Vaccines: What scientific studies reveal.

Scientific research on vaccinations

And they say there is no proof!
Note: Please let me know if a web link doesn’t work, so that I can update it.
Global Vaccine Institute also lists several scientific studies that document hazards associated with vaccines.
Excessive vaccinations can lead to neurological damage in the brains of developing children
**This paper is the one to read, if you only want to read one.**
Blaylock, R.L. 2008. The danger of excessive vaccination during brain development: the case for a link to Autism Spectrum Disorders (ASD). Medical Vertias 5(2008):1727-1741.  (You need Word to open the link above. If you don’t have Word, you can also read it on Dr. Mercola’s website here).
Aluminum adjuvant in vaccines induce the production of IgE antibodies, which can lead to an increase in allergies and sensitivities. 
Fiejka, M. and J. Aleksandrowicz. 1993. Aluminum as an adjuvant in vaccines and post-vaccines reactions. Rocz Panstw Zakl Hig. 1993;44(1):73-80.
 Exposure to hemophilus influenza B (HiB) immunization is associated with an increased risk of insulin dependent diabetes.
Flu vaccines are not effective
Geier, D.A. and M.R. Geier. 2002.Evidence from systematic reviews shows that inactivated flu vaccines have little or no effect on the effects measured.
Jefferson, T. 2006. Influenza vaccination: policy versus evidence. British Medical Journal 2006;333:912.
 Phone survey showed that vaccinated boys were more likely to have a neurological disorder, ADHD and autism than unvaccinated boys (non-peer-reviewed study).
“All vaccinated boys, compared to unvaccinated boys:- Vaccinated boys were 155% more likely to have a neurological disorder (RR 2.55) – Vaccinated boys were 224% more likely to have ADHD (RR 3.24) – Vaccinated boys were 61% more likely to have autism (RR 1.61) Older vaccinated boys, ages 11-17 (about half the boys surveyed), compared to older unvaccinated boys: – Vaccinated boys were 158% more likely to have a neurological disorder (RR 2.58) – Vaccinated boys were 317% more likely to have ADHD (RR 4.17) – Vaccinated boys were 112% more likely to have autism (RR 2.12) (Note: older children may be a more reliable indicator because many children are not diagnosed until they are 6-8 years old, and we captured data beginning at age 4.)”
Adults who have received Hepatitis B vaccinations are statistically associated with neurological changes, gastrointestinal disease, multiple sclerosis and arthritis.
Geier, D.A., M.R. Geier. 2002. Chronic adverse reactions associated with Hepatitis B vaccination. Annals of Pharmacotherapy 36(12):1970-1971.
Children who receive the entire 3-shot series of Hepatitis B Vaccine have a 9x higher rate of developmental disabilities than unvaccinated children.
Hepatitis B triple series vaccine and developmental disability in US children aged 1-9 years
Toxicological and Environmental Chemistry, September 2008, Carolyn Gallagher and Melody Goodman.
Primates receiving the Hepatitis B vaccine experienced developmental delays compared to unvaccinated primates.
A delay in the timing of DPT vaccine lowers the rate of asthma.
Delay in diphtheria, pertussis, tetanus vaccination is associated with a reduced risk of childhood asthma
Journal of Allergy and Clinical Immunology, 2008 Kara L. McDonald, MS, Shamima I. Huq, BS, Lisa M. Lix, PhD, Allan B. Becker, MD, FRCPC, and Anita L. Kozyrskyj, PhD
Read more about this here.
There is a causal relationship between measles vaccines and acute encephalopathy and permanent brain injury or death.
Children with neurological disorders are often suffering from severe gastrointestinal distress and inflammation. A trigger of this inflammation and the resultant behaviors is the MMR vaccine.
Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children
Lancet 1998 Feb 28 Wakefield AJ, Murch SH, Anthony A, Linnell J, Casson DM, [University Department of Medicine, Royal Free Hospital and School of Medicine, London, UK]
The Significance of Ileo-Colonic Lymphoid Nodular Hyperplasia in Children With Autism Spectrum Disorder.
