Development of vaccines and passive immunotherapy against SARS corona virus using SCID-PBL/hu mouse models.
Identifieur interne : 000D48 ( PubMed/Curation ); précédent : 000D47; suivant : 000D49Development of vaccines and passive immunotherapy against SARS corona virus using SCID-PBL/hu mouse models.
Auteurs : Masaji Okada [Japon] ; Yoshinobu Okuno ; Satomi Hashimoto ; Yoko Kita ; Noriko Kanamaru ; Yasuko Nishida ; Yoshie Tsunai ; Ruriko Inoue ; Hitoshi Nakatani ; Reiko Fukamizu ; Yumi Namie ; Junko Yamada ; Kyoko Takao ; Ritsuko Asai ; Ryoko Asaki ; Tetsuo Kase ; Yuji Takemoto ; Shigeto Yoshida ; J S M. Peiris ; Pei-Jer Chen ; Naoki Yamamoto ; Tatsuji Nomura ; Isao Ishida ; Shigeru Morikawa ; Masato Tashiro ; Mitsunori SakataniSource :
- Vaccine [ 0264-410X ] ; 2007.
Descripteurs français
- KwdFr :
- Animaux, Immunisation passive (), Immunothérapie, Lymphocytes T cytotoxiques (immunologie), Modèles animaux de maladie humaine, Souris, Souris SCID, Syndrome respiratoire aigu sévère (), Vaccins antiviraux (administration et posologie), Vaccins à ADN (administration et posologie), Vaccins à ADN (génétique), Virus du SRAS (génétique), Virus du SRAS (immunologie), Virus du SRAS (métabolisme).
- MESH :
- administration et posologie : Vaccins antiviraux, Vaccins à ADN.
- génétique : Vaccins à ADN, Virus du SRAS.
- immunologie : Lymphocytes T cytotoxiques, Virus du SRAS.
- métabolisme : Virus du SRAS.
- Animaux, Immunisation passive, Immunothérapie, Modèles animaux de maladie humaine, Souris, Souris SCID, Syndrome respiratoire aigu sévère.
English descriptors
- KwdEn :
- Animals, Disease Models, Animal, Immunization, Passive (methods), Immunotherapy, Mice, Mice, SCID, SARS Virus (genetics), SARS Virus (immunology), SARS Virus (metabolism), Severe Acute Respiratory Syndrome (prevention & control), T-Lymphocytes, Cytotoxic (immunology), Vaccines, DNA (administration & dosage), Vaccines, DNA (genetics), Viral Vaccines (administration & dosage).
- MESH :
- chemical , administration & dosage : Vaccines, DNA, Viral Vaccines.
- genetics : SARS Virus, Vaccines, DNA.
- immunology : SARS Virus, T-Lymphocytes, Cytotoxic.
- metabolism : SARS Virus.
- methods : Immunization, Passive.
- prevention & control : Severe Acute Respiratory Syndrome.
- Animals, Disease Models, Animal, Immunotherapy, Mice, Mice, SCID.
Abstract
We have investigated novel vaccine strategies against severe acute respiratory syndrome (SARS) CoV using cDNA constructs encoding the structural antigens: (S), (M), (E), or (N) protein, derived from SARS CoV. PBL from healthy human volunteers were administered i.p. into IL-2 receptor gamma-chain disrupted SCID mice, and SCID-PBL/hu mice were constructed. These mice can be used to analyze the human immune response in vivo. SARS M DNA vaccine and N DNA vaccine induced human CTL specific for SARS CoV antigens. Alternatively, SARS M DNA vaccines inducing human neutralizing antibodies and human monoclonal antibodies against SARS CoV are now being developed. These results show that these vaccines can induce virus-specific immune responses and should provide a useful tool for development of protective and therapeutic vaccines.
