Division of Pediatric Hematology-Oncology, Department of Pediatrics, University of California Los Angeles, Los Angeles, California.
Department of Microbiology, Immunology, and Molecular Genetics, University of California Los Angeles, Los Angeles, California.
Cancer Immunol Res. 2023 Dec 1;11(12):1589-1597. doi: 10.1158/2326-6066.CIR-23-0577.
Transgenic T-cell receptor (TCR) T cell-based adoptive cell therapies for solid tumors are associated with dramatic initial response rates, but there remain many instances of treatment failure and disease relapse. The association of infusion product cytokine profiles with clinical response has not been explored in the context of TCR T-cell therapy products. Single-cell antigen-dependent secretomic and proteomic analysis of preinfusion clinical TCR T-cell therapy products revealed that TNFα cytokine functionality of CD8+ T cells and phospho-STAT3 signaling in these cells were both associated with superior clinical responsiveness to therapy. By contrast, CD4+ T-helper 2 cell cytokine profiles were associated with inferior clinical responses. In parallel, preinfusion levels of IL15, Flt3-L, and CX3CL1 were all found to be associated with clinical response to therapy. These results have implications for the development of therapeutic biomarkers and identify potential targets for enrichment in the design of transgenic TCR T-cell therapies for solid tumors.
基于转基因 T 细胞受体 (TCR) T 细胞的过继细胞疗法在治疗实体瘤方面与显著的初始反应率相关,但仍有许多治疗失败和疾病复发的情况。在 TCR T 细胞治疗产品的背景下,输注产品细胞因子谱与临床反应的关联尚未得到探索。对输注前临床 TCR T 细胞治疗产品的单细胞抗原依赖性分泌组学和蛋白质组学分析表明,CD8+T 细胞的 TNFα 细胞因子功能和这些细胞中的磷酸化 STAT3 信号均与对治疗的更好临床反应相关。相比之下,CD4+辅助性 T 细胞 2 细胞细胞因子谱与较差的临床反应相关。同时,IL15、Flt3-L 和 CX3CL1 的预输注水平均与对治疗的临床反应相关。这些结果对治疗生物标志物的开发具有重要意义,并确定了在设计用于实体瘤的转基因 TCR T 细胞治疗的富集潜在目标。