European Journal of Gastroenterology & Hepatology, August 2005. Andrew J. Wakefield, MD [Royal Free & University College Medical School, London].
Detection and Sequencing of Measles Virus from Peripheral Mononuclear Cells from Patients with Inflammatory Bowel Disease and Autism
Digestive Diseases and Sciences, 2000 Hisashi Kawashima, Takayuki Mori, Yasuyo Kashiwagi, Kouji Takekuma
  • This study shows that the measles in the bowels of autistic children is from the MMR vaccine.
  • This study examines the link between autistic behaviors and gastrointestinal disorders and notes a possible link “between GI and behavioral symptoms mediated by innate immune abnormalities.”11
Link between MMR vaccination and autism
Abnormal Measles-Mumps-Rubella Antibodies and CNS Autoimmunity in Children with Autism
Vijendra K. Singh, Sheren X. Lin, Elizabeth Newell, Courtney Nelson. 2002.Abnormal Measles-Mumps-Rubella Antibodies and CNS Autoimmunity in Children with Autism. Journal of Biomedical Science 2002(9):359-364.
  • The team led by Dr Vijendra Singh analysed blood samples from 125 autistic children and 92 children who did not have the developmental disorder.
  • The researchers found a “significant increase” in the level of MMR antibodies in the autistic children.
  • Part of the measles component of the vaccine caused an unusual anti-measles response in 75 of the autistic children, but not in the normal children.
  • More than 90% of the autistic samples, which showed an immune response to MMR, were also positive for antibodies thought to be involved in autism.
  • These antibodies attack the brain by targeting the basic building blocks of myelin, the insulating sheath that covers nerve fibres.
  • Dr Singh has suggested that this autoimmune response may be the root cause of autism.
  • It was determined that there was a close correlation between mercury doses from thimerosal-containing childhood vaccines and the prevalence of autism from the late 1980s through the mid-1990s.
  • In contrast, there was a potential correlation between the number of primary pediatric measles-containing vaccines administered and the prevalence of autism during the 1980s.
  • In addition, it was found that there were statistically significant odds ratios for the development of autism following increasing doses of mercury from thimerosal-containing vaccines (birth cohorts: 1985 and 1990-1995) in comparison to a baseline measurement (birth cohort: 1984).
  • The contribution of thimerosal from childhood vaccines (>50% effect) was greater than MMR vaccine on the prevalence of autism observed in this study.
  • Read more about this article here.
Yazbak, F.E., K.L. Lang-Radosh. 2001. Adverse Outcomes Associated with Postpartum Rubella or MMR Vaccines. Medical Sentinel 2001;6(3):95-99, 108.
 One preservative used in vaccines, Thimerosal (mercury), enters the bloodstream of the child and ends up in the brain after being administered.
Iatrogenic Exposure to Mercury After Hepatitis B Vaccination in Preterm Infants.
Journal of Pediatrics, May 2000. Gregory V. Stajich, PharmD [Mercer University].
Comparison of Blood and Brain Mercury Levels in Infant Monkeys Exposed to Methylmercury or Vaccines Containing Thimerosal.
Environmental Health Perspectives, Aug 2005. Thomas Burbacher, PhD [University of Washington].
The preservatives in vaccines, most notably Thimerosal (mercury) and aluminum, are highly toxic and damaging to the nervous system and immune system of a developing child, and reactions to these toxins may vary greatly by child.
Thimerosal Neurotoxicity is Associated with Glutathione Depletion: Protection with Glutathione Precursors.
Neurotoxicology, Jan 2005. S. Jill James, PhD [University of Arkansas].
  • See this link for 8 other scientific studies on this topic.
 The symptoms of autism and the symptoms of mercury poisoning appear to be very similar.
Autism: A Novel Form of Mercury Poisoning.
Medical Hypothesis, 2001. Sallie Bernard, Albert Enyati, Lynn Redwood, RN, Teresa Binstock, PhD.
The increase in pertussis incidence was higher among vaccinated than among unvaccinated persons of all ages.Re-emergence of pertussis among highly vaccinated population in the Netherlands.
