TL;DRAbstract
The pathogenesis of poliomyelitis is central to understanding the effectiveness of the vaccines that are likely to eradicate the wild-type virus from the world over the next few years. Studies of the molecular biology of the Sabin live polio vaccines have so far concentrated on their virulence or attenuation for primates or transgenic mice carrying the human receptor for poliovirus where the virus is given directly into the central nervous system or parentally. The basis of attenuation or reversion of the Sabin vaccine strains has been studied by comparing the vaccine strain of each serotype with a closely related strain, either the precursor of the vaccine strain or an isolate from a vaccine-associated case of poliomyelitis. Monoclonal antibodies can recognize neutralization sites specific for vaccine rather than wild-type strains, and the most strain-specific antibodies for any serotype are directed against site 3 (Nag III), composed of sequences from VP3 and VPl. A study was conduct
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The pathogenesis of poliomyelitis is central to understanding the effectiveness of the vaccines that are likely to eradicate the wild-type virus from the world over the next few years. Studies of the molecular biology of the Sabin live polio vaccines have so far concentrated on their virulence or attenuation for primates or transgenic mice carrying the human receptor for poliovirus where the virus is given directly into the central nervous system or parentally. The basis of attenuation or reversion of the Sabin vaccine strains has been studied by comparing the vaccine strain of each serotype with a closely related strain, either the precursor of the vaccine strain or an isolate from a vaccine-associated case of poliomyelitis. Monoclonal antibodies can recognize neutralization sites specific for vaccine rather than wild-type strains, and the most strain-specific antibodies for any serotype are directed against site 3 (Nag III), composed of sequences from VP3 and VPl. A study was conduct
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