200+ Future Vaccines: Here’s A Glimpse of What to Expect

In 2013, the Pharmaceutical Research and Manufacturers of America (PhRMA) proudly announced that American biopharmaceutical companies had 271 new vaccines in development [1].

“The 271 vaccines in development span a wide array of diseases, and employ exciting new scientific strategies and technologies. These potential vaccines – all in human clinical trials or under review by the Food and Drug Administration (FDA) – include 137 for infectious diseases, 99 for cancer, 15 for allergies and 10 for neurological disorders”

Here’s a brief glimpse at what we can expect:

  1. A genetically-engineered nasal vaccine for obesity [2].
  2. A vaccine for malaria, using genetically-engineered parasites [3].
  3. A vaccine made from mouse cancer cells, for use in patients with colorectal cancer [4].
  4. A chimeric virus (two viruses genetically engineered/combined into one virus) vaccine for Japanese encephalitis [5].
  5. A genetically-engineered vaccine for Pseudomonas aeruginosa – apparently it is a major cause of hospital-acquired infections [6]. Note that they tested it on ventilated patients in an intensive care unit – as if they didn’t already have enough to deal with! In addition, vaccination made no difference whatsoever to rates of infection…but that didn’t stop them recommending further testing.
  6. A vaccine for Vigoo enterovirus 71…never heard of it, nevertheless, I’m sure they’ll be able to create a market for it [7].
  7. Plant-based oral vaccines for Type-1 diabetes [8].
  8. A vaccine made from genetically-engineered Listeria, for early-stage pancreatic cancer [9].
  9. Genetically-engineered papaya with an inbuilt vaccine for Taenia solium or T. crassiceps – a type of tapeworm found in pigs and humans [10].
  10. A vaccine for stress [11].


[1] Pharmaceutical Research and Manufacturers of America (PhRMA), Medicines in development: Vaccines, http://phrma.org/press-release/medicines-in-development-vaccines. Accessed February, 2017.

[2] Azegami T, Yuki Y, Sawada S, et al. Nano-gel based nasal ghrelin vaccine prevents obesity, Mucosal Immunol, 2017, epub ahead of print.

[3] Kublin JG, Mikolajczak SA, Sack BK, et al. Complete attenuation of genetically engineered plasmodium falciparum sporozoites in human subjects, Sci Transl Med, 2017, 9(371).

[4] Seledtsova GV, Shishkov GV, Kaschenko EA, Seledtsov VI. Xenogeneic cell-based vaccine therapy for colorectal cancer: safety, association of clinical effects with vaccine-induced immune responses, Biomed Pharmac, 2016, 83: 1247-1252.

[5] Kosalaraksa P, Watanaveeradej V, Pancharoen C, et al. Long-term immunogenicity of a single dose of japanese encephalitis chimeric virus vaccine in toddlers and booster response 5 years after primary immunization, Pediatry Infect Dis J, 2016, epub ahead of print.

[6] Rello J, Krenn CG, Locker G, et al. A randomized, placebo-controlled phase II study of a pseudomonas vaccine in ventilated ICU patients, Crit Care, 2017, 21(1): 22.

[7] Wei M, Meng F, Wang S, et al. 2-year efficacy, immunogenicity, and safety of Vigoo enterovirus 71 vaccine in healthy chinese children: a randomized, open-label study, J Infect Dis, 2017, 215(1): 56-63.

[8] Posgai AL, Wasserfall CH, Kwon KC, et al. Plant-based vaccines for oral delivery of type-1 diabetes-related auto-antigens: evaluating oral tolerance mechanisms and disease prevention in NOD mice, Sci Rep, 2017, 7: 42372.

[9] Keenan BP, Saenger Y, Kafrouni MI, et al. A listeria vaccine and depletion of T-regulatory cells activate immunity against early stage pancreatic intraepithelial neoplasms and prolong survival of mice, Gastroenterology, 2014, 146(7): 1784-1794.

[10] Fragoso C, Hernandez M, Cervantes-Torres J, et al. Transgenic papaya: a useful platform for oral vaccines, Planta, 2017, epub ahead of print.

