Antiviral agent, abzyme, primer set, method for producing polynucleotide, and method for producing polypeptide

US9365637B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9365637-B2
Application numberUS-201113579529-A
CountryUS
Kind codeB2
Filing dateFeb 21, 2011
Priority dateFeb 19, 2010
Publication dateJun 14, 2016
Grant dateJun 14, 2016

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  1. Title

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  2. Abstract

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

The present invention provides: a novel antiviral agent containing a human antibody κ light chain, a novel human abzyme containing a human antibody κ light chain; a polynucleotide, a vector, and a transformant, encoding a human antibody κ light chain of the above; a primer set for effectively obtaining a human antibody κ light chain having a function as an antiviral agent or abzyme; and a method for producing a polynucleotide and a method for producing a polypeptide, each of which method utilizes the primer set.

First claim

Opening claim text (preview).

The invention claimed is: 1. A human abzyme comprising one of the following (a) through (f): (a) a human antibody kappa (κ) light chain with a variable domain consisting of SEQ ID NO: 26, and a constant domain with an Ala in the position corresponding to Cys219 in the amino acid sequence shown in SEQ ID NO: 24; (b) a human antibody kappa (κ) light chain with a variable domain consisting of SEQ ID NO: 14, and a constant domain with an Ala in the position corresponding to Cys220 in the amino acid sequence shown in SEQ ID NO: 1; (c) a human antibody kappa (κ) light chain with a variable domain consisting of SEQ ID NO: 50, and a constant domain with an Ala in the position corresponding to Cys220 in the amino acid sequence shown in SEQ ID NO: 48; (d) a human antibody kappa (κ) light chain with a variable domain consisting of SEQ ID NO: 35, and a constant domain with an Ala in the position corresponding to Cys219 in the amino acid sequence shown in SEQ ID NO: 33; (e) a human antibody kappa (κ) light chain with a variable domain consisting of SEQ ID NO: 54, and a constant domain with an Ala in the position corresponding to Cys219 in the amino acid sequence shown in SEQ ID NO: 52; or (f) a human antibody kappa (κ) light chain with a variable domain consisting of SEQ ID NO: 22, and a constant domain with an Ala in the position corresponding to Cys219 in the amino acid sequence shown in SEQ ID NO: 20. 2. The human abzyme as set forth in claim 1 , wherein: the human abzyme has an anti rhabdovirus activity, and anti influenza virus activity; and the variable domain consists of SEQ ID NO: 26, the constant domain has an Ala in the position corresponding to Cys219 in the amino acid sequence shown in SEQ ID NO: 20. 3. The human abzyme as set forth in claim 1 , wherein: the human abzyme has an anti rhabdovirus activity, anti influenza virus activity, and cytotoxicity against cancer cells; and the variable domain consists SEQ ID NO: 14, the constant domain has an Ala in the position corresponding to Cys220 in the amino acid sequence shown in SEQ ID NO: 1. 4. The human abzyme as set forth in claim 1 , wherein: the human abzyme has an anti influenza virus activity and nucleolytic activity; and the variable domain consists of SEQ ID NO: 50, the constant domain has an Ala in the position corresponding to Cys220 in the amino acid sequence shown in SEQ ID NO: 48. 5. The human abzyme as set forth in claim 1 , wherein: the human abzyme has an anti influenza virus activity; and the variable domain consists of SEQ ID NO: 35, the constant domain has an Ala in the position corresponding to Cys219 in the amino acid sequence shown in SEQ ID NO: 33. 6. The human abzyme as set forth in claim 1 , wherein: the human abzyme has an anti influenza virus activity; and the variable domain consists of SEQ ID NO: 54, the constant domain has an Ala in the position corresponding to Cys219 in the amino acid sequence shown in SEQ ID NO: 52. 7. The human abzyme as set forth in claim 1 , wherein: the human abzyme has an anti rhabdovirus activity; and the variable domain consists of SEQ ID NO: 22, the constant domain has an Ala in the position corresponding to Cys219 in the amino acid sequence shown in SEQ ID NO: 20. 8. A method for treating a patient of a rhabdovirus infectious disease by administering a human abzyme comprising a human antibody kappa (κ) light chain with a variable domain consisting of SEQ ID NO: 26, 14, 30, or 22 to the patient, wherein the administering does not comprise administering a human antibody heavy chain. 9. A method for treating a patient of an influenza virus infectious disease by administering a human abzyme comprising a human antibody kappa (κ) light chain with a variable domain consisting of SEQ ID NO: 26, 14, 50, 35 or 54 to the patient.

Assignees

Inventors

Classifications

  • for RNA viruses · CPC title

  • Antivirals · CPC title

  • for influenza or rhinoviruses · CPC title

  • characterized by aspects of specificity or valency · CPC title

  • Complete light chain, i.e. VL + CL · CPC title

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Frequently asked questions

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What does patent US9365637B2 cover?
The present invention provides: a novel antiviral agent containing a human antibody κ light chain, a novel human abzyme containing a human antibody κ light chain; a polynucleotide, a vector, and a transformant, encoding a human antibody κ light chain of the above; a primer set for effectively obtaining a human antibody κ light chain having a function as an antiviral agent or abzyme; and a metho…
Who is the assignee on this patent?
Uda Taizo, Hifumi Emi, Nishizono Akira, and 2 more
What technology area does this patent fall under?
Primary CPC classification C07K16/10. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).