Can A Toxic Metal Found in Vaccines Cause Heart Disease?

Monday, April 18, 2016 by: Dr. Jack Wolfson
Tags: aluminum in vaccines, heart disease, arterial blockage

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(NaturalNews) Aluminum is a metal found in many childhood vaccines. The stated role of aluminum as an adjuvant in vaccines is to enhance the immune response to the main ingredient in the vaccine. This would be either a virus or bacterial component.

Vaccines which currently contain aluminum are: hepatitis A, hepatitis B, diphtheria-tetanus-pertussis (DTaP, Tdap), Haemophilusinfluenzae type b (Hib), human papillomavirus (HPV) and pneumococcal.

Aluminum Stops Cellular Cleaning

Lysosomes are organelles inside of most cells in the body. These are the garbage cans of the cell that digest proteins and other molecules, spitting out their parts to be recycled into other cell components.

The interior of the lysosome is very acidic. This is necessary to break down the garbage. The acidity comes from an energy consuming process that pumps hydrogen ions into the lysosome.

Guess what blocks that hydrogen pump? You guessed it (by the title of the article), aluminum (1).

Yes, aluminum blocks the ability of the lysosome to get acidic. If not acidic, it doesn't work, and cellular garbage starts to collect.

You can imagine the consequences of excess cellular garbage? How would your house look if you didn't take out the garbage? It reminds me of the TV show, Hoarders.

Could Aluminum Link to Autoimmune Disease

The lysosome clears out the garbage. This includes dead cells, old cellular debris, and just about everything else.

If the lysosomes are working, the useless debris floats around the body. The debris is sensed by the immune system as foreign material. The immune system goes into attack mode and this process is linked to subsequent autoimmune conditions. Please read an excellent review by Drs. Shaw and Tomljenovic (2).

Aluminum Leads to Arterial Blockages

Lysosomes breakdown lipid particles that contain cholesterol. As LDL returns to the liver, it is taken up by LDL receptors. These receptors are like little catchers' mitts that trap the LDL and bring it into the liver cell. The LDL particle, along with the receptor travel into the lysosome inside the cell.

But because of aluminum, the lysosome is not acidic enough, and this LDL particle/receptor complex is not broken down. So now, the cell becomes full of cholesterol. In a form of negative feedback, the cell no longer puts out receptors to trap LDL particles.

Without uptake into the liver for breakdown and reprocessing, the LDL particles keep circulating around the body, become damaged by inflammation and oxidation, and are TAKEN UP into plaque.

Aluminum Inhibits Crucial Anti-Oxidant

Glutathione is a major detoxifier in the body. It ushers out toxic metals and other pollutants. Low levels are associated with countless diseases. Scientists have found that glutathione levels are low in heart attack patients. Well, aluminum inhibits glutathione production and function (3).

Aluminum Can Also Cause:

- Cardiomyopathy (4)
- Elevated blood sugar (5)
- Oxidative stress (linked to heart disease (6))
- Heart attacks (7)
- Brain disorders and dementia (8)
- Birth defects (9).

All this, thanks to our "friend" aluminum.

Oh....each of the three Hepatitis B vaccine doses contains 1,000,000,000,000,000,000,000 aluminum atoms. Each atom has the potential to interfere with lysosome function.

Think twice about injecting aluminum into your newborn to supposedly prevent a viral infection linked to IV drugs use and sleeping with prostitutes.

No matter what your opinion is on vaccines, we need to get aluminum out of them. Aluminum serves no biochemical role in the body and inhibits countless enzymes which leads to disease. This is clearly a situation where the medical intervention is more risky than the infection it is designed to prevent.

Learn more about Dr. Jack Wolfson at TheDRsWolfson.com

Sources:

1. J InorgBiochem. 2013 Nov;128:229-36.
2. Immunotherapy. 2014;6(10):1055-71
3. J Cell Biochem. 2004 Dec 15;93(6):1267-71
4. J Saudi Heart Assoc. 2014 Oct;26(4):216-21
5. PLoS One. 2015 Apr 13;10(4):e0123742.
6. J Res Med Sci. 2014 Feb;19(2):196
7. J Expo Sci Environ Epidemiol. 2014 Jan-Feb;24(1):82-8.
8. Expert Rev Neurother. 2014 Jun;14(6):589-91.
9. Birth Defects Res A ClinMolTeratol. 2016 Feb;106(2):95-103.