Inflammation isn't the fire. It's the fire department.
We've been suppressing the body's natural healing mechanisms. The data is starting to show what that costs us.
What inflammation actually does.
When arteries get damaged, macrophages increase up to 20-fold.
They clear approximately 1 million dead cells per second through a process called efferocytosis.
These cells don't just remove debris. They secrete growth factors that regenerate tissue and form new blood vessels.
The REDUCE-IT trial showed that enhancing natural resolution pathways through EPA supplementation reduced cardiovascular events by 25%.
Suppress the fire department. Watch the building burn.
Mice with completely suppressed inflammation develop:
- -Larger necrotic cores in arterial plaques
- -20-fold reduction in plaque repair capacity
How vaccines modulate inflammation.
Vaccines don't just target specific pathogens. They modulate the entire immune system.
Vaccines can expand regulatory T-cell populations, suppressing immune responses
Small molecule immunomodulators can reduce TNF-α and IL-6
Aluminum adjuvants persist in tissues, continuously modulating immune responses
These mechanisms can prevent the transition from inflammatory M1 macrophages to healing M2 macrophages - the ones that clear plaques.
The cardiovascular data.
Increased coronary artery disease risk (COVID vaccine, 2025 meta-analysis)
Increased risk after second dose
Increased myocarditis/pericarditis risk
Myocarditis risk after second dose
This pattern isn't unique to vaccines.
NSAIDs
Increase cardiovascular risk by disrupting thromboxane/prostacyclin balance. Delay bone healing by inhibiting COX-2 - the same pathways needed for cardiovascular repair.
Complete anti-inflammatory therapy
Animals develop impaired reverse cholesterol transport, larger necrotic cores, increased plaque vulnerability.
Block inflammation. Get worse outcomes.
The mortality pattern.
DTP vaccination is associated with a 2.54-fold increase in female mortality from all causes. Not just the target diseases. All causes.
Six different non-live vaccines tested - DTP, pentavalent, inactivated polio, HBV, H1N1 influenza - all showed increased female mortality through:
- -Suppression of innate immunity
- -Induction of T-cell anergy
WHO-sponsored reviews found this pattern affects hundreds of thousands of deaths annually in Africa alone.
The timing problem.
Cardiovascular vaccine studies have median follow-ups of only 19.5 months.
Too short. Long-term consequences of disrupted inflammatory healing may take years to manifest as increased plaque burden and cardiovascular events.
Evidence shows fever suppression increases mortality. Hypothermia trials were terminated early due to increased deaths.
Natural inflammatory responses exist for a reason.
We've been suppressing the fire department.
The natural inflammatory response removes damaged cells at 1 million per second. Produces specialized molecules to resolve inflammation. Maintains arterial health through continuous repair.
Disable it? The body can't maintain its arteries.