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Aging immune cells may drive Alzheimer's and Parkinson's, a review says

A summary of earlier studies · Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · Oct 12, 2026

What this means

This review pulls together earlier studies on aging immune cells and brain disease. It suggests these cells may be a target for future treatments, but it does not prove this.

Plain-English summary written by an AI model from the abstract. The original is below.

Tested inSummary of earlier studies
Who it was tested in
A review of earlier studies, not a new experiment
Kind of research
A summary of earlier studies

The science

Original title
Immunosenescence as a modifiable driver of neurodegenerative diseases: Pathways and multidimensional emerging strategies for Alzheimer's and Parkinson's diseases.
Authors
Zhao J, Qu L, Guan H et al.
Journal
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Published
Oct 12, 2026
Study type
Review

Abstract

Immunosenescence represents a core upstream driver of Alzheimer's disease (AD) and Parkinson's disease (PD), exerting its pathological effects through four mechanistically interconnected cascades: chronic inflammatory imbalance mediated by the senescence-associated secretory phenotype (SASP), oxidative stress arising from immune-metabolic reprogramming, protein homeostasis dysfunction caused by autophagy-lysosomal failure, and disrupted neuro-immune crosstalk secondary to breakdown of central nervous system (CNS) immune privilege. Current clinical practice remains largely constrained to neurotransmitter-based symptomatic management, which can neither arrest upstream pathological progression nor restore lost neuronal populations. Emerging intervention strategies targeting immunosenescence, including senolytic agents, antioxidant and metabolic modulators, autophagy restoration, and precision-targeted nanocarrier delivery, have demonstrated substantial capacity to delay disease progression in preclinical and early clinical investigations. These strategies act through selective clearance of senescent immune cells, remodeling of the neuroinflammatory microenvironment, and restoration of cellular quality-control mechanisms. The multidimensional treatment strategy approaches from the perspectives of artificial intelligence (AI) guided target discovery, nanocarrier engineering, and gut microbiota intervention to simultaneously address multiple nodes in the immunosenescence network, thereby overcoming the inherent limitations of single-target strategies. This review consolidates current mechanistic evidence and translational data to establish immunosenescence as an actionable therapeutic target and to provide a conceptual framework for precision disease-modifying therapy in AD and PD.

Read it on PubMed ↗

Zhao J, Qu L, Guan H et al. Immunosenescence as a modifiable driver of neurodegenerative diseases: Pathways and multidimensional emerging strategies for Alzheimer's and Parkinson's diseases. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics. 2026. doi:10.1016/j.neurot.2026.e01096. PMID: 42863347. https://pubmed.ncbi.nlm.nih.gov/42863347/

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