1120 Danielle Dr, Costa Mesa, CA 92626 606 S Hl St, Los Angeles, CA 90014 608 S Hl St, Los Angeles, CA 90014 633 S Hl St, Los Angeles, CA 90014 (213)4897524, (213)6220889
Genetically engineered, CD20-specific redirected T cells expressing a cell surface protein-having an extracellular domain comprising a receptor which is specific for CD20, an intracellular signaling domain, and a transmembrane domain. Use of such cells for cellular immunotherapy of CD20 malignancies and for abrogating any untoward B cell function. In one embodiment, the cell surface protein is a single chain FvFc: receptor where Fv designates the V and V chains of a single chain monoclonal antibody to CD20 linked by peptide, Fc represents a hinge-CH -CH region of a human IgG , and represents the intracellular signaling domain of the zeta chain of human CD3. A method of making a redirected T cell expressing a chimeric T cell receptor by electroporation using naked DNA encoding the receptor.
Humanized Anti-Cea T84.66 Antibody And Uses Thereof
Paul J. Yazaki - Glendale CA, US Mark A. Sherman - Pasadena CA, US John E. Shively - Arcadia CA, US Andrew A. Raubitschek - San Marino CA, US Anna M. Wu - Sherman Oaks CA, US
Assignee:
City of Hope - Duarte CA
International Classification:
A61K 39/00
US Classification:
4241331
Abstract:
Embodiments of the present invention utilize a more efficient CDR grafting technique to generate humanized versions of the T84. 66 antibody. The technique used to generate these antibodies utilizes crystallographic structural data to select an immunoglobulin framework having maximum structural overlap with a non-human donor molecule. This technique was used to develop humanized T84. 66 antibodies exhibiting in vitro binding affinity and specificity for carcinoembryonic antigen (CEA) nearly identical to that of T84. 66 and the ability to specifically target tumors expressing CEA in vivo.
Engineered Anti-Cd20 Antibody Fragments For In Vivo Targeting And Therapeutics
The present invention provides anti-CD20 antibody fragments for use as in vivo imaging probes and as therapeutic moieties for the diagnosis and treatment of NHL.
Humanized Anti-Cea T84.66 Antibody And Uses Thereof
Paul J. Yazaki - Glendale CA, US Mark A. Sherman - Pasadena CA, US John E. Shively - Arcadia CA, US Andrew A. Raubitschek - San Marino CA, US Anna M. Wu - Sherman Oaks CA, US
Embodiments of the present invention utilize a more efficient CDR grafting technique to generate humanized versions of the T84. 66 antibody. The technique used to generate these antibodies utilizes crystallographic structural data to select an immunoglobulin framework having maximum structural overlap with a non-human donor molecule. This technique was used to develop humanized T84. 66 antibodies exhibiting in vitro binding affinity and specificity for carcinoembryonic antigen (CEA) nearly identical to that of T84. 66 and the ability to specifically target tumors expressing CEA in vivo.
Mark A. Sherman - Pasadena CA, US Anna M. Wu - Sherman Oaks CA, US Robert E. Reiter - Los Angeles CA, US
Assignee:
City of Hope - Duarte CA The Regents of the University of California - Oakland CA
International Classification:
C07H 21/04
US Classification:
536 2353, 536 231
Abstract:
Prostate stem cell antigen (PSCA) is expressed in the majority of prostate cancer patients, making it an ideal target for cancer immunotherapy. Murine monoclonal antibody 1G8 binds to PSCA with nanomolar affinity, but its efficacy as a therapeutic agent is limited by the generation of a HAMA response. The present invention discloses humanized 1G8 antibodies in which the majority of the mouse-derived epitopes have been removed. These humanized antibodies bind PSCA with high affinity and specificity, and have been shown to reduce human bladder tumor take in a nude mouse model. These characteristics make the humanized antibodies of the present invention attractive agents for the treatment and detection of tumors expressing PSCA.
Jonathan Braun - Tarzana CA, US Lynn K. Gordon - Tarzana CA, US Kaori Shimizaki - Los Angeles CA, US Kathy A. Kelly - Sherman Oaks CA, US Anna M. Wu - Sherman Oaks CA, US
Assignee:
The Regents of The University of California - Oakland CA
The present invention provides methods and compositions useful in the treatment or prevention of infections and cancer. The methods and compositions inhibit the entry of into a host cell expressing EMP2 by interfering with the interaction between the and EMP2. The methods and compositions target cancers which express or overexpress EMP2 nucleic acids and polypeptides by targeting EMP2.
Mark A. Sherman - Pasadena CA, US Anna M. Wu - Sherman Oaks CA, US Robert E. Reiter - Los Angeles CA, US
Assignee:
City of Hope - Duarte CA The Regents of the University of California - Oakland CA
International Classification:
C12P 21/08
US Classification:
5303873, 5303911, 5303913, 5303917
Abstract:
Prostate stem cell antigen (PSCA) is expressed in the majority of prostate cancer patients, making it an ideal target for cancer immunotherapy. Murine monoclonal antibody 1G8 binds to PSCA with nanomolar affinity, but its efficacy as a therapeutic agent is limited by the generation of a HAMA response. The present invention discloses humanized 1G8 antibodies in which the majority of the mouse-derived epitopes have been removed. These humanized antibodies bind PSCA with high affinity and specificity, and have been shown to reduce human bladder tumor take in a nude mouse model. These characteristics make the humanized antibodies of the present invention attractive agents for the treatment and detection of tumors expressing PSCA.
Biotin-Ligase System For Secretion Of Biotinylated Protein
Bhaswati Barat - Los Angeles CA, US Anna M. Wu - Sherman Oaks CA, US
Assignee:
The Regents of the University of California - Oakland CA
International Classification:
C12P 21/00 C12P 21/04
US Classification:
435 691, 435 697
Abstract:
The present invention provides methods of metabolically biotinylating recombinant proteins. Cell lines and specific protein and nucleic acid constructs for use in the methods of the present invention are also provided herein.
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California State University, Fullerton - International Business, University of California, Los Angeles - Public Relations Certification, Shanghai Jiao Tong University - Linguistics and Applied Linguistics in Foreign Language
Anna Wu
Work:
Research In Motion - Interaction Design Intern (2010)
Education:
Simon Fraser University - Interaction Design
About:
I create relationships by embedding technologies into social complexities ( it drives me crazies) and i love it; Interaction Design
Anna Wu
Education:
Lane Tech, Holden, Haines
Anna Wu
Work:
SZMG
About:
Experiencing the new +
Anna Wu
Education:
Grand Valley State University - Chinese Studies
Anna Wu
Education:
Peraugymnasium
Anna Wu
About:
GG:45578323
Tagline:
Nie mów nic,kocha się za nic ...nie istnieje żaden powód do milości