Aug 2026· Cell· Vol 189, pp. 5156 - 5173· 0 citations· 187 references
Medicine
TL;DR
Robust data support a model in which neurodegeneration emerges from complex interactions between neural and immune networks, positioning the immune system as both a sensor and driver of brain health and a deeper integration of neuroscience and immunology could transform the future of treating neurodegenerative diseases.
Abstract
SUMMARY Neurodegeneration is increasingly recognized not only as a disorder of neurons but also as a breakdown of dialogue between the nervous and immune systems. Recent discoveries reveal that immune cells and inflammatory signals are deeply interwoven with brain function across the lifespan. Far from passive responders, immune cells act as sentinels and shapers of neuronal resilience, vulnerability, and repair. Together, robust data support a model in which neurodegeneration emerges from complex interactions between neural and immune networks, positioning the immune system as both a sensor and driver of brain health. This perspective synthesizes a growing body of work arguing that neurodegenerative diseases are a failure of neuroimmune crosstalk—where protective signals are lost, and maladaptive responses take hold. By restoring immune homeostasis, fine-tuning inflammatory responses, or targeting epigenetic regulators of the immune state, it may be possible not only to slow degeneration but also to promote recovery. We outline the key challenges and opportunities for this paradigm shift and highlight how a deeper integration of neuroscience and immunology could transform the future of treating neurodegenerative diseases. Lastly, we describe critical focus areas to improve our understanding of neurodegeneration and highlight the development of immune-based therapeutics for neurodegeneration.
Intervention strategies that shift from targeting peripheral immune and glial cells to regulating neuron-derived immunity are systematically integrated, thereby providing a new theoretical framework for overcoming current clinical limitations and identifying effective therapeutic targets for the prevention and treatmen...
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It is proposed that microglia occupy a central position at the interface of these processes because of their dual roles in circuit remodeling and immune surveillance and highlights disease-modifying therapeutic strategies aimed at restoring microglial homeostasis to potentially mitigate the self-sustaining pathology in...
Fan-Qian Yang, Qing Tang, Xiaofang Wang et al.· Frontiers in Immunology· 0 citations
This perspective provides a unifying conceptual framework for understanding neuroimmune pathology in disorders such as Alzheimer’s disease, multiple sclerosis, stroke, and traumatic brain injury, while also pointing toward next-generation strategies that selectively modulate maladaptive cellular programs and promote re...
Moawiah M. Naffaa· Exploration of Immunology· 0 citations
Abstract Sepsis, a life-threatening organ dysfunction caused by a dysregulated host response, is characterized by a dynamic progression from hyperinflammation to immunosuppression. Its persistently high mortality underscores the limitations of therapies focused solely on immune homeostasis. This review advocates a para...
Chuntao Wang, Xiaojiang Huang, Chaoyao Hou et al.· Journal of Inflammation Rese...· 0 citations
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The mechanisms linking systemic inflammation to brain dysfunction are evaluated and emerging translational opportunities are highlighted, including the therapeutic repurposing of cytokine-targeting and immunomodulatory agents for neuropsychiatric interventions.
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