Molecular mechanisms and therapeutic progress in atherosclerosis: bridging immune inflammation and precision medicine
Yimin Han1, Hongyi Xu1, Xinlei Yao1
1Jiangsu Key Laboratory of Tissue Engineering and Neuroregeneration, Key Laboratory of Neuroregeneration of Ministry of Education, Co-innovation Center of Neuroregeneration, Medical School of Nantong University, Nantong University, Nantong, Jiangsu, China.
Insights
This review details atherosclerosis pathogenesis, focusing on lipid-driven inflammation and immune responses. Emerging therapies and precision medicine approaches are highlighted for improved cardiovascular disease treatment.
Area of Science:
- Cardiovascular Research
- Immunology
- Vascular Biology
Background:
- Atherosclerosis is a primary cause of cardiovascular morbidity and mortality.
- It involves lipid-driven inflammation and arterial remodeling.
- Current treatments face limitations in addressing complex pathogenesis.
Purpose of the Study:
- To systematically review recent advances in atherosclerosis pathogenesis.
- To summarize evolving therapeutic strategies.
- To explore the integration of multi-omics and AI for precision medicine.
Main Methods:
- Literature review focusing on endothelial dysfunction, dyslipidemia, and immune activation.
- Discussion of cellular mechanisms like metabolic reprogramming and programmed cell death.
- Analysis of novel therapeutic avenues and traditional Chinese medicine.
Main Results:
- Detailed understanding of the interplay between metabolic, immune, and vascular cells in atherosclerosis.
- Identification of emerging therapies including RNA-based treatments and immunomodulatory vaccines.
- Emphasis on personalized medicine through multi-omics and AI integration.
Conclusions:
- Precision medicine integrating multi-omics, single-cell tech, and AI is crucial.
- Individualized risk prediction and targeted interventions are key.
- Bridging molecular mechanisms and clinical management will improve atherosclerosis treatment.
Abstract:
Atherosclerosis, a chronic vascular disease characterized by lipid-driven inflammation and arterial wall remodeling, remains the leading cause of cardiovascular morbidity and mortality. This review aims to systematically summarize recent advances in our understanding of its multidimensional pathogenesis and the corresponding evolution of therapeutic strategies. We focus on the intricate crosstalk between endothelial dysfunction, dyslipidemia, and immune-inflammatory activation, which collectively drive disease progression. Key mechanisms discussed include metabolic reprogramming of immune cells, phenotypic switching of vascular smooth muscle cells, and novel modes of programmed cell death. Beyond conventional lipid-lowering approaches, we highlight emerging therapeutic avenues such as immunomodulatory vaccines, RNA-based therapeutics, and biodegradable stents with inherent anti-ferroptotic properties. Furthermore, we explore the potential of modernized traditional Chinese medicine formulations that target multiple pathways. Looking forward, we conclude that integrating multi-omics data, single-cell technologies, and artificial intelligence is pivotal for advancing precision medicine. This integration will enable the development of individualized risk prediction models and targeted interventions, ultimately bridging the gap between molecular mechanisms and effective clinical management to overcome current bottlenecks in atherosclerosis prevention and treatment.
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