[11] Elliot D. Preventing Mental Illness with a Stress Vaccine, The Atlantic, Nov 26, 2016.

7 Reasons Why Antibodies Can’t Possibly Provide Immunity

There is a massive vaccine industry that rakes in billions in profits, based on the belief that if you have antibodies, you are ‘protected’. Here’s 7 reasons why that belief needs a re-think…


There are numerous cases in the scientific literature, of people succumbing to illness, even though they had high antibody counts [1-3]. In fact, some of those had antibody titres 100x higher than what is considered sufficient to provide ‘immunity’. On the other hand, there are people with little to no antibody counts (and supposedly susceptible) passing through disease outbreaks completely untouched [4].

Actually, the discovery that antibodies are not responsible for immunity was made more than 80 years ago, by immunologist Dr. Merrill Chase, and his discovery was largely ignored by mainstream medicine, despite a long and illustrious career, and publishing more than 150 research papers [5].


According to vaccine logic, the more antibodies you have, the better, but in a NORMALLY functioning immune system, antibody production is tightly restricted (for good reason – more on that later). It’s now common knowledge that Vitamin D is necessary for a healthy immune system…but did you know Vitamin D LIMITS antibody production [6]? It begs the question why, if antibodies really are as vital as we have been led to believe…


The presence of prior antibodies has been found to ENHANCE some diseases. It’s called ‘antibody-dependant enhancement’ and, so far, it has been demonstrated to enhance dengue fever, zika virus, HIV, Ebola, and others [7-12].


Antibodies are created in the body as a last resort. It only occurs AFTER the cells have become infected. Remember the selling point of vaccines – about having a ‘primed’ immune system, so that antibodies could respond faster? Well, technically that’s true, but they neglected to mention that, even in a ‘primed’ immune system, antibodies are STILL not called into action, until after infection occurs [13]. Therefore, it’s a biological impossibility for antibodies to prevent infection, even in a ‘primed’ immune system.


By now, you may be wondering why the human body is designed to limit, restrict or delay antibody production. There’s a good reason for this – because antibodies are highly inflammatory and uncomfortable. Those unpleasant symptoms that you experience when ‘sick’ are not symptoms of disease, they are the result of antibodies. Antibodies place a large burden on the body’s excretory systems and, if not excreted in a timely manner, they conglomerate and form ‘antibody complexes’, which are rather large and tend to get stuck in the soft tissues and joints, causing inflammation and tissue damage [14]. If you get ‘arthritis’ after a vaccine or illness, now you know why! Antibodies!


True immunity requires a robust innate immune system (also known as Th1 immunity). This is the very first line of defence. As already mentioned, vaccines target antibody production, which is part of the humoral immune system (also known as Th2 immunity) – and the last function called into play by the immune system.

We can look upon these two arms of the immune system (innate and humoral) as being antagonistic – when one is dominant, the other is suppressed. So, a dominant antibody response (caused/exacerbated by repeat vaccinations), means that the innate immune system (first line of defence) is suppressed, leaving you more vulnerable to infection [15].

It should be noted here, that the disease known as ‘AIDS’ is characterised by this very same thing – high antibody counts, and poor function of the innate immune system [16]

Also of note – studies have shown that cancer and autism patients have this particular immune imbalance – high antibody counts and suppressed innate immunity [17-20].


Antibodies are extracellular, meaning that they are active outside the cells, but cannot actually enter cells…although scientists are trying to genetically engineer antibodies that will do just that [21].

Now, this is quite a conundrum, because antibodies are not called into action until after a pathogen has entered the cells, and antibodies can only bind to antigens on the surface of the cell (NOT inside the cell).

Now you have to rely on T-cells to orchestrate the killing of infected cells, in order to stop the spread of infection – this is the realm of the innate immune system (the one that is suppressed by repeated vaccinations, remember?). Such is the natural sequence of events when a th1-type response is generated, such as seen in natural infection [22].

