parvofighter
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Here's some interesting info on a patented antiretroviral dialysis-like "machine" that is making a buzz in the biotech investment blogs. It's called the Hemopurifier , from Aethlon Medical Inc. and it has been proven to reduce viral load of HIV and other viruses, and improve immune function.
Why do I think this technology might have relevance for XMRV ME/CFS patients?
Excerpts of info on Aethlon Medical Inc.
From: http://messages.finance.yahoo.com/Stocks_(A_to_Z)/Stocks_H/threadview?m=tm&bn=27865&tid=388347&mid=388347&tof=12&frt=2
From: http://www.aethlonmedical.com/technology/hemopurifier.htm
The Hemopurifier - Aethlon Medical (OTC BB: AEMD.OB)
From: http://www.aethlonmedical.com/pdfs/IndustryReport.pdf
More publications on plasmapharesis at: http://www.aethlonmedical.com/technology/publications.htm

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Why do I think this technology might have relevance for XMRV ME/CFS patients?
- Some ME/CFS patients are highly drug-intolerant. The Hemopurifier might provide a viable non-drug option for these patients.
- It might provide a means to reduce maternal/fetal transmission of XMRV (if that indeed happens) after birth, preventing XMRV from entering cells and organs.
- If government guidelines result in delay of antiretrovirals for XMRV patients (something that I don't recall being discussed yet on this forum), the Hemopurifier could "be used as a first line therapy, reducing viral load and delaying the need to start antiviral therapy."
- If XMRV - despite its low replication rate - eventually proves to mutate in the way HIV does, developing resistance to drug therapies, the Hemopurifier could forestall XMRV resistance to antiretrovirals by removing mutant strains.
- If used in a clinical trial with Canadian-criteria, XMRV+ve ME/CFS patients, treatment success might provide yet another source of proof that we are dealing with a virus, and abnormal cytokine profile.
- Since retroviruses (and ME/CFS) are known to be associated with opportunistic infections, use of the Hemopurifier might be invaluable in eliminating opportunistic infections within ME/CFS patients, as well as XMRV. This is especially relevant for as-yet unidentified opportunistic infections... namely viruses known to be positive in tissue, and below the limit of detection in bloodwork. I.E. You might have a false negative result (as I had) for, say, Parvovirus B19 or HHV-6. But you need to treat that too, as well as the XMRV (if indeed XMRV is proven to be causal for ME/CFS).
- And the list goes on... very intriguing stuff.
Excerpts of info on Aethlon Medical Inc.
From: http://messages.finance.yahoo.com/Stocks_(A_to_Z)/Stocks_H/threadview?m=tm&bn=27865&tid=388347&mid=388347&tof=12&frt=2
- Established Exosome Sciences, Inc. (ESI) as a wholly owned subsidiary of Aethlon Medical to leverage the discovery that our Hemopurifier captures exosomes known to suppress the immune system in cancer patients.
- Completed and reported on the "first-in-man" study of a medical device to treat the Human Immunodeficiency Virus (HIV), which demonstrated a 92% reduction of viral load and improved immune function resulting from short-term intermittent application of our Hemopurifier in the absence of any antiviral drug therapy.
- OK, so how do we get Aethlon interested in doing research on XMRV?
- Entered into an agreement that extends studies of our Hemopurifier with the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) under a cooperative research and development agreement.
- I wonder if USAMRIID might be enticed by Veterans associations - possibly Dr Klimas and/or WPI? - to do a study on the Hemopurifier with Gulf War Illness and/or ME/CFS patients?
- Documented our Hemopurifier effectively captures the current pandemic strain of the H1N1 Swine Flu Virus. During invitro studies, the Hemopurifier removed 68% of H1N1 virus from blood plasma in 30 minutes, 80% of the virus in two hours, and a 96% reduction of H1N1 was observed at six hours. The studies were performed by third party researchers approved by the United States Department of Health and Human Services (HHS) to house and conduct research with pandemic strains of H1N1 virus.
- Reported compelling human clinical outcomes against Hepatitis-C virus (HCV) infection; then disclosed a data supported strategy to improve HCV cure rates; and subsequently discovered a clinical validation by Asahi Kasei Kuraray Medical (Asahi) that confirms moderate levels of viral filtration at the outset of standard of care (SOC) therapy can dramatically impact HCV cure rates.
From: http://www.aethlonmedical.com/technology/hemopurifier.htm
Aethlon Medical has developed a patented extracorporeal device, known as the Hemopurifier, to address the treatment of viral conditions that are either resistant or evolve resistance to drug and vaccine therapies. The Hemopurifier converges the established scientific principals of hollow-fiber dialysis and affinity chromatography with the discovery of affinity agents that selectively bind envelope viruses. The result is an affinity treatment cartridge that separates and captures circulating viruses, viral proteins, and toxins before the occurrence of cell and organ infection. The treatment goal is to reduce viral load burden without drug toxicity so that the patient's natural immunity can recover to wage an effective battle against viral infection. However, the mechanical nature of the Hemopurifier also allows it to be deployed in conjunction with other therapies including drugs and vaccines, if available. An additional benefit stems from treatment access, as the Hemopurifier has been designed for utilization in the global infrastructure of dialysis and continuous renal replacement machines already present in hospitals and clinics.
