About us

In the name of the Almighty
C.V. of Saleh Mohaghegh Hazrati, Ph.D.
ISTITUTION AND LOCATION DEGREE YEAR(s) FIELD OF STUDY
Tehran University, Tehran, IRAN B.Sc. 1977 Biology
Institute of Biochemistry & Biophysics, Tehran, IRAN M.Sc. 1983 Cell Biology
School of Public Health, Tehran University, Tehran MPH 1987 Master of Public Health
School of Public Health, Tehran Med. Sci. University Ph.D. 1993 Immunology

Research Activities (Papers, Presentations)

1. Kia SJ., Sahebjamee M., Mighani G., Mohaghegh hazrati S. ,Tohidast ekrad Z.,Vahedi M..The Impact of Immunotherapeutic G2 Vaccine on Treatment of Oral Lichen Planus. Shiraz Univ Dent J 2011; Vol.11, Supplement.
2. Khodaberdi Kalavi, and Saleh Mohaghegh Hazrati. Treatment of Chronic wounds: Time for Immunologic Concern on drug design? Accepted for publication.
3. JAFARZADEH A, HASSAN ZM, EBTEKAR M, MOHAGHEGH-HAZRATI S, AND TIRAIHI T. TIME-DEPENDENT CHANGES OF IMMUNOLOGIC RESPONSES AFTER BURN INJURY AND IMMUNOMODULATION BY CIMETIDINE AND PYRIMETHAMINE IN AN ANIMAL MODEL. Pak. J. Pharm. Sci., Vol.23, No.4, October 2010, pp.367-373.
4. Neamati A, Boskabady MH, Afshari JT, Hazrati SM, and Rohani A. The Effect of natural adjuvants on tracheal responsiveness and cell count in lung lavage of sensitized quinea pigs.Respirology 2009, 14, 877-884.
5. Kalavi K, Mordi AV, Keshtkar AA, Kalavi M, Namazi G & Mohaghegh Hazrati S. Diabetes foot Ulcers: A Novel treatment strategy. Iranian J Med Hypotheses and Ideas.
6. Latifynia A, Mohaghegh Hazrati S. Safety and toxicity of a new formulated Leishmania major preliminary vaccine in animal model Balb/c and small white conventional laboratory mice. Türkiye Parazitoloji Dergisi, 32 (2): XX – XX, 2008 Türkiye Parazitol Derg. Türkiye Parazitoloji Derneði, Turkish Society for Parasitology.
7. Neamati A, Boskabady MH, Tavakol Afshari J, Mohaghegh Hazrati S. The effect of the natural adjuvants on cell count in lung lavage of sensitized guinea pigs. Pharmacology online 2008;1:270-278.
8. Mohaghegh Hazrati S. Immunotherapy of Cancer with Th-1 activator (case report). The second international congress of cancer genetics: tumors of the upper body. 30Nov-2Dec 2006. http://iccg2006.tums.ac.ir/
9. Mohaghegh Hazrati S. Effect of Th-1 activators on treatment of adeno carcinoma of breast cancer in mice. The second international congress of cancer genetics: tumours of the upper body. 30Nov-2Dec 2006. http://iccg2006.tums.ac.ir/
10. Mohaghegh Hazrati S., Aghazadeh J., Mohtarami F, Abouzari M., Rashidi A. Immunotherapy of Prolactinoma with a T Helper 1 Activator Adjuvant and Autoantigens: A Case Report. Neuro-immuno-modulation 2006;13:205-208.
11. Mohaghegh Hazrati S. T helper Cell Activators (G2, PC, G2F) as Adjuvants (Biotherapy and prevention of Cancers and Allergies). New Approaches to Vaccine Development from the bench to the field. 8-10 September 2005, Berlin, Germany; pp26:90.
12. Jafarzadeh A, Khoshnoodi J, Ghorbani S, Mohaghegh Hazrati S, Faraj Mazaheri B, Shokri F. Differential Immunogenicity of a recombinant Hepatitis B vaccine in Iranian neonates: influence of ethnicity and environmental factors. I. J. I. 2004; 1 (2): 29-104.

