- Redmond WA, US - Chengdu, Sichuan, CN Dong XIA - Redmond WA, US David JELLYMAN - Duvall WA, US Katrina BYKOVA - Seattle WA, US Anne-Marie ROUSSEAU - Seattle WA, US Bill BRADY - Bothell WA, US Blair RENSHAW - Renton WA, US Brian KOVACEVICH - Snohomish WA, US Yu LIANG - Redmond WA, US Camilla WANG - Sammamish WA, US Zeren GAO - Redmond WA, US Hui Huang - Redmond WA, US
International Classification:
C07K 16/28 A61P 35/02 C12N 5/0783 C12N 5/09
Abstract:
The application provides guidance and navigation control (GNC) proteins. In one embodiment, the guidance and navigation control (GNC) protein, comprising a binding domain for a T cell activating receptor, a binding domain for a tumor associated antigen, a bind domain for an immune checkpoint receptor, and a binding domain for a T cell co-stimulating receptor. The binding domain for the tumor associated antigen is not adjacent to the binding domain for the T cell co-stimulating receptor. In one embodiment, the binding domain for the T cell activating receptor is adjacent to the binding domain for the tumor associated antigen (TAA).
Methods Of Making And Using Guidance And Navigation Control Proteins
- Redmond WA, US - Chengdu, Sichuan, CN Jahan KHALILI - Everett WA, US Dong XIA - Redmond WA, US David JELLYMAN - Duvall WA, US Katrina BYKOVA - Seattle WA, US Anne-Marie ROUSSEAU - Seattle WA, US Camilla WANG - Sammamish WA, US Zeren GAO - Redmond WA, US Hui HUANG - Redmond WA, US Steven K. LUNDY - Woodinville WA, US
The application provides methods for generating a therapeutic composition. The method includes the steps of providing a cell material comprising a cytotoxic cell, incubating the cell material with a first GNC protein to provide an activated cell composition, wherein the activated cell composition comprises a first therapeutic cell, and formulating the activated cell composition to provide a therapeutic composition, wherein the therapeutic composition is substantially free of exogenous viral and non-viral DNA or RNA. The first GNC protein comprises a first cytotoxic binding moiety and a first cancer targeting moiety, wherein the first cytotoxic binding moiety has a specificity to a first cytotoxic cell receptor and is configured to activate the first cytotoxic cell, and wherein the first cancer targeting moiety has a specificity to a first cancer cell receptor. The first therapeutic cell comprises the first GNC protein bound to the cytotoxic cell through the first cytotoxic cell receptor.
Multi-Specific Antibodies And Methods Of Making And Using Thereof
- Redmond WA, US - Chengdu, CN Dong XIA - Redmond WA, US David JELLYMAN - Duvall WA, US Katrina BYKOVA - Seattle WA, US Anne-Marie K. ROUSSEAU - Seattle WA, US Bill BRADY - Bothell WA, US Blair RENSHAW - Renton WA, US Brian KOVACEVICH - Snohomish WA, US Yu LIANG - Redmond WA, US Zeren GAO - Redmond WA, US
International Classification:
C07K 16/28 A61K 47/68 A61K 39/395 A61K 45/06
Abstract:
The application provides tri-specific antibody monomers having a N-terminal and a C-terminal, comprising in tandem from the N-terminal to the C-terminal, a first scFv domain at the N-terminal, a Fab domain, a Fc domain, and a second scFv domain at the C-terminal. In one embodiment, the first scFv domain, the Fab domain, and the second scFv domain each has a binding specificity against a different antigen.
Anti-Cd3 Antibodies And Methods Of Making And Using Thereof
- Redmond WA, US - Chengdu, Sichuan, CN Dong XIA - Redmond WA, US David JELLYMAN - Duvall WA, US Brian KOVACEVICH - Snohomish WA, US Bill BRADY - Bothell MA, US Blair RENSHAW - Renton WA, US Zeren GAO - Redmond WA, US Yi ZHU - Chengdu, CN
International Classification:
C07K 16/28 A61K 47/68 C12N 15/85
Abstract:
The applications provides the anti-CD3 monoclonal antibodies, antigen-binding portions thereof, therapeutic compositions thereof and/or nucleic acid encoding the same, and their use to active CD3+ T-cells to enhance cell-mediated immune responses in the treatment of cancer and other T-cell dysfunctional disorders.
Multi-Specific Antibodies And Methods Of Making And Using Thereof
- Redmond WA, US - Chengdu, CN Dong XIA - Redmond WA, US David JELLYMAN - Duvall WA, US Katrina BYKOVA - Seattle WA, US Anne-Marie K. ROUSSEAU - Seattle WA, US Bill BRADY - Bothell WA, US Blair RENSHAW - Renton WA, US Brian KOVACEVICH - Snohomish WA, US Yu LIANG - Redmond WA, US Zeren GAO - Redmond WA, US
International Classification:
C07K 16/28 C07K 16/32 A61K 35/16
Abstract:
The disclosure provides a tetra-specific antibody monomer having a N-terminal and a C-terminal, comprising in tandem from the N-terminal to the C-terminal, a first scFv domain at the N-terminal, a second scFv domain, a Fab domain, a Fc domain, and a third scFv at the C-terminal, wherein the first scFv domain, the second scFv domain, the Fab domain, and the third scFv domain each has a binding specificity against a different antigen. In one embodiment, the antigen is a tumor antigen, an immune signaling antigen, or a combination thereof. In one embodiment, the antigen includes CD19, CD3, CD137, 4-1BB, and PD-L1. Multi-specific antibodies comprising the disclosed tetra-specific antibodies are also provided.
Research Associate at Theraclone Sciences at Theraclone Sciences
Location:
Greater Seattle Area
Industry:
Biotechnology
Work:
Theraclone Sciences - Greater Seattle Area since Sep 2009
Research Associate at Theraclone Sciences
University of Bristol - Bristol, United Kingdom Sep 2002 - Sep 2006
Lab assistant, tutor and grad student
Education:
University of Bristol 2005 - 2008
MSc, Biochem
The University of Sheffield 1999 - 2002
BSc, Pharmacology
Skills:
Platform development and innovation Experiment designee Protocol righting FACS, 8 years experience, 8 color panel designe, high throughput B cell culture, 4 years experience including platform development Cell enrichment 11year experience including enrichment designee tissue culture 10years experience including culture of primary cells× FACS sorting experience Molecular Biology Microsoft Excel Word and PowerPoint Laboratory Robotics