ChAdOx1 nCoV-19 protection against SARS-CoV-2 in rhesus macaque and ferret challenge models

T Lambe, AJ Spencer, KM Thomas, KE Gooch… - Communications …, 2021 - nature.com
T Lambe, AJ Spencer, KM Thomas, KE Gooch, S Thomas, AD White, HE Humphries…
Communications biology, 2021nature.com
Vaccines against SARS-CoV-2 are urgently required, but early development of vaccines
against SARS-CoV-1 resulted in enhanced disease after vaccination. Careful assessment of
this phenomena is warranted for vaccine development against SARS CoV-2. Here we report
detailed immune profiling after ChAdOx1 nCoV-19 (AZD1222) and subsequent high dose
challenge in two animal models of SARS-CoV-2 mediated disease. We demonstrate in
rhesus macaques the lung pathology caused by SARS-CoV-2 mediated pneumonia is …
Abstract
Vaccines against SARS-CoV-2 are urgently required, but early development of vaccines against SARS-CoV-1 resulted in enhanced disease after vaccination. Careful assessment of this phenomena is warranted for vaccine development against SARS CoV-2. Here we report detailed immune profiling after ChAdOx1 nCoV-19 (AZD1222) and subsequent high dose challenge in two animal models of SARS-CoV-2 mediated disease. We demonstrate in rhesus macaques the lung pathology caused by SARS-CoV-2 mediated pneumonia is reduced by prior vaccination with ChAdOx1 nCoV-19 which induced neutralising antibody responses after a single intramuscular administration. In a second animal model, ferrets, ChAdOx1 nCoV-19 reduced both virus shedding and lung pathology. Antibody titre were boosted by a second dose. Data from these challenge models on the absence of enhanced disease and the detailed immune profiling, support the continued clinical evaluation of ChAdOx1 nCoV-19.
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