MX393649B - Vacunas y anticuerpos contra el dengue - Google Patents
Vacunas y anticuerpos contra el dengueInfo
- Publication number
- MX393649B MX393649B MX2017001017A MX2017001017A MX393649B MX 393649 B MX393649 B MX 393649B MX 2017001017 A MX2017001017 A MX 2017001017A MX 2017001017 A MX2017001017 A MX 2017001017A MX 393649 B MX393649 B MX 393649B
- Authority
- MX
- Mexico
- Prior art keywords
- dimer
- denv
- ede
- envelope
- dengue virus
- Prior art date
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Classifications
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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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
- A61K47/6839—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting material from viruses
- A61K47/6841—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting material from viruses the antibody targeting a RNA virus
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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
- C07K14/18—Togaviridae; Flaviviridae
- C07K14/1816—Flaviviridae, e.g. pestivirus, mucosal disease virus, bovine viral diarrhoea virus, classical swine fever virus (hog cholera virus), border disease virus
- C07K14/1825—Flaviviruses or Group B arboviruses, e.g. yellow fever virus, japanese encephalitis, tick-borne encephalitis, dengue
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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
- C07K16/116—Togaviridae (F); Matonaviridae (F); Flaviviridae (F)
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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
- A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
- A61K2039/525—Virus
- A61K2039/5258—Virus-like particles
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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
- A61K2039/545—Medicinal preparations containing antigens or antibodies characterised by the dose, timing or administration schedule
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- 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
- C07K2317/33—Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
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- 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
- C07K2317/34—Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
-
- 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
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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
- 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
- C12N2770/24011—Flaviviridae
- C12N2770/24111—Flavivirus, e.g. yellow fever virus, dengue, JEV
- C12N2770/24122—New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
-
- 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
- C12N2770/24011—Flaviviridae
- C12N2770/24111—Flavivirus, e.g. yellow fever virus, dengue, JEV
- C12N2770/24134—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Virology (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Gastroenterology & Hepatology (AREA)
- Communicable Diseases (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Peptides Or Proteins (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
La presente invención se refiere a un epítopo del dímero de envoltura (EDE) del virus del dengue, en donde el EDE:c) abarca los polipéptidos de un dímero del polipéptido de envoltura del virus del dengue; y/od) se presenta en un dímero de las proteínas de envoltura; y/oc) se forma de residuos consecutivos o no consecutivos del dímero del polipéptido de envoltura,en donde el dímero es un homodímero o un heterodímero de polipéptidos de envoltura nativos y/o mutantes, de cualquiera de uno o dos de DENV-1, DENV-2, DENV-3 y DENV-4. El EDE puede ser un dímero estabilizado del ectodominio de la glucoproteína E de envoltura del virus del dengue recombinante (sE), en donde el dímero:se estabiliza de