Mice immunogenicity after vaccination by DNA vaccines containing individual genes of a new type of reovirus.
Identifieur interne : 001899 ( Main/Exploration ); précédent : 001898; suivant : 001900Mice immunogenicity after vaccination by DNA vaccines containing individual genes of a new type of reovirus.
Auteurs : B. Bai ; H. Shen ; Y. Hu ; J. Hou ; R. Li ; Z. Liu ; S. Luo ; P. MaoSource :
- Acta virologica [ 0001-723X ] ; 2013.
Descripteurs français
- KwdFr :
- Animaux, Anticorps antiviraux (immunologie), Femelle, Humains, Infections à Reoviridae (immunologie), Infections à Reoviridae (virologie), Lymphocytes T CD4+ (immunologie), Lymphocytes T CD8+ (immunologie), Orthoréovirus mammalien (génétique), Orthoréovirus mammalien (immunologie), Orthoréovirus mammalien (isolement et purification), Protéines virales (génétique), Protéines virales (immunologie), Souris, Souris de lignée BALB C, Vaccination, Vaccins antiviraux (administration et posologie), Vaccins antiviraux (génétique), Vaccins antiviraux (immunologie), Vaccins à ADN (administration et posologie), Vaccins à ADN (génétique), Vaccins à ADN (immunologie).
- MESH :
- administration et posologie : Vaccins antiviraux, Vaccins à ADN.
- génétique : Orthoréovirus mammalien, Protéines virales, Vaccins antiviraux, Vaccins à ADN.
- immunologie : Anticorps antiviraux, Infections à Reoviridae, Lymphocytes T CD4+, Lymphocytes T CD8+, Orthoréovirus mammalien, Protéines virales, Vaccins antiviraux, Vaccins à ADN.
- isolement et purification : Orthoréovirus mammalien.
- virologie : Infections à Reoviridae.
- Animaux, Femelle, Humains, Souris, Souris de lignée BALB C, Vaccination.
English descriptors
- KwdEn :
- Animals, Antibodies, Viral (immunology), CD4-Positive T-Lymphocytes (immunology), CD8-Positive T-Lymphocytes (immunology), Female, Humans, Mice, Mice, Inbred BALB C, Orthoreovirus, Mammalian (genetics), Orthoreovirus, Mammalian (immunology), Orthoreovirus, Mammalian (isolation & purification), Reoviridae Infections (immunology), Reoviridae Infections (virology), Vaccination, Vaccines, DNA (administration & dosage), Vaccines, DNA (genetics), Vaccines, DNA (immunology), Viral Proteins (genetics), Viral Proteins (immunology), Viral Vaccines (administration & dosage), Viral Vaccines (genetics), Viral Vaccines (immunology).
- MESH :
- chemical , administration & dosage : Vaccines, DNA, Viral Vaccines.
- chemical , genetics : Vaccines, DNA, Viral Proteins, Viral Vaccines.
- chemical , immunology : Antibodies, Viral, Vaccines, DNA, Viral Proteins, Viral Vaccines.
- genetics : Orthoreovirus, Mammalian.
- immunology : CD4-Positive T-Lymphocytes, CD8-Positive T-Lymphocytes, Orthoreovirus, Mammalian, Reoviridae Infections.
- isolation & purification : Orthoreovirus, Mammalian.
- virology : Reoviridae Infections.
- Animals, Female, Humans, Mice, Mice, Inbred BALB C, Vaccination.
Abstract
In this study, we investigated humoral and cellular immune responses in mice to DNA vaccines containing individual S or M genes of a new type of reovirus (nRV) isolate from a severe acute respiratory syndrome (SARS) patient in Beijing, China. Mice were immunized intramuscularly (i.m.) with 100 μg of S1, S2, S3, S4, M1, M2, and M3 DNA vaccine each 4 times in 2-week intervals and assayed for humoral IgG, IgG1, IgG2, and IgG2b antibodies by ELISA and for cellular immune response, particularly IFN-γ induction by ELISpot assay. Moreover, CD4+ and CD8+ T cell levels in peripheral blood mononuclear cells were assayed by flow cytometry. We found that all DNA vaccines induced IgG antibodies, predominantly of the IgG2a class and S3 DNA vaccine was the strongest inducer. M2 and S3 DNA vaccines elicited Th1- and Th2-based immune responses, respectively, while S1 and M3 DNA vaccines induced a mixed Th1/Th2 response. M1, S2, and S4 DNA vaccines were poorly immunogenic. To our knowledge, this is the first report characterizing mammalian reovirus DNA vaccines applied to a mouse model.
DOI: 10.4149/av_2013_04_397
PubMed: 24294952
Affiliations:
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Le document en format XML
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<term>CD8-Positive T-Lymphocytes (immunology)</term>
<term>Female</term>
<term>Humans</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
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<term>Orthoreovirus, Mammalian (immunology)</term>
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<term>Reoviridae Infections (virology)</term>
<term>Vaccination</term>
<term>Vaccines, DNA (administration & dosage)</term>
<term>Vaccines, DNA (genetics)</term>
<term>Vaccines, DNA (immunology)</term>
<term>Viral Proteins (genetics)</term>
<term>Viral Proteins (immunology)</term>
<term>Viral Vaccines (administration & dosage)</term>
<term>Viral Vaccines (genetics)</term>
<term>Viral Vaccines (immunology)</term>
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<term>Infections à Reoviridae (virologie)</term>
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<term>Protéines virales (immunologie)</term>
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<term>Souris de lignée BALB C</term>
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<term>Vaccins antiviraux (administration et posologie)</term>
<term>Vaccins antiviraux (génétique)</term>
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<front><div type="abstract" xml:lang="en">In this study, we investigated humoral and cellular immune responses in mice to DNA vaccines containing individual S or M genes of a new type of reovirus (nRV) isolate from a severe acute respiratory syndrome (SARS) patient in Beijing, China. Mice were immunized intramuscularly (i.m.) with 100 μg of S1, S2, S3, S4, M1, M2, and M3 DNA vaccine each 4 times in 2-week intervals and assayed for humoral IgG, IgG1, IgG2, and IgG2b antibodies by ELISA and for cellular immune response, particularly IFN-γ induction by ELISpot assay. Moreover, CD4+ and CD8+ T cell levels in peripheral blood mononuclear cells were assayed by flow cytometry. We found that all DNA vaccines induced IgG antibodies, predominantly of the IgG2a class and S3 DNA vaccine was the strongest inducer. M2 and S3 DNA vaccines elicited Th1- and Th2-based immune responses, respectively, while S1 and M3 DNA vaccines induced a mixed Th1/Th2 response. M1, S2, and S4 DNA vaccines were poorly immunogenic. To our knowledge, this is the first report characterizing mammalian reovirus DNA vaccines applied to a mouse model.</div>
</front>
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<name sortKey="Hu, Y" sort="Hu, Y" uniqKey="Hu Y" first="Y" last="Hu">Y. Hu</name>
<name sortKey="Li, R" sort="Li, R" uniqKey="Li R" first="R" last="Li">R. Li</name>
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