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Phagocytic cells contribute to the antibody-mediated elimination of pulmonary-infected SARS coronavirus.

Identifieur interne : 001602 ( Main/Exploration ); précédent : 001601; suivant : 001603

Phagocytic cells contribute to the antibody-mediated elimination of pulmonary-infected SARS coronavirus.

Auteurs : Fumihiko Yasui [Japon] ; Michinori Kohara [Japon] ; Masahiro Kitabatake [Japon] ; Tetsu Nishiwaki [Japon] ; Hideki Fujii [Japon] ; Chise Tateno [Japon] ; Misako Yoneda [Japon] ; Kouichi Morita [Japon] ; Kouji Matsushima [Japon] ; Shigeo Koyasu [Japon] ; Chieko Kai [Japon]

Source :

RBID : pubmed:24725942

Descripteurs français

English descriptors

Abstract

While the 2002-2003 outbreak of severe acute respiratory syndrome (SARS) resulted in 774 deaths, patients who were affected with mild pulmonary symptoms successfully recovered. The objective of the present work was to identify, using SARS coronavirus (SARS-CoV) mouse infection models, immune factors responsible for clearing of the virus. The elimination of pulmonary SARS-CoV infection required the activation of B cells by CD4(+) T cells. Furthermore, passive immunization (post-infection) with homologous (murine) anti-SARS-CoV antiserum showed greater elimination efficacy against SARS-CoV than that with heterologous (rabbit) antiserum, despite the use of equivalent titers of neutralizing antibodies. This distinction was mediated by mouse phagocytic cells (monocyte-derived infiltrating macrophages and partially alveolar macrophages, but not neutrophils), as demonstrated both by adoptive transfer from donors and by immunological depletion of selected cell types. These results indicate that the cooperation of anti-SARS-CoV antibodies and phagocytic cells plays an important role in the elimination of SARS-CoV.

DOI: 10.1016/j.virol.2014.02.005
PubMed: 24725942


Affiliations:


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Le document en format XML

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<term>Antibodies, Viral (immunology)</term>
<term>B-Lymphocytes (immunology)</term>
<term>CD4-Positive T-Lymphocytes (immunology)</term>
<term>Disease Models, Animal</term>
<term>Female</term>
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<term>Lung (immunology)</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Mice, SCID</term>
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<term>Severe Acute Respiratory Syndrome (immunology)</term>
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<term>Femelle</term>
<term>Immunisation passive</term>
<term>Lymphocytes B (immunologie)</term>
<term>Lymphocytes T CD4+ (immunologie)</term>
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<term>Female</term>
<term>Immunization, Passive</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Mice, SCID</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Animaux</term>
<term>Femelle</term>
<term>Immunisation passive</term>
<term>Modèles animaux de maladie humaine</term>
<term>Souris</term>
<term>Souris SCID</term>
<term>Souris de lignée BALB C</term>
<term>Transfert adoptif</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">While the 2002-2003 outbreak of severe acute respiratory syndrome (SARS) resulted in 774 deaths, patients who were affected with mild pulmonary symptoms successfully recovered. The objective of the present work was to identify, using SARS coronavirus (SARS-CoV) mouse infection models, immune factors responsible for clearing of the virus. The elimination of pulmonary SARS-CoV infection required the activation of B cells by CD4(+) T cells. Furthermore, passive immunization (post-infection) with homologous (murine) anti-SARS-CoV antiserum showed greater elimination efficacy against SARS-CoV than that with heterologous (rabbit) antiserum, despite the use of equivalent titers of neutralizing antibodies. This distinction was mediated by mouse phagocytic cells (monocyte-derived infiltrating macrophages and partially alveolar macrophages, but not neutrophils), as demonstrated both by adoptive transfer from donors and by immunological depletion of selected cell types. These results indicate that the cooperation of anti-SARS-CoV antibodies and phagocytic cells plays an important role in the elimination of SARS-CoV.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Japon</li>
</country>
<region>
<li>Région de Kantō</li>
</region>
<settlement>
<li>Tokyo</li>
</settlement>
<orgName>
<li>Université de Tokyo</li>
</orgName>
</list>
<tree>
<country name="Japon">
<region name="Région de Kantō">
<name sortKey="Yasui, Fumihiko" sort="Yasui, Fumihiko" uniqKey="Yasui F" first="Fumihiko" last="Yasui">Fumihiko Yasui</name>
</region>
<name sortKey="Fujii, Hideki" sort="Fujii, Hideki" uniqKey="Fujii H" first="Hideki" last="Fujii">Hideki Fujii</name>
<name sortKey="Kai, Chieko" sort="Kai, Chieko" uniqKey="Kai C" first="Chieko" last="Kai">Chieko Kai</name>
<name sortKey="Kitabatake, Masahiro" sort="Kitabatake, Masahiro" uniqKey="Kitabatake M" first="Masahiro" last="Kitabatake">Masahiro Kitabatake</name>
<name sortKey="Kohara, Michinori" sort="Kohara, Michinori" uniqKey="Kohara M" first="Michinori" last="Kohara">Michinori Kohara</name>
<name sortKey="Koyasu, Shigeo" sort="Koyasu, Shigeo" uniqKey="Koyasu S" first="Shigeo" last="Koyasu">Shigeo Koyasu</name>
<name sortKey="Matsushima, Kouji" sort="Matsushima, Kouji" uniqKey="Matsushima K" first="Kouji" last="Matsushima">Kouji Matsushima</name>
<name sortKey="Morita, Kouichi" sort="Morita, Kouichi" uniqKey="Morita K" first="Kouichi" last="Morita">Kouichi Morita</name>
<name sortKey="Nishiwaki, Tetsu" sort="Nishiwaki, Tetsu" uniqKey="Nishiwaki T" first="Tetsu" last="Nishiwaki">Tetsu Nishiwaki</name>
<name sortKey="Tateno, Chise" sort="Tateno, Chise" uniqKey="Tateno C" first="Chise" last="Tateno">Chise Tateno</name>
<name sortKey="Yoneda, Misako" sort="Yoneda, Misako" uniqKey="Yoneda M" first="Misako" last="Yoneda">Misako Yoneda</name>
</country>
</tree>
</affiliations>
</record>

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