 Vaccination and Allergy citations
Fries, J H, Coleman, M, “Anaphylactoid Allergic Reaction to Influenza and Poliomyelitis Vaccines”, Ann Allerg, Oct 1960; 18:1130-1137.
Bernard, JG, et al, “Vaccination Complications and Cutaneous Allergic Reactions in Young Adults”, Rey Corps Sante Armees, Feb 1962; 3:35-46.
Smith, RE, “Allergic Reactions to Immunization Materials In Children and Approach to Diagnosis”, Ann Allerg, Dec 1965; 23:600-603.
Erdmann, G, “Vaccination Allergy”, Muenchen Med Wachr, Jun 16, 1961; 103:1217-1219 & 103:1256-1259.
Kreinin, LS, et al, “On the Problem of the Allergizing Effect on the Respiratory Organs of Aerosol Vaccination and Revaccination against Typhoid and Tetanus”,Zh Mikrobiol, Aug 1968, 45:130-132.
Fedotova, AM, “The Pathogenesis of Manifestations of Non-specific Allergy During Vaccination, Pediatria, Jan 1967; 46:56-60.
D’iakova, R M, “Allergic Reaction in Children”, Pediat Akush Ginek, Jan-Feb 1966, 1:20-21. [Listed under Vaccines.]
Isacson, P et al, “Allergic Reactions Associated with Viral Vaccines”, Prog Med Virol, 1971, 13:239-270.
Kantchourine, AK, et al, “Role of Delayed Allergic Reactions in the Pathogenesis of Post-Vaccinal Typhoid Complications”, Rev Franc Allerg, Jan-Mar 1969, 9:19-24.
Bawa YS, Wahi PL, “Allergic Encephalomyelitis after Vaccination and Serum Therapy: Report of Ten Cases”, Indian J Med Sci, Apr 1961;15:290-297.
Nazareth, B, et al, “Systemic Allergic Reactions to Japanese Encephalitis Vaccines”, Vaccine, May 1994, 12(7):666.
Weisse, ME, et al, “Tetanus Toxoid Allergy”, JAMA, Nov 14, 1990, 264 (18):2448.
Mazurin, A V, et al, “Severe Allergic Reaction with Hemorrhagic Syndrome Following the Administration of DPT Vaccine”, Vop Okhr Materin Dets, Mar 1964, 9:87-89.
Ehrengut, W, “Vaccinal Allergy, Systemic Vaccinia and Ulcerous Vaccinia”, Presse Med, July 4, 1964, 72:1957-1958.
Vaccination and Anaphylaxis Citations: 
Koval’skala Sia, “Anaphylactogenic Properties of ADT, PDT, and APDT Vaccines…”, Zh Mikrobiol, Jan 1969; 46:65-71.
Egorova, NB, “Anaphylactic Reaction And Anti-toxin Titre Following Aerosol and Subcutaneous Immunization Against Tetanus”, Zh Mikrobiol, Apr 1968, 45:63-68.
Ovens, H, “Anaphylaxis Due to Vaccination in the Office”, Can Med Assoc J, Feb 15, 1986, 134(4):369-370.
NA, “Anaphylaxis Due to Vaccination in the Office”, Can Med Assoc J, May 15, 1986, 134(10): 1109.
James, LP, Jr, et al, “Fatal Systemic Anaphylaxis in man”, NEJM, Mar 19, 1964; 270:597-603.
Wiseman, “Anaphylactoid Reaction to Tetanus Toxoid”, Ann Allerg, Nov 1982, 49(5):308.
Proctor, JW, et al, “Anaphylactoid Reaction to Intralesional BCG”, Lancet, Jul 15, 1978, 2(8081):162.
Kelleher, PC, et al, “Anaphylactoid Reaction After Typhoid Vaccination”, Am J Med, Dec 1990, 89(6):822-824.
Lear, J T, et al, “Anaphylaxis After Hepatitis B Vaccination”, Lancet, May 13, 1995, 345(8959): 1249.
