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Cell Rep ; 25(7): 1982-1993.e4, 2018 11 13.
Artigo em Inglês | MEDLINE | ID: mdl-30428362

RESUMO

Synthetically engineered DNA-encoded monoclonal antibodies (DMAbs) are an in vivo platform for evaluation and delivery of human mAb to control against infectious disease. Here, we engineer DMAbs encoding potent anti-Zaire ebolavirus (EBOV) glycoprotein (GP) mAbs isolated from Ebola virus disease survivors. We demonstrate the development of a human IgG1 DMAb platform for in vivo EBOV-GP mAb delivery and evaluation in a mouse model. Using this approach, we show that DMAb-11 and DMAb-34 exhibit functional and molecular profiles comparable to recombinant mAb, have a wide window of expression, and provide rapid protection against lethal mouse-adapted EBOV challenge. The DMAb platform represents a simple, rapid, and reproducible approach for evaluating the activity of mAb during clinical development. DMAbs have the potential to be a mAb delivery system, which may be advantageous for protection against highly pathogenic infectious diseases, like EBOV, in resource-limited and other challenging settings.


Assuntos
Anticorpos Monoclonais/imunologia , DNA/administração & dosagem , Ebolavirus/imunologia , Doença pelo Vírus Ebola/imunologia , Doença pelo Vírus Ebola/prevenção & controle , Animais , Modelos Animais de Doenças , Mapeamento de Epitopos , Epitopos/imunologia , Feminino , Glicoproteínas/imunologia , Células HEK293 , Doença pelo Vírus Ebola/virologia , Humanos , Camundongos Endogâmicos BALB C , Músculos/metabolismo , Mutagênese , Proteínas Recombinantes/metabolismo
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