Anti-Gliadin Antibodies
US-2024101651-A1 · Mar 28, 2024 · US
US10081672B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10081672-B2 |
| Application number | US-201615088944-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 1, 2016 |
| Priority date | Jun 10, 2011 |
| Publication date | Sep 25, 2018 |
| Grant date | Sep 25, 2018 |
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The present invention relates to anti-ricin antibodies and uses thereof. More specifically, the invention relates to anti-ricin antibodies and fragments thereof as well as their use in therapy or prophylaxis.
Opening claim text (preview).
The invention claimed is: 1. A method of preventing deleterious effects caused by ricin exposure or of treating exposure to ricin, comprising administering an antibody or fragment thereof, or a composition comprising an antibody or fragment thereof and a pharmaceutically acceptable diluent, excipient, or carrier to a subject in need thereof, wherein the antibody or fragment thereof comprises a CDR L1 of sequence KASQDVTAAVA (SEQ ID NO:4), a CDR L2 of sequence SASYRYT (SEQ ID NO:8), and a CDR L3 of sequence QQYYNTPLT (SEQ ID NO:12); and a variable heavy chain comprising CDR H1 of sequence EHIIN (SEQ ID NO:16), a CDR H2 of sequence LINPNSGGTNYNQKFKD (SEQ ID NO:20), and a CDR H3 of sequence LRYDAAY (SEQ ID NO:24), and wherein the antibody or fragment thereof specifically binds ricin toxin lectin-B protein. 2. The method of claim 1 , wherein the subject is a mouse or a human. 3. The method of claim 1 , wherein the antibody or fragment thereof comprises the variable light chain sequence: (SEQ ID NO: 31) DIELTQSHKFMSTSVGDRVSITCKASQDVTAAVAWYQQKPGQSPKLLIHS ASYRYTGVPDRFTGSGSGSDFTFTISSVQAEDLAVYYCQQYYNTPLTFGA GTKLELKR or a sequence at least 95% identical thereto: and the variable heavy chain sequence: (SEQ ID NO: 32) QVQLQESGPELVKPGASMKISCKASGYSFTEHIINWVKQTHRENLEWIGL INPNSGGTNYNQKFKDKATLTVDTASNTAYMELLSLTSEDSAVYYCARLR YDAAYWGQGTTVTVSS, or a sequence at least 95% identical thereto. 4. The method of claim 1 , wherein the antibody or fragment thereof of claim 1 , is an IgG. 5. The method of claim 1 , wherein the one or more than one antibody or fragment thereof is administered to the subject several hours following exposure to the ricin toxin to treat ricin exposure. 6. The method of claim 1 , wherein the one or more than one antibody or fragment thereof is administered to the subject several weeks prior to exposure to the ricin toxin to protect the subject against ricin exposure. 7. The method of claim 1 , further comprising administering a second antibody or fragment thereof said second antibody or fragment thereof comprising the variable light chain sequence: (SEQ ID NO: 27) DIVLTQSPSSMYASLGERVTITCKASQDINNYLRWFQQKPGKSPKTLIYR ANRLVDGVPSRFSGSGSGQDYSLTISSLEYEDMGFYSCLQYDEFPYTFGG GTKLEIKR or a sequence at least 95% identical thereto; and the variable heavy chain sequence: (SEQ ID NO: 23) QVQLQESGPELVKPGASMKISCKASGYSFTEHIINWVKQTHRENLEWIGL INPNSGGTNYNQKFKDKATLTVDTASNTAYMELLSLTSEDSAVYYCARLR YDAAYWGQGTTVTVSS, or a sequence at least 95% identical thereto. 8. The method of claim 7 , wherein at least one of the antibodies or fragments thereof is humanized. 9. The method of any one of claim 1 - 4 , wherein preventing deleterious effects caused by ricin exposure is achieved by conferring immunity against ricin by administering the antibody or fragment thereof prior to exposure. 10. The method of claim 9 , wherein administering the antibody or fragment thereof occurs at least 1 day prior to exposure.
comprising antibodies · CPC title
against material from plants · CPC title
Antidotes · CPC title
variable (Fv) region, i.e. VH and/or VL · CPC title
Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value · CPC title
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