13. Mohaghegh Hazrati S, Nasiri Khalaj S, Mohtarami F, Rahimi A. G2, PC and G2F in allergic asthma. Iranian J of Pediatrics 2004; 13 (2) suppl. 2 :30-31.
14. Mohaghegh Hazrati S , Nasiri Khalaj S , Mohtarami F. Vaccines Against Allergic Asthma. Third Iranian National Congress for Biotechnology, Sept. 2003.
15. Jafarzadeh A, Hassan ZA, Ebtekar M, Mohaghegh Hazrati S. Modulation of Cell- Mediated Immune Response Following Burn Injury in an Animal Model of Balb/c Mice. Journal of Rafsanjan University of Medical Sciences 2003;2:2; 94-101.
16. Mohaghegh Hazrati S. ,Mohtarami F. Combined non-specific Th-1 cells activator adjuvants and specific immunotherapy with auto-antigens of cancer. 3rd International Symposium on Genetic Anti-cancer Agents. Feb. 28-2 march, 2002, Amsterdam, The Netherlands .
17. Mohaghegh Hazrati S, et. al. Effect of Auto-antigens and Th-1 activator adjuvants on pituitary adenoma of prolactinoma. 6th International congress of endocrine disorders. Oct 5-9, 2001, Iranian J. of Endocrine and Metabolism, O-28, pp 22.
18. Mohaghegh Hazrati S, et al. Review of Immunotherapy with Th-1 activator and Auto-vaccines against cancers. Seminar on Diagnostic and new methods of Cancer treatment. June 6-8 2001, Babol University of Medical Sciences, IR of Iran.
19. Mohaghegh Hazrati S, et al. Immunotherapy of brain tumors and other cancers with immunopotent adjuvants and auto-antigens (case report). 23 April 2001, 11th International congress of Immunology, Sweden.
20. Mohaghegh Hazrati S & Mohtarami F. Why Th-1 activator vaccines could effective for Immunotherapy of chemical gas injured patients. The Role of Basic Sciences on defense against new wars. 12-13 March 2001 Tehran, University of Imam Hossein (A), IR of Iran.
21. Mohaghegh Hazrati S, Mohtarmai F, Ghoharani R, Pakrou M, Rohi D, Mohaghegh Hazrati F. Biotherapy of brain tumors and other cancers with immunopotent adjuvants and auto-antigens (case repot). The First North & North West Biotechnology Congress Islamic Republic of Iran. August 15-16, 2001, Urmia.
22. Latifynia A, Mohaghegh Hazrati S, Mohebali M. Pereperation of a new formulation of leihsmanial antigen and the evaluation of its effects on cell mediated induction in BALB/c and small white laboratory mice. The 9th Iranian congress on infectious diseases and tropical medicine 14 – 18 Jan. 2001, O24, pp20.
23. Mohaghegh Hazrati S, et al. The Role of GW-1, GM-1, PPD-A, PPD-B as immunopotent Adjuvants in cell Mediated Immune response against recombinant gp63 in BALB/c Mice. April 10-13, 2000, 9th International Congress on Infectious Diseases Buenos Aires, Argentina.
24. Mohaghegh Hazrati S, et al. Immunotherapy of pituitary Adenoma of Prolactinoma with Adjuvants (Cases Report). 17-19 May 2000, 5th Iranian congress of Immunology and Allergy, Tehran IR of Iran.
25. Baban B, Soubebielle B, Sharafi J, Mohaghegh Hazrati S and Safara M. Use of Mycobacterium vaccae (SRL 172) as an immunomodulating agent in association with Murine Melanoma Model B16-F10. Arch Razi Ins. 2000;51:4752.
26. Mohaghegh Hazrati S, et al. A novel an invasive and metastatic adenocarcinoma of breast cancer (HAZ-1) in small white laboratory mice. (Complementary Report). Sept. 6-9, 1999, The Fifth Biochemistry Congress of Uromia, IR of Iran.
27. Mohaghegh Hazrati S., et al. Biotherapy in Cancers, Asthma and Infectious and other diseases.. Nov 1999, First Azarbidjanian Congress on Biotechnology Uromia, IR of Iran.
28. Mohaghegh Hazrati S, Mohtarmai F, Ghoharani R, Pakrou M, Rohi D, Mohaghegh Hazrati F. Biotherapy of brain tumors and other cancers with immunopotent adjuvants and auto-antigens (case repot). The First North & North West Biotechnology Congress Islamic Republic of Iran. August 15-16, 2001, Urmia.
29. Mohaghegh Hazrati S, Mohtarami F, Ghoharani R, Pakrou M, Rohe D, Mohaghegh Hazrati F. Immunotherapy of brin tumors and other cancer with immunopetent adjunvants and auto- antigen (case report). 11th International congress of Immunology, 23-27 July 2001.
30. Mohaghegh Hazrati S, Hasumi KI, Sharfi J, Ali-Nedjad M, Khiri M, Ghadiri AA, Amani M, Mahbodi F, Mohtarami F, Djabbari H. The Role of GW-1, GM-1, PPD-A and PPD-B as immunopotent Adjuvants in Cell Mediated Immune Response against recombinant gp63 in BABL/c mice. 9th Internatioanl Congress on Infectious Diseases Buenos Aires, Argentina, April 10-13 2000. Abst. No 10808.
31. Sharafi J Mohaghegh Hazrati S. Immunotherapy in Cancer. The Fourth International Congress of Immunology & Allergry, Iran, Isfahan 13-15 May 1998.