Leung AK, “Anaphylaxis to DPT vaccine.” J R Soc Med 1985 Feb; 78(2):175.
Wilkins J, “Circulating immune complexes after DTP vaccination.”, J Pediatr 1987 Jul; 111(1):162.
Valovirta E, “Circulating immune complexes during immunotherapy in allergy to dog.” Allergy 1989 Feb; 44(2):123-131.
 Bunnag C, Dhorranintra B, “A preliminary study of circulating immune complexes during allergen immuno-therapy in Thai patients.” Asian Pac J Allergy Immunol 1989 Jun; 7(1):15-21.
 Spinozzi F, et al, “Circulating immune complexes and serum lysozyme levels in untreated Hodgkin’s disease. Their relationship to immune function.” J Clin Lab Immunol 1983 Oct; 12(2):87-92.
 Vaccines and Immune Suppression citations:
Toraldo, R, et al, “Effect of Measles-Mumps-Rubella Vaccination on Polymorphonuclear Neutrophil Functions in Children”, Acta Paediatr, 1992 Nov; 81(11):887-890.
Munyer, et al, “Depressed Lymphocyte Function after Measles-Mumps-Rubella Vaccination”, JourInfection Disorder, vol 132, No 1, July 1975, p 75-80.
Oski and Naiman, “Effect of Live Measles Vaccine on the Platelet Count”, NEJM, Aug 18, 1966, p 352-356.
Reik, L Jr, “Disseminated Vasculomyelinopathy: An Immune Complex Disease”,Ann Neurol, Apr 1980, 7(4):291-296.
Wilkins and Wehrle, “Additional Evidence Against Measles Vaccine Administration to Infants Less than 12 months of Age: Altered Immune Response Following Active-Passive Immunization, Jour Ped, 1979, Vol 94, p 865-869.
Futton, A et al, “Vaccines May Cause Immune Suppression”, Vaccine, Jan 1999, 17(2):126-133.
Ehrland, W, “Susceptibility to Infection After Vaccination”, Br Med J, Mar 11, 1972, 1:683.
Bastin, R et al, “Repeated Cholera Vaccination. Immunological “Depressive” effect,”Ann Med Interne (Paris), Jun-July 1974, 125(6-7):513-518.
Kumar, L et al, “Cell-Mediated Immuno-deficiency with Normal Immunoglobulins (Nezelof’s Syndrome) with Progressive Vaccinia”, Indian Pediatr, Jan 1977, 14(1):69-72.
Stickl, H, “Iatrogenic Immunosuppression as a Result of Vaccination”, Fortschr Med, Mar 5, 1981, 99(9):289-292.
Daniliuk, O S et al, “Immunodepressive action Vaccinia Virus”, Biull Eksp Biol Med, Jul 1982, 94(7):73-74.
Castan, P et al, “Coma Revealing an acute Leukosis in a child, 15 days after an Oral Anti-poliomyelitis Vaccination,” Acta Neurol Bekg, May 1965, 65:349-367.
Pletsityl, DF, et al, “The Effect of the Vaccinal Process on the Non-specific Phagocytic Activity of Peripheral Blood Leukocytes”, Biull Eksp Biol Med, Mar 1973, 75(3):76-79.
Green, MS, et al , “Depression of Immune Response to an Inactivated Hepatitis A Vaccine Administered Concomitantly with Immune Globulin”, J Infect Dis, 1993 Sep; 168(3):740-743.
Beckenhauer, W H, et al, “Immunosuppression with Combined Vaccines”, J AM Vet Med Assoc, Aug 15, 1983, 183(4):389-390.
Green, MS, et al , “Depression of Immune Response to an Inactivated Hepatitis A Vaccine Administered Concomitantly with Immune Globulin”, J Infect Dis, 1993 Sep; 168(3):740-743.
Kotwal, G j et al, “Inhibition of the Complement Cascade by the Major Secretory Protein of Vaccinia Virus”, Science, Nov 9, 1990, 250(4982):827-830.
