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Quantitative Analysis of Cellular Composition in Advanced Atherosclerotic Lesions of Smooth Muscle Cell Lineage-Tracing Mice
Published on: February 20, 2019
Opportunities for an atherosclerosis vaccine: From mice to humans
Payel Roy1, Amal J Ali1, Kouji Kobiyama2
1Division of Inflammation Biology, La Jolla Institute for Immunology, 9420, Athena Circle Drive, La Jolla, CA 92037, USA.
Abstract:
Atherosclerosis, the major underlying cause of cardiovascular diseases (CVD), is the number one killer globally. The disease pathogenesis involves a complex interplay between metabolic and immune components. Although lipid-lowering drugs such as statins curb the risks associated with CVD, significant residual inflammatory risk remains. Substantial evidence from experimental models and clinical studies has established the role of inflammation and immune effector mechanisms in the pathogenesis of atherosclerosis. Several stages of the disease are affected by host-mediated antigen-specific adaptive immune responses that play either protective or proatherogenic roles. Therefore, strategies to boost an anti-atherogenic humoral and T regulatory cell response are emerging as preventative or therapeutic strategies to lowering inflammatory residual risks. Vaccination holds promise as an efficient, durable and relatively inexpensive approach to induce protective adaptive immunity in atherosclerotic patients. In this review, we discuss the status and opportunities for a human atherosclerosis vaccine. We describe (1) some of the immunomodulatory therapeutic interventions tested in atherosclerosis (2) the immune targets identified in pre-clinical and clinical investigations (3) immunization strategies evaluated in animal models (4) past and ongoing clinical trials to examine the safety and efficacy of human atherosclerosis vaccines and (5) strategies to improve and optimize vaccination in humans (antigen selection, formulation, dose and delivery).
Insights
Developing a human atherosclerosis vaccine could reduce residual inflammatory risks associated with cardiovascular diseases (CVD). This approach aims to induce protective adaptive immunity, offering a promising preventative and therapeutic strategy.
Area of Science:
- Cardiovascular Research
- Immunology
- Vaccinology
Background:
- Atherosclerosis, a primary cause of global mortality from cardiovascular diseases (CVD), involves complex metabolic and immune interactions.
- Despite statin therapy, significant residual inflammatory risk persists in CVD patients.
- Inflammation and adaptive immune responses critically influence atherosclerosis development, with roles that can be protective or detrimental.
Purpose of the Study:
- To review the current status and future opportunities for developing a human atherosclerosis vaccine.
- To explore immunomodulatory interventions, identified immune targets, and immunization strategies for atherosclerosis.
- To discuss clinical trials and optimization strategies for human atherosclerosis vaccines.
Main Methods:
- Review of immunomodulatory therapies and immune targets in atherosclerosis.
- Analysis of pre-clinical immunization strategies in animal models.
- Examination of clinical trial data and optimization approaches for human vaccines.
Main Results:
- Several immunomodulatory interventions have been tested for atherosclerosis.
- Key immune targets and immunization strategies have been identified through pre-clinical and clinical research.
- Past and ongoing clinical trials are evaluating the safety and efficacy of atherosclerosis vaccines.
Conclusions:
- Vaccination presents a viable strategy to induce protective adaptive immunity against atherosclerosis.
- Boosting anti-atherogenic humoral and T regulatory cell responses can mitigate residual inflammatory risks.
- Optimizing antigen selection, formulation, dose, and delivery is crucial for effective human atherosclerosis vaccines.
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Atherosclerosis I: Introduction
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Atherosclerosis II: Clinical Manifestations and Diagnostic Tests

