<p>Combining chemoradiotherapy with immunotherapy increases the risk of immune-related adverse events (irAEs), but the underlying mechanisms remain poorly understood. To address this, we conducted a longitudinal single-cell multi-omics analysis of patients with locally advanced cervical cancer. Here we show that the proportions of CD4<sup>+</sup> and CD8<sup>+</sup> terminally differentiated effector memory or effector T cells are elevated in patients with irAEs. Chemoradiotherapy reduces B cell clonality while increasing the abundance and somatic hypermutation frequencies of IgA<sup>+</sup> and IgG<sup>+</sup> B cells in irAE patients. In the myeloid compartment, combined treatment expands specific monocyte subclusters associated with irAEs. Spatial transcriptomics and immunofluorescence analyses further reveal that these irAE-associated immune cells aggregate within the tumor microenvironment. Finally, we develop the predictive models for irAEs and integrate them, along with all datasets, into a user-friendly data portal. Our findings suggest that chemoradiotherapy and immunotherapy exert distinct effects on different immune cells, contributing to irAE development.</p>

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Distinct immune cell dynamics associated with immune-related adverse events during combined chemoradiation and immune checkpoint inhibitor therapy

  • Lei Zhang,
  • Xiaokai Fan,
  • Jun Ma,
  • Jun Zhang,
  • Ying Wei,
  • Bin Hu,
  • Di Zhou,
  • Junjun Zhou,
  • Yongrui Bai,
  • Xiumei Ma,
  • Jian Song,
  • Jianming Tang,
  • Haiyan Chen,
  • Ying Jing

摘要

Combining chemoradiotherapy with immunotherapy increases the risk of immune-related adverse events (irAEs), but the underlying mechanisms remain poorly understood. To address this, we conducted a longitudinal single-cell multi-omics analysis of patients with locally advanced cervical cancer. Here we show that the proportions of CD4+ and CD8+ terminally differentiated effector memory or effector T cells are elevated in patients with irAEs. Chemoradiotherapy reduces B cell clonality while increasing the abundance and somatic hypermutation frequencies of IgA+ and IgG+ B cells in irAE patients. In the myeloid compartment, combined treatment expands specific monocyte subclusters associated with irAEs. Spatial transcriptomics and immunofluorescence analyses further reveal that these irAE-associated immune cells aggregate within the tumor microenvironment. Finally, we develop the predictive models for irAEs and integrate them, along with all datasets, into a user-friendly data portal. Our findings suggest that chemoradiotherapy and immunotherapy exert distinct effects on different immune cells, contributing to irAE development.