Strauss, J et al, “Loss of Maternal Measles Antibodies Acquired By Vaccination Against Measles,” Cesk epidemiol Mikrobiol Immunol, May 1991, 40(3):137-143.
 Fattom, A, Cho, Y.H, Chu, C.Y, Fuller, S, Fries, L, Naso, R, “Vaccines May Cause Immune Suppression ….”, Vaccine, Jan 1999;17(2):126-133.
Blumberg DA, “Leukocyte responses to diphtheria-tetanus-pertussis and diphtheria-tetanus immunization”, Pediatr Infect Dis J 1991 Mar; 10(3):247-248.
Vaccinations and AIDS Citations:
Scheier, R, Hepatitis vaccine: the Danger of AIDS Transmission, Z Hautkr, 1984 Apr 15; 59(8):502-506.
Macek, C, “AIDS Transmission: What about the Hepatitis B Vaccine?”, JAMA, 1983 Feb 11; 249(6):685-686.
NA, “The Risk of AIDS after Hepatitis Vaccination,” JAMA, 1985 May 24-31; 253(20):2960-2961.
Taubman, L B, et al, “The Question of Possible Relationship Between Hepatitis B Vaccine and AIDS”, AM J Med, 1984 Apr; 76(4): A 59.
Kato, S et al, “Hepatitis B Vaccination and AIDS,” JAMA, 1985 Jul 5; 254(1):53.
Schwartz, AM, et al, “Hepatitis Vaccine and the Acquired Immunodeficiency Syndrome”, 1983, JAMA, Oct: 99(4):567-568.
Sacks, H S, et al, “Should the Risk of Acquired Immunodeficiency Syndrome deter Hepatitis B Vaccination?” A Decision Analysis.” JAMA, 1984 Dec 28; 252(24): 3375-3377.
Papaevangelou, G et al, “Risk of AIDS in Recipients of Hepatitis B Vaccine”, NEJM, 1985 Feb 7; 312(6):376-377.
Francis, DP, et al, “The Safety of the Hepatitis B Vaccine. Inactivation of the AIDS virus During Routine Manufacture”, JAMA, 1986 Aug 15; 256(7): 869-872.
Schultz, TF, “Origin of AIDS,” Lancet, Mar 7, 1992, 339(8797):867


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 is 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 that exposure to bacterial pathogens may prolong the normally transient immune responsiveness to 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, egg, legumes, milk, seeds, etc., depending on what proteins the mother ate at the time of pregnancy?
Is the introduction of the HiB vaccine connected to the increase in food analphyaxis 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 Bordetella 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 Bronchial hyper-reactivity to histamine induced by Haemophilus influenzae vaccination states “……This suggests a hyper-reactivity 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
Can multiple vaccinations cause immune dysfunction related to asthma, allergies and anaphylaxis?
Read more about this here.
Taylor-Robinson, A.W. 1999. Multiple vaccination effects on atopy. Can vaccinations cause immune dysfunction resulting in allergies, asthma and anaphylaxis? Allergy 54: 398-399.
Rook GAW, Zumla A. Gulf War syndrome: is it due to a systemic shift in cytokine balance towards a Th2 profile? Lancet 1997;349:1831-1833.
Butler D. Admission on Gulf War vaccines spurs debate on medical records. Nature 1997;390:3-4.
Kemp T, Pearce N, Fitzharris Pet al. Is infant immunization a risk factor for childhood asthma or allergy? Epidemiology 1997;8:678-680.
Del Prete G. The concept of type-1 and type-2 helper T cells and their cytokines in humans. Int Rev Immunol 1998;16:427-455.
Is there a link between the pertussis vaccines and 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 immunization 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 1mg 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 received 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 vaccine 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?
J Allergy 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 together with alum produced IgE and IgG1 antibodies. PMID 7369497
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
Pediatric 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 808719
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).” PMID 10923599
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 1523881
Can J Comp Med 1985 Apr;49(2):149-51 compared 6 different adjuvants in swine including four mineral oil compounds, one peanut oil compound 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 influenza vaccine.PMID 811378
Are vaccines responsible for the epidemic of anaphylaxis in young children?