32. Mohaghegh Hazrati S, Sharafi J, Kochmeshki R & Mohtarami F. Venous Ozone Therapy in Cancer. The Fourth International Congress of Immunology & Allergry, Iran, Isfahan 13-15 May 1998.
33. Eskandarpour M, Elahi E, Mohaghegh Hazrati S, Amir Moghaddam and Hasumi KI. The Study of CD44 Variant Isoforms in Different Tumors. UICC Symposium, Familial Cancer and Prevention, Molecular Epidemiology. May 14-16 1997, Kobe Japan. (Presentation).
34. Mohagheh Hazrati S, Rabani, Mohebeali M, Eslami MB. Evaluation of vaccination against Tetanous Toxoid within Defense Army during Iraq and Iran War. The First Seminar of Infectious Diseases in War and Unexpected events. Bagiyatalah Medical Sience University; 21-23 Oct 1997: p21.
35. Mahmodzadeh A, Mohaghegh Hazrati S, Sobati R & Mohtarami M. Evaluation of Leishmanization after Stopping this Method of Control of Leishmaniasis in Islamic Rep. of Iran. XIV International Congress for Tropical medicine and Malaria, Nov. 17-22, 1996, Nagasaki, Japan , O-34-4.
36. Mohaghegh Hazrati S. The Function of Viruses in water and their treatment. The National Congress on Environmental Health 1996. (Presentation).
37. Mohaghegh Hazrati S, Valizadeh M, Shojaei S. Establishing Macrophage culture for evaluation Itraconazole and Ketakonazole against leishmaniasis parasites (In vitro model) . May 1995, 8th International Congress of Geographic Medicine, (Infectious Diseases), Shiraz University of Medical Sciences, Shiraz, Iran. (Presentation).
38. Mohaghegh Hazrati S. Controversial role of BCG on treatment of cancers. First Seminar of Immunotherapy of cancer. Tehran Medical Sciences University Dec 1995. (Presentation)
39. Mohaghegh Hazrati S. Immunoregulation of Antibody Synthesis in Sjogren’s Syndrome. May 1995, 8th International Congress of Geographic Medicine, (Infectious Diseases), Shiraz University of Medical Sciences, Shiraz, Iran. (Presentation).
40. Mohaghegh Hazrati S, Majidi J & Zahir Mohammed-Hassan. Effect of BCG on Leishmanization within the mice. May 1995, 8th International Congress of Geographic Medicine, (Infectious Diseases), Shiraz University of Medical Sciences, Shiraz, Iran. (Presentation).
41. Mohaghegh Hazrati S, Valizadeh M, Shojaei S. In vitro effect of intaconazole and keteconazol on L. major infected mouse macrophages. May 1995, 8th International Congress of Geographic Medicine, (Infectious Diseases), Shiraz University of Medical Sciences, Shiraz, Iran. (Presentation).
42. Mohaghegh Hazrati S. Immunoregulation of Antibody Synthesis in Sjogren’s Syndrome. May 1995, 8th International Congress of Geographic Medicine, (Infectious Diseases), Shiraz University of Medical Sciences, Shiraz, Iran. (Presentation).
43. Mohaghegh Hazrati S. Mohebali M, Latifinia A. Preparation of vaccine against cutaneous leishmaniasis (Phse I). May 1995, 8th International Congress of Geographic Medicine, (Infectious Diseases), Shiraz University of Medical Sciences, Shiraz, Iran. (Presentation).
44. Sharafi J, Mohaghgh Hazrati S, Hasumi KI. Combined surgery, chemo, Radio- Immunotherapy of cancers. May 1995, 8th International Congress of Geographic Medicine, (Infectious Diseases), Shiraz University of Medical Sciences, Shiraz, Iran. (Presentation).
45. Mohaghegh Hazrati S, Valizadeh M. NNN Modified Medium for prolonged and mass cultivationg of Leishmania promastigotes (SPH media and HVMA 273). May 1995, 8th International Congress of Geographic Medicine, (Infectious Diseases), Shiraz University of Medical Sciences, Shiraz, Iran. (Presentation).
46. Mohaghegh Hazrati S, Pezeshki M, Khodadadi A. Evaluation of vaccination against Tetanus within the pregnant women under PHC and Hospital Helath Cared System. May 1995, 8th International Congress of Geographic Medicine, (Infectious Diseases), Shiraz University of Medical Sciences, Shiraz, Iran. (Presentation).
47. Baban B, Soubebielle B, Sharafi J, Mohaghegh Hazrati S and Safara M. Use of Mycobacterium vaccae (SRL 172) as an immunomodulating agent in association with Murine Melanoma Model B16-F10. Arch Razi Ins. 2000;51:4752.
48. Eskandarpour M, Elahi E, Mohaghegh Hazrati S & Moghaddam A. A study of CD44 variant isoforms in esophagus and stomach cancers. Iranian Academic Association , Second Annual Congerence Proceedings (Science and Technology in Medicine and Engineering) , 1997; 1:43-59.

