Long-lived effector/central memory T-cell responses to severe acute respiratory syndrome coronavirus (SARS-CoV) S antigen in recovered SARS patients
Identifieur interne : 000E96 ( Pmc/Curation ); précédent : 000E95; suivant : 000E97Long-lived effector/central memory T-cell responses to severe acute respiratory syndrome coronavirus (SARS-CoV) S antigen in recovered SARS patients
Auteurs : Li-Tao Yang [République populaire de Chine] ; Hui Peng [République populaire de Chine] ; Zhao-Ling Zhu [République populaire de Chine] ; Gang Li [République populaire de Chine] ; Zi-Tong Huang [République populaire de Chine] ; Zhi-Xin Zhao [République populaire de Chine] ; Richard A. Koup [États-Unis] ; Robert T. Bailer [États-Unis] ; Chang-You Wu [République populaire de Chine]Source :
- Clinical Immunology (Orlando, Fla.) [ 1521-6616 ] ; 2006.
Abstract
The role of cell-mediated immunity in human SARS-CoV infection is still not well understood. In this study, we found that memory T-cell responses against the spike (S) protein were persistent for more than 1 year after SARS-CoV infection by detecting the production of IFN-γ using ELISA and ELISpot assays. Flow cytometric analysis showed that both CD4+ and CD8+ T cells were involved in cellular responses against SARS-CoV infection. Interestingly, most of SARS-CoV S-specific memory CD4+ T cells were central memory cells expressing CD45RO+ CCR7+ CD62L−. However, the majority of memory CD8+ T cells revealed effector memory phenotype expressing CD45RO− CCR7− CD62L−. Thus, our study provides the evidence that SARS-CoV infection in humans can induce cellular immune response that is persistent for a long period of time. These data may have an important implication in the possibility of designing effective vaccine against SARS-CoV infection, specifically in defining T-cell populations that are implicated in protective immunity.
Url:
DOI: 10.1016/j.clim.2006.05.002
PubMed: 16781892
PubMed Central: 7106132
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<author><name sortKey="Peng, Hui" sort="Peng, Hui" uniqKey="Peng H" first="Hui" last="Peng">Hui Peng</name>
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<author><name sortKey="Wu, Chang You" sort="Wu, Chang You" uniqKey="Wu C" first="Chang-You" last="Wu">Chang-You Wu</name>
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<series><title level="j">Clinical Immunology (Orlando, Fla.)</title>
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<front><div type="abstract" xml:lang="en"><p>The role of cell-mediated immunity in human SARS-CoV infection is still not well understood. In this study, we found that memory T-cell responses against the spike (S) protein were persistent for more than 1 year after SARS-CoV infection by detecting the production of IFN-γ using ELISA and ELISpot assays. Flow cytometric analysis showed that both CD4<sup>+</sup>
and CD8<sup>+</sup>
T cells were involved in cellular responses against SARS-CoV infection. Interestingly, most of SARS-CoV S-specific memory CD4<sup>+</sup>
T cells were central memory cells expressing CD45RO<sup>+</sup>
CCR7<sup>+</sup>
CD62L<sup>−</sup>
. However, the majority of memory CD8<sup>+</sup>
T cells revealed effector memory phenotype expressing CD45RO<sup>−</sup>
CCR7<sup>−</sup>
CD62L<sup>−</sup>
. Thus, our study provides the evidence that SARS-CoV infection in humans can induce cellular immune response that is persistent for a long period of time. These data may have an important implication in the possibility of designing effective vaccine against SARS-CoV infection, specifically in defining T-cell populations that are implicated in protective immunity.</p>
</div>
</front>
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</TEI>
<pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Clin Immunol</journal-id>
<journal-id journal-id-type="iso-abbrev">Clin. Immunol</journal-id>
<journal-title-group><journal-title>Clinical Immunology (Orlando, Fla.)</journal-title>
</journal-title-group>
<issn pub-type="ppub">1521-6616</issn>
<issn pub-type="epub">1521-7035</issn>
<publisher><publisher-name>Elsevier Inc.</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">16781892</article-id>
<article-id pub-id-type="pmc">7106132</article-id>
<article-id pub-id-type="publisher-id">S1521-6616(06)00735-2</article-id>
