tetrahedron.org Autism, Allergy, Asthma and Vaccine Induced Autoimmunity

Foreword by Dr. Leonard G. Horowitz

Author of Emerging Viruses: AIDS & Ebola�Nature, Accident or Intentional? and

Death in the Air: Globalism, Terrorism and Toxic Warfare

I hate to say I told you so, but read the following information, wake up, or weep.

Since the initial publication in 1996 of my national bestsellerEmerging Viruses: AIDS & Ebola�Nature, Accident or Intentional?(1-888-508-4787) and subsequent release of the related audiotape package, Horowitz �On Vaccines,� a rapidly growing mountain of scientific evidence has accumulated in support of my early claims. Not only are the skyrocketing rates of autoimmune diseases and childhood illnesses including allergy, asthma, autism, and many many more, linked, if not routinely caused, by vaccine ingredients, vaccine contaminants, or just pain vaccine injuries, but politically, vaccines are the most lethal weapons being used today, under the guise of �public health,� for accomplishing global genocide and depopulation.

I know this later statement transcends credulity and most people�s comprehension. �Genocide,� however, is simply defined in Webster�s Dictionary as �the mass killing of people for economic, political and/or ideological reasons.� It shocks most people to learn that the primary institutions, organizations, and agencies that fund vaccination campaigns, �public health� initiatives, American medicine, the cancer industry, and pharmaceutics also fund global depopulation (e.g. the Merck Pharmaceutical Company Fund and the Rockefeller Foundation). Currently, for instance, the Population Council, principally funded by Rockefeller-related entities, as is the National Academy of Science�s National Research Council�publisher of Beyond Six Billion, the recent depopulation advocacy assessment�licenses the birth control pill RU 486. (Are you for 86-ing life?) This organization is currently calling for a fifty percent reduction of the population of the United States. Might vaccines be playing a significant role in this outcome? Obviously so.

My latest book, published months before the September 11, 2001 �terrorist� attacks, entitled Death in the Air: Globalism, Terrorism and Toxic Warfare, examines the art and science of depopulation conducted on behalf of leading globalists by their affiliated organizations and agencies using various means of �non-lethal warfare.� The book urges an examination of vaccination in the context of this �non-lethal warfare.� It proposes that vaccinations, with their concomitant toxic and immune-compromising side effects, serve as an efficient substitute/alternative for standard depopulation methods and military-sustained economies. Chapter 14 entitled, �Vaccinations for Global Genocide� provides ample evidence that definitive risk/benefit scientific support for vaccinations is sorely lacking. Given the dearth of risk/benefit analyses concerning vaccinations, abysmal injury reporting systems, and the rising tide of articles such as the following, it is clear that the vast majority of those professing vaccination attributes are well-meaning Manchurian candidates�mind controlled operatives for a medical system gone mad in the practice of �iatrogenocide.�

One family�s story exemplifies this issue. Mrs. Rita Hoffman had heard me present a lecture on this topic in Toronto in March, 2002. She e-mailed me her concerns regarding her little girl who had developed multiple allergies immediately following receipt of the MMR vaccine. She wrote about �the silent epidemic of children with anaphylaxis,� directly attributable to vaccination campaigns. She sent querries to the Institute of Medicine, which in the book Death in the Air: Globalism, Terrorism and Toxic Warfare is exposed for the subservient role it plays on behalf of vaccine makers. Mrs. Hoffman summarized documented research in her letter to IOM officials regarding why her child could now die from eating foods containing �peanuts, nuts, eggs, milk, sesame seeds or kiwi fruit.� To her dismay, the IOM issued a report stating that they could not accept or reject a link between vaccines and allergies/asthma. According to Mrs. Hoffman, �They also suggested further research, which got them off the hook.�

