| Literature DB >> 28978751 |
Takahiro Ishiguro1, Yuji Sano2, Shun-Ichiro Komatsu3, Mika Kamata-Sakurai3, Akihisa Kaneko3, Yasuko Kinoshita2, Hirotake Shiraiwa3, Yumiko Azuma2, Toshiaki Tsunenari2, Yoko Kayukawa2, Yukiko Sonobe2, Natsuki Ono3, Kiyoaki Sakata2, Toshihiko Fujii2, Yoko Miyazaki2, Mizuho Noguchi2, Mika Endo2, Asako Harada3, Werner Frings3, Etsuko Fujii2, Eitaro Nanba3, Atsushi Narita3, Akihisa Sakamoto3, Tetsuya Wakabayashi3, Hiroko Konishi3, Hiroaki Segawa3, Tomoyuki Igawa3, Takashi Tsushima2, Hironori Mutoh2, Yukari Nishito2, Mina Takahashi2, Lorraine Stewart4, Ehab ElGabry4, Yoshiki Kawabe2,3, Masaki Ishigai3, Shuichi Chiba3, Masahiro Aoki2, Kunihiro Hattori2, Junichi Nezu5.
Abstract
Cancer care is being revolutionized by immunotherapies such as immune checkpoint inhibitors, engineered T cell transfer, and cell vaccines. The bispecific T cell-redirecting antibody (TRAB) is one such promising immunotherapy, which can redirect T cells to tumor cells by engaging CD3 on a T cell and an antigen on a tumor cell. Because T cells can be redirected to tumor cells regardless of the specificity of T cell receptors, TRAB is considered efficacious for less immunogenic tumors lacking enough neoantigens. Its clinical efficacy has been exemplified by blinatumomab, a bispecific T cell engager targeting CD19 and CD3, which has shown marked clinical responses against hematological malignancies. However, the success of TRAB in solid tumors has been hampered by the lack of a target molecule with sufficient tumor selectivity to avoid "on-target off-tumor" toxicity. Glypican 3 (GPC3) is a highly tumor-specific antigen that is expressed during fetal development but is strictly suppressed in normal adult tissues. We developed ERY974, a whole humanized immunoglobulin G-structured TRAB harboring a common light chain, which bispecifically binds to GPC3 and CD3. Using a mouse model with reconstituted human immune cells, we revealed that ERY974 is highly effective in killing various types of tumors that have GPC3 expression comparable to that in clinical tumors. ERY974 also induced a robust antitumor efficacy even against tumors with nonimmunogenic features, which are difficult to treat by inhibiting immune checkpoints such as PD-1 (programmed cell death protein-1) and CTLA-4 (cytotoxic T lymphocyte-associated protein-4). Immune monitoring revealed that ERY974 converted the poorly inflamed tumor microenvironment to a highly inflamed microenvironment. Toxicology studies in cynomolgus monkeys showed transient cytokine elevation, but this was manageable and reversible. No organ toxicity was evident. These data provide a rationale for clinical testing of ERY974 for the treatment of patients with GPC3-positive solid tumors.Entities:
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Year: 2017 PMID: 28978751 DOI: 10.1126/scitranslmed.aal4291
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956