R
Rin Nakamura
Researcher at Genentech
Publications - 8
Citations - 238
Rin Nakamura is an academic researcher from Genentech. The author has contributed to research in topics: Antibody & T cell. The author has an hindex of 5, co-authored 8 publications receiving 168 citations.
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Journal ArticleDOI
Membrane-Proximal Epitope Facilitates Efficient T Cell Synapse Formation by Anti-FcRH5/CD3 and Is a Requirement for Myeloma Cell Killing
Ji Li,Nicola J. Stagg,Jennifer Johnston,Michael J. Harris,Sam A. Menzies,Danielle DiCara,Vanessa Clark,Maria Hristopoulos,Ryan Cook,Dionysos Slaga,Rin Nakamura,Luke McCarty,Siddharth Sukumaran,Elizabeth Luis,Zhengmao Ye,Thomas D. Wu,Teiko Sumiyoshi,Dimitry M. Danilenko,Genee Y. Lee,Klara Totpal,Diego Ellerman,Isidro Hötzel,John R. James,Teemu T. Junttila +23 more
TL;DR: The potential for the anti-FcRH5/CD3 TDB, alone or in combination with inhibition of PD-1/PD-L1 signaling, in the treatment of MM and other B cell malignancies is demonstrated.
Journal ArticleDOI
Prevalence Study of PD-L1 SP142 Assay in Metastatic Triple-negative Breast Cancer.
Yijin Li,Bharathi Vennapusa,Ching-Wei Chang,David Tran,Rin Nakamura,Teiko Sumiyoshi,Priti S. Hegde,Luciana Molinero +7 more
TL;DR: The results suggest that the anatomic location of metastases and time of collection may influence the detection of PD-L1, which was highest in lymph nodes and lowest in liver metastases while breast tissue was intermediate.
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Tigit, CD226 and PD-L1/PD-1 Are Highly Expressed By Marrow-Infiltrating T Cells in Patients with Multiple Myeloma
Mahesh Yadav,Cherie Green,Connie Ma,Alberto Robert,Andrew Glibicky,Rin Nakamura,Teiko Sumiyoshi,Ray Meng,Yu-Waye Chu,Jenny Wu,John Byon,Woodard Joseph Paul,Joanne I. Adamkewicz,Jane L. Grogan,Jeffrey M. Venstrom +14 more
TL;DR: Evaluation of expression of TIGIT, CD226, PD-1 and PD-L1 in patients with MM to inform novel immunotherapy combinations finds additional benefit of TigIT blockade through elaboration of CD226-mediated anti-tumor immunity, analogous to CTLA-4/CD28 regulation of T-cell immunity.
Journal ArticleDOI
Early Pharmacodynamic Changes in T-Cell Activation, Proliferation, and Cytokine Production Confirm the Mode of Action of BFCR4350A, a FcRH5/CD3 T-Cell-Engaging Bispecific Antibody, in Patients with Relapsed/Refractory Multiple Myeloma
Rin Nakamura,Sean Lear,Deanna Grant Wilson,Hartmut Koeppen,Anjali Vaze,Suzanne Trudel,Andrew Spencer,Simon J. Harrison,Adam D. Cohen,Bernard M. Fine,Mengsong Li,James R. Cooper,Teiko Sumiyoshi +12 more
TL;DR: Preliminary biomarker data are presented that demonstrate the mode of action (MOA) of BFCR4350A, provide support for Cycle (C) 1 step-up dosing, and offer preliminary insights into markers that may predict response.
Journal ArticleDOI
Myeloid cell biology and inhibition of anti-tumor immune responses by MPDL3280A in urothelial bladder cancer
Yuanyuan Xiao,Christina Rabe,Marcin Kowanetz,Thomas Powles,Nicholas J. Vogelzang,Daniel P. Petrylak,Yohann Loriot,Mitchell Denker,Rin Nakamura,Qun J Wu,Teiko Sumiyoshi,Zachary Boyd,Siew-leng Melinda Teng,Xiaodong Shen,Gregg Fine,Daniel S. Chen,Priti S. Hegde +16 more
TL;DR: In this article, gene expression analyses of metastatic urothelial bladder cancer (UBC) patients were conducted to interrogate the tumor immune microenvironment in PD-L1-positive tumors and to identify potential mechanisms associated with response or resistance to MPDL3280A.