Gram-positive bacteria specific binding compounds

US2016168232A9 · US · A9

Patent metadata
FieldValue
Publication numberUS-2016168232-A9
Application numberUS-201313786206-A
CountryUS
Kind codeA9
Filing dateMar 5, 2013
Priority dateJul 15, 2009
Publication dateJun 16, 2016
Grant date

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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 present invention provides improved binding compounds capable of specifically binding Gram-positive bacteria. Binding compounds are provided that are fully human, enabling therapeutic applications in human individuals.

First claim

Opening claim text (preview).

1 - 43 . (canceled) 44 . An antibody or functional part thereof capable of binding a serine-aspartate (SD) repeat-dependent epitope. 45 . The antibody of claim 44 , wherein the SD repeat epitope is a domain of an SD repeat (sdr) protein. 46 . The antibody of claim 45 , wherein the sdr protein is located on the surface of a bacterium. 47 . The antibody of claim 45 , wherein the sdr protein is anchored to the peptidoglycan cell wall of a gram-positive bacterium. 48 . The antibody of claim 47 , wherein the gram positive bacterium is a Staphylococcus species. 49 . The antibody of claim 48 , wherein the bacterium is S. aureus. 50 . The antibody of claim 49 , wherein the sdr protein is selected from the group consisting of C1fA (SdrA), C1fB (SdrB), SdrC, SdrD and SdrE. 51 . The antibody of claim 48 , wherein the bacterium is S. epidermidis. 52 . The antibody of claim 51 , wherein the sdr protein is selected from the group consisting of SdrF, SdrG and SdrH. 53 . The antibody of claim 48 , wherein the bacterium is S. saprophyticus. 54 . The antibody of claim 53 , wherein the sdr protein is SdrI. 55 . The antibody of claim 48 , wherein the bacterium is S. capitis. 56 . The antibody of claim 55 , wherein the sdr protein is SdrX. 57 . The antibody of claim 48 , wherein the bacterium is S. caprae. 58 . The antibody of claim 57 , wherein the sdr protein is selected from the group consisting of SdrY and SdrZ. 59 . The antibody of claim 44 , wherein the epitope comprises a molecule that binds to or is associated with an Sdr protein. 60 . The antibody of claim 59 , wherein the molecule that binds to or is associated with an Sdr protein is a component of a cell wall of a gram-positive bacteria. 61 . The antibody of claim 60 , wherein the molecule is peptidoglycan. 62 . The antibody of claim 60 , wherein the molecule is selected from the group consisting of peptides, proteins, sugars and sugar residues. 63 . The antibody of claim 44 , wherein the antibody or functional part thereof is coupled to another moiety to form an antibody-drug conjugates. 64 . The antibody of claim 61 , wherein said another moiety is a cytotoxic agent. 65 . The antibody of claim 62 , wherein the cytotoxic agent is an antibiotic. 66 . The antibody of claim 44 , wherein the antibody binds to cell wall lysates from S. aureus and/or S. epidermis. 67 . The antibody of claim 44 , wherein the antibody is able to compete with an antibody comprising (a) a heavy chain CDR1 sequence RFAMS (SEQ ID NO:1), and (b) a heavy chain CDR2 sequence SINNGNNPYYARSVQY (SEQ ID NO:2) or SINSGNNPYYARSVQY (SEQ ID NO:60), and (c) a heavy chain CDR3 sequence DHPSSGWPTFDS (SEQ ID NO:3), and (d) a light chain CDR1 sequence RASENVGDWLA (SEQ ID NO:4), and (e) a light chain CDR2 sequence KTSILES (SEQ ID NO:5), and (f) a light chain CDR3 sequence QHYXRFPYT (SEQ ID NO:6), wherein X is I or M. 68 . The antibody of claim 67 , wherein the antibody binds to a Staphylococcus species selected from the group consisting of S. aureus, S. epidermidis, S. caprae, S. saprophyticus, S. capitis , or methicillin-resistant S. aureus (MRSA). 69 . A pharmaceutical composition comprising the antibody of claim 44 .

Assignees

Inventors

Classifications

  • Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics · CPC title

  • Immunosuppressants, e.g. drugs for graft rejection · CPC title

  • Immunostimulants · CPC title

  • Antibacterial agents · CPC title

  • Complementarity determining region [CDR] · CPC title

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Frequently asked questions

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What does patent US2016168232A9 cover?
The present invention provides improved binding compounds capable of specifically binding Gram-positive bacteria. Binding compounds are provided that are fully human, enabling therapeutic applications in human individuals.
Who is the assignee on this patent?
Genentech Inc, Aimm Therapeutics Bv
What technology area does this patent fall under?
Primary CPC classification G01N33/5091. Mapped technology areas include Physics.
When was this patent published?
Publication date Thu Jun 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A9). 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).