manera covalente con al menos un puente de disulfuro intercatenario entre los dos monómeros de sE, y/o se estabiliza de manera covalente con al menos un reticulador que reacciona con sulfhidrilo entre dos monómeros de sE, y/ose estabiliza de manera covalente mediante la unión de dos monómeros de sE a través de azúcares modificados; y/ose estabiliza de manera covalente mediante la formación como una cadena de polipéptidos simple, opcionalmente con una región ligadora, opcionalmente una región ligadora rica en glicina-serina, que separa las secuencias de sE, y/ose estabiliza de manera no covalente mediante la sustitución de al menos un residuo de aminoácido en la secuencia de aminoácidos de al menos un monómero de sE con al menos un aminoácido de la cadena lateral voluminosa, en la interfaz dimérica o en el ligador de dominio 1 (D1) / dominio 3 (D3) de cada monómero.Un compuesto, por ejemplo, un anticuerpo o un fragmento de anticuerpo que puede neutralizar más de un serotipo del virus del dengue, por ejemplo, un anticuerpo que se puede fijar a un EDE de la invención.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1413086.8A GB201413086D0 (en) | 2014-07-23 | 2014-07-23 | Methods |
| PCT/GB2015/052139 WO2016012800A1 (en) | 2014-07-23 | 2015-07-23 | Anti-dengue vaccines and antibodies |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MX2017001017A MX2017001017A (es) | 2017-08-10 |
| MX393649B true MX393649B (es) | 2025-03-21 |
Family
ID=51495027
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2017001017A MX393649B (es) | 2014-07-23 | 2015-07-23 | Vacunas y anticuerpos contra el dengue |
Country Status (7)
| Country | Link |
|---|---|
| US (3) | US11198706B2 (es) |
| EP (3) | EP3172229B1 (es) |
| JP (3) | JP7433744B2 (es) |
| CA (1) | CA2988499A1 (es) |
| GB (1) | GB201413086D0 (es) |
| MX (1) | MX393649B (es) |
| WO (1) | WO2016012800A1 (es) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK3059246T3 (en) | 2007-09-26 | 2018-10-01 | Chugai Pharmaceutical Co Ltd | Modified constant region of an antibody |
| GB201413086D0 (en) * | 2014-07-23 | 2014-09-03 | Imp Innovations Ltd And Inst Pasteur | Methods |
| WO2016125495A1 (en) | 2015-02-05 | 2016-08-11 | Chugai Seiyaku Kabushiki Kaisha | Antibodies comprising an ion concentration dependent antigen-binding domain, fc region variants, il-8-binding antibodies, and uses therof |
| EP3359652A1 (en) * | 2015-10-07 | 2018-08-15 | The University of North Carolina at Chapel Hill | Methods and compositions for dengue virus vaccines and diagnostistics |
| WO2017142831A1 (en) * | 2016-02-16 | 2017-08-24 | Albert Einstein College Of Medicine, Inc. | Dengue virus glycoprotein e diii variants and uses thereof |
| GB2550418A (en) | 2016-05-20 | 2017-11-22 | Laing Peter | An improved vaccine against flaviviruses avoiding elicitation or stimulation of infection-enhancing antibodies |
| MX374731B (es) | 2016-06-06 | 2025-03-06 | Univ Wien Med | Método para la detección de un anticuerpo igm específico para un flavivirus en una muestra. |
| GB201610162D0 (en) * | 2016-06-10 | 2016-07-27 | Imp Innovations Ltd And Inst Pasteur | Methods |
| CN109689099B (zh) | 2016-08-05 | 2023-02-28 | 中外制药株式会社 | 用于预防或治疗il-8相关疾病的组合物 |
| SG10201607778XA (en) | 2016-09-16 | 2018-04-27 | Chugai Pharmaceutical Co Ltd | Anti-Dengue Virus Antibodies, Polypeptides Containing Variant Fc Regions, And Methods Of Use |
| JP2020500007A (ja) | 2016-10-13 | 2020-01-09 | マサチューセッツ インスティテュート オブ テクノロジー | ジカウイルスエンベロープタンパク質に結合する抗体およびその使用 |
| US20190358313A1 (en) * | 2016-12-23 | 2019-11-28 | Expres2Ion Biotechnologies Aps | New flavivirus vaccine |
| IL277375B2 (en) | 2018-03-15 | 2025-08-01 | Chugai Pharmaceutical Co Ltd | Anti-dengue virus antibodies having cross-reactivity to zika virus and methods of use |
| EP4477230A3 (en) * | 2019-08-06 | 2025-05-14 | The University of North Carolina at Chapel Hill | Methods and compositions for stabilized recombinant flavivirus e protein dimers |
