Therapeutic methods using anti-cd200 antibodies
US-2016009803-A1 · Jan 14, 2016 · US
US10118969B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10118969-B2 |
| Application number | US-201615011544-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 30, 2016 |
| Priority date | May 27, 2014 |
| Publication date | Nov 6, 2018 |
| Grant date | Nov 6, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present disclosure relates to compositions and methods of use comprising antibodies or binding fragments thereof further comprising universal Fc glycoforms.
Opening claim text (preview).
What is claimed is: 1. An isolated monoclonal antibody or antigen-binding fragment thereof that binds to Neu5Acα2→3Galβ1→3GalNAcβ1→3Galα1→4Galβ1→4Glcβ1, wherein the antibody or antigen-binding fragment thereof comprises a glycan attached to Asn-297 of the Fc region, wherein the glycan has the formula: Sia 2 ( α2-6)Gal 2 GlcNAc 2 Man 3 GlcNAc 2 , as in the structure shown in FIG. 1 , and wherein the antibody or antigen-binding fragment thereof comprises an H-CDR1, an H-CDR2, an H-CDR3, an L-CDR1, an L-CDR2, and an L-CDR3, wherein: (i) the H-CDR1 comprises the sequence of SEQ ID NO:152 (GFSLTSYG); (ii) the H-CDR2 comprises the sequence of SEQ ID NO:153 (IWGEGST); (iii) the H-CDR3 comprises the sequence of SEQ ID NO:154 (AMTGTAY); (iv) the L-CDR1 comprises the sequence of SEQ ID NO:149 (SSVSY); (v) the L-CDR2 comprises the sequence of SEQ ID NO:150 (DTS); and (vi) the L-CDR3 comprises the sequence of SEQ ID NO:151(HQWSSSPHT). 2. The isolated monoclonal antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody is an IgG1. 3. The isolated monoclonal antibody or antigen-binding fragment thereof of claim 2 wherein the antibody comprises a VH having SEQ ID NO:147 and a VL having SEQ ID No:148. 4. The isolated monoclonal antibody or antigen-binding fragment thereof of claim 1 wherein the antibody is a humanized antibody. 5. A pharmaceutical composition comprising the isolated monoclonal antibody or antigen-binding fragment thereof of claim 1 and a pharmaceutically acceptable carrier. 6. The isolated monoclonal antibody or antigen-binding fragment thereof of claim 2 , wherein the antibody comprises a VH having SEQ ID NO:137 and a VL having SEQ ID NO:138. 7. The isolated monoclonal antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof further comprises an H-FR1, an H-FR2, an H-FR3, an HFR4, an L-FR1, an L-FR2, an L-FR3, and an L-FR4, wherein: (i) the H-FR1 comprises the sequence of SEQ ID NO: 159 (QVQLKESGPGLVAPSQSLSITCTVS); (ii) the H-FR2 comprises the sequence of SEQ ID NO:160 (VSWIRQPPGKGLEWIGV); (iii) the H-FR3 comprises the sequence of SEQ ID NO:161 (NYHSVLISRLTISKDNSKSQVFLKLNSLQTDDTATYYC); (iv) the H-FR4 comprises the sequence of SEQ ID NO:162 (WGQGTLVTVSS); (v) the L-FR1 comprises the sequence of SEQ ID NO:155 (QIVLTQSPAIMSASPGEKVTMTCSAS); (vi) the L-FR2 comprises the sequence of SEQ ID NO 156 (MHWYQQKSGTSPKRWIY); (vii) the L-FR3 comprises the sequence of SEQ ID NO:157 (KLSSGVPGRFSGSGSGTSYSLTISRLEAEDAATYYC); and (viii) the L-FR4 comprises the sequence of SEQ ID NO:158 (FGGGTKVEIKR). 8. An isolated monoclonal antibody or antigen-binding fragment thereof that binds to Neu5Acα2→3Galβ1→3GalNAcβ1→3Galα1→4Galβ1→4Glcβ1, wherein the antibody or antigen-binding fragment thereof comprises a glycan attached to Asn-297 of the Fc region, wherein the glycan has the formula: Sia 2 (α2-6)Gal 2 GlcNAc 2 Man 3 GlcNAc 2 , as in the structure shown in FIG. 1 , and wherein the antibody or antigen-binding fragment thereof comprises an H-CDR1, an H-CDR2, an H-CDR3, an L-CDR1, an L-CDR2, and an L-CDR3, wherein: (i) the H-CDR1 comprises the sequence of SEQ ID NO:207; (ii) the H-CDR2 comprises the sequence of SEQ ID NO:208; (iii) the H-CDR3 comprises the sequence of SEQ ID NO:209; (iv) the L-CDR1 comprises the sequence of SEQ ID NO:204; (v) the L-CDR2 comprises the sequence of SEQ ID NO:205; and (vi) the L-CDR3 comprises the sequence of SEQ ID NO:206. 