First Immune GcMAF

treatment for cancer, aids and immune diseases

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GcMAF information


What are Macrophages?

munching_macrophagemunching_macrophageMacrophages (Greek: "big eaters", makros = large, phagein = eat) are cells within the tissues that originate from specific white blood cells called monocytes. Monocytes and macrophages are phagocytes, acting in both nonspecific defence (or innate immunity) as well as specific defense (or cell-mediated immunity) of vertebrate animals. Their role is to phagocytize (engulf and then digest) cellular debris and pathogens either as stationary or mobile cells, and to stimulate lymphocytes and other immune cells to respond to the pathogen.  The picture shows a macrophage eating a tumour cell.

 

GcMAF: macrophages also attack other diseases

macrophagemacrophageThe GcMAF activated macrophages rapidly phagocytize various bacteria (E. coli, Salmonella typhimurium, Pseudomonas aeruginosa, B.subtilis, Clostridium perfringens and Mycobacterium tuberculosis) and various viruses (rubella, measles, herpes simplex, parainfluenza (Sendai), influenza virus and HIV type 1) (unpublished data).

There are indications that GcMAF may be effective against other diseases such as lupus, MS, Parkinson’s and fibromyalgia. No side effects are reported. (unpublished data)

Macrophage phagocytosing (eating) bateria.

 

GcMAF and EBV / Herpes Zoster

Similarly, treatment of peripheral blood macrophages of patients chronically infected with Epstein-Barr virus (EBV) and with herpes zoster with 100 ng GcMAF/ml resulted in a greatly enhanced macrophage activation. Like HIV, EBV infects lymphocytes (B cells). Since these enveloped viruses code for ?-N-acetylgalactosaminidase and infected cells secrete it into blood stream. Thus this enzyme activity in patient sera can be used as a prognostic index during therapy.

After approximately 25 administrations of GcMAF (100 ng/week) to patients chronically infected with EBV and with herpes zoster, the enzyme activity decreased to that of healthy control levels.

Source:  http://www.freepatentsonline.com/6410269.html

 

GcMAF and HIV

Since latently HIV-infected cells are unstable and constantly release HIV virions, the activated macrophages rapidly intercept the released HIV virions to prevent reinfection resulting in exhaustion of infected cells.

After less than 18 weekly administrations of 100 ng GcMAF for nonanemic patients, they exhibited low serum Nagalase activities equivalent to healthy controls, indicating eradication of HIV-infection, which was also confirmed by no infectious center formation by provirus inducing agent-treated patient PBMCs. No recurrence occurred and their healthy CD + cell counts were maintained for 7 years

Source: http://www3.interscience.wiley.com/journal/121531612/abstract

 

Causes of Cancer

 

  Table 1. Acceptance of  causes of human cancers.


Cancer Parasite or Virus Year accepted

Cholangioma liver cancers Opisthorchid trematodes 1970
Bladder cancer Schistosome trematodes 1970
Burkitt's lymphoma Epstein–Barr virus   jointly with Plasmodium falciparum 1975
Adult T cell leukaemia Human T lymphotropic virus I 1980
Cervical cancer Human papilloma virus (HPV) 1985
Nasopharyngeal cancer Epstein–Barr virus (EBV) 1990
Liver cancer Hepatitis B & C viruses 1995
Kaposi's sarcoma Human herpesvirus 8 1995
Stomach cancer Helicobacter pylori 2000
Oropharyngeal cancer HPV 2005

  Persistent viruses. Years of acceptance are approximate because the transition to acceptance generally has been gradual and controversial.

 

 

  Table 2. Cancers that have been associated with particular parasites or viruses for which a causal role has not yet been generally accepted.


Cancer Virus or Parasite

Colorectal cancer Schistosoma japonicum
Liver cancer Schistosoma japonicum
Merkel cell cancer Merkel cell polyomavirus
Mesothelioma Simian virus 40 (SV40)
Breast cancer MMTV, EBV, HPV
Acute lymphoblastic leukaemia EBV
Hodgkin's lymphoma EBV
Non-Hodgkin's lymphomas EBV, SV40
Skin cancers HPV
Oesophageal cancer HPV
Colon cancer JC virus
Ovarian cancer Unknown retrovirus, EBV
Prostrate XMRV, BK virus

  Known to be persistent viruses. EBV, Epstein–Barr virus; HPV, human papilloma virus; MMTV, mouse mammary tumour virus; JC virus, John Cunningham virus; XMRV, xenotropic murine leukemia virus-related virus.

Source: http://www3.interscience.wiley.com/cgi-bin/fulltext/123320093/HTMLSTART?CRETRY=1&SRETRY=0

 

 

 

September Issue of Heartbeat

Some interesting reading in fairly plain English on page 8 (VDBP)  9 (GcMAF) and 14 (XMRV)

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