| US20250188154A1 (en) * | 2020-09-15 | 2025-06-12 | Duke University | Coronavirus antibodies and uses thereof |
| GB2603567B (en) * | 2021-02-03 | 2024-11-20 | D Silver Joshua | Viral load tester and applications thereof |
| WO2025101126A1 (en) * | 2023-11-06 | 2025-05-15 | Agency For Science, Technology And Research | Modified flavivirus polypeptide and uses thereof |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999006068A2 (en) * | 1997-07-31 | 1999-02-11 | Hawaii Biotechnology Group, Inc. | Recombinant dimeric envelope vaccine against flaviviral infection |
| CA2441986A1 (en) | 2001-03-27 | 2002-10-03 | Massachusetts Institute Of Technology | Methods and products related to fgf dimerization |
| JP4990621B2 (ja) * | 2003-07-02 | 2012-08-01 | ピーティーシー セラピューティクス,インコーポレーテッド | Rnaプロセシングタンパク質複合体及びその使用 |
| CA2894300A1 (en) * | 2003-12-08 | 2005-06-23 | The Government Of The United States Of America, As Represented By The Secreatary, Department Of Health And Human Services | Monoclonal antibodies that bind or neutralize dengue virus |
| CA2567741A1 (en) | 2004-05-25 | 2006-03-30 | Chimeracore, Inc. | Self-assembling nanoparticle drug delivery system |
| EP1948688A2 (en) | 2005-11-14 | 2008-07-30 | Psma Development Company, L.L.C. | Compositions of and methods of using stabilized psma dimers |
| DK2257624T5 (da) | 2008-02-05 | 2012-09-10 | Medical Res Council | Fremgangsmåder og sammensætninger |
| US7923016B2 (en) | 2008-02-27 | 2011-04-12 | Medical College Of Wisconsin | Engineered CXCL12 α locked dimer polypeptide |
| US20120315270A1 (en) | 2009-10-21 | 2012-12-13 | The United States Of America, As Represented By The | Rsv immunogens, antibodies and compositions thereof |
| KR20130138789A (ko) * | 2010-10-29 | 2013-12-19 | 머크 샤프 앤드 돔 코포레이션 | 재조합 서브유닛 뎅기 바이러스 백신 |
| EP2834265A4 (en) * | 2012-04-02 | 2015-10-14 | Univ North Carolina | METHOD AND COMPOSITIONS FOR DENGUE VIRUS EPITOPES |
| US9267114B2 (en) | 2012-11-07 | 2016-02-23 | Southern Research Institute | Flavivirus envelope protein mutations affecting virion disassembly |
| GB201413086D0 (en) * | 2014-07-23 | 2014-09-03 | Imp Innovations Ltd And Inst Pasteur | Methods |
-
2014
- 2014-07-23 GB GBGB1413086.8A patent/GB201413086D0/en not_active Ceased
-
2015
- 2015-07-23 EP EP15781974.9A patent/EP3172229B1/en active Active
- 2015-07-23 EP EP23196992.4A patent/EP4282483A3/en active Pending
- 2015-07-23 CA CA2988499A patent/CA2988499A1/en active Pending
- 2015-07-23 JP JP2017524124A patent/JP7433744B2/ja active Active
- 2015-07-23 US US15/328,441 patent/US11198706B2/en active Active
- 2015-07-23 EP EP23165672.9A patent/EP4223773A3/en active Pending
- 2015-07-23 WO PCT/GB2015/052139 patent/WO2016012800A1/en not_active Ceased
- 2015-07-23 MX MX2017001017A patent/MX393649B/es unknown
-
2021
- 2021-10-26 US US17/510,930 patent/US12415836B2/en active Active
-
2023
- 2023-12-08 JP JP2023207737A patent/JP2024037829A/ja active Pending
-
2025
- 2025-07-24 US US19/278,838 patent/US20260055145A1/en active Pending
- 2025-07-31 JP JP2025127851A patent/JP2025172747A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JP2017529096A (ja) | 2017-10-05 |
| JP7433744B2 (ja) | 2024-02-20 |
| WO2016012800A1 (en) | 2016-01-28 |
| US20260055145A1 (en) | 2026-02-26 |
| JP2024037829A (ja) | 2024-03-19 |
| EP3172229A1 (en) | 2017-05-31 |
| US20180037611A1 (en) | 2018-02-08 |
| US11198706B2 (en) | 2021-12-14 |
| EP4282483A3 (en) | 2024-09-11 |
| US12415836B2 (en) | 2025-09-16 |
| EP4282483A2 (en) | 2023-11-29 |
| US20220127307A1 (en) | 2022-04-28 |
| JP2025172747A (ja) | 2025-11-26 |
| CA2988499A1 (en) | 2016-01-28 |
| BR112017001340A2 (pt) | 2017-11-14 |
| EP4223773A2 (en) | 2023-08-09 |
| MX2017001017A (es) | 2017-08-10 |
| EP3172229B1 (en) | 2023-05-10 |
| EP4223773A3 (en) | 2023-12-06 |
| GB201413086D0 (en) | 2014-09-03 |
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