49. Mahmoodzadeh A, Mohaghegh Hazrati S, Sobaty H, Faghizadeh S. Evaluation of Leishmanization in the military Forces. Kowsar Medical Journal 1997; 2:4. (Parsian paper).
50. Mohaghegh Hazrati S, Sharafi J & Kochmeshki R. Venous Ozone Therapy in Cancer and Other Diseases 1996 (One Vol. ; 1-56).
51. Adam S Hay, Thor G Theander, Lars Hviid, Saleh Mohaghegh Hazrati, Micheal Kemp and Arsalan Kharazmi. The major surface glycoprotein (gp63) from Leishmania major and Leishmania and Leishmania donovni cleaves CD4 molecules on human T cells. J Immunol 1994; 152: 4542-4548.
52. Mohebali M, Mohaghegh Hazrati S. Evaluation of the effectiveness of leishmanization in Revolutionary Guards of the Islamic Republic of Iran. Paper presented at the National Seminar on Leishmaniasis, Teheran, 1990 (in Farsi).

Memberships;
1. Member of European Tissue Culturs Society
2. British Society for Cell Biology
3. The American Society for Cell Biology
4. Iranian Society for Immunology and Allergy
5. Iranian Society for Biotechnology
6. West Azarbidjan Society for Biotechnology
7. Iranian Society for Asthma & Allergy
8. International Society for Infectious Diseases PROFESSIONAL EXPERIENCE

1974-1978 Laboratory Instructor, Department of Biochemistry, IRAN Pasteur Institute,
1978-1984 Pathobiologist, (Department of Pathobiology of School of Public Health, Tehran Medical Sciences University
1984-1993 Assistant Lecturer, School of Public Health and Institute of Public Health Researches, Tehran Medical Science University, IR of IRAN
!991-1992 Vice president of Basic and Health Sciences Committee of Ministry of Health, Treatment and Education
1993- Count. Lecturer in Field of Immunology, Teaching for B.Sc., M.Sc. and Ph.D. Students.
1995- 2007 Dean of Euromieh Training and Research Health Center,
1993- Count Supervising of different M.Sc. & Ph.D. Thesis’s 1999-2001 President of West Azerbaijan Biotechnology Society. 2002- 2004. President of Iranian Biotechnology Society,(Website: http://ibs.nrcgeb.ac.ir)
1993 – Count. Head of Different Research Projects.
2003 –2005 Head of Incubators Center of Biotechnology and Herbal Plants of West Azerbaijan State of IR of IRAN.
1999-2002 Head of Park of Biotechnology In West Azerbaijan State of IR of IRAN Project. 2002-2006. Member of Herbal Medicine Committee of Minstary of Health, Treatment and
Education.
2002-2006t. Member of UNEP-GEF Project of National Biosafety Frameworks (Department of Environment I.R. IRAN.
2001-2005. Member of Recycle Committee Of West Azarbidjan.
2000- Count. Reviewer of Iranian Biomedical Journal (Institute Pastor of IRAN)
2005-Count. Regional Editors of Ansi-Biotechnology and Molecular Sciences Journal. 2005- 2006. National Biosafety Framework: the National Coordinating Committee
member.
Inoviations;
1. G2 Vaccine as a cell mediated activator registered in the Iranian Patent office on 2007.
2. PC Vaccine as a cell mediated activator registered in the Iranian Patent office on 2007.
3. G2F Vaccine as a cell mediated activator registered in the Iranian Patent office on 2007.

