possible HIV vaccine and cure
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andrew j langham

UK

#24 Aug 6, 2010
Methyl octadecanoic acid (tuberculostearic acid) is present at the sn-2 position in the phosphatidylinositol mannosides found mainly in several Mycobacterium species and form esters with testosterone and estradiol which carries across the brain barrier into dentritic cells may be responsible for brain cancers and neuron diseases and complicates HIV treatment;

Later, a similar position of tuberculostearic has been described in phosphatidylethanolamines from Mycobacterium tuberculosis. The detection of this fatty acid in saliva and cerebrospinal fluid was proposed as a possibility for rapid and specific diagnosis of tuberculous meningitis. The presence of this fatty acid in sputum lipids was successively utilized for the diagnosis of tuberculous pneumonia. note; methyl nonadecanoic acid (phytomonic acid) is also found in Mycobacterium, along with mrsa staph'
andrew j langham

UK

#25 Aug 7, 2010
AIDS-related dementia complex.and relevent glyco protein having specific gravity of 1.20 exsisted before HIV it is not just the coating of the HIV virus;
gp120, the coat protein of HIV, can be neurotoxic and is thought to contribute to AIDS-related dementia complex. Such toxicity involves activation of glutomate receptors, mobilization of free cytosolic calcium; as previously known, shows that estrogen 17β-estradiol, in concentrations of 100 nM or higher, lessens the neurotoxicity of gp120 in hippocampas and cortical cultures, slows gp120-induced calcium mobilization;
In this examined protective potential of other estrogens, gp120 neurotoxicity in hippocampas cultures are significantly lessened by estrone, equilin and estriol, although with an order of magnitude less potent than 17β-estradiol. all four estrogens to gp120-induced calcium mobilization, with estriol being more efficacious than the other three estrogens,note aluminium ion take up in these areas block cells leading to a tremendous build up of calcium ions outside brain cells; These findings give insight both into the mechanisms of estrogenic protection (e.g. receptor-dependent versus independent actions) and show that even small amounts of aluminium ions cause significant blocking of brain cells; ie little or no calcium ions enter the brain cells because the the receptors of A globulin are blocked with aluminium ions;
andrew j langham

UK

#26 Aug 8, 2010
The gp120 gene, env, is around 1.5 kb long and codes for around 500 amino acids; Three gp120s, bound as heterodimers to a transmembrane glycoprotein, gp41, are thought to combine in a trimer to form the envelope spike, which is involved in virus-cell attachment.

Note well; testosterone estrifiction with Hiv proteins using pylori toxin acting as a catalyst is the major way in which HIV virions gain access to all bodily cells; fact;

The glycoprotein gp120 is anchored electrostaically to the viral membrane, via non-covalent bonds with the transmembrane glycoprotein, gp41. It is involved in entry into cells by stimulating CD4 receptors, which helper CD4 T-cells then should stimulate a cyctokine cascade, which due to Hiv contamination does not fuction;

note in the future it may be possible to use the RF frequency of hydrogen in multple short bursts in order to dis-enguage Hiv gp 120 electro-statically + a vaccine that acts against corrupt testosterone hiv esters thus irradicating and blocking hiv virions completely;
andrew j langham

UK

#27 Aug 8, 2010
The gp120 gene, env, is around 1.5 kb long and codes for around 500 amino acids; Three gp120s, bound as heterodimers to a transmembrane glycoprotein, gp41, are thought to combine in a trimer to form the envelope spike, which is involved in virus-cell attachment.

Note well; testosterone estrification with Hiv proteins, using pylori toxin acting as a catalyst is the major way in which HIV virions gain access to all bodily cells; fact;

The glycoprotein gp120 is anchored electro-statically to the Hiv viral membrane, via 'non-covalent bonds' with the transmembrane glycoprotein, gp41. It is involved in complex entry into cells by stimulating CD4 receptors, which helper CD4 T-cells then should stimulate a cytokine cascade, which due to Hiv contamination does not function;

note in the future it may be possible to use the RF frequency of hydrogen (1400MHz), in multiple short bursts, in order to dis-engage Hiv gp 120 electro-statically + the use of an administered vaccine that acts against corrupt testosterone hiv esters, thus irradicating and blocking hiv virions completely;
andrew j langham

Derby, UK

#33 Jun 12, 2013
note; CCR5 delta can isolated and given by injection; and is not toxic' early on in HIV patients immune system can learn to acquire the ccr5 & cxr4 genes so might be able to sustain immunity against HIV progressing to AIDS;
andrew john langham

Derby, UK

#40 Jun 30, 2013
CCR5 has the ability to communicate with B memory cells and can instruct an epsin derived coating that recognizes HIV protein' so whether or not the CCR5 is a type of gate it unlikely' its more of a protein recognition that is able to domainate surrounding cells in the same class'so that clathrin only is coated on cells that need down grading' so that the dominant remaining CCR5 protein coated cells then class homologize and remain resistant to HIV
andrew john langham

Derby, UK

#41 Jun 30, 2013
VERY VERY IMPORTANT:_>>>> >

The Clathrin' endocytosis and exocytosis of vesicles allows cells to transfer nutrients, to import signaling receptors, to mediate an immune response after sampling the extracellular world, and to clean up the cell debris left by tissue inflammation. On occasion, this mechanism also provides a pathway for raiding pathogens or toxins.
andrew john langham

Derby, UK

#42 Jun 30, 2013
CCR5 means Clathrin Coated Reductase of 5 B CELL instructed proteins' which form the cell coating, of which people immune to HIV have as a written Gene on spry 1 & 2 upon zinc fingure arrays; this very important and is the hub clue process'and the writes corrupt HIV genes that produce HIV protein amino chains of extreme length'and forms lipidoidal tertiary Globule known as the full tractioned HIV capsid' which is disengaged inside T cells by acidification by reductase;
andrew john langham

Derby, UK

#43 Jun 30, 2013
SPRY1 derived proteins function as an antagonist of fibroblast growth factor (FGF) pathways and negatively modulate respiratory organogenesis. part of the sprouty family. Induced by FGF growth factoring & signaling. and plays apart in neuro-transmitters associate to B cells of which Hiv shuts the process down so B cells do not recognize antigens' CCxR5 protein can block SPRY 1 & 2 proteins so therefore HIV cannot DOWN GRADE' B CELLS from recognizing HIV amino acid chains as marked or unmarked antigens and will instruct an antibody phage and phagocite response by natural killer cells' even if T HELPER cell information is lacking' so allows tyrosine kinase to dock which then down grades HIV in all cells especially T CELLS and phages;
andrew john langham

Derby, UK

#53 Jul 11, 2013
We now have the answer for a viable HIV vaccine…….

NOTE- Genetic cell engineering involves isolating the CCR5 Delta 5 CCXR5 delta protein incorporated in donars B cells’ and in vitro incorporating into a safe adenoids virus’ or safe lentivirus and then in vivo inserting into the body by oral capsule vaccine so that when transcription takes place’ new CCXR5 Delta genes will be formed’ thus then providing B cell update recovery in new B cells’ this will work for everyone as a safe Hiv vaccine and Hiv cure; Thanks be to Almighty God/Allah' thanks to Jesus my best friend; who is the one with the 'real Knowledge'''''

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