Sunday, August 03, 2008

Robert Kennedy on the Vaccine Autism Coverup



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Another Plum Island link- Brucella's TLR2?

Plum Island is a bio-weapons military/Big Pharma chemical and biological weapons research center located between Long Island, New York, and Connecticut, located in Long Island Sound.

Was West Nile virus and Lyme Disease an "accidental" release of bio-weapons to the general public?

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The below from PubMed [found here]

1: Hoppe Seylers Z Physiol Chem. 1983 May;364(5):593-606.

Synthesis of the mitogenic S-[2,3-bis(palmitoyloxy)propyl]-N-palmitoylpentapeptide from Escherichia coli lipoprotein.



Wiesmüller KH, Bessler W, Jung G.

The N-terminal pentapeptide of the lipoprotein from the outer membrane of Escherichia coli was obtained by coupling S-[2,3-bis(palmitoyloxy)-(2RS)-propyl]-N-palmitoyl-(R)-cysteine to O-tert-butylseryl-O-tert-butyl-seryl-asparaginyl-alanine tert-butyl ester followed by deprotection with trifluoroacetic acid. The tetrapeptide was built up from alanine tert-butyl ester with N-9-fluorenylmethyloxycarbonyl protected amino acids. S-[2,3-Bis(palmitoyloxy)propyl]-N-palmitoylcysteine was obtained from N,N'-dipalmitoylcystine di-tert-butyl ester via reduction to the thiol, and S-alkylation with racemic 3-bromo-1,2-propanediol followed by esterification with palmitic acid in the presence of dicyclohexylcarbodiimide/dimethylaminopyridine and deprotection with trifluoroacetic acid. The compounds were characterized unequivocally by 13C-NMR and mass spectra. The diastereomers of S-[2,3-bis(palmitoyloxy)propyl]-N-palmitoylcysteine tert-butyl ester with opposite configuration at the propyl-C-2 atom could be separated on a silica-gel column.



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http://www.jimmunol.org/cgi/content/full/173/4/2683
LPS binding protein (LBP) is an acute-phase protein synthesized predominantly in the liver of the mammalian host. It was first described to bind LPS of Gram-negative bacteria and transfer it via a CD14-enhanced mechanism to a receptor complex including TLR-4 and MD-2, initiating a signal transduction cascade leading to the release of proinflammatory cytokines. In recent studies, we found that LBP also mediates cytokine induction caused by compounds derived from Gram-positive bacteria, including lipoteichoic acid and peptidoglycan fragments. Lipoproteins and lipopeptides have repeatedly been shown to act as potent cytokine inducers, interacting with TLR-2, in synergy with TLR-1 or -6. In this study, we show that these compounds also interact with LBP and CD14. We used triacylated lipopeptides, corresponding to lipoproteins of Borrelia burgdorferi, mycobacteria, and Escherichia coli, as well as diacylated lipopeptides, corresponding to, e.g., 2-kDa macrophage activating lipopeptide of Mycoplasma spp. Activation of Chinese hamster ovary cells transfected with TLR-2 by both lipopeptides was enhanced by cotransfection of CD14. Responsiveness of human mononuclear cells to these compounds was greatly enhanced in the presence of human LBP. Binding of lipopeptides to LBP as well as competitive inhibition of this interaction by LPS was demonstrated in a microplate assay. Furthermore, we were able to show that LBP transfers lipopeptides to CD14 on human monocytes using FACS analysis. These results support that LBP is a pattern recognition receptor transferring a variety of bacterial ligands including the two major types of lipopeptides to CD14 present in different receptor complexes.

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From Kathleen Dickson:

http://www.actionlyme.org/BIOWEAPONEERS_CORIXA_YALE_TLRS.htm

Keep in mind that the CDC, the HIV and the Lyme crooks are totally
flipping over the HIV link to the Lyme (LYMErix) crymes.

OspA suppresses the immune system, which is *probably* why it did
not work as an adjuvant or as part of the natural vaccine, even though
it is possible that whatever is in tick saliva blocks anti-HIV, which
has Pam3Cys scrambled into it.
http://www.actionlyme.org/PAM3CYS_LYME_HIV.htm

Remember, you can't recrystalize a lipid, so you can't shoot
it with X-rays to determine it's structure in the natural form.
Creating this vaccine, it also was not easy to get E. coli to exactly
produce three C14s. There was uneven lipidation even in the production
of the vaccine, and as the Korean report shows, this stuff gummed up
the HPLC columns, so they really could not assess the finished product:
http://www.actionlyme.org/PAM3CYS_LYME_HIV.htm

READ ABOUT IT.


They almost certainly worked with Brucella on Plum Island since that was
one of the main goodies the Navy brought back from Japan's Unit 731- something
we learned from Edward McSweegan:
http://www.actionlyme.org/GOLDWATER_LETTER.htm


Lyme is the Yuppie AIDS. It is not an inflammatory disease. The immune
suppression outcomes are the New Great Imitator outcomes.

The Yale Lyme criminals wrecked research in all known chronic/deadly diseases:
Cancer, HIV, ALS, Lupus, Multiple Sclerosis, Alzheimer's, and a whole slew of
half-known, partially understood immune disorders (allergies, toxins, etc).


LYMErix was the New Great Imitator Vaccine, when of course, they tried to
sell it as the first-ever vaccine against hypochondria or hysteria or
Lakkanukki,... while simultaneously claiming it was a stealth disabler;
a brain and nerve specific Trojan Horse or a time-bomb:
http://www.actionlyme.org/JohnDunn_Brookhaven.htm
http://www.actionlyme.org/SIKAND.htm


I would like everyone to note that the CDC and NIH make no corrections
to all these lies on their website. Did everyone watch Bobby Kennedy
Junior in his interview with Joe Scarborough re autism and vaccines?
http://www.youtube.com/watch?v=zrIM2hwrLoc

Don't miss it. It reveals *absolute* *deliberateness* in the cover-up.
That confirms what we already knew CDC has said about vaccines damage:
"It's a calculated risk."

They've known for at least 16 years (since 1992).

The solution is to get rid of the CDC. We cannot afford the screw
ups of any more secret government entities.


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