WO2021062212A4 - Vaccines and immunoglobulins targeting african swine fever virus, methods of preparing same, and methods of using same - Google Patents
Vaccines and immunoglobulins targeting african swine fever virus, methods of preparing same, and methods of using same Download PDFInfo
- Publication number
- WO2021062212A4 WO2021062212A4 PCT/US2020/052805 US2020052805W WO2021062212A4 WO 2021062212 A4 WO2021062212 A4 WO 2021062212A4 US 2020052805 W US2020052805 W US 2020052805W WO 2021062212 A4 WO2021062212 A4 WO 2021062212A4
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- WIPO (PCT)
- Prior art keywords
- asf
- virus particles
- naturally expressed
- viral components
- asfv
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/08—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses
- C07K16/081—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses from DNA viruses
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/12—Viral antigens
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N7/00—Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
- A61K2039/525—Virus
- A61K2039/5252—Virus inactivated (killed)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/55—Medicinal preparations containing antigens or antibodies characterised by the host/recipient, e.g. newborn with maternal antibodies
- A61K2039/552—Veterinary vaccine
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
- C12N2710/00011—Details
- C12N2710/12011—Asfarviridae
- C12N2710/12021—Viruses as such, e.g. new isolates, mutants or their genomic sequences
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
- C12N2710/00011—Details
- C12N2710/12011—Asfarviridae
- C12N2710/12034—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Immunology (AREA)
- Medicinal Chemistry (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pharmacology & Pharmacy (AREA)
- Molecular Biology (AREA)
- Animal Behavior & Ethology (AREA)
- Mycology (AREA)
- Biophysics (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Biotechnology (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- General Engineering & Computer Science (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
The present disclosure provides a method of isolating and preparing live African Swine Fever (ASF) viruses (ASFV) and an ASFV vaccine composed of whole ASF virus particles, viral components, and/or immunosuppressive protein factors. The ASFV vaccine can be used to immunize pigs and wild boars, or can be used to immunize species other than pig or wild boar, such as fowl, bovine, goat, rabbit, donkey or horse, to generate polyclonal immunoglobulins with broad-spectrum specificity to the ASFV. The ASFV-specific immunoglobulins then can be extracted and purified. The ASFV-specific immunoglobulins can provide acute treatment of ASF-infected pigs or wild boars or preventative treatment for pigs or wild boars at risk of ASF, for example that may have been exposed to ASFV or ASFV-infected subjects.
Claims
AMENDED CLAIMS received by the International Bureau on 26 April 2021 (26.04.2021)
Claim 1 : A method of treating African swine fever (ASF) viral (ASFV) infection in an infected pig or wild boar, the method comprising administering to the infected pig or wild boar an effective amount of a composition comprising IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors.
Claim 2: The method of Claim 1, wherein the composition is administered in an amount that provides a dose of the IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors that is about 0.5 mg to about 1.0 mg per kg body weight of the infected pig or wild boar.
Claim 3 : The method of Claim 1 , wherein the composition comprising the IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors is administered for a time period comprising at least once per week or 7 consecutive days.
Claim 4: The method of Claim 1, wherein the composition comprising the IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors is administered parenterally by intramuscular or intraperitoneal injection.
Claim 5: The method of Claim 1, wherein the composition comprising the IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors is a food product administered orally.
Claim 6: A method of preventing, decreasing incidence of, and/or decreasing severity of ASF viral infection in a pig or wild boar at risk thereof, the method comprising administering to the pig or wild boar an effective amount of a composition comprising IgY immunoglobulins
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specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors.
Claim 7: The method of Claim 6, wherein the composition is administered in an amount that provides a dose of the IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors that is about 0.5 to about 1.0 mg per kg of body weight of the pig or wild boar at risk thereof.
Claim 8: The method of Claim 6, wherein the composition comprising the IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors is administered for a time period comprising at least once per week or 7 consecutive days.
Claim 9: The method of Claim 6, wherein the composition comprising the IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors is administered parenterally.
Claim 10: The method of Claim 6, wherein the composition comprising the IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors is a food product administered orally.
Claim 11: A method of producing ASFV-specific immunoglobulins wherein a ASFV vaccine comprised of whole live ASF virus particles, naturally expressed ASF viral components, and/or immunosuppressive protein factors, is administered to a non-swine species host for ASFV-specific immunoglobulin production.
Claim 12: The method of Claim 11, wherein the host is an egg-laying fowl.
Claim 13: A unit dosage form comprising a therapeutically or prophylactically effective amount of a composition comprising IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors.
Claim 14: The unit dosage form of Claim 13, wherein the composition is a food product formulated for oral administration.
Claim 15: A method of preventing, decreasing incidence of, and/or decreasing severity of ASF viral infection in a pig or wild boar at risk thereof, the method comprising administering to the pig or wild boar an effective amount of an ASFV vaccine composition comprising (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors.
Claim 16: The method of Claim 15, wherein the naturally expressed ASF viral components and whole live ASF virus particles are inactiv[e]ated using gamma irradiation.
Claim 17: The method of Claim 15, wherein the ASFV vaccine composition is administered parenterally by intramuscular or intraperitoneal injection.
Claim 18: The method of Claim 15, wherein the ASFV vaccine composition is administered in an amount that provides a dose of the naturally expressed ASF viral components that is about 0.05 mg to about 1.0 mg per pig or wild boar.