The natural Th-1 type response is to eliminate infection via externalising it – this is the classic disease symptoms we know so well, such as rash, fever, cough, mucus, swelling etc [23]. Th2 dominance inhibits this natural response, which inevitably must lead to either:

  • altered disease manifestation, so for example, the vaccinated person who has whooping cough, may have a cough, but without the tell-tale ‘whoop’ sound [24].
  • chronic underlying infection, inflammation or auto-immune disease [25-26].

Let’s just re-emphasize that last point, because it’s really important, and once understood, you’ll never again look at vaccines the same way again…

First: Vaccines are designed to stimulate antibody production (Th2 immune system).

Second: Antibodies cannot stop infection, nor can they enter cells that are infected.

Third: Due to immune imbalance caused by vaccination, infected cells harbour infection chronically, causing inflammation and auto-immune conditions.

Fourth: person shows only mild or no signs of acute illness, but becomes progressively burdened down by chronic health issues.

So, what actually happens is that the vaccine has not prevented infection, it has simply prevented the body from expelling the infection.

It goes without saying, that such a state of affairs does wonders for the vaccine ‘efficacy’ statistics, since the vaccinated are less likely to show overt signs of acute disease, and therefore, less likely to be diagnosed, or even tested – meanwhile, chronic ‘non-communicable’ diseases continue to spiral out of control…

Now you know why.


[1] Crone NE, Reder AT. Severe tetanus in immunized patients with high anti-tetanus titers, Neurology, 1992, 42(4): 761-764.

[2] Maselle SY, Matre R, Mbise R, Hofstad T. Neonatal tetanus despite protective serum antitoxin concentration, FEMS Microbiol Immunol, 1991, 3(3): 171-175.

[3] Pitisuttithum P, Gilbert P, Gurwith M, et al. Randomized, double-blind, placebo-controlled efficacy trial of a bivalent recombinant glycoprotein 120 HIV-1 vaccine among injection drug users in Bangkok, Thailand. J Infect Dis, 2006, 194(12):1661-1761.

[4] Brodie M, Park W. Active Immunization Against Poliomyelitis, Am J Pub Health, 1936, 26:119–125.

[5] O’Connor A, Merrill W Chase, 98, Scientist Who Advanced Immunology, New York Times, Jan 22, 2004. https://www.nytimes.com/2004/01/22/nyregion/merrill-w-chase-98-scientist-who-advanced-immunology.html. Accessed October, 2018.

[6] Røsjø, E., Lossius, A., Abdelmagid, N., Lindstrøm, J. C., Kampman, M. T., Jørgensen, L., … Holmøy, T. (2017). Effect of high-dose vitamin D3 supplementation on antibody responses against Epstein–Barr virus in relapsing-remitting multiple sclerosis. Multiple Sclerosis Journal, 23(3), 395–402.

[7] Halstead SB, O’Rourke EJ. Antibody-enhanced dengue virus infection in primate leukocytes, Nature, 1977, 265(5596):739-741.

[8] ] Dejnirattisai W, Jumnainsong A, Onsirisakul N, et al. Cross-reacting antibodies enhance dengue virus infection in humans, Science, 2010, 328(5979):745-748.

[9] Dejnirattisai W, Supasa P, Wongwiwat W, et al. Dengue virus sero-cross-reactivity drives antibody-dependent  enhancement of infection with zika virus, Nat Immunol, 2016, 17(9):1102-1108.

[10] Homsy J, Meyer M, Tateno M, et al. The fc and not CD4 receptor mediates antibody enhancement of HIV infection in human cells, Science, 1989, 244(4910):1357+.

[11] Furuyama W, Marzi A, Carmody AB, et al. Fcy-receptor Ila-mediated Src signaling pathway is essential for the antibody-dependent enhancement of ebola virus infection, PLoS Pathogen, 2016, 12(12):e1006139.

[12] Biryukov S, Angov E, Landmesser ME, et al. Complement and antibody-mediated enhancement of red blood cell invasion and growth of malaria parasites, EBioMedicine, 2016, 9:207-216.

