DK2731967T3 - Humane bindingsmolekyler, der er i stand til at neutralisere influenza a-virus fra fylogenetisk gruppe 1 og fylogenetisk gruppe 2 og influenza b-virus - Google Patents

Humane bindingsmolekyler, der er i stand til at neutralisere influenza a-virus fra fylogenetisk gruppe 1 og fylogenetisk gruppe 2 og influenza b-virus Download PDF

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DK2731967T3
DK2731967T3 DK12735516.2T DK12735516T DK2731967T3 DK 2731967 T3 DK2731967 T3 DK 2731967T3 DK 12735516 T DK12735516 T DK 12735516T DK 2731967 T3 DK2731967 T3 DK 2731967T3
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seq
influenza
binding
region
heavy chain
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DK12735516.2T
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Theodorus Hendrikus Jacobus Kwaks
David A T M Zuijdgeest
Ronald Vogels
Robert Heinz Edward Friesen
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Janssen Vaccines & Prevention Bv
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    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/08Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses
    • C07K16/10Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses from RNA viruses
    • C07K16/1018Orthomyxoviridae, e.g. influenza virus
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    • C07K16/10Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses from RNA viruses
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    • GPHYSICS
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    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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    • G01N33/569Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
    • G01N33/56983Viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
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    • C07ORGANIC CHEMISTRY
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    • C07K2317/00Immunoglobulins specific features
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    • C07ORGANIC CHEMISTRY
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    • C07K2317/00Immunoglobulins specific features
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    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
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    • C07K2317/00Immunoglobulins specific features
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    • C07K2317/90Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
    • C07K2317/92Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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    • G01N2333/005Assays involving biological materials from specific organisms or of a specific nature from viruses
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    • G01N2333/11Orthomyxoviridae, e.g. influenza virus

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Claims (7)

