研究概要
整合先天免疫和适应性免疫激活以对抗癌症的策略是迫切需要的。
中文摘要
整合先天性和适应性免疫激活以对抗癌症的策略是迫切需要的。我们建立了一个新型平台,即表达Wilms瘤抗原1(WT1)的人工佐剂载体细胞(aAVC-WT1),将iNKT细胞介导的树突状细胞激活与T细胞免疫连接起来。在此,我们报告了aAVC-WT1在9例复发和难治性急性髓系白血病患者中的首次人体应用。未观察到剂量限制性毒性,而在所有患者中均观察到iNKT和/或NK细胞的激活。5例患者出现了客观的白血病消退,这与WT1特异性T细胞反应相关。配对单细胞RNA和TCR测序显示骨髓中存在效应CD8+ T细胞克隆。一些骨髓CD8+ T细胞从预先存在的前体耗竭T细胞转变为功能性T细胞,或作为新激活的T细胞出现,其中一些被长期维持。这些结果证明了aAVC-WT1治疗的可行性和安全性,以及该平台在人体中激活先天性和适应性免疫的能力。
展开英文摘要原文
Strategies integrating activation of innate and adaptive immunity against cancer are desired. We established a novel platform, Wilms' tumor antigen 1 (WT1)-expressing artificial adjuvant vector cells (aAVC-WT1), linking invariant natural killer T (iNKT)-mediated dendritic cell activation to T cell immunity. Here, we report the first-in-human application of aAVC-WT1 in nine patients with relapsed and refractory acute myelogenous leukemia. No dose-limiting toxicities were observed, whereas activation of iNKT and/or NK cells was observed in all patients. Five patients experienced objective leukemic regression, which correlated with WT1-specific T cell responses. Paired single-cell RNA and T cell receptor (TCR) sequencing demonstrated effector CD8 + T cell clones in the bone marrow. Some bone marrow CD8 + T cells underwent transition from pre-existing precursor exhausted T cells to functional T cells or emerged as newly activated T cells, some of which were maintained long term. These demonstrate the feasibility and safety of aAVC-WT1 therapy and the capacity of this platform to activate both innate and adaptive immunity in humans.
论文信息
- 作者
- Fujii SI、Kawamata T、Shimizu K、Nakabayashi J、Yamasaki S、Iyoda T、Shinga J、Nakazato H
- 第一作者单位
- Laboratory for Immunotherapy, RIKEN Center for Integrative Medical Science (IMS), 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan.Japan
- 通讯作者单位
- Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo (IMSUT): Minato-ku, Tokyo 108-8639, Japan.Japan
- 期刊
- Molecular therapy oncolytics2022 Dec 15