The present invention relates to Her3 specific antibodies, preferably fully human or humanized antibodies and antigen-binding portions thereof. Nucleic acid molecules encoding the Her3 antibodies as well as methods of use thereof are also disclosed. Also included are pharmaceutical compositions comprising these antibodies and methods of using the antibodies and compositions thereof for treatment and diagnosis of pathological hyperproliferative oncogenic disorders associated with aberrant expression of Her3 or Her2 including aberrant activation of each of these receptors.
Renee C. Gaspar - Souderton PA, US Paul J. Shughrue - West Chester PA, US Fubao Wang - Dresher PA, US Weirong Wang - Harleysville PA, US Ningyan Zhang - Ambler PA, US Wei-Qin Zhao - North Wales PA, US Min Xu - Ambler PA, US Alexander McCampbell - Chalfont PA, US
Disclosed are antibodies that bind amyloid beta-derived diffusible ligands, also known as ADDLs. The antibodies are selective for ADDLs, can penetrate the brain, and are useful in methods of detecting ADDLs and diagnosing Alzheimer's disease. The antibodies also block binding of ADDLs to neurons, assembly of ADDLS, and tau phosphorylation and are there useful in methods for the preventing and treating diseases associated with ADDLs.
Generation And Characterization Of Anti-Notch Antibodies For Therapeutic And Diagnostic Use
Ningyan Zhang - Ambler PA, US Fubao Wang - Dresher PA, US Andrew Bett - Lansdale PA, US Anna Demartis - Rome, IT Maurizio Nuzzo - Rome, IT Paolo Monaci - Rome, IT Stephen Blacklow - Cambridge MA, US Jon Aster - Lexington MA, US
The present invention relates to mammalian antibodies, preferably fully human monoclonal antibodies and antigen-binding portions thereof that specifically bind to a cell surface receptor, wherein the receptor protein is a Notch1 receptor protein. Some of the disclosed antibodies bind Notch1 to the exclusion of other members of the Notch receptor family, while other antibodies bind Notch 1 and Notch3. Nucleic acid molecules encoding the Notch antibodies as well as methods of use thereof are also disclosed. Also included are pharmaceutical compositions comprising these antibodies and methods of using the antibodies and compositions thereof for treatment and diagnosis of pathological hyperproliferative oncogenic disorders associated with expression of Notch1 or Notch3 including aberrant activation of each of these receptors.
Multimeric Sars-Cov-2 Binding Molecules And Uses Thereof
- Austin TX, US - Mountain View CA, US Paul HINTON - Sunnyvale CA, US Ningyan ZHANG - Houston TX, US Bruce KEYT - Hillsborough CA, US Dean NG - San Francisco CA, US Stephen CARROLL - Walnut Creek CA, US Zhiqiang AN - Houston TX, US
Assignee:
The Board of Regents of The University of Texas System - Austin TX IGM Biosciences, Inc. - Mountain View CA
International Classification:
C07K 16/10 A61P 31/14
Abstract:
This disclosure provides multimeric binding molecules that bind to SARS-CoV-2. This disclosure also provides compositions comprising the multimeric binding molecules, polynucleotides that encode the multimeric binding molecules, and host cells that can produce the binding molecules. Further this disclosure provides methods of using the multimeric binding molecules, including methods for treating and preventing coronavirus disease 2019 (COVID-19).
- Austin TX, US - Palo Alto CA, US Ningyan ZHANG - Houston TX, US Xun GUI - Houston TX, US Mi DENG - Dallas TX, US Tao HUANG - Palo Alto CA, US Qiang LIU - Palo Alto CA, US
The present disclosure provides an isolated monoclonal antibody or an antigen-binding fragment thereof that binds specifically to leukocyte immunoglobulin-like receptor 4 (LILRB4). In certain embodiments, the antibody or antigen-binding fragment, when bound to LILRB4, modulates the activation of LILRB4. In certain embodiments, the antibody or antigen-binding fragment, when bound to LILRB4, activates LILRB4. In certain embodiments, the antibody or antigen binding fragment, when bound to LILRB4, suppresses activation of LILRB4. In certain embodiments, the antibody or antigen-binding fragment, when bound to LILRB4, specifically blocks binding of ApoE to LILRB4. In another aspect, there is provided a method of treating or ameliorating the effects of a cancer in a subject, comprising administering to the subject a therapeutically effective amount of the antibody or an antigen-binding fragment thereof or an engineered cell as provided herein.
- Austin TX, US Zhiqiang AN - Houston TX, US Ningyan ZHANG - Houston TX, US Mi DENG - Plano TX, US Jaehyup KIM - Houston TX, US Xun GUI - Houston TX, US
International Classification:
G01N 33/574 G01N 33/50 G01N 15/14 G01N 21/64
Abstract:
Provided herein are methods and compositions for the identification of modulators of ApoE-induced LILRB activation. Also provided herein are methods of treating cancer comprising the administration of an inhibitor of ApoE-induced LILRB activation. Also provided are methods of treating autoimmune disease or inhibiting the onset of transplant rejection or treating an inflammatory disorder comprising administering an agonist of ApoE-induced LILRB activation to a subject.
Connexin (Cx) 43 Hemichannel-Binding Antibodies And Uses Thereof
- Austin TX, US Zhiqiang An - Houston TX, US Ningyan Zhang - Houston TX, US Wei Xiong - Houston TX, US Manuel A. Riquelme - San Antonio TX, US Sumin Gu - San Antonio TX, US Naomi Ledene Sayre - San Antonio TX, US
Antibodies that bind to connexin 43 hemichannels and inhibit, or activate, channel opening are provided. In certain aspects, methods for detecting or treating cancers with antibodies that activate Cx43 channel opening are also provided. Likewise, methods for treating inflammatory diseases (e.g., osteoarthritis) and neurological injuries (e.g., spinal cord injury) with antibodies that inhibit Cx43 channel opening arc provided.
Anti-Lilrb Antibodies And Their Use In Detecting And Treating Cancer
- Austin TX, US Mi DENG - Plano TX, US Wei XIONG - Pearland TX, US Zhiqiang AN - Houston TX, US Ningyan ZHANG - Houston TX, US Xun GUI - Houston TX, US Junke ZHENG - Shanghai, CN