WO2022162012A3 - Anticorps ciblant sur un large spectre des coronavirus et leurs utilisations - Google Patents
Anticorps ciblant sur un large spectre des coronavirus et leurs utilisations Download PDFInfo
- Publication number
- WO2022162012A3 WO2022162012A3 PCT/EP2022/051776 EP2022051776W WO2022162012A3 WO 2022162012 A3 WO2022162012 A3 WO 2022162012A3 EP 2022051776 W EP2022051776 W EP 2022051776W WO 2022162012 A3 WO2022162012 A3 WO 2022162012A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- antibodies
- coronaviruses
- relates
- protein
- antigen binding
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/005—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from viruses
- C07K14/08—RNA viruses
- C07K14/165—Coronaviridae, e.g. avian infectious bronchitis virus
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/08—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from viruses
- C07K16/10—RNA viruses
- C07K16/102—Coronaviridae (F)
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/08—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from viruses
- C07K16/10—RNA viruses
- C07K16/102—Coronaviridae (F)
- C07K16/104—Severe acute respiratory syndrome coronavirus 2 [SARS‐CoV‐2]
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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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/33—Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
-
- 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
- C12N2770/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses positive-sense
- C12N2770/00011—Details
- C12N2770/20011—Coronaviridae
- C12N2770/20034—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Virology (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Peptides Or Proteins (AREA)
Abstract
La présente invention concerne des anticorps et des fragments de liaison à l'antigène de ceux-ci, qui se lient à la protéine de spicule (S) des coronavirus. Les anticorps, et des fragments de liaison à l'antigène de ceux-ci, ciblent sur un large spectre des coronavirus, comprenant différents alpha-et bêta-coronavirus. L'invention concerne également des acides nucléiques qui codent pour de tels anticorps et fragments d'anticorps et des cellules qui expriment de tels anticorps et fragments d'anticorps. De plus, l'invention concerne l'utilisation des anticorps et des fragments d'anticorps dans le traitement et le diagnostic d'une infection à coronavirus. En outre, l'invention concerne un peptide, un polypeptide ou une protéine de recombinaison comprenant l'épitope, auquel les anticorps se lient, et pouvant être utile dans la vaccination.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/EP2021/051745 WO2022161598A1 (fr) | 2021-01-26 | 2021-01-26 | Anticorps ciblant largement des coronavirus et leurs utilisations |
| EPPCT/EP2021/051745 | 2021-01-26 | ||
| EP2021078062 | 2021-10-11 | ||
| EPPCT/EP2021/078062 | 2021-10-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2022162012A2 WO2022162012A2 (fr) | 2022-08-04 |
| WO2022162012A3 true WO2022162012A3 (fr) | 2022-09-09 |
Family
ID=80222205
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2022/051776 Ceased WO2022162012A2 (fr) | 2021-01-26 | 2022-01-26 | Anticorps ciblant sur un large spectre des coronavirus et leurs utilisations |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2022162012A2 (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN118440186A (zh) * | 2023-01-05 | 2024-08-06 | 郴州市第一人民医院 | 一种广谱抗SARS-like冠状病毒和/或新冠突变株的抗体及其应用 |
| CN118852420B (zh) * | 2024-08-16 | 2025-11-11 | 东北农业大学 | 一种猪δ冠状病毒中和性单克隆抗体及其应用 |
| CN119592517B (zh) * | 2024-10-08 | 2025-09-19 | 河南农业大学 | 一种抗猪δ冠状病毒S2亚基的单克隆抗体及其杂交瘤细胞株和应用 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100355470B1 (ko) | 1993-11-17 | 2003-02-17 | 도이체 오엠 아르 쯔나이미텔 게엠바하 | 글루코사민이당류,그의제조방법,이를함유하는제약학적조성물,및그의용도 |
| WO1999064301A1 (fr) | 1998-06-08 | 1999-12-16 | Sca Emballage France | Emballage a remise a plat rapide |
| AU761396B2 (en) | 1998-06-30 | 2003-06-05 | Om Pharma | Novel acyl pseudodipeptides, preparation method and pharmaceutical compositions containing same |
| AU1581400A (en) | 1999-12-22 | 2001-07-03 | Om Pharma | Acyl pseudopeptides bearing a functionalised auxiliary spacer |
