Children’s vaccines do not induce cross reactivity against SARS-CoV
Identifieur interne : 000254 ( Istex/Curation ); précédent : 000253; suivant : 000255Children’s vaccines do not induce cross reactivity against SARS-CoV
Auteurs : Yang Yu [République populaire de Chine] ; Huali Jin [République populaire de Chine] ; Ze Chen [République populaire de Chine] ; Qingling L. Yu [République populaire de Chine] ; Yijie J. Ma [République populaire de Chine] ; Xiaolin L. Sun [République populaire de Chine] ; Bin Wang [République populaire de Chine]Source :
- Journal of Clinical Pathology [ 0021-9746 ] ; 2007-02.
English descriptors
- KwdEn :
- Teeft :
- Ampv, Attenuated, Bacille, Beijing, Biological science, Bovine serum albumin, Cell proliferation, Clinical analysis, Cona, Elisa, Encephalitis, Haemophilus influenzae type, Immune responses, Immunisation, Immunised, Immunised mice, Inbred, Inbred mice, Individual vaccine, Japanese encephalitis vaccine, Kunming mice, Measles, Meningococcal polysaccharide, Mice immunised, Mmrv, Mumps, Nixed1 nixed2, Optical density, Oral poliovirus vaccine, Other factors, Parainfluenza virus, Poliovirus, Polysaccharide, Positive control, Respiratory syndrome, Results show, Rubella, Rubella vaccine, Rubella virus, Sars, Second immunisation, Several vaccines, Specific antibodies, Streptococcus, Streptococcus pneumoniae vaccine, Syndrome, Tetanus, Third immunisation, Vaccine, Vero cells, Virus vaccine, Wang.
Abstract
In contrast with adults, children infected by severe acute respiratory syndrome-corona virus (SARS-CoV) develop milder clinical symptoms. Because of this, it is speculated that children vaccinated with various childhood vaccines might develop cross immunity against SARS-CoV. Antisera and T cells from mice immunised with various vaccines were used to determine whether they developed cross reactivity against SARS-CoV. The results showed no marked cross reactivity against SARS-CoV, which implies that the reduced symptoms among children infected by SARS-CoV may be caused by other factors.
Url:
DOI: 10.1136/jcp.2006.038893
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Yu</name><affiliation wicri:level="1"><mods:affiliation>State Key Laboratory for Agro-Biotechnology, College of Biological Science, China Agricultural University, Beijing, China</mods:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>State Key Laboratory for Agro-Biotechnology, College of Biological Science, China Agricultural University, Beijing</wicri:regionArea></affiliation></author><author><name sortKey="Ma, Yijie J" sort="Ma, Yijie J" uniqKey="Ma Y" first="Yijie J" last="Ma">Yijie J. 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Sun</name><affiliation wicri:level="1"><mods:affiliation>State Key Laboratory for Agro-Biotechnology, College of Biological Science, China Agricultural University, Beijing, China</mods:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>State Key Laboratory for Agro-Biotechnology, College of Biological Science, China Agricultural University, Beijing</wicri:regionArea></affiliation></author><author><name sortKey="Wang, Bin" sort="Wang, Bin" uniqKey="Wang B" first="Bin" last="Wang">Bin Wang</name><affiliation wicri:level="1"><mods:affiliation>State Key Laboratory for Agro-Biotechnology, College of Biological Science, China Agricultural University, Beijing, China</mods:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>State Key Laboratory for Agro-Biotechnology, College of Biological Science, China Agricultural University, Beijing</wicri:regionArea></affiliation></author></analytic><monogr></monogr><series><title level="j">Journal of Clinical Pathology</title><title level="j" type="abbrev">J Clin Pathol</title><idno type="ISSN">0021-9746</idno><idno type="eISSN">1472-4146</idno><imprint><publisher>BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><date type="published" when="2007-02">2007-02</date><biblScope unit="volume">60</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="208">208</biblScope></imprint><idno type="ISSN">0021-9746</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0021-9746</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>SARS CoV, SARS coronavirus</term><term>SARS, severe acute respiratory syndrome</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Ampv</term><term>Attenuated</term><term>Bacille</term><term>Beijing</term><term>Biological science</term><term>Bovine serum albumin</term><term>Cell proliferation</term><term>Clinical analysis</term><term>Cona</term><term>Elisa</term><term>Encephalitis</term><term>Haemophilus influenzae type</term><term>Immune responses</term><term>Immunisation</term><term>Immunised</term><term>Immunised mice</term><term>Inbred</term><term>Inbred mice</term><term>Individual vaccine</term><term>Japanese encephalitis vaccine</term><term>Kunming mice</term><term>Measles</term><term>Meningococcal polysaccharide</term><term>Mice immunised</term><term>Mmrv</term><term>Mumps</term><term>Nixed1 nixed2</term><term>Optical density</term><term>Oral poliovirus vaccine</term><term>Other factors</term><term>Parainfluenza virus</term><term>Poliovirus</term><term>Polysaccharide</term><term>Positive control</term><term>Respiratory syndrome</term><term>Results show</term><term>Rubella</term><term>Rubella vaccine</term><term>Rubella virus</term><term>Sars</term><term>Second immunisation</term><term>Several vaccines</term><term>Specific antibodies</term><term>Streptococcus</term><term>Streptococcus pneumoniae vaccine</term><term>Syndrome</term><term>Tetanus</term><term>Third immunisation</term><term>Vaccine</term><term>Vero cells</term><term>Virus vaccine</term><term>Wang</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">In contrast with adults, children infected by severe acute respiratory syndrome-corona virus (SARS-CoV) develop milder clinical symptoms. Because of this, it is speculated that children vaccinated with various childhood vaccines might develop cross immunity against SARS-CoV. Antisera and T cells from mice immunised with various vaccines were used to determine whether they developed cross reactivity against SARS-CoV. The results showed no marked cross reactivity against SARS-CoV, which implies that the reduced symptoms among children infected by SARS-CoV may be caused by other factors.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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