[13] Janeway CA Jr, Travers P, Walport M, et al. Immunobiology: The Immune System in Health and Disease. 5th edition. New York: Garland Science; 2001

[14] Cochrane CG, Dixon FJ. Cell and tissue damage through antigen-antibody complexes. Calif Med. 1969;111(2):99-112.

[15] Brad Spellberg, John E. Edwards; Type 1/Type 2 Immunity in Infectious Diseases, Clinical Infectious Diseases, Volume 32, Issue 1, 1 January 2001, Pages 76–102.

[16] Kaur R, Dhakad MS, Goyal R, Bhalla P, Dewan R (2016) Study of TH1/TH2 Cytokine Profiles in HIV/AIDS Patients in a Tertiary Care Hospital in India. J Med Microb Diagn 5:214

[17] Sato M, Goto S, Kaneko R, et al. Impaired production of Th1 cytokines and increased frequency of Th2 subsets in pBMC from advanced cancer patients. Anticancer Res, 1998, 18:3951-3955.

[18] Huang M, Wang J, Lee p, et al. Human non-small cell lung cancer cells express a type 2 cytokine pattern. Cancer Res, 1995, 55:3847-3853.

[19] Filella X, Alcover J, Zarco MA, et al. Analysis of type T1 and T2 cytokines in patients with prostate cancer, prostate, 2000, 44:271-274.

[20] Gupta, S., Aggarwal, S., Rashanravan, B., Lee, T., TH1 and TH2-like cytokines in CD4+ and CD8+ T cells in autism, J of Neuroimmunol, 1998; 85:106-109.

[21] Coghlan A. Super-antibodies break the cell barrier, New Scientist, https://www.newscientist.com/article/dn4881-super-antibodies-break-the-cell-barrier/. Accessed December 2018.

[22] Kim EJ, Cho D, Kim TS. Efficient induction of T helper type 1-mediated immune responses in antigen-primed mice by anti-CD3 single-chain Fv/interleukin-18 fusion DNA, Immunology, 2004, 111(1): 27–34.

[23] Abbas AK, Murphy KM, Sher A. Functional diversity of helper T lymphocytes, Nature, 1996, 383(6603):787-93.

[24] Nelson KE, Williams C. Infectious Disease Epidemiology: Theory and practice 2007), Jones and Bartlett Learning, pp 131.

[25] Hayflick, L. Slow Viruses, Executive Health Report, Feb. 1981, pp 4.

[26] Talai, N., “Autoimmunity,” in Fudenberg, Basic Clinical Immunology, 3rd Ed., Lange, 1980, p. 222.

10 Reasons Why The Flu Shot is Worse Than Useless

  1. The number of “flu deaths” each year, used to scare people into getting vaccinated, is grossly inaccurate. There are several reasons for this, the main one being that so-called “flu deaths” are lumped in with deaths from pneumonia and ‘influenza-like illnesses’, and ‘respiratory and circulatory causes’ [1]. Out of all those deaths, the CDC ‘estimates’ how many were caused by influenza. Given that a) states are not even required to report flu cases or deaths in adults, and b) the ‘CDC feels it is important to convey the full burden of seasonal flu to the public’ (their words, not mine), one can just imagine how inflated their ‘guesstimates’ are!
  2. Seasonal flu vaccine makes you more susceptible to other respiratory infections [2].
  3. Influenza-related deaths have actually increased, as vaccination rates have increased [3].
  4. Numerous reviews have found that there is evidence of widespread manipulation of data in flu vaccine studies, and what’s more, no measurable benefits in vaccinating healthcare workers, young children, healthy adults, pregnant women or the elderly [4-8]. Actually, let’s just say that there are no measurable benefits for anybody [9].
  5. Flu vaccine induces auto-antibodies against gangliosides in the brain [10]. Gangliosides are found throughout the body, especially the central nervous system and play an important role in many cell functions.
  6. Flu vaccine makes people more susceptible to pandemic influenza strains [11].
  7. After three consecutive years, people who receive the annual flu vaccine, are more likely to get influenza [12].
  8. The prestigious Cochrane Review found that 71 people would need to be vaccinated in order to prevent one case of influenza…while at the same time concluding that only 10% of the studies included in their review had good methodological quality. Therefore, even this unimpressive finding is likely to be vastly over-inflated [4].
  9. Vaccines only target A and B strains of influenza, which account for approximately 10% of known circulating strains. Remembering that “efficacy” is based on ability to produce antibodies, which does not equal immunity anyway [4].
  10. Multidose flu vaccines (such as trivalent and quadrivalent vaccines) contain thimerosal, which is 50% ethylmercury by weight. Ethylmercury is highly toxic, converts to inorganic mercury, persists in the brain for many years. Oh, and it also suppresses the immune system… [13].