<article-id pub-id-type="doi">10.1016/j.clim.2006.05.002</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Long-lived effector/central memory T-cell responses to severe acute respiratory syndrome coronavirus (SARS-CoV) S antigen in recovered SARS patients</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Yang</surname>
<given-names>Li-Tao</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Peng</surname>
<given-names>Hui</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Zhu</surname>
<given-names>Zhao-Ling</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Li</surname>
<given-names>Gang</given-names>
</name>
<xref rid="aff2" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Huang</surname>
<given-names>Zi-Tong</given-names>
</name>
<xref rid="aff3" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Zhao</surname>
<given-names>Zhi-Xin</given-names>
</name>
<xref rid="aff2" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Koup</surname>
<given-names>Richard A.</given-names>
</name>
<xref rid="aff4" ref-type="aff">d</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Bailer</surname>
<given-names>Robert T.</given-names>
</name>
<xref rid="aff4" ref-type="aff">d</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Wu</surname>
<given-names>Chang-You</given-names>
</name>
<email>Changyou_wu@yahoo.com</email>
<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="cor1" ref-type="corresp">⁎</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>a</label>
Department of Immunology, Zhongshan Medical School, Sun Yat-sen University, 74 Zhongshan 2nd Road, Guangzhou 510080, China</aff>
<aff id="aff2"><label>b</label>
Third affiliated hospital of the Sun Yat-sen University, Guangzhou 510630, China</aff>
<aff id="aff3"><label>c</label>
Second affiliated hospital of the Sun Yat-sen University, Guangzhou 510120, China</aff>
<aff id="aff4"><label>d</label>
Vaccine Research Center, NIAID/NIH, Bethesda, MD 20892, USA</aff>
<author-notes><corresp id="cor1"><label>⁎</label>
Corresponding author. Fax: +86 20 87331552. <email>Changyou_wu@yahoo.com</email>
</corresp>
</author-notes>
<pub-date pub-type="pmc-release"><day>16</day>
<month>6</month>
<year>2006</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><month>8</month>
<year>2006</year>
</pub-date>
<pub-date pub-type="epub"><day>16</day>
<month>6</month>
<year>2006</year>
</pub-date>
<volume>120</volume>
<issue>2</issue>
<fpage>171</fpage>
<lpage>178</lpage>
<history><date date-type="received"><day>22</day>
<month>11</month>
<year>2005</year>
</date>
<date date-type="rev-recd"><day>21</day>
<month>4</month>
<year>2006</year>
</date>
<date date-type="accepted"><day>1</day>
<month>5</month>
<year>2006</year>
</date>
</history>
<permissions><copyright-statement>Copyright © 2006 Elsevier Inc. All rights reserved.</copyright-statement>
<copyright-year>2006</copyright-year>
<copyright-holder>Elsevier Inc.</copyright-holder>
<license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p>
</license>
</permissions>
<abstract><p>The role of cell-mediated immunity in human SARS-CoV infection is still not well understood. In this study, we found that memory T-cell responses against the spike (S) protein were persistent for more than 1 year after SARS-CoV infection by detecting the production of IFN-γ using ELISA and ELISpot assays. Flow cytometric analysis showed that both CD4<sup>+</sup>
and CD8<sup>+</sup>
T cells were involved in cellular responses against SARS-CoV infection. Interestingly, most of SARS-CoV S-specific memory CD4<sup>+</sup>
T cells were central memory cells expressing CD45RO<sup>+</sup>
CCR7<sup>+</sup>
CD62L<sup>−</sup>
. However, the majority of memory CD8<sup>+</sup>
T cells revealed effector memory phenotype expressing CD45RO<sup>−</sup>
CCR7<sup>−</sup>
CD62L<sup>−</sup>
. Thus, our study provides the evidence that SARS-CoV infection in humans can induce cellular immune response that is persistent for a long period of time. These data may have an important implication in the possibility of designing effective vaccine against SARS-CoV infection, specifically in defining T-cell populations that are implicated in protective immunity.</p>
</abstract>
<kwd-group><title>Keywords</title>
<kwd>SARS</kwd>
<kwd>SARS-CoV</kwd>
<kwd>S protein</kwd>
<kwd>IFN-γ</kwd>
<kwd>Cellular immune response</kwd>
<kwd>Memory T cells</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>
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