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56 <strong>Suppressed</strong> <strong>Inventions</strong> <strong>and</strong> Other <strong>Discoveries</strong><br />

MILITARY ORDERS FOR AIDS-LIKE VIRUSES:<br />

THE BIOLOGICAL WEAPONS CONTRACTORS<br />

As early as 1970, the U.S. Department <strong>of</strong> Defense (DOD) appropriated at<br />

least $10 million to "initiate an adequate program through the National<br />

Academy <strong>of</strong> Sciences-National Research Council (NAS-NRC)" to make<br />

a new infective microorganism which could differ in certain important<br />

aspects from any known disease-causing organisms. Most important <strong>of</strong><br />

these [aspects] is that it might be refractory to the immunological <strong>and</strong><br />

therapeutic processes upon which we depend to maintain our relative freedom<br />

from infectious disease. Members <strong>of</strong> the NAS-NRC had instructed<br />

scientific leaders in the DOD this work might be accomplished "within 5<br />

years." 4 This research was then carried out by American defense contractors<br />

despite the authorization <strong>and</strong> signing <strong>of</strong> the Geneva accord by Dr.<br />

Henry Kissinger <strong>and</strong> President Nixon outlawing the production <strong>and</strong> testing<br />

<strong>of</strong> such biological weapons. 5<br />

Also in 1970 Gallo <strong>and</strong> his co-workers presented research describing<br />

the experimental entry <strong>of</strong> bacterial ribonucleic acid (RNA) into human<br />

white blood cells (WBCs) before a special symposium sponsored by<br />

NATO. 6 The paper published in the Proceedings <strong>of</strong> the National Academy<br />

<strong>of</strong> Sciences discussed several possible mechanisms prompting the "entry<br />

<strong>of</strong> foreign nucleic acids" into lymphocytes—the cells principally attacked<br />

by HIV. Prior to this, Gallo et al. had published studies identifying:<br />

1. mechanisms responsible for reduced amino acid <strong>and</strong> protein synthesis<br />

by T-lymphocytes required for immunosuppression; 7<br />

2. specific enzymes required to produce such effects along with a "base<br />

pair switch mutation" in the genes <strong>of</strong> WBCs to create immune system<br />

dysfunction; 8 <strong>and</strong><br />

3. methods by which WBC "DNA degradation" <strong>and</strong> immune system<br />

decay may be prompted by the "pooling" <strong>of</strong> purine bases <strong>and</strong>/or the<br />

addition <strong>of</strong> specific reagents. 9<br />

Subsequent studies published in 1970 by Gallo <strong>and</strong> co-workers identified<br />

"RNA dependent DNA polymerase" (i.e., the unique AIDS-linked<br />

enzyme, reverse transcriptase) responsible for "gene amplification . . .<br />

biochemical cytodifferentiation," (i.e., the development <strong>of</strong> unique WBC<br />

characteristics including cancer cell production) <strong>and</strong> "leukaemogenesis";<br />

10 <strong>and</strong> identified L-Asparaginase synthetase—a key enzyme that, if<br />

repressed, will induce treatment resistant leukemias <strong>and</strong> <strong>other</strong> cancers. 11<br />

The year following the $10 million appropriation by the DOD for<br />

AIDS-like biological weapons research, the NCI acquired the lion's share

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