In The Name of God,

Saleh MohagheghHazratPh.D in Immunology,

Assistant Professor of Tehran University of Medical Sciences

B.Sc., M.Sc., M.P.H., Ph.D., WAIM (Integrated Medicine) FellowShip& Post Doct. (Immunotherapy & Biotherapy)

Introduction, Over twenty-six years of research conducted by me and various colleagues has resulted in the invention of an injectable, immune-enhancing and modulating drug called G2 and G2F vaccine. The G2 ingredients originated in completely natural and harmless resources, have prepared from animal lipids with addition of some other materials which I am going to mention in details.

  1. All pharmacological  studies,  including:  cytotoxicity,  examination  of  the pathological effects on nine organs in mice, mutagenicity tests, amyloidosis, tissue  culture  and  animal  studies  showed  no  adverse    A  detailed description of all reports is available.
  2. Evaluation of the G2 vaccine effect on mouse cellular immune system using delayed hypersensitivity and blastogenesis assay showed that this vaccine is an immune system stimulator by stimulating T helper (Th-1) cells immune response. That stimulates and strengthens this immune response more than ten times.
  1. Creating an animal model of breast cancer in mice and therapeutically studies have shown that G2 vaccine can make about 42% of  mice completely cancer-free and significantly increase the life expectancy and survival.
  2. Initial studies of the use of G2 vaccine in end-stage patients with various cancers showed that they had gone from complete treatment to control or noBut almost all of these patients benefited from longer life expectancy and better quality of life.
  3. One of the cancer patients with concomitant asthma, recovered from asthma following the injection of the G2
  4. Three volunteer patients with chronic asthma were screened for the G2 vaccine followed by 12 injections that experienced 85% asthma
  5. So, we went one step back and the studies of animal model of asthma (sensitivity) were examined in one research center in Urmia city and two centers in Mashhad city. All three studies showed that the G2 and G2F vaccines reduced serum IgE levels as well as Eos. Cell counts also elevatedfor Th-1 cells cytokines pattern,
  6. Phase I clinical trials of G2 vaccine in three healthy volunteers showed no adverse
  7. Phase II study of human studies of the G2 vaccine among 33 asthma and allergy patients in Tabriz city has been done by a colleague in his personal clinic. He reported that between 40% and 100% of illness improved and become healthy. A detailed report of the late Dr. NasiriKhalaji is
  8. The G2 and G2F vaccines of the immersion type (injectable oil type) vaccines were
  9. We presented these results to the Medical Ethics Committee of the Tehran Med. , University. After two years, the committee authorized the study of the drug among asthmatic patients.
  10. Phase III Clinical trials of the G2 vaccine in more than 160 asthmatic patients showed decreased serum IgE levels and Eos cell counts. Their breath problems were significantly reduced and the clinical symptoms of asthma patients showed about 70% improvement in patient satisfaction and their physician evaluation. The written report of the analysis of the findings was reflected in the research deputy of Tehran Medical Sciences of University.
  11. Phase IV clinical trials of asthma patients continued until approximately one thousand asthma patients and confirmed the result of phase III. (Full written report of the late Dr. NasiriKhalaji is )
  12. Simultaneous evaluation of G2 vaccine in more than one hundred asthmatic children in Rasht These surveys were conducted in accordance with a contract with the Country Support of Charitable Association of Diabetic Patients (CSCADP) in Rasht city and the results showed that about 90% of children asthma recovered. (The letter of manager of CSCADP is available). (CSCADP is the biggest NGO with more than 3.5 million members in my country).
  13. All human studies in asthma and allergies have shown that the G2 vaccine has no side effects.
  14. At the same time, these studies were launched at one ofTehran Hospital of Immunology and Allergy Clinic and were offered one year of asthma and allergy immunotherapy services to asthma and allergy

Mechanisms of Effect:

  1. Our basic research has shown that G2 can stimulate and proliferate immune Th-1 cells. This stimulation and increased in the number and activity of Th-1 cells can be up to Th-1 cells are key cells of the immune system. Their activation stimulates a network of other cells including Natural killer cells (NK cells) via by releasing gamma-IFN. It has been shown in texts, activated NK cells release IL-12 which is an autocrine cytokine. IL-12 causes more NK cells to proliferate, and this proliferation and activity destroy all kinds of virus-infected cells as non-specific immune response.
  2. This means that the proliferation and activation of NK cells causes our body to react quickly to any virus cell that is infected and immediately destroy them. It doesn’t matter what kind of virus has entered cells of the body. Our colleagues (Khodadi et al 2016) also showed that the G2 vaccine increased NKG2DR receptors on NK cells, which play an important role in the lethal activity of these By releasing viruses from dead cells, they are killed and excreted by other immune mechanisms.

