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.

Vaccine
|January 23, 2020
PubMed

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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