[1] CDC. Influenza (Flu): Estimating seasonal influenza-associated deaths in the United States, https://www.cdc.gov/flu/about/disease/us_flu-related_deaths.htm. Accessed December, 2018.

[2] Cowling BJ, Fang VJ, Nishiura H, et al. Increased risk of non-influenza respiratory virus infections associated with receipt of inactivated influenza vaccine, Clin Infect Dis, 2012, 54(12):1778-1783.

[3] Simonson L, Reichert TA, Blackwelder WC, Miller MA, Benefits of influenza vaccination on influenza-related mortality among elderly in the US: an unexpected finding, Intern Cong Series, 2004, 1263: 163-167.

[4] Jefferson T, Di Pietrantoni C, Rivetti A, et al. Vaccines for preventing influenza in healthy adults, Cochrane Database Syst Rev, 2010, 7(7): CD001269.

[5] Thomas RE, Jefferson T, Lasserson TJ. Influenza vaccination for healthcare workers who work with the elderly, Cochrane Database Syst Rev, 2010, 17(2): CD005187.

[6] Szilagyi PG, Faibrother G, Griffin MR, et al. Influenza vaccine effectiveness among children 6-59 months of age during 2 influenza seasons: a case-cohort study, Arch Pediatr Adolesc Med, 2008, 162(10): 943-951.

[7] France EK, Smith-Ray R, McClure D, et al. Impact of maternal influenza vaccination during pregnancy on the incidence of acute respiratory illness visits among infants, Arch Pediatr Adolesc Med, 2006, 160(12): 1277-1283.

[8] Osterholm MT, Kelley NS, Sommer A, Belongia EA. Efficacy and effectiveness of influenza: a systematic review and meta-analysis, Lancet Infect Dis, 2012, 12(1)36-44.

[9] Simonsen L, Reichert TA, Viboud C, et al. Impact of influenza vaccination on seasonal mortality in the US elderly population, Arch Intern Med, 2005, 165(3): 265-272.

[10] Nachamkin I, Shadomy SV, Moran AP, et al. Anti-ganglioside antibody induction by swine and other influenza vaccines: insights into vaccine-associated Guillain-Barre syndrome, J Infect Dis, 2008, 198(2): 226-233.

[11] Bodewes R, Kreigtz JH, Baas C, et al. Vaccination against human influenza A/H3N2 virus prevents the induction of heterosubtypic immunity against lethal infection with avian influenza A/H5N1 virus, PLoS One, 2009, 4(5): e5538.

[12] Skowronski D, Chambers C, Sabaiduc S, et al. A perfect storm: impact of genomic variation and serial vaccination on low influenza vaccination effectiveness during 2014-2015 season, Clin Infect Dis, 2016, 63(1): 21-32.

[13] Loison E, Poirier-Beaudouin B, Seffer V, et al. Suppression by thimerosal of ex-vivo CD4+ T-cell response to influenza vaccine and induction of apoptosis in primary memory T cells, PLoS One, 2014, 9(4): e92705

Vaccines: A Real Pain In The…BACK?