This schematic figure shows how Th-1, Th-2 cells development and balance form Th-p cells. Th-2 plays a specific role in the production of antibodies like IgE resulting hypersensitivities (Asthma and Allergies). Unfortunately in most infectious and even non-infectious diseases that are associated with Th-2 cells, this will result in severe reactions. By G2 injection this balance changes in the favor of Th-1 cells increasing up to tenfold. As a result, the number and activity of natural killer cells have increased, killing viruses infected cells and releasing viruses that are destroyed by other immune mechanisms. NK cells are ready to kill any new cells that are infected with viruses and could prevent COVID-19 like infections.

  1. In other words, injecting G2 vaccine enhances immunity as a sophisticated and very powerful method in the prevention and treatment of viral diseases such as seasonal flu, influenza, corona virus COVID-19, Dengue virus, Zika virus, Nipah virus It has been used in the treatment and prevention of seasonal flu and influenza in hundreds of cases and more recently in several cases in the prevention and treatment of COVID-19. That is, while having a preventive role against viral diseases, it shortens the recovery time of infected people.
  2. Immunology reference books also say that between ten days to two weeks, other cells called Cytotoxic T Lymphocytes (CTLs) are formed and equipped to kill cells infected with a particular virus like COVID-19 that the body has infected with help of NK cells produced IL-12 and gamma
  3. We were also able to show that the G2 vaccine can increase the number of cells with a CD+ markers (Kia SJ et 2011). In normal people the ratio is

But in many diseases, such as cancers, viral illnesses  can

be reversed and sometimes reversed, even reducing to one-fourth (1/4). This is offset by the 12 injection with interval of two per week of G2 vaccine injection.

  1. Another effective mechanism of the G2 vaccine that emerged from research that are enzymes in the body outer cells membrane called MMPs (Matrix MetalloProteinases) which have role in cancers and many diseases is well known. These extracellular metalloenzymes can break down cancer cells, thereby causing metastasis and causing new cancer in another area of the body. MMPs can also cause angiogenesis in tumors to make branch vein from the main vein to feed tumors. This phenomenonis called angiogenesis. Our research on G2 vaccine has shown that can reduce the expression and activity of MMPs by up to 50%.Gene expression and activity of MMPs are increased in many diseases like: all viral diseases, asthma and allergies, inflammatory disorders of the brain like MS and subgroups of MS, rheumatic diseases in chronic wounds and also in diabetes which can sometimes be up to 64-fold higher than normal one.That is, one of the important reasonswhy G2 vaccine could help these patients via increasing their immunity.
  2. Therefore, the G2 vaccine has been used and continues to be used in more than 2500 diabetic patients as recommended by the Scientific Committee of the (CSCADP) in Rasht city to improve the safety of these patients against viral flu, influenza and microbial infection during last several The numbers of injection were performed 5 up to 10 injections with interval of 5-

7 days. This has been done according to the letter from the country’s (CSCADP) scientific committee, as well as articles published in the Azad Anditishan weekly newspaper which were published years ago and in the December 2020 which because of epidemic of influenza N1H1 in our country. Furthermore, I should also add that due to the severe COVID- 19 epidemic in Rasht city, a report came from stating CSCADP that all diabetic patients who had previously received the G2 vaccine and due to quarantine conditions were able to call them. None of them have COVID-19. This means that the G2 vaccine has been shown to prevent COVID-19 in diabetic patients. Or if they have been infected, they have not shown any symptoms. This was important news, indicating that the G2 vaccine has the potential to prevent COVID-19 infection. And it can be used as a non-specific vaccine to prevent COVID-19 in high risk population.