Scientific articles classify the Hemopurifier to be both an immunotherapy and fusion inhibitor treatment. The Food And Drug Administration (FDA) has indicated that the Hemopurifier will be treated as a Class III Medical Device in U.S. regulatory submissions. Pre-clinical human blood studies have documented the effectiveness of the Hemopurifier in capturing HIV (The AIDS Virus), HCV (Hepatitis-C), and Orthopox Viruses related to human Smallpox. The mechanism of capture has been shown to be via the polysaccharide chains that reside on the surface glycoproteins of envelope viruses. Since the polysaccharide portions of the viral glycoproteins are attached via normal host cell (functions not under control of the virus), they are highly invariant. Moreover, the high abundance of polysaccharides allows viruses to escape immune surveillance. Thus, while many viral proteins are highly variable in their primary structure, the polysaccharide chains are nearly invariant, allowing for the capture of all strains and clades of many viruses. In fact, lectin derived affinity agents immobilized within the Hemopurifier have been shown to inhibit the growth of all tested strains of HIV and can capture of inhibit the growth of other envelope viruses including SIV, FIV, HCV, Measles, Mumps, Influenza, Ebola, Marburg, and Orthopox viruses. Recent studies indicate that the Hemopurifier affinity agent is also able to capture Dengue hemorrhagic fever virus. In conclusion, the Hemopurifier has expansive therapeutic capabilities that address: global pandemics (HIV-AIDS); chronic infectious diseases (Hepatitis-C); naturally evolving pathogens; and pathogens weaponized for bioterrorism attacks against U.S. military and civilian populations.
Scientific articles classify the Hemopurifier to be both an immunotherapy and fusion inhibitor treatment. The Food And Drug Administration (FDA) has indicated that the Hemopurifier will be treated as a Class III Medical Device in U.S. regulatory submissions. Pre-clinical human blood studies have documented the effectiveness of the Hemopurifier in capturing HIV (The AIDS Virus), HCV (Hepatitis-C), and Orthopox Viruses related to human Smallpox. The mechanism of capture has been shown to be via the polysaccharide chains that reside on the surface glycoproteins of envelope viruses. Since the polysaccharide portions of the viral glycoproteins are attached via normal host cell (functions not under control of the virus), they are highly invariant. Moreover, the high abundance of polysaccharides allows viruses to escape immune surveillance. Thus, while many viral proteins are highly variable in their primary structure, the polysaccharide chains are nearly invariant, allowing for the capture of all strains and clades of many viruses. In fact, lectin derived affinity agents immobilized within the Hemopurifier have been shown to inhibit the growth of all tested strains of HIV and can capture of inhibit the growth of other envelope viruses including SIV, FIV, HCV, Measles, Mumps, Influenza, Ebola, Marburg, and Orthopox viruses. Recent studies indicate that the Hemopurifier affinity agent is also able to capture Dengue hemorrhagic fever virus. In conclusion, the Hemopurifier has expansive therapeutic capabilities that address: global pandemics (HIV-AIDS); chronic infectious diseases (Hepatitis-C); naturally evolving pathogens; and pathogens weaponized for bioterrorism attacks against U.S. military and civilian populations.
The Hemopurifier - Aethlon Medical (OTC BB: AEMD.OB)
From: http://www.aethlonmedical.com/pdfs/IndustryReport.pdf
Researchers from Aethlon Medical have developed a potentially promising extracorporeal entry inhibitor, the Hemopurifier (HIV dialysis). The Hemopurifier, by decreasing viral load, appears to have a number of attributes necessary for a globally practical therapy for HIV, both as a conjunctive and salvage therapy. And by removing mutant strains, could extend the life of currently approved drugs and could represent a valuable lifecycle management strategy. The Hemopurifier is able to clear infectious HIV, gp120 and other related toxins before infection occurs. Also, since the Hemopurifier does not cause cross-resistance, and given the new government guidelines that encourage the delay of initial drug regimens, it may be utilized as a first line therapy, reducing viral load and delaying the need to start antiviral therapy. Aethlon Medicals dialysis approach could also represent an important adjunct therapy for current dialysis patients that are co-infected with HIV (estimated to be a significant percent of the current kidney dialysis population). Aethlon also has plans to use the Hemopurifier as a treatment countermeasure against drug and vaccine resistant biological weapons. In one hour of treatment The Hemopurifier has cleared 90% of the toxic protein gp-120, which depletes healthy immune cells.58 Aethlon scientists are also researching the capability of the Hemopurifier to regulate the overproduction of Cytokines, which could improve the treatment outcomes of both infectious and autoimmune diseases.
The Hemopurifier, by removing mutant strains that cause resistances, could extend the life of currently approved drugs, and represent a valuable lifecycle management strategy for patients and pharmaceutical companies.
The Hemopurifier, by removing mutant strains that cause resistances, could extend the life of currently approved drugs, and represent a valuable lifecycle management strategy for patients and pharmaceutical companies.
More publications on plasmapharesis at: http://www.aethlonmedical.com/technology/publications.htm
Now we just have to get Judy Mikovits and Jim Joyce
(Chairman & CEO of Aethlon Medical Inc.) talking.

[FONT="] P.S. Just wish I had some income so I could buy stock!(Chairman & CEO of Aethlon Medical Inc.) talking.
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