🛰️ Daily AI Frontier
‹ back to 2026-08-18

Cancer Cell | 单细胞 TCR 联合免疫肽组解析骨髓肿瘤 T 细胞特征精准预测血液肿瘤免疫治疗疗效

Research Medical/Healthcare AI

Ranking

Overall 74
Content 85
Popularity 47

Observed public metrics from 1 member.

Representative image for Cancer Cell | 单细胞 TCR 联合免疫肽组解析骨髓肿瘤 T 细胞特征精准预测血液肿瘤免疫治疗疗效

Merged summary

TL;DR - A Cancer Cell study combines single-cell RNA/TCR sequencing, functional screening, and HLA immunopeptidomics to characterize tumor-reactive T cells in multiple myeloma and acute myeloid leukemia. Its 15-gene TFiT classifier identifies these cells and predicts immunotherapy response, potentially enabling better patient stratification.

  • Tumor-reactive bone-marrow T cells showed strong cytotoxic effector programs without the deep exhaustion commonly observed in solid tumors.
  • Immunopeptidomics identified 17,161 HLA-bound peptides, largely from noncanonical rather than mutation-derived antigens.
  • TFiT achieved an AUC of 0.895 in an independent cohort and outperformed published solid-tumor T-cell classifiers.
  • TFiT predicted responses to BCMA×CD3 therapy in myeloma and nivolumab-based treatment in AML, but not standard AML chemotherapy.

Sources (1)

Cancer Cell | 单细胞 TCR 联合免疫肽组解析骨髓肿瘤 T 细胞特征精准预测血液肿瘤免疫治疗疗效

WeChat: 单细胞天地 2026-08-15 doi:10.1016/j.ccell.2026.07.011
Public signals OpenAlex citations 1
Providers: Hugging Face · N/A OpenAlex · Citations 1 Publisher · N/A Semantic Scholar · N/A X · N/A Fetched 2026-09-17 14:33:08.792101 UTC

TL;DR - A Cancer Cell study combines single-cell RNA/TCR sequencing, functional screening, and HLA immunopeptidomics to characterize tumor-reactive T cells in multiple myeloma and acute myeloid leukemia. Its 15-gene TFiT classifier identifies these cells and predicts immunotherapy response, potentially enabling better patient stratification.

  • Tumor-reactive bone-marrow T cells showed strong cytotoxic effector programs without the deep exhaustion commonly observed in solid tumors.
  • Immunopeptidomics identified 17,161 HLA-bound peptides, largely from noncanonical rather than mutation-derived antigens.
  • TFiT achieved an AUC of 0.895 in an independent cohort and outperformed published solid-tumor T-cell classifiers.
  • TFiT predicted responses to BCMA×CD3 therapy in myeloma and nivolumab-based treatment in AML, but not standard AML chemotherapy.
item →