Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Erin Willert"'
Autor:
Eric T Williams, Roger J. Waltzman, Jack P. Higgins, Asis K. Sarkar, Aimee Iberg, Erin Willert
Publikováno v:
Cancer Research. 80:P1-18
Engineered toxin bodies (ETBs) are differentiated, targeted therapeutics comprised of a proprietarily engineered form of Shiga-like Toxin A subunit (SLTA) genetically fused to antibody-like binding domains. ETBs work through novel mechanisms of actio
Autor:
John Newcomb, Wenrou Zheng, Wassilis S. C. Bruins, Niels W.C.J. van de Donk, Erin Willert, Tuna Mutis, Jack P. Higgins, Sonja Zweegman, Ajeeta B Dash
Publikováno v:
Blood. 136:11-12
Monoclonal antibodies (daratumumab, anti-CD38; elotuzumab, anti-SLAMF7) and BCMA-targeting T-cell redirecting therapies are highly effective in a large proportion of multiple myeloma (MM) patients. Nonetheless, age, prior (chemo)therapy, and the tumo
Autor:
Garrett L. Robinson, Aimee Iberg, Melissa M. Singh, Joseph D. Dekker, Hilario J. Ramos, Jay Zhao, Sara LeMar, Erin Willert
Publikováno v:
Cancer Research. 80:521-521
CD45 is highly expressed on the cell surface of all nucleated hematopoietic cells, including malignant cells of B, T and myeloid lineage. CD45, a receptor tyrosine phosphatase that has important roles in antigen receptor signaling, has multiple isofo
Autor:
Sara LeMar, Hilario J. Ramos, Garrett L. Robinson, Joseph D. Dekker, Aimee Iberg, Asis K. Sarkar, Banmeet Anand, Brigitte Brieschke, Melissa M. Singh, Jack P. Higgins, Jay Zhao, Erin Willert
Publikováno v:
Cancer Research. 80:3366-3366
Engineered toxin bodies (ETBs) comprised of a proprietarily engineered Shiga-like Toxin A subunit (SLTA) genetically fused to antibody-like binding domains work through novel mechanisms of action and can force internalization, self-route through intr
Autor:
Aimee Iberg, Joseph D. Dekker, Garrett L. Robinson, Edith Acquaye-Seedah, Erin Willert, Hilario J. Ramos, Lilia A. Rabia, Jay Zhao
Publikováno v:
Cancer Research. 80:2278-2278
Tumor resident regulatory T cells (Tregs) are important mediators of an immunosuppressive tumor microenvironment (TME) promoting tumor immune evasion. The presence of Tregs, and a higher ratio of Tregs to effector T cells in the TME, are associated w
Autor:
Hilario J. Ramos, Erin Willert, Jay Zhao, Caleigh Howard, Garrett L. Cornelison, Garrett L. Robinson, Aimee Iberg
Publikováno v:
Cancer Research. 80:539-539
Engineered toxin bodies (ETBs) are comprised of a proprietarily engineered form of Shiga-like Toxin A subunit (SLT-A) genetically fused to antibody-like binding domains. ETBs work through novel mechanisms of action and are capable of forcing internal
Autor:
Roger J. Waltzman, Sara LeMar, Hilario J. Ramos, Garrett L. Robinson, Joseph D. Dekker, Brigitte Brieschke, Garrett L. Cornelison, Aimee T. Iberg, Asis K. Sarkar, Erin Willert, Jay Zhao
Publikováno v:
Journal of Clinical Oncology. 38:12-12
12 Background: Engineered toxin bodies (ETBs) comprised of a proprietarily engineered Shiga-like Toxin A subunit (SLT-A) genetically fused to antibody-like binding domains work through novel mechanisms of action and can force internalization, self-ro
Autor:
Jack T. Higgins, Roger J. Waltzman, Aimee T. Iberg, Asis K. Sarkar, Eric T Williams, Erin Willert
Publikováno v:
Journal of Clinical Oncology. 38:433-433
433 Background: Engineered toxin bodies (ETBs) are comprised of a proprietarily engineered Shiga-like Toxin A subunit genetically fused to antibody-like binding domains. MT-5111 is a de-immunized ETB targeting HER2 for solid tumors. MT-5111 works thr
Autor:
Garrett L. Robinson, Erin Willert, Jack P. Higgins, Sangeetha Rajagopalan, Brigitte Brieschke, Jennifer Erdman, William Null
Publikováno v:
Cancer Research. 75:P4-15
The HER2 receptor is overexpressed in 20-30% of breast cancers. HER2 overexpression in breast cancer has been successfully targeted by both antibody and antibody-drug conjugate (ADC) approaches. The recently approved trastuzumab-emtansine (T-DM1, Kad
Autor:
Richard Labotka, Yuhong Zhang, Divya Manoharan, Ajeeta B Dash, Erin Willert, Robert F. Cornell, Jack P. Higgins, Roger J. Waltzman, Michael J. Hanley, Jianchang Lin, Alexander Vorog, Ola Landgren, Morgan Leichter, Sikander Ailawadhi, Anya Lublinsky, Sean Ottinger, Shaji Kumar, John Newcomb
Publikováno v:
Blood. 134:1867-1867
Background CD38 is highly expressed on MM cells, hence anti-CD38 agents are of interest as a therapeutic approach in MM. The anti-CD38 monoclonal antibody, dara, as mono- or combination therapy, has substantially improved efficacy outcomes in RRMM, i