| EP1597280B2 (fr) | 2003-02-26 | 2016-08-24 | Institute for Research in Biomedicine | Production d'anticorps monoclonaux par transformation de lymphocytes b par le virus d'epstein barr |
| US20090252729A1 (en) | 2007-05-14 | 2009-10-08 | Farrington Graham K | Single-chain Fc (scFc) regions, binding polypeptides comprising same, and methods related thereto |
| NZ592036A (en) | 2008-10-22 | 2012-12-21 | Inst Research In Biomedicine | Methods for producing antibodies from plasma cells |
| US8326547B2 (en) | 2009-10-07 | 2012-12-04 | Nanjingjinsirui Science & Technology Biology Corp. | Method of sequence optimization for improved recombinant protein expression using a particle swarm optimization algorithm |
-
2022
- 2022-01-26 WO PCT/EP2022/051776 patent/WO2022162012A2/fr not_active Ceased
Non-Patent Citations (9)
| Title |
|---|
| ALSAADI ENTEDAR A. J. ET AL: "A Fusion Peptide in the Spike Protein of MERS Coronavirus", VIRUSES, vol. 11, no. 9, 5 September 2019 (2019-09-05), pages 825, XP055917114, Retrieved from the Internet <URL:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784214/pdf/viruses-11-00825.pdf> [retrieved on 20220502], DOI: 10.3390/v11090825 * |
| CHEK MENG POH ET AL: "Two linear epitopes on the SARS-CoV-2 spike protein that elicit neutralising antibodies in COVID-19 patients", NATURE COMMUNICATIONS, vol. 11, no. 1, 1 June 2020 (2020-06-01), XP055746936, DOI: 10.1038/s41467-020-16638-2 * |
| DUAN J ET AL: "A human SARS-CoV neutralizing antibody against epitope on S2 protein", BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, ELSEVIER, AMSTERDAM NL, vol. 333, no. 1, 22 July 2005 (2005-07-22), pages 186 - 193, XP027218787, ISSN: 0006-291X, [retrieved on 20050623], DOI: 10.1016/J.BBRC.2005.05.089 * |
| JONES BRYAN E. ET AL: "Title: LY-CoV555, a rapidly isolated potent neutralizing antibody, provides protection in a non-human primate model of SARS-CoV-2 infection", BIORXIV, 9 October 2020 (2020-10-09), XP055806789, Retrieved from the Internet <URL:https://www.biorxiv.org/content/10.1101/2020.09.30.318972v3.full.pdf> [retrieved on 20210523], DOI: 10.1101/2020.09.30.318972 * |
| LADNER JASON T. ET AL: "Epitope-resolved profiling of the SARS-CoV-2 antibody response identifies cross-reactivity with endemic human coronaviruses", vol. 2, no. 1, 1 January 2021 (2021-01-01), pages 100189, XP055847640, ISSN: 2666-3791, Retrieved from the Internet <URL:https://www.cell.com/cell-reports-medicine/pdfExtended/S2666-3791(20)30244-5> [retrieved on 20211013], DOI: 10.1016/j.xcrm.2020.100189 * |
| PINTO DORA ET AL: "Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody", NATURE, NATURE PUBLISHING GROUP UK, LONDON, vol. 583, no. 7815, 18 May 2020 (2020-05-18), pages 290 - 295, XP037289888, ISSN: 0028-0836, [retrieved on 20200518], DOI: 10.1038/S41586-020-2349-Y * |
| WANG CHUNYAN ET AL: "Isolation of cross-reactive monoclonal antibodies against divergent human coronaviruses that delineate a conserved and vulnerable site on the spike protein", BIORXIV, 20 October 2020 (2020-10-20), pages 1 - 40, XP055916872, Retrieved from the Internet <URL:https://www.biorxiv.org/content/10.1101/2020.10.20.346916v1.full.pdf> [retrieved on 20220502], DOI: 10.1101/2020.10.20.346916 * |
| WEC ANNA Z. ET AL: "Broad neutralization of SARS-related viruses by human monoclonal antibodies", SCIENCE, vol. 369, no. 6504, 15 June 2020 (2020-06-15), US, pages 731 - 736, XP055845076, ISSN: 0036-8075, DOI: 10.1126/science.abc7424 * |
| ZHENG ZHIQIANG ET AL: "Monoclonal antibodies for the S2 subunit of spike of SARS-CoV-1 cross-react with the newly-emerged SARSCoV-2", vol. 25, no. 28, 16 July 2020 (2020-07-16), FR, pages 1560 - 7917, XP055850940, ISSN: 1560-7917, Retrieved from the Internet <URL:https://www.eurosurveillance.org/deliver/fulltext/eurosurveillance/25/28/eurosurv-25-28-4.pdf?itemId=/content/10.2807/1560-7917.ES.2020.25.28.2000291&mimeType=pdf&containerItemId=content/eurosurveillance> [retrieved on 20211013], DOI: 10.2807/1560-7917.ES.2020.25.28.2000291 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2022162012A2 (fr) | 2022-08-04 |
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