Sars-cov-2 vaccines
US-2024408193-A1 · Dec 12, 2024 · US
US10144917B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10144917-B2 |
| Application number | US-201515507620-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 28, 2015 |
| Priority date | Aug 29, 2014 |
| Publication date | Dec 4, 2018 |
| Grant date | Dec 4, 2018 |
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Official abstract text for this publication.
The present invention relates to a method for preparing a vaccine antigen, which includes a step of fragmenting a biological membrane associated with said vaccine antigen by treating said biological membrane with at least one calixarene of formula (II): wherein: X is a —(CH2)-CO2Y group and Y is an alkaline metal or one of the pharmaceutically acceptable salts thereof, wherein said resulting vaccine antigen also includes a fragment of the biological membrane associated with said antigen. The present invention also relates to a vaccine that can be produced by implementing the method, including a calixarene of formula (II) in carrier format, with a quantity of 0.1 to 1,000 μg in the total weight of the vaccine. The present invention further relates to the use of a calixarene as defined above for the preparation of a vaccine or a vaccine antigen, and to the vaccine for use as a drug in the treatment or prevention of an infectious disease.
Opening claim text (preview).
The invention claimed is: 1. A process for preparing a vaccine antigen, comprising a step of fragmenting a biological membrane associated with said vaccine antigen by bringing said biological membrane into contact with at least one calixarene of formula (II): in which: X is a (CH 2 )—CO 2 Y group, and Y is an alkali metal, or a pharmaceutically acceptable salt thereof, wherein said vaccine antigen obtained also comprises a fragment of the biological membrane, said fragment being associated with said antigen, and wherein the vaccine antigen is a membrane protein of flu virus. 2. The process as claimed in claim 1 , wherein Y is sodium. 3. The process as claimed in claim 1 , wherein said biological membrane is derived from the flu virus. 4. The process as claimed in claim 1 , wherein said biological membrane is derived from an embryonated egg. 5. The process as claimed in claim 1 , wherein said vaccine antigen comprises a biological membrane of the flu virus. 6. The process as claimed in claim 1 , wherein said viral origin is chosen from the group comprising: the orthomyxoviridae virus family and the paramyxoviridae virus family. 7. The process as claimed in claim 6 , wherein said flu virus is chosen from influenza viruses A and influenza viruses B. 8. The process as claimed in claim 1 , also comprising a step of dialyzing said vaccine antigen. 9. A vaccine that can be produced by carrying out the process as defined in claim 1 , comprising a calixarene of formula (II) in excipient format in an amount of from 0.1 to 1000 μg in the total weight of the vaccine. 10. The vaccine as claimed in claim 9 , for application thereof as a medicament in the treatment or prevention of an infectious disease. 11. A process for preparing a vaccine antigen, consisting of a step of fragmenting a biological membrane associated with said vaccine antigen by bringing said biological membrane into contact with at least one calixarene of formula (II): in which: X is a (CH 2 )—CO 2 Y group, and Y is an alkali metal, or a pharmaceutically acceptable salt thereof, wherein said vaccine antigen obtained also comprises a fragment of the biological membrane, said fragment being associated with said antigen, and wherein the vaccine antigen is a membrane protein of flu virus.
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