論文 - 詳細
| RRC ID | 58841 |
|---|---|
| 著者 | Kato D, Yaguchi T, Iwata T, Katoh Y, Morii K, Tsubota K, Takise Y, Tamiya M, Kamada H, Akiba H, Tsumoto K, Serada S, Naka T, Nishimura R, Nakagawa T, Kawakami Y. |
| タイトル | GPC1 specific CAR-T cells eradicate established solid tumor without adverse effects and synergize with anti-PD-1 Ab. |
| ジャーナル | Elife |
| Abstract |
Current xenogeneic mouse models cannot evaluate on-target off-tumor adverse effect, hindering the development of chimeric antigen receptor (CAR) T cell therapies for solid tumors, due to limited human/mouse cross-reactivity of antibodies used in CAR and sever graft-versus-host disease induced by administered human T cells. We have evaluated safety and antitumor efficacy of CAR-T cells targeting glypican-1 (GPC1) overexpressed in various solid tumors. GPC1-specific human and murine CAR-T cells generated from our original anti-human/mouse GPC1 antibody showed strong antitumor effects in xenogeneic and syngeneic mouse models, respectively. Importantly, the murine CAR-T cells enhanced endogenous T cell responses against a non-GPC1 tumor antigen through the mechanism of antigen-spreading and showed synergistic antitumor effects with anti-PD-1 antibody without any adverse effects in syngeneic models. Our study shows the potential of GPC1 as a CAR-T cell target for solid tumors and the importance of syngeneic and xenogeneic models for evaluating their safety and efficacy. |
| 巻・号 | 9 |
| 公開日 | 2020-3-31 |
| DOI | 10.7554/eLife.49392 |
| PII | 49392 |
| PMID | 32228854 |
| PMC | PMC7108862 |
| MeSH | Animals Cell Line Cell Line, Tumor Female Glypicans / genetics Glypicans / immunology* Humans Immunotherapy, Adoptive Male Mice Mice, Inbred C57BL Programmed Cell Death 1 Receptor / immunology* Receptors, Antigen, T-Cell / immunology* Receptors, Chimeric Antigen / immunology* Receptors, Chimeric Antigen / therapeutic use T-Lymphocytes / immunology* Xenograft Model Antitumor Assays |
| IF | 7.08 |
| 引用数 | 3 |
| リソース情報 | |
| ヒト・動物細胞 | TE-14(RCB2101) |