Coronavirus Constructs and Vaccines
US-2024252619-A1 · Aug 1, 2024 · US
US12473570B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12473570-B2 |
| Application number | US-202017609496-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 20, 2020 |
| Priority date | May 21, 2019 |
| Publication date | Nov 18, 2025 |
| Grant date | Nov 18, 2025 |
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Provided are Zika virus constructs and methods of using Zika virus constructs and Zika viruses to treat subjects in need thereof.
Opening claim text (preview).
What is claimed is: 1 . A Zika virus construct comprising a Zika virus genome, wherein said Zika virus genome consists of SEQ ID NO: 7, and wherein said Zika virus construct optionally includes a gene that encodes a mutated E protein comprising SEQ ID NO: 1, wherein the amino acid at position 154 of SEQ ID NO: 1 is any amino acid residue other than asparagine. 2 . The Zika virus construct according to claim 1 , wherein said Zika virus construct comprises (a) the gene that encodes the mutated E protein; (b) a nucleic acid sequence that encodes an immunomodulatory agent; or (c) the gene that encodes the mutated E protein and a nucleic acid sequence that encodes an immunomodulatory agent. 3 . The Zika virus construct according to claim 1 , wherein the amino acid at position 154 of SEQ ID NO: 1 is Thr, His, Asp, Tyr, Ser, Leu, or Lys. 4 . The Zika virus construct according to claim 2 , wherein the amino acid at position 154 of SEQ ID NO: 1 is Thr or Asp. 5 . The Zika virus construct according to claim 2 , wherein the immunomodulatory agent is interleukin 2 (IL2), interleukin 15 (IL15), interleukin 18 (IL18), chemokine (C-C) ligand 5 (CCL5), or tumor necrosis factor superfamily member 14 (TNFSF14). 6 . A pharmaceutical composition comprising, consisting essentially of, or consisting of the Zika virus construct according to claim 1 , and a pharmaceutically acceptable carrier. 7 . The pharmaceutical composition according to claim 6 , wherein the pharmaceutical composition comprises a therapeutically effective amount of the Zika virus construct. 8 . A method of treating a cancer and/or aberrant neuroprogenitor cells in a subject, which comprises administering to the subject one or more Zika virus constructs according to claim 1 and/or a pharmaceutical composition comprising the one or more Zika virus constructs. 9 . The method according to claim 8 , wherein a therapeutically effective amount of the Zika virus construct is administered to the subject by subcutaneous delivery, intravenous delivery, intratumoral delivery, intracerebral delivery, and/or intracarotid delivery. 10 . The method according to claim 8 , wherein the Zika virus construct is administered to the subject at a ratio of about 1:1 to about 10:1 of the cells to be treated or infected by the Zika virus and/or the Zika virus construct. 11 . The method according to claim 8 , wherein the cancer is a glioma, a glioblastoma, a neuroblastoma, or a retinoblastoma. 12 . The Zika virus construct according to claim 2 , wherein the nucleic acid sequence that encodes an immunomodulatory agent is SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, or SEQ ID NO: 6.
Demonstrated in vivo effect · CPC title
viral genome or elements thereof as genetic vector · CPC title
Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title
Use of virus as therapeutic agent, other than vaccine, e.g. as cytolytic agent · CPC title
New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes · CPC title
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