Consistent with my lecture revelations, Mrs. Hoffman wrote about the world�s leading vaccine maker, the Merck, Sharp & Dohme, �I have noticed the following interesting connections to Merck & Co. and increasing allergies. Merck has the market on much of the asthma, allergy, anaphylaxis medication and treatments. (Click Here) Merck acquired a majority share in 1991 – the beginning of the anaphylaxis epidemic – of Dey Laboratories (makers of Epi-Pen, injectible epinephrine), carried by hundreds of thousands of people at a cost of at least $90 Cdn. (See:http://www.deyinc.com/about/aboutDey.cfm) She provided much of the information below that, in her accurate words, �proves that MMR vaccine causes allergy.�

Mrs. Hoffman closed her correspondence this way: � God Bless You Dr. Horowitz. I think I would have lost all hope by now if not for your uplifting statements, especially the one on your vaccines tape (Horowitz �On Vaccines� 1-888-508-4787), “We know who wins in the end.”

I only hope that more of these surfacing truths will be widely distributed to help save more lives and curtail the ongoing vaccine-induced genocide.

“Abnormal Measles Serology and Autoimmunity in Autistic Children,” Journal of Allergy and Clinical Immunology, vol. 109, no. 1, S232, January 2002 (abstract #702)

Vijendra K. Singh (Scientific Board member, Autism Autoimmunity Project) and Courtney Nelson, Utah State University, Logan

Immune factors such as autoimmunity may play a causal role in autism. We recently showed that many autistic children have autoantibodies to brain myelin basic protein (MBP) as well as elevated levels of measles virus antibodies. To extend this research further, we conducted a serological study of measles virus (MV), mumps virus (MuV), rubella virus (RV), cytomegalovirus (CMV), human herpesvirus-6 (HHV-6), measles-mumps-rubella (MMR), diptheria-pertussis-tetanus (DPT), diptheria-tetanus (DT) and hepatitis B (Hep B) and studied correlations with MBP autoantibodies. Antibodies were assayed in sera of autistic children (n=125) and normal children (n=92) by ELISA or immunoblotting methods. We found that autistic children have significantly (p=0.001) higher than normal levels of MV and MMR antibodies whereas the antibody levels of MuV, RV, CMV, HHV-6, DPT, DT or Hep B did not significantly differ between autistic and normal children. Immunoblotting analysis showed the presence of an unusual MMR antibody in 60% (75 of 125) of autistic children, but none of the 92 normal children had this antibody. Moreover, by using MMR blots and monoclonal antibodies, we found that the specific increase of MV antibodies or MMR antibodies was related to measles hemagglutinin antigen (MV-HA), but not to mumps or rubella viral proteins, of the MMR vaccine. In addition, over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a causal association between MMR and brain autoimmunity in autism. Stemming from this evidence, we suggest that an “atypical” measles infection in the absence of a rash but with neurological symptoms might be etiologically linked to autoimmunity in autism.

Clinical Immunology

Vol. 100, No. 3, September, pp. 355-361, 2001

Infection of Human B Lymphocytes with MMR Vaccine Induces IgE Class Switching

Farhad Imani and Kelly E. Kehoe

Division of Clinical Immunology, Department of Medicine, The John Hopkins University School of Medicine, Asthma and Allergy Center, 5501 Hopkins Bayview Circle, Baltimore, Maryland 21224 Correspondence should be addressed. E-mail: fimani@mail.jhmi.edu

Circulating immunoglobulin E (IgE) is one of the characteristics of human allergic diseases including allergic asthma. We recently showed that infection of human B cells with rhinovirus or measles virus could lead to the initial steps of IgE class switching. Since many viral vaccines are live viruses, we speculated that live virus vaccines may also induce IgE class switching in human B cells. To examine this possibility, we selected the commonly used live attenuated measles mumps rubella (MMR) vaccine. Here, we show that infection of a human IgM+ B cell line with MMR resulted in the expression of germline e transcript. In addition, infection of freshly prepared human PBLs with this vaccine resulted in the expression of mature IgE mRNA transcript. Our data suggest that a potential side effect of vaccination with live attentuated viruses may be an increase in the expression of IgE.