Read more here.
Van Odijk J. et al, Specific IgE antibodies to peanut in western Sweden – has the occurrence of peanut allergy increased without an increase in consumption? Allergy 2001 Jun;56(6):573-7
Ewan, PW, Clinical study of peanut and nut allergy in 62 consecutive patients: new features and associations. BMJ 1996 Apr 27;312(7038):1074-8.
Vadas, P, et al, Detection of peanut allergens in breast milk of lactating women. JAMA 2001 Apr 4;285(13):1746-8.
Zimmerman B, et al. Highly atopic children: formation of IgE antibody to food protein, especially peanut. J Allergy Clin Immunol 1989 Apr;83(4):764-70 PMID 2708736
Study Acquits Peanuts in Allergic Reaction – Finds condition stems from abnormal immune response. Accessed April 6, 2006
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Pichichero, ME. New Combination Vaccines. Pediatr Clin North Am 2000 Apr;47(2):497-26 PMID: 10761511
Scheifele et al. Breastfeeding and antibody responses to routine vaccination in infants. Lancet. 1992 Dec 5;340(8832):1406.
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Redhead K et al. Combination of DTP and Haemophilus influenzae type b conjugate vaccines can affect laboratory evaluation of potency and immunogenicity. Biologicals 1994 Dec;22(4);339-45 PMID 7779360
Primeau MN, Adkinson NF Jr, Hamilton RG. Natural rubber pharmaceutical vial closures release latex allergens that produce skin reactions. J Allergy Clin Immunol 2001 Jun;107(6):958-62 PMID: 11398071
Granoff DM, Munson RS Jr. Prospects for prevention of Haemophilus influenzae type b disease by immunization. J Infect Dis 1986 Mar;153(3):448-61 PMID: 3485160
Munson RS Jr, Granoff DM. Purification and partial characterization of outer membrane proteins P5 and P6 from Haemophilus influenzae type b. Infect Immun. 1985 Sep;49(3):544-9. PMID: 2411657
Munson RS Jr, et al. Purification and comparison of outer membrane protein P2 from Haemophilus influenzae type b isolates. J Clin Invest. 1983 Aug;72(2):677-84. PMID: 6603479
Pichichero ME, et al. Do pili play a role in pathogenicity of Haemophilus influenzae type B? Lancet. 1982 Oct 30;2(8305):960-2. PMID: 6127463
Hetherington SV, et al. Outer membrane protein binding sites of complement component 3 during opsonization of Haemophilus influenzae. Infect Immun. 1993 Dec;61(12):5157-63. PMID: 7693595
Coulton JW, Wan DT. The outer membrane of haemophilus influenzae type b: cell envelope associations of major proteins. Can J Microbiol. 1983 Feb;29(2):280-7. PMID: 6406024
Barenkamp SJ, Munson RS Jr, Granoff DM. Subtyping isolates of Haemophilus influenzae type b by outer-membrane protein profiles. J Infect Dis. 1981 May;143(5):668-76. PMID: 6972422
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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.” PMID 9540269
From the journal Allergy 1999, 54, 398-399, Multiple Vaccination effects 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 vaccination from birth is worth the price of a higher prevalence of atopy.” PMID 10371102
Journal of Manipulative and Physiological Therapeutics, Feb. 2000; 23(2):81-90, Effects of diphtheria-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 immunisation with whole cell pertussis vaccine and treatment with oral antibiotics 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; in the 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 life 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. PMID 10686503
 Want to read more? 
  • Generation Rescue has several more peer-reviewed scientific papers on vaccinations here.
  • Vaccination Risk Awareness Network discusses a lot of scientific research on vaccinations as well.
  • What about the 14 studies that support the false assertion that vaccines do not cause autism? Read more about them here.
  • Refer to Dr. Sherri Tenpenny’s Saying No to Vaccines book, which lists more than 350 scientific references documenting vaccine problems.
  • Vaccine Information Coalition – More links to research about autism here.
  • 60 lab studies confirm link between polio vaccine and cancer.