  1. The method of using G2 vaccine to prevent of seasonal flu are injections of two to three injections per week for 10 to 20 injections in normal individuals can provide relative immunity. Injections can be continued if needed. And to help treat viral flu and influenza in the first week of treatment, a daily injection will help,and if the disease persists, two injections can be taken daily. The number of injections can easily be increased in the treatment of cancers, especially because of the weaken immune system of cancerous patients.
  2. Reported Complications: Following Injection of G2 Vaccines has been used by several thousand different patients, and some complications have been reported. One case of in the Urmia city:
    1. A woman presented with asthma symptoms who stated after the sixth injection that she had pain in the injection site. Therefore, injections were One vial of Betamethasone was injected in half with one hand and half with the other. After this injection, the pain disappeared and the patient’s asthma recovered.
    2. Another case was reported from Ardabil Who was a mustard gas injured man from the Iraq war against in Iran, which was similar to the patient mentioned above. This time, complications were eliminated by injecting a betamethasone into two vaccine injection sites. And the pulmonary complications of mustard gas declined dramatically.
  • And the third case: a woman presented with asthma symptoms that also had a slight swelling in the armpit and breast lymph nodes after 5-6 injections. It was also recommended that she should be given a betamethasone injection at the vaccine site or use corticosteroids
  1. One case was reported from the city of A 12-year-old child had symptoms of asthma, but no details were reported. It seems it was not important matter.
  • In some cases, people who have received the G2 vaccine say that they have increased sweating that we do not know the
  1. Some normal people after injection of G2 give them a lethargy, which seems to be the main cause of a slight drop in blood So, it seems that another application of G2 could control of blood pressure. A physician colleague who had unmanageable blood pressure mentioned that, his blood pressure was controlled after injection of G2 vaccine. So, if people blood pressure is low, instead of infusion, use a cream or honey containing G2.
  2. The latest case was reported about a month ago when a woman with symptoms of asthma and allergies used the vaccine, which had

She was also advised to inject betamethasone, and his inflammation improved. However, in any case where complications occur it is recommended to inject betamethasone into the injection site as well as discontinue the G2 vaccine.

  1. In several cases it was reported that people who had difficulty falling asleep at night or had to use sleeping medications were asleep. With the G2 vaccine, this can be resolved and they can easily fall asleep at night without taking any
  2. Therefore, given that over 3,500 people have used the G2 vaccine and averaged between 20 up to 40 and more in cancerous patient, injections each for treatment. Therefore, over 60,000 to 100,000 injections have been performed during last 20 years and no other side effects
  3. It should be noted that the immersion type of these vaccines was also developed as G2F Vaccine for long-term release, which has been shown to be highly effective for injecting tumors mainly. Also, when a relatively high safety is required, only one injection of 0.05 CC – 0.1 CC is injected subcutaneously. In some cases, Erythema or Induration may occur, sometimes with a slight itching and Then it means that good safety is activated. And if this does not happen, one week later another injection will provide sufficient and strong immunity.
  4. One colleague used G2F vaccines with five times the volume of several allergic patients because of lack of G2 vaccines several years (0.5 CC volume instead of 0.1 CC was used to cause swelling of the axillaries lymph nodes of the patients. Following the above discontinued injections and one or two injections of corticosteroid this control and recovery condition was achieved. And their allergies recovered.

30.   Contraindications for the use of G2 vaccines.

These vaccines should not be used in pregnant women. Also, in all cases where immunity to the type of Th-1 cell activity is severe. Such as Helicobacter pylori and similar diseases should not be consumed.

Finally,as mentioned by WHO, and other Ministries of Health of different countries, COVID-19 has raised control points, such as regular hand washing, quarantine to control outbreaks and postponement of public outbreaks of disease control,will happen about,50- 70% of people of around the world. If we could immunize human being with G2 vaccine the rate of death will decrease significantly and we do not hesitate spreading of the virus. Because most people immunity will be high enough to become healthy, and if an individual become infects with COVID-19, he or she will become healthy after a few days, without needs hospitalized which we need at the moment.

So, for controlling this pandemic COVID-19 problem, there are two very important points that should mention.

  1. One is to develop a vaccine against COVID-19, for control and prevention, which is seems not available
  2. And the other way to control of distributing of COVID-19 to boost

communities’bodies’ immunity with G2 vaccine (or any things like that) to prevent or treat the infected people that have a long history of usage without any important side effects. Therefore, it seems that the G2 vaccine can partially accomplish this goal. Because it already has an operational history in diabetic asthmatic, virus infected people, cancers and other illness prevention and treatment.

Also, the G2F vaccine, which is oil type G2 vaccine and are very potent one. When injected gradually releases G2 components. As a result, it constantly stimulates and enhances immunity. In other words, with just one or two single s.c. injections (0.05-0.1CC), the normal people and patient’s immunity increases so much that he or she can resist to most of diseases such as flu, influenza viral and possibly COVID-19.As it well known that corona virus could not do important sign of illness within the people who have strong immunity.