November 6, 2001

Immunization Safety Review Committee
National Academy of Sciences
Institute of Medicine FO 3009
2101 Constitution Avenue NW
Washington, DC 20418

Dear Dr. McCormick, Chair & Committee,

Re: Epidemic of Children with Anaphylaxis

Thank you for the opportunity to submit the following information for your review of the possible association between multiple immunizations in newborns and infants and immune system dysfunction. We are writing in particular about the potentially life threatening allergic response called anaphylaxis.

The exact numbers of children affected by anaphylaxis are difficult to pinpoint. A study in Arch Intern Med 2001 Jan 8; 161 (1): 15-2, Anaphylaxis in the United States: an investigation into its epidemiology, concluded with “The occurrence of anaphylaxis in the US is not as rare as is generally believed. On the basis of our figures, the problem of anaphylaxis may, in fact, affect 1.21% (1.9 million) to 15.04% (40.9 million) of the US population.” PMID 11146694

In June of this year an article by Associated Press Writer Jim Fitzgerald entitled Peanut Butter Wars Rage in Schools stated “Schools that haven’t had a dangerously allergic pupil can expect one soon.” And “peanut allergies among schoolchildren were ‘barely on the radar’ a decade ago, said Dr. Robert Goldman, a New York allergist and immunologist who specializes in pediatric cases.” “Now I’m seeing a tremendous number of cases,” he said. “It seems like the incidence is really increasing. As to why, I don’t think anyone in the world could tell you for sure.”

In Canada, the Anaphylaxis Canada’s Summer 2001 newsletter states that”20% of Canadians suffer from some form of allergy and approximately 4% of children and 2% of adults have developed a potentially lethal allergy to food.”

The cover story in the September 2000 issue of Professionally Speaking, the magazine of the Ontario College of Teachers is “An Abnormal Response to Normal Things.” The article begins with “Teachers have to be aware that allergies can kill. A growing number of children are at risk – and a well-prepared teacher can make all the difference.” The article explains that “About a decade ago, the sudden surge in highly allergic children entering school systems across the province caught many educators off guard.”

Why the “surge” in anaphylactic children entering school a decade ago? These children were among the first to receive an additional vaccination, Hib meningitis. Is it possible that the Pertussis and Hib vaccine, both shown below to cause allergic responses, are creating a hypersensitive immune system in some children? Has any study looked into what happens to atopy incidence and IgE levels when 5 vaccines are given concurrently in infants?

CAN VACCINES CAUSE FOOD ALLERGIES?

JAMA 2001 Apr 4;285(13): 1746-8 Detection of peanut allergens in breast milk of lactating women states, “Most individuals who react to peanuts do so on their first known exposure”………and concluded “Peanut protein secreted into breast milk of lactating women following maternal dietary ingestion. Exposure to peanut protein during breastfeeding is a route of occult exposure that may result in sensitization of at-risk infants.” PMID 11277829

Women have been ingesting peanut protein while breastfeeding for decades. What has changed in the last 15 years to cause infants to develop life-threatening allergies to this legume? One change has been the vaccination schedule.

The Int Arch Allergy Immunol 1999 Jul, 119(3):205-11 Pertussis adjuvant prolongs intestinal hypersensitivity concludes: Our findings indicate nanogram quantities of PT (pertussis toxin), when administered with a food protein, result in long-term sensitization to the antigen, and altered intestinal neuroimmune function. These data suggest exposure to bacterial pathogens may prolong the normally transient immune responsiveness tio inert food antigens. PMID 10436392

Does this study explain why babies and toddlers react on their first exposure to the peanuts or other antigens? The babies may have been sensitized by the vaccines to the proteins through breast milk or formula ingested at the time of vaccination. This would also explain why children are anaphylactic to a variety of proteins, such as different tree nuts, peanuts, eggs, legumes, milk, seeds, etc., depending on what proteins the mother ate at the time of vaccination.

