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1.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;48(5): 420-426, 05/2015. tab, graf
Article de Anglais | LILACS | ID: lil-744378

RÉSUMÉ

An enterovirus 71 (EV71) vaccine for the prevention of hand, foot, and mouth disease (HMFD) is available, but it is not known whether the EV71 vaccine cross-protects against Coxsackievirus (CV) infection. Furthermore, although an inactivated circulating CVA16 Changchun 024 (CC024) strain vaccine candidate is effective in newborn mice, the CC024 strain causes severe lesions in muscle and lung tissues. Therefore, an effective CV vaccine with improved pathogenic safety is needed. The aim of this study was to evaluate the in vivo safety and in vitro replication capability of a noncirculating CVA16 SHZH05 strain. The replication capacity of circulating CVA16 strains CC024, CC045, CC090 and CC163 and the noncirculating SHZH05 strain was evaluated by cytopathic effect in different cell lines. The replication capacity and pathogenicity of the CC024 and SHZH05 strains were also evaluated in a neonatal mouse model. Histopathological and viral load analyses demonstrated that the SHZH05 strain had an in vitro replication capacity comparable to the four CC strains. The CC024, but not the SHZH05 strain, became distributed in a variety of tissues and caused severe lesions and mortality in neonatal mice. The differences in replication capacity and in vivo pathogenicity of the CC024 and SHZH05 strains may result from differences in the nucleotide and amino acid sequences of viral functional polyproteins P1, P2 and P3. Our findings suggest that the noncirculating SHZH05 strain may be a safer CV vaccine candidate than the CC024 strain.


Sujet(s)
Humains , Anti-infectieux/usage thérapeutique , Revue des pratiques de prescription des médicaments , Anti-infectieux/effets indésirables , Anti-infectieux/économie , Maîtrise des coûts , Coûts des médicaments , Résistance microbienne aux médicaments , Utilisation médicament , Revue des pratiques de prescription des médicaments/méthodes , Revue des pratiques de prescription des médicaments/organisation et administration , Revue des pratiques de prescription des médicaments/normes , Évaluation des résultats et des processus en soins de santé , Sécurité des patients
2.
Braz J Med Biol Res ; 48(5): 420-6, 2015 May.
Article de Anglais | MEDLINE | ID: mdl-25831207

RÉSUMÉ

An enterovirus 71 (EV71) vaccine for the prevention of hand, foot, and mouth disease (HMFD) is available, but it is not known whether the EV71 vaccine cross-protects against Coxsackievirus (CV) infection. Furthermore, although an inactivated circulating CVA16 Changchun 024 (CC024) strain vaccine candidate is effective in newborn mice, the CC024 strain causes severe lesions in muscle and lung tissues. Therefore, an effective CV vaccine with improved pathogenic safety is needed. The aim of this study was to evaluate the in vivo safety and in vitro replication capability of a noncirculating CVA16 SHZH05 strain. The replication capacity of circulating CVA16 strains CC024, CC045, CC090 and CC163 and the noncirculating SHZH05 strain was evaluated by cytopathic effect in different cell lines. The replication capacity and pathogenicity of the CC024 and SHZH05 strains were also evaluated in a neonatal mouse model. Histopathological and viral load analyses demonstrated that the SHZH05 strain had an in vitro replication capacity comparable to the four CC strains. The CC024, but not the SHZH05 strain, became distributed in a variety of tissues and caused severe lesions and mortality in neonatal mice. The differences in replication capacity and in vivo pathogenicity of the CC024 and SHZH05 strains may result from differences in the nucleotide and amino acid sequences of viral functional polyproteins P1, P2 and P3. Our findings suggest that the noncirculating SHZH05 strain may be a safer CV vaccine candidate than the CC024 strain.


Sujet(s)
Infections à virus coxsackie/prévention et contrôle , Entérovirus humain A/immunologie , Entérovirus humain A/pathogénicité , Vaccination/méthodes , Vaccins antiviraux/immunologie , Réplication virale/physiologie , Séquence d'acides aminés/génétique , Animaux , Animaux nouveau-nés , Séquence nucléotidique/génétique , Lignée cellulaire , Infections à virus coxsackie/sang , Infections à virus coxsackie/anatomopathologie , Entérovirus humain A/physiologie , Souris de lignée ICR , Culture de cellules primaires , ARN viral/isolement et purification , Alignement de séquences , Spécificité d'espèce , Virulence
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