Vaccines cause back pain
My son told me recently that the nurses had been to his high school to administer HPV vaccines. He didn’t get one, but all his classmates did. He said many complained of having sore arms, and one boy was crying in class, because of severe pain in his back.
Now, don’t get me wrong. I’m 100% convinced that vaccines are nasty, and cause all kinds of problems, but really! Back pain, too?!
I mulled over it for a week or so, and the more I thought about it, the more it all began to make sense.
Back pain is one of the major symptoms of KIDNEY STRESS or DIS-EASE. This is fairly common knowledge in the world of medicine [1-3].
There are numerous reports and case studies in the scientific literature, of kidney problems and diseases following vaccination [4-6]. Dr. Suzanne Humphries was a nephrologist (kidney specialist) who began to question vaccines when she saw first-hand the damage they caused in her patients [7].
It seems fairly straightforward.
1)      The kidneys contain millions of microscopic little filters (known as glomerulus/glomeruli), which filter 140 – 180 litres of blood per day.
2)      Vaccines contain toxins, which end up in the bloodstream.
3)      The kidneys have to filter those toxins from the bloodstream.
But actually, that’s only part of the story.
The whole point of vaccines is to induce antibody production. The more the merrier! Those antibodies produced by the body (over the course of days/weeks/months following vaccination or infection) bind together with the antigen in vaccines, which then form antigen-antibody complexes. These are rather large (in the scheme of things), and tend to get stuck in small areas – like the blood vessels, the joints…and the tiny little filters in your hard-working kidneys. This causes inflammation and tissue damage in the kidneys [8].
This process is called Type III Hypersensitivity reaction, and can occur hours, days or even years after exposure to the original antigen [8].
But wait, there’s more!

The aluminium, contained in many vaccines, also form complexes with the antigen found in vaccines. Antigen-aluminium complexes are a higher molecular weight (24 – 83 kDa) than the molecular weight cut-off of the glomeruli (~18 kDa) [9]. So, then you end up with aluminium lodged in your kidneys, too, causing chronic inflammation.

With billions of vaccines being administered worldwide, maybe this partly explains why back pain is the leading cause of disability in the world [10]?

Or why more than $50 billion is spent every year, on back pain treatment, in the US alone [10]?

Or why 6 million people are dealing with chronic back pain in the US alone [10]?

And, why my son’s classmate was crying in agony following the HPV vaccination?

PS. Since the kidneys also regulate blood pressure, is it possible that vaccines are indirectly contributing to the epidemic of high blood pressure? Ah, that’s a whole other can of worms…


[1] Healthline: The Most Common Symptoms of Kidney Cancer, https://www.healthline.com/health/kidney-cancer-symptoms#takeaway. Accessed October, 2018.


[2] National Kidney Foundation: 3 Early Warning Signs of Kidney Disease, https://www.kidney.org/blog/kidney-cars/3-early-warning-signs-kidney-disease. Accessed October, 2018.


[3] MedicineNet: Kidney Pain (Location, Symptoms, Relief) https://www.medicinenet.com/kidney_pain/article.htm. Accessed October, 2018.


[4] Tan SY, Cumming AD. Vaccine related glomerulonephritis. BMJ : British Medical Journal. 1993;306(6872):248.


[5] NOVATI R, NEBIOLO PE, GALOTTO C, MASTAGLIA M, MANES M. Acute renal failure after influenza vaccination: a case report. Journal of Preventive Medicine and Hygiene. 2014;55(1):31-32.


[6] Debiec, H. et al., 2011, Early Childhood Membranous Nephropathy Due to Cationic Bovine Serum Albumin,” NEJM. Jun 2;364(22):2101-10.


[7] Humphries S, Bystrianyk R. Dissolving Illusions: Disease, Vaccines and the Forgotten History, CreateSpace Independent Publishing Platform, 2013.


[8] Eggleton P. Hypersensitivity: Immune Complex Mediated (Type III). In eLS. John Wiley & Sons Ltd, Chichester, 2013.


[9] Exley C. Aluminium and Medicine. In Molecular and Supramolecular Bioinorganic Chemistry: Applications in Medical Sciences. Merce ALR, Felcman J, Recio MAL, Nova Biomedical Books: New York, 2009, pp 45 – 68.


[10] Pain Doctor: Chronic Pain Statistics, https://paindoctor.com/resources/chronic-pain-statistics. Accessed October, 2018.