IS THE INTRODUCTION OF THE HIB VACCINE CONNECTED TO THE INCREASE IN FOOD ANAPHYLAXIS IN CHILDREN?

Rates of anaphylaxis have increased dramatically since the introduction of the Hib vaccine.

Clin Exp Pharmacol Physiol 1979 Mar-Apr; 6 (2): 139-49 Comparison of vaccination of mice and rats with Haemophilus influenzae and Bordetta pertussis as models of atopy, states “The Haemophilus influenzae vaccinated experimental animal provides a model that is possibly more related to human atopy than the Bordetella pertussis vaccinated animal.”

PMID 311260

Ann Allergy 1979 Jan;42(1):36-40 states “To determine whether Haemophilus influenzae could be a factor in human atopy its effects were studied on the (para-)Sympathic Cyclic nucleotide-histamine axis in rats. Haemophilus influenzae vaccination induced changes in the cholinergic system compatible with higher cyclic GMP levels and enhanced histamine release. The authors suggest an involvement of the cholinergic system in Haemophilus influenzae vaccination effects. PMID 216288

Agents Actions 1984 Oct;15(3-4):211-5 entitled Brochial hyperreactivity to histamine induced by Haemophilus influenzae vaccination states”…… This suggests hyperreactivity of the parasympathethic, cholinergic pathways as a result of H influenzae vaccination.” PMID 6335351

Eur J. Pharmacol 1980 Apr 4;62(4):261-8 entitled The effects of Haemophilus influenzae vaccination on anaphylactic mediator release and isoprenaline-induced inhibition of mediator release states”These results indicate an increased sensitivity to antigenic challenge and suggest that the functioning of beta-adrenoceptors was decreased as a result of H. Influenzae vaccination.” PMID 6154589

DOES THE PERTUSSIS VACCINE CAUSE ASTHMA, ALLERGIES AND ANAPHYLAXIS?

Pediatrics 1988 Jun (81) Supplement – Report on the Task Force on Pertussis and Pertussis Immunization – extract states, For more than 25 years, it has been known that pertussis vaccine is a reliable adjuvant for the production of experimental allergic encephalitis.

Bull Eur Physiopathol Respir 1987;23 Suppl 10:111s-113s A model for experimental asthma provocation in guinea-pigs immunized with Bordetella pertussis states, “Guinea-pigs were sensitized with killed Bordetella pertussis….the presence of the immediate type of immune response was verified by passive cutaneous anaphylaxis….B. pertussis not only alters adrenergic function but provocation in B. pertussis-sensitized guinea-pigs seems to be a good model for bronchial asthma. PMID 2889487

Pediatr Res 1987 Sep; 22(3): 262-7 Murine responses to immunizations with pertussis toxin and bovine serum albumin: I. Mortality observed after bovine albumin challenge is due to an anaphylactic reaction……the results of our experiments have established that the disease induced by coimmunizing mice with Ptx and BSA is due to an immediate type hypersensitivity PMID 3309858

Infect Immun 1987 Apr.; 55(4):1004-8 Anaphylaxis or so-called encephalopathy in mice sensitized to an antigen with the aid of pertussigen (pertussis toxin), states, Sensitization of mice with 1 mg of bovine serum albumin (BSA) or chicken egg albumin (EA)…induced a high degree of anaphylactic sensitivity when the mice were challenged i.v. with 1 mg of antigen 14 days later. PMID 3557617

JAMA 1994 Aug 24-31;272(8):592-3 Pertussis vaccination and asthma: is there a link? A study of 450 children, 11% of the children who had recived the pertussis vaccination suffered from asthma, as compared with only 2% of the children who had not been vaccinated. PMID 8057511

Allergy 1983 May; 38(4):261-71

The non-specific enhancement of allergy. III. Precipitation of bronchial anaphylactic reactivity in primed rats by injection of alum or B. pertussis vaccine: relation of response capacity to IgE and IgG2a antibody levels….These results show that injection of alum or B. pertussis without antigen can precipitate/enhance anaphylactic response capacity and production of specific and non-specific IgE and IgG2a.