Claim 19: A unit dosage form comprising an effective amount of an ASFV vaccine composition comprising naturally expressed ASF viral components, whole live ASF virus particles, and/or immunosuppressive protein factors.
Claim 20: The unit dosage form of Claim 19, wherein the naturally expressed ASF viral components and whole live ASF virus particles are derived from ASF-infected spleen mononuclear cells (SMNCs), ASF-infected peripheral blood and mononuclear cells (PBMCs), and/or ASF-infected primary alveolar macrophages (PAMs).
Claim 21: The unit dosage form of Claim 19, wherein the naturally expressed ASF viral components are inactivated using gamma irradiation.
Claim 22: ASFV vaccine, comprising IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors for use in the treatment and/or prevention of ASF infection in a pig or wild boar at risk thereof.
Claim 23: A composition comprising IgY immunoglobulins specific against (a) naturally expressed ASF viral components, (b) whole live ASF virus particles, and/or (c) immunosuppressive protein factors for use in the treatment and/or prevention of ASF infection in a pig or wild boar at risk thereof.
Claim 24: The method of Claim 1, wherein the naturally expressed ASF viral components, whole live ASF virus particles, and/or immunosuppressive protein factors are derived from cells, tissues, and/or organs of an ASFV-infected pig or wild boar.
Claim 25: The method of Claim 1, wherein the naturally expressed ASF viral components and whole live ASF virus particles are inactivated by gamma irradiation.
Claim 26: The method of Claim 6, wherein the naturally expressed ASF viral components, whole live ASF virus particles, and/or immunosuppressive protein factors are derived from cells, tissues, and/or organs of an ASFV-infected pig or wild boar.
Claim 27: The method of Claim 11, wherein the naturally expressed ASF viral components, whole live ASF virus particles, and/or immunosuppressive protein factors are derived from cells, tissues, and/or organs of an ASFV-infected pig or wild boar.
Claim 28: The method of Claim 13, wherein the naturally expressed ASF viral components, whole live ASF virus particles, and/or immunosuppressive protein factors are derived from cells, tissues, and/or organs of an ASFV-infected pig or wild boar.
Claim 29: The method of Claim 13, wherein the naturally expressed ASF viral components and whole live ASF virus particles are inactivated by gamma irradiation.
Claim 30: The unit dosage form of Claim 19, wherein the naturally expressed ASF viral components, whole live ASF virus particles, and/or immunosuppressive protein factors are derived from ASF-infected spleen mononuclear cells (SMNCs) and/or ASF-infected peripheral blood and mononuclear cells (PBMCs).
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Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202080080011.9A CN114746110A (en) | 2019-09-26 | 2020-09-25 | Vaccine and immunoglobulin targeting African swine fever virus, and methods of making and using the same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201962906357P | 2019-09-26 | 2019-09-26 | |
US62/906,357 | 2019-09-26 |
Publications (2)
Publication Number | Publication Date |
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WO2021062212A1 WO2021062212A1 (en) | 2021-04-01 |
WO2021062212A4 true WO2021062212A4 (en) | 2021-05-20 |
Family
ID=75166857
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/US2020/052805 WO2021062212A1 (en) | 2019-09-26 | 2020-09-25 | Vaccines and immunoglobulins targeting african swine fever virus, methods of preparing same, and methods of using same |
Country Status (3)
Country | Link |
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CN (1) | CN114746110A (en) |
TW (1) | TW202126328A (en) |
WO (1) | WO2021062212A1 (en) |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PL2275132T3 (en) * | 2005-12-29 | 2021-09-13 | Boehringer Ingelheim Animal Health USA Inc. | Multivalent PCV2 immunogenic compositions and methods of producing them |
WO2015091322A1 (en) * | 2013-12-18 | 2015-06-25 | Boehringer Ingelheim Vetmedica Gmbh | Cd2 deficient african swine fever virus as live attenuated or subsequently inactivated vaccine against african swine fever in mammals |
CN104262484A (en) * | 2014-10-17 | 2015-01-07 | 深圳出入境检验检疫局动植物检验检疫技术中心 | Specific IgY antibody for resisting African swine fever virus as well as preparation method and application thereof |
WO2017096341A2 (en) * | 2015-12-04 | 2017-06-08 | The Texas A&M University System | Adenovirus-vectored multivalent vaccine |
WO2018086686A1 (en) * | 2016-11-09 | 2018-05-17 | Probiogen Ag | Novel porcine cell line for virus production |
CN109734810A (en) * | 2019-01-24 | 2019-05-10 | 深圳市雅臣智能生物工程有限公司 | Anti- African swine fever virus and CD dual-target pig source antibody, the preparation method and application |
CN110845604B (en) * | 2019-11-22 | 2020-05-26 | 苏州世诺生物技术有限公司 | African swine fever preventing and/or treating neutralizing antibody, preparation method and application thereof |
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2020
- 2020-09-25 WO PCT/US2020/052805 patent/WO2021062212A1/en active Application Filing
- 2020-09-25 TW TW109133411A patent/TW202126328A/en unknown
- 2020-09-25 CN CN202080080011.9A patent/CN114746110A/en active Pending
Also Published As
Publication number | Publication date |
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TW202126328A (en) | 2021-07-16 |
CN114746110A (en) | 2022-07-12 |
WO2021062212A1 (en) | 2021-04-01 |
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