Inflammation and atherosclerosis: signaling pathways and therapeutic intervention
Open accessAbstract
Atherosclerosis is a chronic inflammatory vascular disease driven by traditional and nontraditional risk factors. Genome-wide association combined with clonal lineage tracing and clinical trials have demonstrated that innate and adaptive immune responses can promote or quell atherosclerosis. Several signaling pathways, that are associated with the inflammatory response, have been implicated within atherosclerosis such as NLRP3 inflammasome, toll-like receptors, proprotein convertase subtilisin/kexin type 9, Notch and Wnt signaling pathways, which are of importance for atherosclerosis development and regression. Targeting inflammatory pathways, especially the NLRP3 inflammasome pathway and its regulated inflammatory cytokine interleukin-1β, could represent an attractive new route for the treatment of atherosclerotic diseases. Herein, we summarize the knowledge on cellular participants and key inflammatory signaling pathways in atherosclerosis, and discuss the preclinical studies targeting these key pathways for atherosclerosis, the clinical trials that are going to target some of these processes, and the effects of quelling inflammation and atherosclerosis in the clinic.
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Inflammation is critically implicated in the pathogenesis and progression of numerous diseases.
“Inflammation, as a basic pathological process, is critically implicated in the pathogenesis and progression of numerous diseases.”
From Picroside II as a Potential Anti-Inflammatory Agent (2026) · cites this paper as [4]
The Introduction identifies atherosclerosis as chronic vascular inflammation and describes inflammatory processes that promote plaque progression. The paper supports the claim for atherosclerosis, but the broader assertion about the pathogenesis and progression of numerous diseases is not established by these passages. (LLM, conf=0.86)
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In Vitro Modeling of Atherosclerosis Using iPSC‐Derived Blood Vessel Organoids
Kong, D., Ryu, J., Shin, N., Lee, S., Kim, N. G., Kim, H., Kim, M., Choi, J., Kim, D., & Kang, K. (2025) · Advanced Healthcare Materials · doi:10.1002/adhm.202400919 · Cited by 36 · see citing works
Cao, C., Liu, W., Guo, X., Weng, S., Chen, Y., Luo, Y., Wang, S., Zhu, B., Liu, Y., & Peng, D. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1460431 · Cited by 16 · see citing works
Borges, A. L. S., Bittar, V. P., Justino, A. B., Carrillo, M. S. P., Duarte, R. F. M., Silva, N. B. S., Gonçalves, D. S., Prado, D. G., Araújo, I. A. C., Martins, M. M., et al. (2024) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2024.116143 · Cited by 6 · see citing works
Picroside II as a Potential Anti-Inflammatory Agent
Ren, Y., Liu, Z., Wei, L., Wang, Y., Wang, Y., Guo, Y., & Ma, Z. (2026) · Pharmaceutics · doi:10.3390/pharmaceutics18040499 · Cited by 2 · see citing works
- Authors
- Kong, P., Cui, Z.-Y., Huang, X.-F., Zhang, D.-D., Guo, R.-J., & Han, M.
- Affiliations
- Hebei Medical University (CN)
- Corresponding author
- Han, Mei
- ORCID
- Han, Mei
- Venue
- Signal Transduction and Targeted Therapy
- Published
- 2022-04-22
- Volume
- 7
- Issue
- 1
- Pages
- 131-131
- ISSN
- 2059-3635 (ISSN-L)
- PMC
- PMC9033871
- OpenAlex
- W4224251997
- Cited by
- 1,183
- References
- 33
- Citations by year
- 2026: 262 · 2025: 456 · 2024: 301 · 2023: 139 · 2022: 25
- FWCI
- 24.21
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Signal Transduction and Targeted Therapy (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation of China (91739301, 91849102, QN2020167, H2019206028, H2021206006)
- Natural Science Foundation of Hebei Province (H2019206028, H2021206006, 91849102, 91739301)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Keywords
- atherosclerosis, inflammation, NLRP3 inflammasome, IL-1β, Toll-like receptors, PCSK9, Notch signaling, Wnt signaling, innate and adaptive immunity, atherosclerosis regression, anti-inflammatory therapy, inflammatory signaling
- MeSH terms
- NLR Family, Pyrin Domain-Containing 3 Protein, Humans, Inflammation, Signal Transduction, Atherosclerosis, Genome-Wide Association Study, Inflammasomes
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