H.</creatorcontrib><creatorcontrib>Goto, T.</creatorcontrib><creatorcontrib>Sung, W. C.</creatorcontrib><creatorcontrib>Yang, C. H.</creatorcontrib><creatorcontrib>Cheng, Y. F.</creatorcontrib><creatorcontrib>Jawan, B.</creatorcontrib><creatorcontrib>Chiu, K. W.</creatorcontrib><creatorcontrib>Goto, S.</creatorcontrib><collection>Pascal-Francis</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>Nucleic Acids Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical and experimental immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hsu, L. W.</au><au>Chen, C. L.</au><au>Nakano, T.</au><au>Lai, C. Y.</au><au>Chiang, K. C.</au><au>Lin, Y. C.</au><au>Kao, Y. H.</au><au>Chen, S. H.</au><au>Goto, T.</au><au>Sung, W. C.</au><au>Yang, C. H.</au><au>Cheng, Y. F.</au><au>Jawan, B.</au><au>Chiu, K. W.</au><au>Goto, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of a nuclear protein, histone H1, on signalling pathways for the maturation of dendritic cells</atitle><jtitle>Clinical and experimental immunology</jtitle><addtitle>Clin Exp Immunol</addtitle><date>2008-06</date><risdate>2008</risdate><volume>152</volume><issue>3</issue><spage>576</spage><epage>584</epage><pages>576-584</pages><issn>0009-9104</issn><eissn>1365-2249</eissn><coden>CEXIAL</coden><abstract>Summary
We have demonstrated previously that liver allograft tolerance is associated with the immunosuppressive activity of anti‐histone H1 autoreactive antibodies induced in the serum of liver transplantation. Furthermore, we and others have shown that nuclear proteins such as histone H1 and high mobility group box 1 play an important role in maturation of dendritic cells (DCs), although the precise mechanisms are still unknown. In the present study, we focus upon the significance of histone H1 on DCs in terms of the intracellular signalling pathway of DCs. Our immunostaining and immunoblot studies demonstrated that histone H1 was detected in cytoplasm and culture supernatants upon the activation of DCs. Histone H1 blockage by anti‐histone H1 antibody down‐regulated the intracellular activation of mitogen‐activated protein kinases (MAPKs) (p38) and IκBα of DCs, and inhibited DC activity in the proliferation of CD4+ T cells. On the other hand, the addition of histone H1 without endotoxin stimulation up‐regulated major histocompatibility complex class II, the CD80 and CD86 surface markers of DCs and the activation of MAPKs (p38 and extracellular‐regulated kinase 1/2) and IκBα. These results suggest that the translocation of histone H1 from nuclei to cytoplasm and the release of their own histone H1 are necessary for the maturation of DCs and the activation for T lymphocytes.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18435805</pmid><doi>10.1111/j.1365-2249.2008.03652.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-9104 |
ispartof | Clinical and experimental immunology, 2008-06, Vol.152 (3), p.576-584 |
issn | 0009-9104 1365-2249 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2453206 |
source | PubMed Central (Open Access) |
subjects | Analytical, structural and metabolic biochemistry Animals antigen‐presenting cells Basic Immunology Biological and medical sciences Bone Marrow Cells - metabolism CD4-Positive T-Lymphocytes - immunology Cell Differentiation - drug effects Cell Differentiation - physiology Cell Proliferation Cells, Cultured Coculture Techniques Cytosol - metabolism dendritic cells (myeloid, plasmacytoid, monocyte‐derived) Dendritic Cells - cytology Dendritic Cells - metabolism Extracellular Matrix - metabolism flow cytometry/FACS Fundamental and applied biological sciences. Psychology Histones - immunology Histones - metabolism Histones - pharmacology Histones - physiology I-kappa B Kinase - physiology immune regulation Lymphocyte Activation - immunology Male Molecular biophysics p38 Mitogen-Activated Protein Kinases - physiology proliferation Rats Signal Transduction - physiology Translocation, Genetic |
title | The role of a nuclear protein, histone H1, on signalling pathways for the maturation of dendritic cells |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T14%3A30%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20role%20of%20a%20nuclear%20protein,%20histone%20H1,%20on%20signalling%20pathways%20for%20the%20maturation%20of%20dendritic%20cells&rft.jtitle=Clinical%20and%20experimental%20immunology&rft.au=Hsu,%20L.%20W.&rft.date=2008-06&rft.volume=152&rft.issue=3&rft.spage=576&rft.epage=584&rft.pages=576-584&rft.issn=0009-9104&rft.eissn=1365-2249&rft.coden=CEXIAL&rft_id=info:doi/10.1111/j.1365-2249.2008.03652.x&rft_dat=%3Cproquest_pubme%3E20438552%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5332-e7939f76e82975f88fcec6b6dcfe0200a9d806b9e5474d7113cd8eab0ebc24ba3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=20438552&rft_id=info:pmid/18435805&rfr_iscdi=true |