Methods for the induction of ebola virus-specific immune responses comprising administering a replication-defective chimpanzee adenovirus vector expressing the ebola virus glycoprotein
US-9526777-B2 · Dec 27, 2016 · US
US11173201B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11173201-B2 |
| Application number | US-201916655516-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 17, 2019 |
| Priority date | Sep 3, 2014 |
| Publication date | Nov 16, 2021 |
| Grant date | Nov 16, 2021 |
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The present invention provides compositions, vaccines and methods for inducing protective immunity against filovirus infection, particularly protective immunity against infection of one or more subtypes of Ebola viruses and Marburg virus.
Opening claim text (preview).
What is claimed is: 1. A method of inducing a protective immune response against a filovirus in a subject, the method comprising: a. administering to the subject a first composition comprising an immunologically effective amount of an adenovirus vector comprising a nucleic acid encoding an antigenic glycoprotein of a first filovirus subtype, wherein the antigenic glycoprotein has the amino acid sequence of SEQ ID NO:1; and b. administering to the subject a second composition comprising an immunologically effective amount of an MVA vector comprising a nucleic acid encoding antigenic glycoproteins of at least two strains of filovirus subtypes; wherein step (b) is conducted at least 8 weeks after step (a), and wherein the administration of (a) and (b) induces a protective immune response in the subject. 2. The method according to claim 1 wherein the first composition further comprises an adenovirus vector comprising a nucleic acid encoding an antigenic glycoprotein of a second filovirus subtype. 3. The method according to claim 2 , wherein the first composition further comprises an adenovirus vector comprising a nucleic acid encoding an antigenic glycoprotein of a third filovirus subtype. 4. The method according to claim 1 , wherein the first composition further comprises an adenovirus vector comprising a nucleic acid encoding the antigenic protein with SEQ ID NO:2. 5. The method according to claim 4 , wherein the first composition further comprises an adenovirus vector comprising a nucleic acid encoding the antigenic protein with SEQ ID NO:3. 6. The A method according to claim 1 , wherein the MVA vector in the second composition comprises a nucleic acid encoding antigenic proteins of at least four filovirus subtypes. 7. The method according to claim 1 , wherein the MVA vector in the second composition comprises a nucleic acid encoding antigenic proteins from four different filovirus subtypes having the amino acid sequences set forth in SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO: 5. 8. The method according to claim 1 , wherein the adenovirus vectors are rAd26 or rAd35 vectors.
Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title
Demonstrated in vivo effect · CPC title
Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title
humoral response · CPC title
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