Broadly neutralizing human immunodeficiency virus type 1 (HIV-1) GP120-specific monoclonal antibody

US10087239B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10087239-B2
Application numberUS-201615152630-A
CountryUS
Kind codeB2
Filing dateMay 12, 2016
Priority dateAug 31, 2010
Publication dateOct 2, 2018
Grant dateOct 2, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The invention provides a method for obtaining a broadly neutralizing antibody (bNab), including screening memory B cell cultures from a donor PBMC sample for neutralization activity against a plurality of HIV-1 species, cloning a memory B cell that exhibits broad neutralization activity; and rescuing a monoclonal antibody from that memory B cell culture. The resultant monoclonal antibodies may be characterized by their ability to selectively bind epitopes from the Env proteins in native or monomeric form, as well as to inhibit infection of HIV-1 species from a plurality of clades. Compositions containing human monoclonal anti-HIV antibodies used for prophylaxis, diagnosis and treatment of HIV infection are provided. Methods for generating such antibodies by immunization using epitopes from conserved regions within the variable loops of gp120 are provided. Immunogens for generating anti-HIV1 bNAbs are also provided. Furthermore, methods for vaccination using suitable epitopes are provided.

First claim

Opening claim text (preview).

What is claimed is: 1. An immortalized B cell clone expressing a PGT-121 monoclonal antibody comprising a light chain sequence of SEQ ID NO: 148 and a heavy sequence of SEQ ID NO: 66. 2. One or more vectors containing and expressing a PGT-121 light chain sequence of SEQ ID NO: 148 and/or a PGT-121 heavy chain sequence of SEQ ID NO: 66. 3. One or more vectors containing a nucleic acid comprising a PGT-121 light chain sequence of SEQ ID NO.: 146 and/or a PGT-121 heavy chain sequence of SEQ ID NO.: 62. 4. The one or more vectors of claim 2 or 3 , wherein one vector encodes the light chain sequence and another vector encodes the heavy chain sequence. 5. The one or more vectors of claim 2 or 3 , wherein one vector encodes the light chain sequence and the heavy chain sequence. 6. The one or more vectors of claim 2 or 3 , wherein the vector is an adeno-associated virus vector. 7. An isolated or purified cell containing and expressing the one or more vectors of claim 2 or 3 .

Assignees

Inventors

Classifications

  • Lentivirus (G), e.g. human immunodeficiency virus [HIV], feline immunodeficiency virus [FIV] or simian immunodeficiency virus [SIV] · CPC title

  • Env proteins, e.g. gp41, gp110/120, gp160, V3, principal neutralising domain [PND] or CD4-binding site · CPC title

  • Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value · CPC title

  • Retroviridae, e.g. equine infectious anemia virus · CPC title

  • comprising antibodies · CPC title

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What does patent US10087239B2 cover?
The invention provides a method for obtaining a broadly neutralizing antibody (bNab), including screening memory B cell cultures from a donor PBMC sample for neutralization activity against a plurality of HIV-1 species, cloning a memory B cell that exhibits broad neutralization activity; and rescuing a monoclonal antibody from that memory B cell culture. The resultant monoclonal antibodies may …
Who is the assignee on this patent?
Theraclone Sciences Inc, Scripps Research Inst, Int Aids Vaccine Initiative
What technology area does this patent fall under?
Primary CPC classification C07K16/1145. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 02 2018 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 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).