PMID 6307077

CAN VACCINE ADJUVANTS CAUSE ALLERGIES AND ANAPHYLAXIS?

Requests for information on the types of adjuvants used in human vaccines have not been answered to date. We did find that adjuvants are used to create allergic animals for scientific study and also that peanut oil has been used as an adjuvant. Peanut is by far the most common food to cause anaphylaxis in young children. Is peanut oil, or a similar protein or portion of a protein used in human vaccines as an adjuvant or “protein coat” in the Hib vaccine?? Aluminum has also been used as an adjuvant and is known to cause allergies according to the studies below. Could the adjuvants used in vaccines over the last 15 years be creating anaphylactic and allergic children?

J allerhy Clin Immunol 2001 Apr.;107(4):693-702 Murine model of atopic dermatitis associated with food hypersensitivity states,”Female C3H/HeJ mice were sensitized orally to cow’s milk or peanut with a cholera toxin adjuvant and then subjected to low-grade allergen exposure…..An eczematous eruption developed in approximately one third of mice after low-grade exposure to milk or peanut proteins……This eczematous eruption resembles AD (atopic dermatitis) in human subjects and should provide a useful model for studying immunopathogenic mechanisms of food hypersensitivity in AD.” PMID 11295660

Allergy 1980 Jan;35(1):65-71 Antigen-induced bronchial anaphylaxis in actively sensitized guinea-pigs. Pattern of response in relation to immunization regimen….guinea-pigs sensitized with small amounts of antigen with alum produced IgE and IgG1 antibodies. PMID 11295660

Allergy 1978 Jun:33(3):155-9 Aluminum phosphate but not calcium phosphate stimulates the specific IgE response in guinea-pigs to tetanus toxoid. It is hypothesized that the regular application of aluminum compound-containing vaccines on the entire population could be one of the factors leading to the observed increase of allergic diseases. PMID 707792

Pediatr Allergy Immunol 1994 May;5(2):118-23 Immunoglobulin E and G responses to pertussis toxin after booster immunization in relation to atopy, local reactions and aluminum content of the vaccines. The role of aluminum for IgG and IgE responses to pertussis toxin (PT), as well as for side effects, was investigated in 49 children with known atopy status…..the addition of aluminum to the pertussis vaccine was, thus, associated with a stronger IgG antibody response, but tended also to induce a stronger IgE antibody response. The correlation between total IgE and PT-IgE, which was most prominent in children with atopy, indicates that the role of immunization for the development of allergy merits further studies. PMID 8087191

Adv Drug Deliv Rev 1998 Jul 6;32(3):155-172 entitled Aluminum compounds as vaccine adjuvants stated, “Limitations of aluminum adjuvants include local reactions, augmentation of IgE antibody responses, ineffectiveness for some antigens and inability to augment cell-mediated immune responses, especially cytotoxic T-Cell responses. PMID 10837642

Annals of Asthma, Allergy and Immunology, Vol. 85, Number 1, July 2000 article T-cell subsets (Th1 versus Th2) includes figure 7 on page 15 – “Factors responsible for the imbalance of the Th1/Th2 responses which is partly responsible for the increased prevalence of allergy in Western countries. Risk for atopy – Th2, increased exposure to some allergens and Th2-biasing vaccines (alum as adjuvant).”

