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Radiotherapy and immunotherapy in cancer treatment: mechanisms of clinical synergy
Lu Lu, Liufu Deng
Lu Lu, Liufu Deng
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Review

Radiotherapy and immunotherapy in cancer treatment: mechanisms of clinical synergy

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Abstract

Synergizing radiotherapy (RT) with immune checkpoint inhibitors has emerged as a promising strategy for solid tumors. RT acts as a potent immunomodulator, capable of functioning as an in situ vaccine through the induction of immunogenic cell death and activation of innate immune sensing, thereby promoting DC maturation and CD8+ T cell responses. However, RT also triggers counter-regulatory immunosuppression, including PD-L1 upregulation and the recruitment of suppressive cells, providing the biological rationale for synergy. Here, we systematically review advances in radioimmunotherapy, covering immunomodulatory mechanisms, clinical optimization of dose and sequencing, and the emerging role of artificial intelligence (AI) in guiding treatment paradigms. We adopt a spatial interaction–centric perspective to synthesize current knowledge on how RT governs the DC/CD8+ T cell interaction axis across the tumor microenvironment and tumor-draining lymph nodes, aiming to chart a rational course from empirical combination toward personalized, precision radioimmunotherapy. Furthermore, we explore how AI-driven analysis of radiomics and multiomics data is being applied to predict responders and personalize treatment planning.

Authors

Lu Lu, Liufu Deng

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Figure 1

RT-induced innate immune sensing.

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RT-induced innate immune sensing.
(A) RT functions as an in situ vaccine...
(A) RT functions as an in situ vaccine by inducing ICD, which promotes the release of tumor-associated antigens, neoantigens, and DAMPs, including ATP, calreticulin, and HMGB1. These signals promote DC activation and antigen uptake. (B) DC-intrinsic DNA and RNA sensing pathways are indispensable for type I IFN–dependent effective CD8+ T cell priming after RT, whereas canonical RIG-I/MAVS signaling in DCs can paradoxically impair cross-priming through inhibiting IL-12 production. ZBP1 further functions as a dual RNA/DNA sensor that detects RT-induced nucleic acids, triggers necroptosis, and amplifies STING-dependent immune activation, thereby reinforcing DC-dependent adaptive antitumor immunity.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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