It should be borne in mind that the preparation of the G2 vaccine is not easy and time-consuming and should take three to six months between approval and order. But at moment there are a few thousands single doses to start the injection.

Mass production requires special facilities. The most important part is to provide Clean Rooms and ampoule filing and division machines in sterile conditions. Fortunately, all the raw materials for this vaccine can be produced domestically.Moreover, the G2 vaccine last article presented as a lecture at the International Conference on Iranian herbal and Islamic Medicine, held in September 2019, was selected as the top paper and presentation.

I am readyto join the battle against ongoing pandemics and discuss in details for mass production. Please feel freeto reach out and do not hesitate to reflect on any suggestions or comments.

Yours Faithfully MohagheghHazrati

Tel. +98-9125142743 (also Whats app), dr.mohaghegh.foundation@gmail.com

References:

 

Boskabady MS, Neamati A, MohagheghHazrati S, Khakzad MR, Moosavi SH, Gholamnezhad Z. The preventive effects of natural adjuvants, G2 and G2F on tracheal responsiveness and serum IL-4 and IFN-c (th1/th2 balance) in sensitized guinea pigs. Clinics vol.69 no.7 São Paulo July 2014. https://doi.org/10.6061/clinics/2014(07)09

Hazrati SM, Aghazadeh J, Mohtarami F, Abouzari M, Rashidi A.Neuroimmunomodulation. 2006;13(4):205-8. Epub 2007 Mar 2. Immunotherapy of prolactinoma with a T helper 1 activator adjuvant and autoantigens: a case report.

Kalavi K, Mohagheghhazrati S. Treatment of DFUs: an immunologic concern.Endocrinologys Conference, Dec 19–23, Cochin, India [Oral]. (Abstract). 5 Kalavi K, Maleki A,

KalaviMergen, Hazrati SM.   Kalavi K, Moradi A, Keshtkar A, Kalavi M, Namazi G, MohagheghHazrati S. Diabetic foot ulcers: a novel treatment strategy.Irn J Med hypothesis Ideas 2008;2:1–5..Can we prevent amputation by immunologic concern? Student conference, Oct 2009, Antwerp, Belgium [Oral]. (Abstract).

Khodadadi A, Abdoli Z, Boroujerdnia MG, Assarehzadegan MA, Ghasemi M, Hazrati SM, Gerdabi ND. Cancer BiotherRadiopharm. 2016 May;31(4):119-24. doi: 10.1089/cbr.2015.1883.The Effect of G2 Adjuvant on Gene Expression and Delivery of NKG2D Receptor on NK Cells in Peripheral Blood.Original Article

KiaSJ,Sahebjamee M., Mighani G., MohagheghHazrati S., Tohidastekrad Z., Vahedi M. Shiraz Univ Dent J 2011; Vol.11, 29-34. Supplement. The Impact of Immunotherapeutic G2 Vaccine on Treatment of Oral Lichen Planus. Document Type: Original Article

Neamati A , Boskabady MH, MohagheghHazrati S , Khakzad MR, Moosav SH. Avicenna Journal of Phytomedicine 3(4):364-70 · June 2013. The effect of natural adjuvants (G2, G2F) on lung inflammation of sensitized guinea pigs.

 

Neamati A, BoskabadyMH, Tabatabaei A, MohagheghHazrati S. Iran Red Crescent Med J. 2014 February; 16(2): e14267. DOI: 10.5812/ircmj.14267 Published online 2014 February 5. Research Article. The Effect of Natural Adjuvants on Pathological Changes in Sensitized Guinea Pig Lungs.

Mirsadraee M, MohagheghHazratiS, Khakzad MR, Ghafarzadegan K, Boskabady MH. Iranian Journal of Basic Medical Sciences www.mums.ac.ir Vol. 15, No. 5, Sep-Oct 2012, 1068-1075 Dec 24, 2011 1068 Iran J Basic Med Sci, Vol. 15, No. 5, Sep-Oct 2012 Preventive Effect of Novel Bacterial Polysaccharide and Animal Splenic Protein as Natural Adjuvants on Animal Model of Asthma.

 

Shafie S, Soltani E, Soltani M, HazratiMohaghehg S. Fish Shellfish Immunol. 2018 Nov;82:115-120. doi: 10.1016/j.fsi.2018.08.011. Epub 2018

Aug 7. Adjuvant efficacy of G2 (buffalo spleen extraction) against Yersinia septicemia in rainbow trout (Onchorhynchus mykiss).