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1.
Nat Mater ; 2022 Nov 28.
Artículo en Inglés | MEDLINE | ID: covidwho-2278861

RESUMEN

Messenger RNA has now been used to vaccinate millions of people. However, the diversity of pulmonary pathologies, including infections, genetic disorders, asthma and others, reveals the lung as an important organ to directly target for future RNA therapeutics and preventatives. Here we report the screening of 166 polymeric nanoparticle formulations for functional delivery to the lungs, obtained from a combinatorial synthesis approach combined with a low-dead-volume nose-only inhalation system for mice. We identify P76, a poly-ß-amino-thio-ester polymer, that exhibits increased expression over formulations lacking the thiol component, delivery to different animal species with varying RNA cargos and low toxicity. P76 allows for dose sparing when delivering an mRNA-expressed Cas13a-mediated treatment in a SARS-CoV-2 challenge model, resulting in similar efficacy to a 20-fold higher dose of a neutralizing antibody. Overall, the combinatorial synthesis approach allowed for the discovery of promising polymeric formulations for future RNA pharmaceutical development for the lungs.

2.
Nat Biotechnol ; 39(6): 717-726, 2021 06.
Artículo en Inglés | MEDLINE | ID: covidwho-1065901

RESUMEN

Cas13a has been used to target RNA viruses in cell culture, but efficacy has not been demonstrated in animal models. In this study, we used messenger RNA (mRNA)-encoded Cas13a for mitigating influenza virus A and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in mice and hamsters, respectively. We designed CRISPR RNAs (crRNAs) specific for PB1 and highly conserved regions of PB2 of influenza virus, and against the replicase and nucleocapsid genes of SARS-CoV-2, and selected the crRNAs that reduced viral RNA levels most efficiently in cell culture. We delivered polymer-formulated Cas13a mRNA and the validated guides to the respiratory tract using a nebulizer. In mice, Cas13a degraded influenza RNA in lung tissue efficiently when delivered after infection, whereas in hamsters, Cas13a delivery reduced SARS-CoV-2 replication and reduced symptoms. Our findings suggest that Cas13a-mediated targeting of pathogenic viruses can mitigate respiratory infections.


Asunto(s)
COVID-19/terapia , Gripe Humana/terapia , ARN Mensajero/farmacología , SARS-CoV-2/genética , Animales , COVID-19/genética , COVID-19/virología , Sistemas CRISPR-Cas/genética , Cricetinae , Modelos Animales de Enfermedad , Humanos , Gripe Humana/genética , Gripe Humana/virología , Ratones , Orthomyxoviridae/efectos de los fármacos , Orthomyxoviridae/genética , Orthomyxoviridae/patogenicidad , ARN Mensajero/genética , ARN Viral/genética , Sistema Respiratorio/efectos de los fármacos , Sistema Respiratorio/metabolismo , SARS-CoV-2/patogenicidad
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