This review critically evaluates the translational potential of targeting these neuro-immune interactions, highlighting combination strategies designed to enhance the efficacy of cancer immunotherapy.
Abstract
The tumor microenvironment (TME) is a complex and dynamic ecosystem composed of cancer cells, stromal cells, immune cells, and the extracellular matrix, which significantly influences the initiation, progression, and therapeutic response of cancer. Emerging evidence indicates a crucial interaction between the nervous and immune systems within the TME, forming a “neuro-immune axis” that profoundly impacts tumor biology. This review not only synthesizes current knowledge on this critical bidirectional crosstalk but also offers a fresh perspective by critically evaluating underappreciated aspects such as the neural differentiation of cancer stem cells and the challenges in translating preclinical findings into clinical therapies. On one hand, tumor cells actively promote nerve recruitment and remodeling through tumor innervation, neurogenesis, and perineural invasion. In turn, neural signals-including adrenergic, cholinergic, and sensory neuropeptides-orchestrate immunosuppression by modulating key immune cell populations such as T cells, macrophages, and myeloid-derived suppressor cells (MDSCs). Consequently, neural signaling promotes immune escape, tumor progression and therapeutic resistance. This review further critically evaluates the translational potential of targeting these neuro-immune interactions, highlighting combination strategies designed to enhance the efficacy of cancer immunotherapy.
Targeting the mechanisms regulating Treg recruitment, stability, or suppressive function may represent a promising strategy to enhance the efficacy of immunotherapies including Bacillus Calmette–Guérin therapy.
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This review systematically summarizes the classification and identification of myeloid-derived suppressor cells, their biological properties in the context of tumors and autoimmune diseases, genetic and signaling pathway regulatory mechanisms, differentiation skewing in the TME, and cellular interactions with the TME.
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Within the CRC microenvironment, neural and immunological systems constitute a regulatory axis with strong dynamism and bidirectionality, thereby profoundly influencing tumor initiation, immune evasion, and therapeutic resistance. Here, we systematically outline the anatomical as well as functional underpinnings, the m...
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