Nobuto Yamamoto dichiara di aver CURATO 15 pazienti
Inviato: 22 dicembre 2008, 12:27
Dottore.. vorrei ricevere dei commenti, è una balla gigantesca o le balle sono state raccontate fino adesso a tutti i sieropositivi con la litania della non curabilità ?
Se è una balla gigantesca, risultano balle anche le stesse pubblicazioni scientifiche nei stessi siti e stesse riviste che tempo indietro puntualizzavano costantemente la non eradicabilità dell hiv.
QUALCOSA NON QUADRA.
E stavolta sono negli USA.
http://www.ncbi.nlm.nih.gov/pubmed/19031451
1: J Med Virol. 2009 Jan;81(1):16-26
Yamamoto N, Ushijima N, Koga Y.
Division of Molecular Immunology and Immunotherapy, Socrates Institute for Therapeutic Immunology, Philadelphia, Pennsylvania 19126-3305, USA. nobutoyama@verizon.net
Serum Gc protein (known as vitamin D3-binding protein) is the precursor for the principal macrophage activating factor (MAF). The MAF precursor activity of serum Gc protein of HIV-infected patients was lost or reduced because Gc protein is deglycosylated by alpha-N-acetylgalactosaminidase (Nagalase) secreted from HIV-infected cells. Therefore, macrophages of HIV-infected patients having deglycosylated Gc protein cannot be activated, leading to immunosuppression. Since Nagalase is the intrinsic component of the envelope protein gp120, serum Nagalase activity is the sum of enzyme activities carried by both HIV virions and envelope proteins. These Nagalase carriers were already complexed with anti-HIV immunoglobulin G (IgG) but retained Nagalase activity that is required for infectivity. Stepwise treatment of purified Gc protein with immobilized beta-galactosidase and sialidase generated the most potent macrophage activating factor (termed GcMAF), which produces no side effects in humans. Macrophages activated by administration of 100 ng GcMAF develop a large amount of Fc-receptors as well as an enormous variation of receptors that recognize IgG-bound and unbound HIV virions. 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.
PMID: 19031451 [PubMed - indexed for MEDLINE]
http://www.sciencedirect.com/science?_o ... 3d83d6accf
OR.7. Treatment of HIV-Infected Patients with Gc Protein-derived Macrophage Activating Factor (GcMAF) Eradicates HIV-infection
References and further reading may be available for this article. To view references and further reading you must purchase this article.
Nobuto Yamamoto1, Kazuya Hashinaka1, Masumi Ueda1, Theodore Sery1 and Charles Benson2
1Socrates Institute for Therapeutic Immunology, Philadelphia, PA
2University of Pennsylvania, Philadelphia
Se è una balla gigantesca, risultano balle anche le stesse pubblicazioni scientifiche nei stessi siti e stesse riviste che tempo indietro puntualizzavano costantemente la non eradicabilità dell hiv.
QUALCOSA NON QUADRA.
E stavolta sono negli USA.
http://www.ncbi.nlm.nih.gov/pubmed/19031451
1: J Med Virol. 2009 Jan;81(1):16-26
Yamamoto N, Ushijima N, Koga Y.
Division of Molecular Immunology and Immunotherapy, Socrates Institute for Therapeutic Immunology, Philadelphia, Pennsylvania 19126-3305, USA. nobutoyama@verizon.net
Serum Gc protein (known as vitamin D3-binding protein) is the precursor for the principal macrophage activating factor (MAF). The MAF precursor activity of serum Gc protein of HIV-infected patients was lost or reduced because Gc protein is deglycosylated by alpha-N-acetylgalactosaminidase (Nagalase) secreted from HIV-infected cells. Therefore, macrophages of HIV-infected patients having deglycosylated Gc protein cannot be activated, leading to immunosuppression. Since Nagalase is the intrinsic component of the envelope protein gp120, serum Nagalase activity is the sum of enzyme activities carried by both HIV virions and envelope proteins. These Nagalase carriers were already complexed with anti-HIV immunoglobulin G (IgG) but retained Nagalase activity that is required for infectivity. Stepwise treatment of purified Gc protein with immobilized beta-galactosidase and sialidase generated the most potent macrophage activating factor (termed GcMAF), which produces no side effects in humans. Macrophages activated by administration of 100 ng GcMAF develop a large amount of Fc-receptors as well as an enormous variation of receptors that recognize IgG-bound and unbound HIV virions. 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.
PMID: 19031451 [PubMed - indexed for MEDLINE]
http://www.sciencedirect.com/science?_o ... 3d83d6accf
OR.7. Treatment of HIV-Infected Patients with Gc Protein-derived Macrophage Activating Factor (GcMAF) Eradicates HIV-infection
References and further reading may be available for this article. To view references and further reading you must purchase this article.
Nobuto Yamamoto1, Kazuya Hashinaka1, Masumi Ueda1, Theodore Sery1 and Charles Benson2
1Socrates Institute for Therapeutic Immunology, Philadelphia, PA
2University of Pennsylvania, Philadelphia