9. The isolated monoclonal antibody or antigen-binding fragment thereof of claim 8 , wherein the antibody is a humanized antibody. 10. The isolated monoclonal antibody of claim 8 , wherein the monoclonal antibody or antigen-binding fragment thereof comprises a VH having SEQ ID NO:202 and a VL having SEQ ID No:203. 11. A pharmaceutical composition comprising the isolated monoclonal antibody or antigen-binding fragment thereof of claim 8 and a pharmaceutically acceptable carrier. 12. An isolated monoclonal antibody or antigen-binding fragment thereof that binds to Neu5Acα2→3Galβ1→3GalNAcβ1→3Galα1→4Galβ1→4Glcβ1, wherein the antibody or antigen-binding fragment thereof comprises a glycan attached to Asn-297 of the Fc region, wherein the glycan has the formula: Sia 2 (α2-6)Gal 2 GlcNAc 2 Man 3 GlcNAc 2 , as in the structure shown in FIG. 1 , and wherein the antibody or antigen-binding fragment thereof comprises an H-CDR1, an H-CDR2, an H-CDR3, an L-CDR1, an L-CDR2, and an L-CDR3, wherein: (i) the H-CDR1 comprises the sequence of SEQ ID NO:217; (ii) the H-CDR2 comprises the sequence of SEQ ID NO:218; (iii) the H-CDR3 comprises the sequence of SEQ ID NO:219; (iv) the L-CDR1 comprises the sequence of SEQ ID NO:214; (v) the L-CDR2 comprises the sequence of SEQ ID NO:215; and (vi) the L-CDR3 comprises the sequence of SEQ ID NO:216. 13. The isolated monoclonal antibody or antigen-binding fragment thereof of claim 12 , wherein the antibody is a humanized antibody. 14. The isolated monoclonal antibody or antigen-binding fragment thereof of claim 12 , wherein the antibody comprises a VH having SEQ ID NO:212 and a VL having SEQ ID NO:213. 15. A pharmaceutical composition comprising the isolated monoclonal antibody or antigen-binding fragment thereof of claim 12 and a pharmaceutically acceptable carrier. 16. An isolated monoclonal antibody or antigen-binding fragment thereof that binds to Neu5Acα2→3Galβ1→3GalNAcβ1→3Galαl→4Galβ1→4Glcβ1, wherein the antibody or the antigen-binding fragment thereof comprises a glycan attached to Asn-297 of the Fc region, wherein the glycan has the formula: Sia 2 (α2-6)Gal 2 GlcNAc 2 Man 3 GlcNAc 2 , as in the structure shown in FIG. 1 , and wherein the antibody or antigen-binding fragment thereof comprises an H-CDR1, an H-CDR2, an H-CDR3, an L-CDR1, an L-CDR2, and an L-CDR3, wherein: (i) the H-CDR1 comprises the sequence of SEQ ID NO:227; (ii) the H-CDR2 comprises the sequence of SEQ ID NO:228; (iii) the H-CDR3 comprises the sequence of SEQ ID NO:229; (iv) the L-CDR1 comprises the sequence of SEQ ID NO:224; (v) the L-CDR2 comprises the sequence of SEQ ID NO:225; and (vi) the L-CDR3 comprises the sequence of SEQ ID NO:226. 17. The isolated monoclonal antibody or antigen-binding fragment thereof of claim 16 , wherein the antibody is a humanized antibody. 18. The isolated monoclonal antibody or antigen-binding fragment thereof of claim 16 , wherein the antibody comprises a VH having SEQ ID NO:222 and a VL having SEQ ID NO:223. 19. A pharmaceutical composition comprising the isolated monoclonal antibody or antigen-binding fragment thereof of claim 16 and a pharmaceutically acceptable carrier.
Orthomyxoviridae (F), e.g. influenza virus · CPC title
against material from animals or humans · CPC title
Chemistry & Metallurgy · mapped topic
Constant or Fc region; Isotype · CPC title
acting on glycosyl compounds (3.2) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.