Vaccine 1992;10(10):714-20 Parameters affecting the immunogenicity of microencapsulated tetanus toxoid states “As expected, incomplete Freund’s adjuvant (IFA) proved to be a more potent adjuvant than peanut oil…….” PMID 1523381

Can J Comp Med 1985 Apr;49(2):149-51 compared 6 different adjuvants in swine including four mineral oil compounds, one peanut oil compond and aluminum hydroxide. PMID 4016580

C R Acad Sci Hebd Seances Acad Sci D 1975 Apr 7;280(13):1629-32 states….a stable water in oil emulsion can be produced by using metabolizable peanut oil with arlacel. When mycobacteria are added, a potent emulsified oil adjuvant is obtained which increases the immune response to BSA and to influenzae vaccine. PMID 811378

ARE MULTIPLE VACCINES CAUSING OUR IMMUNE SYSTEMS TO FAIL?

Immunology Today, March 1998, Volume 19, p. 113-116 states, “Modern vaccinations, fear of germs and obsession with hygiene are depriving the immune system of information input upon which it is dependent. This fails to maintain the correct cytokine balance and fine-tune T-cell regulation, and may lead to increased incidences of allergies and autoimmune diseases.”

>From the journal Allergy 1999, 54, 398-399, Multiple Vaccinations

>effect

on atopy, “An increase in the incidence of childhood atopic diseases may be expected as a result of concurrent vaccination strategies that induce a Th2-biased immune response. What should be discussed is whether the prize of a reduction of common infectious diseases through a policy of mass vaccinations from birth is worth the price of a higher prevalence of atopy.”

Journal of Manipulative and Physiological Therapeutics, Feb 2000;23(2):81-90, Effects of diptheria-tetanus-pertussis or tetanus vaccination on allergies and allergy-related respiratory symptoms among children and adolescents in the United States, “The odds of having a history of asthma was twice as great among vaccinated subjects than among unvaccinated subjects. The odds of having any allergy-related respiratory symptom in the past 12 months was 63% greater among vaccinated subjects than unvaccinated subjects.” PMID 10714532

Thorax 1998 Nov;53(11):927-32 Early childhood infection and atopic disorder, stated “Interpretation of the prediction of atopic disorders by immunization with wholecell pertussis vaccine and treatment with oral antibotics needs to be very cautious because of the possibilities of confounding effects and reverse causation. However, plausible immune mechanisms are identifiable for the promotion of atopic disorders by both factors and further investigation of these association is warranted.” PMID 10193389

Epidemiology 1997 Nov;8(6):678-80 Is infant immunization a risk factor for childhood asthma or allergy? This study followed 1,265 children born in 1977. The 23 children who received no DPT and polio immunizations had no recorded asthma episodes or consultations for asthma or other allergic illness before age 10 years;inthe immunized children, 23.1% had asthma episodes, 22.5% asthma consultations, and 30% consultations for other allergic illness. Similar differences were observed at ages 5 and 16 years. PMID 9345669

Arerugi 2000 Jul;49(7):585-92, The Effect of DPT and BCG vaccinations on atopic disorders findings include, “From these results we conclude that DPT vaccination has some effect in the promotion of atopic disorders…..” PMID 10944825

International Archives of Allergy and Immunology 121;1:2000,2-9, Genetic and environmental factors contributing to the onset of allergic disorders. “The increasing prevalence of allergy in developed countries suggests that environmental factors acting either before or after birth also contribute to regulate the development of Th2 cells and/or their function. The reduction of infectious diseases in early klife due to increasing vaccinations, antimicrobial treatments as well as changed lifestyle are certainly important in influencing the individual outcome in the Th response to ubiquitous allergens.

In conclusion, living with anaphylaxis is to be continually on guard for minute quantities of everyday food or other substances that may cause death. Keeping anaphylactic children safe involves the whole community including the child, parents, teachers, bus drivers, caregivers, friends and family.

It is our hope that the Committee will investigate the questions we have raised and will recommend further investigation into the connection between vaccines and this most distressing allergic disease called anaphylaxis.

Your time is greatly appreciated.

Respectfully yours,

Rita Hoffman