1. Isoleret antistof eller antigenbindende fragment deraf, der er i stand til at binde specifikt til en epitop i stilkregionen af hæmagglutininproteinet (HA) fra influenza A-virusundertyper af fylogenetisk gruppe 1 og influenza A-virusundertyper af fylogenetisk gruppe 2-undertyper og er i stand til at neutralisere mindst en eller flere gruppe 1- influenza A-virusundertyper udvalgt fra gruppen, der består af influenza A-virus, der omfatter HA af Hl-, H2-, H5-, H6-, H8-, H9- og Hl1-undertypen, og mindst en eller flere gruppe 2- influenza A-virusundertyper udvalgt fra gruppen, der består af influenza A-virus, der omfatter HA af H3-, H4-, H7- og H10- undertypen, der er kendetegnet ved, at antistoffet eller det antigenbindende fragment deraf også er i stand til at binde specifikt til hæmagglutininproteinet (HA) fra influenza B-virusundertyper.
2. Antistof eller antigenbindende fragment deraf ifølge krav 1, hvor antistoffet eller det antigenbindende fragment deraf ikke har nogen hæmagglutinationshæmmende aktivitet.
3. Antistof eller antigenbindende fragment deraf ifølge et hvilket som helst af ovennævnte krav, hvor antistoffet eller det antigenbindende fragment deraf er udvalgt fra gruppen, der består af: et antistof eller et antigenbindende fragment deraf, der omfatter en tung kædes CDRl-region ifølge SEQ ID NO: 139, en tung kædes CDR2-region ifølge SEQ ID NO: 134 og en tung kædes CDR3-region ifølge SEQ ID NO: 145 og en let kædes CDRl-region ifølge SEQ ID NO: 146, en let kædes CDR2-region ifølge SEQ ID NO: 174 og en let kædes CDR3-region ifølge SEQ ID NO: 147, en tung kædes CDRl-region ifølge SEQ ID NO: 139, en tung kædes CDR2-region ifølge SEQ ID NO: 134 og en tung kædes CDR3-region ifølge SEQ ID NO: 145 og en let kædes CDRl-region ifølge SEQ ID NO: 148, en let kædes CDR2-region ifølge SEQ ID NO: 149 og en let kædes CDR3-region ifølge SEQ ID NO: 150, en tung kædes CDRl-region ifølge SEQ ID NO: 139, en tung kædes CDR2-region ifølge SEQ ID NO: 134 og en tung kædes CDR3-region ifølge SEQ ID NO: 145 og en let kædes CDRl-region ifølge SEQ ID NO: 142, en let kædes CDR2-region ifølge SEQ ID NO: 143 og en let kædes CDR3-region ifølge SEQ ID NO: 173; et antistof eller et antigenbindende fragment deraf, der omfatter en tung kædes CDRl-region ifølge SEQ ID NO: 139, en tung kædes CDR2-region ifølge SEQ ID NO: 134 og en tung kædes CDR3-region ifølge SEQ ID NO: 152 og en let kædes CDRl-region ifølge SEQ ID NO: 148, en let kædes CDR2-region ifølge SEQ ID NO: 149 og en let kædes CDR3-region ifølge SEQ ID NO: 150, en tung kædes CDRl-region ifølge SEQ ID NO: 139, en tung kædes CDR2-region ifølge SEQ ID NO: 134 og en tung kædes CDR3-region ifølge SEQ ID NO: 152 og en let kædes CDRl-region ifølge SEQ ID NO: 156, en let kædes CDR2-region ifølge SEQ ID NO: 157 og en let kædes CDR3-region ifølge SEQ ID NO: 158, en tung kædes CDRl-region ifølge SEQ ID NO: 139, en tung kædes CDR2-region ifølge SEQ ID NO: 130 og en tung kædes CDR3-region ifølge SEQ ID NO: 152 og en let kædes CDRl-region ifølge SEQ ID NO: 171, en let kædes CDR2-region ifølge SEQ ID NO: 164 og en let kædes CDR3-region ifølge SEQ ID NO: 172 og en tung kædes CDRl-region ifølge SEQ ID NO: 139, en tung kædes CDR2-region ifølge SEQ ID NO: 134 og en tung kædes CDR3-region ifølge SEQ ID NO:152 og en let kædes CDRl-region ifølge SEQ ID NO: 142, en let kædes CDR2-region ifølge SEQ ID NO: 143 og en let kædes CDR3-region ifølge SEQ ID NO: 144.
4. Nukleinsyremolekyle, der koder for et antistof eller et antigenbindende fragment deraf ifølge et hvilket som helst af kravene 1-3.
5. Antistof eller antigenbindende fragment deraf ifølge et hvilket som helst af kravene 1-3 og/eller et nukleinsyremolekyle ifølge krav 4 til anvendelse som et medikament.
6. Antistof eller antigenbindende fragment deraf ifølge krav 5 til anvendelse til profylaktisk og/eller terapeutisk behandling af influenzainfektion.
7. Farmaceutisk sammensætning, der omfatter et antistof eller et antigenbindende fragment deraf ifølge et hvilket som helst af kravene 1-3 og/eller et nukleinsyremolekyle ifølge krav 4 og et farmaceutisk acceptabelt excipiens.
DK12735516.2T 2011-07-14 2012-07-12 Humane bindingsmolekyler, der er i stand til at neutralisere influenza a-virus fra fylogenetisk gruppe 1 og fylogenetisk gruppe 2 og influenza b-virus DK2731967T3 (da)

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US201161572417P 2011-07-14 2011-07-14
EP11173953 2011-07-14
PCT/EP2012/063637 WO2013007770A1 (en) 2011-07-14 2012-07-12 Human binding molecules capable of neutralizing influenza a viruses of phylogenetic group 1 and phylogenetic group 2 and influenza b viruses

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US (2) US8961978B2 (da)
EP (1) EP2731967B1 (da)
JP (1) JP5683752B2 (da)
KR (1) KR101941724B1 (da)
CN (1) CN103906763B (da)
AU (1) AU2012282504B2 (da)
BR (1) BR112014000263B1 (da)
CA (1) CA2838999C (da)
DK (1) DK2731967T3 (da)
EA (1) EA027054B1 (da)
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HR (1) HRP20161740T1 (da)
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MY166282A (en) 2018-06-25
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KR20140095017A (ko) 2014-07-31
CN103906763A (zh) 2014-07-02
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