Recombinant adenoviruses carrying transgenes
US-2018369404-A1 · Dec 27, 2018 · US
US11339374B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11339374-B2 |
| Application number | US-201816230114-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 21, 2018 |
| Priority date | Jan 16, 2014 |
| Publication date | May 24, 2022 |
| Grant date | May 24, 2022 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention relates to defective interfering viruses and defective interfering virus RNAs that are effective as antiviral agents. The invention also relates to methods for identifying defective interfering virus RNAs that can be used as effective antiviral agents.
Opening claim text (preview).
The invention claimed is: 1. A method to identify an antiviral agent, comprising: in a host cell, exposing an influenza A virus to a test defective interfering (DI) influenza A virus RNA having a deletion in one of RNA segments 1, 2, or 3; monitoring for the production of RNA from each of segments 1, 2, and 3 of the influenza A virus in the presence of the test DI influenza A virus RNA; and identifying the antiviral agent as being a test DI virus RNA that interferes with production of RNA from each of segments 1, 2, and 3 of the influenza A virus. 2. The method according to claim 1 , wherein the RNA production from each of segments 1, 2 and 3 of the influenza A virus is monitored in a separate assay. 3. The method according to claim 1 , wherein the RNA production from each of segments 1, 2, or 3 of the influenza A virus comprises cRNA, mRNA and/or vRNA. 4. The method according to claim 3 , wherein both cRNA and mRNA production are monitored. 5. The method according to claim 1 , wherein one or more of segments 1, 2 or 3 of the influenza A virus is provided as a construct. 6. The method according to claim 5 , wherein the host cell is transfected with one or more nucleic acids each comprising one or more of segments 1, 2, and 3 of the influenza A virus. 7. The method according to claim 5 , wherein each of said segments 1, 2, and 3 of the influenza A virus is provided on a separate plasmid. 8. The method according to claim 5 , wherein the construct comprises a reporter gene, such that a reduction in production of RNA from a segment reduces expression of the reporter gene.
Pseudoviral particles; Non infectious pseudovirions, e.g. genetically engineered · CPC title
Use of virus as therapeutic agent, other than vaccine, e.g. as cytolytic agent · CPC title
Viruses; Subviral particles; Bacteriophages · CPC title
in screening processes · CPC title
for influenza or rhinoviruses · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.