Intranasal vaccination with recombinant receptor-binding domain of MERS-CoV spike protein induces much stronger local mucosal immune responses than subcutaneous immunization: Implication for designing novel mucosal MERS vaccines
Identifieur interne : 001C13 ( Main/Exploration ); précédent : 001C12; suivant : 001C14Intranasal vaccination with recombinant receptor-binding domain of MERS-CoV spike protein induces much stronger local mucosal immune responses than subcutaneous immunization: Implication for designing novel mucosal MERS vaccines
Auteurs : Cuiqing Ma [États-Unis, République populaire de Chine] ; Ye Li [États-Unis] ; Lili Wang [États-Unis] ; Guangyu Zhao [République populaire de Chine] ; Xinrong Tao [États-Unis] ; Chien-Te K. Tseng [États-Unis] ; Yusen Zhou [République populaire de Chine] ; Lanying Du [États-Unis] ; Shibo Jiang [États-Unis, République populaire de Chine]Source :
- Vaccine [ 0264-410X ] ; 2014.
Descripteurs français
- KwdFr :
- Administration par voie nasale, Animaux, Anticorps antiviraux (sang), Anticorps neutralisants (sang), Cellules HEK293, Coronavirus (), Coronavirus (immunologie), Femelle, Fragments Fc des immunoglobulines (immunologie), Glycoprotéine de spicule des coronavirus (immunologie), Humains, Immunité cellulaire, Immunité humorale, Immunité muqueuse, Immunoglobuline G (sang), Injections sous-cutanées, Poumon (immunologie), Protéines recombinantes (immunologie), Rate (immunologie), Souris, Souris de lignée BALB C, Vaccins antiviraux (immunologie).
- MESH :
- immunologie : Coronavirus, Fragments Fc des immunoglobulines, Glycoprotéine de spicule des coronavirus, Poumon, Protéines recombinantes, Rate, Vaccins antiviraux.
- sang : Anticorps antiviraux, Anticorps neutralisants, Immunoglobuline G.
- Administration par voie nasale, Animaux, Cellules HEK293, Coronavirus, Femelle, Humains, Immunité cellulaire, Immunité humorale, Immunité muqueuse, Injections sous-cutanées, Souris, Souris de lignée BALB C.
English descriptors
- KwdEn :
- Administration, Intranasal, Animals, Antibodies, Neutralizing (blood), Antibodies, Viral (blood), Coronavirus (classification), Coronavirus (immunology), Female, HEK293 Cells, Humans, Immunity, Cellular, Immunity, Humoral, Immunity, Mucosal, Immunoglobulin Fc Fragments (immunology), Immunoglobulin G (blood), Injections, Subcutaneous, Lung (immunology), Mice, Mice, Inbred BALB C, Recombinant Proteins (immunology), Spike Glycoprotein, Coronavirus (immunology), Spleen (immunology), Viral Vaccines (immunology).
- MESH :
- chemical , blood : Antibodies, Neutralizing, Antibodies, Viral, Immunoglobulin G.
- classification : Coronavirus.
- immunology : Coronavirus, Immunoglobulin Fc Fragments, Lung, Recombinant Proteins, Spike Glycoprotein, Coronavirus, Spleen, Viral Vaccines.
- Administration, Intranasal, Animals, Female, HEK293 Cells, Humans, Immunity, Cellular, Immunity, Humoral, Immunity, Mucosal, Injections, Subcutaneous, Mice, Mice, Inbred BALB C.
Abstract
We compared MERS-CoV RBD-induced immune responses I.n. induced comparable systemic humoral immune responses as s.c. I.n. induced similar neutralization but more robust cellular responses than s.c. I.n. elicited significantly higher local mucosal immune responses than s.c. Has potential to be developed as an effective and safe MERS mucosal vaccine.
Url:
DOI: 10.1016/j.vaccine.2014.02.004
PubMed: 24560617
PubMed Central: 4194189
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en"><title>Highlights</title>
<p><list list-type="simple" id="lis0005"><list-item id="lsti0005"><label>•</label>
<p id="par0005">We compared MERS-CoV RBD-induced immune responses <italic>via</italic>
i.n. and s.c. routes.</p>
</list-item>
<list-item id="lsti0010"><label>•</label>
<p id="par0010">I.n. induced comparable systemic humoral immune responses as s.c.</p>
</list-item>
<list-item id="lsti0015"><label>•</label>
<p id="par0015">I.n. induced similar neutralization but more robust cellular responses than s.c.</p>
</list-item>
<list-item id="lsti0020"><label>•</label>
<p id="par0020">I.n. elicited significantly higher local mucosal immune responses than s.c.</p>
</list-item>
<list-item id="lsti0025"><label>•</label>
<p id="par0025">Has potential to be developed as an effective and safe MERS mucosal vaccine.</p>
</list-item>
</list>
</p>
</div>
</front>
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</div1>
</back>
</TEI>
<affiliations><list><country><li>République populaire de Chine</li>
<li>États-Unis</li>
</country>
<region><li>Texas</li>
<li>État de New York</li>
</region>
<settlement><li>Pékin</li>
</settlement>
</list>
<tree><country name="États-Unis"><region name="État de New York"><name sortKey="Ma, Cuiqing" sort="Ma, Cuiqing" uniqKey="Ma C" first="Cuiqing" last="Ma">Cuiqing Ma</name>
</region>
<name sortKey="Du, Lanying" sort="Du, Lanying" uniqKey="Du L" first="Lanying" last="Du">Lanying Du</name>
<name sortKey="Jiang, Shibo" sort="Jiang, Shibo" uniqKey="Jiang S" first="Shibo" last="Jiang">Shibo Jiang</name>
<name sortKey="Li, Ye" sort="Li, Ye" uniqKey="Li Y" first="Ye" last="Li">Ye Li</name>
<name sortKey="Tao, Xinrong" sort="Tao, Xinrong" uniqKey="Tao X" first="Xinrong" last="Tao">Xinrong Tao</name>
<name sortKey="Tseng, Chien Te K" sort="Tseng, Chien Te K" uniqKey="Tseng C" first="Chien-Te K." last="Tseng">Chien-Te K. Tseng</name>
<name sortKey="Tseng, Chien Te K" sort="Tseng, Chien Te K" uniqKey="Tseng C" first="Chien-Te K." last="Tseng">Chien-Te K. Tseng</name>
<name sortKey="Wang, Lili" sort="Wang, Lili" uniqKey="Wang L" first="Lili" last="Wang">Lili Wang</name>
</country>
<country name="République populaire de Chine"><noRegion><name sortKey="Ma, Cuiqing" sort="Ma, Cuiqing" uniqKey="Ma C" first="Cuiqing" last="Ma">Cuiqing Ma</name>
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<name sortKey="Jiang, Shibo" sort="Jiang, Shibo" uniqKey="Jiang S" first="Shibo" last="Jiang">Shibo Jiang</name>
<name sortKey="Zhao, Guangyu" sort="Zhao, Guangyu" uniqKey="Zhao G" first="Guangyu" last="Zhao">Guangyu Zhao</name>
<name sortKey="Zhou, Yusen" sort="Zhou, Yusen" uniqKey="Zhou Y" first="Yusen" last="Zhou">Yusen Zhou</name>
</country>
</tree>
</affiliations>
</record>
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