DOI: 10.1016/j.vaccine.2007.01.032
PubMed: 17289225
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pubmed:17289225Le document en format XML
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<author><name sortKey="Yamamoto, Naoki" sort="Yamamoto, Naoki" uniqKey="Yamamoto N" first="Naoki" last="Yamamoto">Naoki Yamamoto</name>
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<author><name sortKey="Nomura, Tatsuji" sort="Nomura, Tatsuji" uniqKey="Nomura T" first="Tatsuji" last="Nomura">Tatsuji Nomura</name>
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<term>Immunotherapy</term>
<term>Mice</term>
<term>Mice, SCID</term>
<term>SARS Virus (genetics)</term>
<term>SARS Virus (immunology)</term>
<term>SARS Virus (metabolism)</term>
<term>Severe Acute Respiratory Syndrome (prevention & control)</term>
<term>T-Lymphocytes, Cytotoxic (immunology)</term>
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<term>Immunothérapie</term>
<term>Lymphocytes T cytotoxiques (immunologie)</term>
<term>Modèles animaux de maladie humaine</term>
<term>Souris</term>
<term>Souris SCID</term>
<term>Syndrome respiratoire aigu sévère ()</term>
<term>Vaccins antiviraux (administration et posologie)</term>
<term>Vaccins à ADN (administration et posologie)</term>
<term>Vaccins à ADN (génétique)</term>
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<term>Viral Vaccines</term>
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<term>Vaccins à ADN</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>SARS Virus</term>
<term>Vaccines, DNA</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Vaccins à ADN</term>
<term>Virus du SRAS</term>
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<term>Virus du SRAS</term>
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<front><div type="abstract" xml:lang="en">We have investigated novel vaccine strategies against severe acute respiratory syndrome (SARS) CoV using cDNA constructs encoding the structural antigens: (S), (M), (E), or (N) protein, derived from SARS CoV. PBL from healthy human volunteers were administered i.p. into IL-2 receptor gamma-chain disrupted SCID mice, and SCID-PBL/hu mice were constructed. These mice can be used to analyze the human immune response in vivo. SARS M DNA vaccine and N DNA vaccine induced human CTL specific for SARS CoV antigens. Alternatively, SARS M DNA vaccines inducing human neutralizing antibodies and human monoclonal antibodies against SARS CoV are now being developed. These results show that these vaccines can induce virus-specific immune responses and should provide a useful tool for development of protective and therapeutic vaccines.</div>
</front>
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<ArticleTitle>Development of vaccines and passive immunotherapy against SARS corona virus using SCID-PBL/hu mouse models.</ArticleTitle>
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<Abstract><AbstractText>We have investigated novel vaccine strategies against severe acute respiratory syndrome (SARS) CoV using cDNA constructs encoding the structural antigens: (S), (M), (E), or (N) protein, derived from SARS CoV. PBL from healthy human volunteers were administered i.p. into IL-2 receptor gamma-chain disrupted SCID mice, and SCID-PBL/hu mice were constructed. These mice can be used to analyze the human immune response in vivo. SARS M DNA vaccine and N DNA vaccine induced human CTL specific for SARS CoV antigens. Alternatively, SARS M DNA vaccines inducing human neutralizing antibodies and human monoclonal antibodies against SARS CoV are now being developed. These results show that these vaccines can induce virus-specific immune responses and should provide a useful tool for development of protective and therapeutic vaccines.</AbstractText>
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<Initials>M</Initials>
<AffiliationInfo><Affiliation>Clinical Research Center, National Hospital Organization Kinki-Chuo Chest Medical Center, 1180 Nagasone, Kitaku, Sakai, Osaka 591-8555, Japan. okm@kch.hosp.go.jp</Affiliation>
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<Initials>PJ</Initials>
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<Author ValidYN="Y"><LastName>Yamamoto</LastName>
<ForeName>Naoki</ForeName>
<Initials>N</Initials>
</Author>
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<ForeName>Tatsuji</ForeName>
<Initials>T</Initials>
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<ForeName>Isao</ForeName>
<Initials>I</Initials>
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<ForeName>Shigeru</ForeName>
<Initials>S</Initials>
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<ForeName>Masato</ForeName>
<Initials>M</Initials>
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<Author ValidYN="Y"><LastName>Sakatani</LastName>
<ForeName>Mitsunori</ForeName>
<Initials>M</Initials>
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<Month>01</Month>
<Day>23</Day>
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