Très à la mode en ce moment, alors que l’on assiste à une sorte de débat de caricaturiste dans la presse et les réseaux sociaux au sujet du vaccin covid, où l’on monte les provax contre les antivax avec des arguments plutôt simplistes et sans-doute peu objectifs.
Il faut se rendre compte que la réalité n’est ni pro, ni anti-vaccins : Les vaccins ont des effets bénéfiques et protecteurs certains mais aussi des effets secondaires potentiellement très sérieux dont les maladies auto-immunes très graves, voire mortelles dans des proportions autour de 1/10 000 -1/100 000, comme nous allons en discuter ci-dessous. En vaccinant massivement, on va toucher une population beaucoup plus large et donc il faut peser la balance bénéfices risques. Il y a également le problème de savoir comment on prouve les effets secondaires des vaccins, de comment les déterminer de façon objective, car la médecine n’est pas une sciences exacte, mais se base sur des outils statistiques. Nous vous renvoyons à notre article Vaccin Covid-19 et (absense d’) effets secondaires pour plus d’information à ce sujet.
Vaccin et maladie auto-immunes:
Il est possible que les anticorps formes contre l’agent pathogène trouvent des cellules propres de notre corps très semblables et les attaques (« molecular mimicry »). D’où l’estimation de Bill Gates, un ardent défenseur des vaccins, qui a d’énormes intérêts financiers derrières ceux-ci d’ailleurs, de dire lui-même que vacciner 7 milliards d’individus contre le Covid pourrait causer à peu près 700 000 morts (https://perma.cc/QN6C-T445 ) et que c’est tout à fait acceptable… ce que personnellement je ne pense pas ( car ça touchera principalement des gens jeunes et en bonne santé qui ne sont pas à risques). Dans le cas du vaccin ARN covid, on n’a pas de recul sur ces nouvelles techniques vaccinales. On ne connait donc pas les risques à plus long termes, qui pourrait nécessiter plusieures années d’observations avant que l’on ne les décèlent (les compagnies pharmaceutiques ont d’ailleurs refusé d’assumer le risque financiers d’indemnisation des effets secondaires).
Un article scientifique par un expert dans le domaine des vaccins et de l’immunologie (image et quelques extraits ci-dessous) :
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129276/
3. The vaccines
3.1. Measles, mumps, rubella (MMR) vaccine
Thrombocytopenia has been reported as the main adverse event following MMR vaccine. After MMR vaccine the onset of immune thrombocytopenic purpura (ITP) usually occurred within 6 weeks at a risk rate of 1:22,000–25,000 MMR vaccine doses, while the incidence of ITP following infections is 1:6000 for measles and 1:3000 for rubella [108]. As the risk of thrombocytopenia is higher in patients who experience natural infection with measles, mumps or rubella than in those receiving the vaccine, vaccination is encouraged. Arthralgia complaints have also been reported and they may present as transient arthralgia, acute arthritis and rarely chronic arthritis [109].
Some risk factors have been found to be associated with the development of arthritis in vaccinated patients such as: female gender, older age, prior seronegativity and specific HLA alleles [110].
3.5. Human papilloma virus (HPV) vaccine
Up to 90% of cervical cancer deaths, occur in developing countries that lack the ability to fully implement the Papanicolau (Pap) screening programs.
HPV poses a special challenge in vaccine safety. HPV is necessary for the development of cervical cancer. However, most women infected with HPV will not develop the disease since 70% of infections will resolve within a year and up to 90% within 2 years without specific treatment. Over the course of decades, cancer may result in a small proportion of the remaining infected women. Death rate from cervical cancer in 9–20 year old girls is zero and long-term benefits are yet to be proven. In this specific case, short term risks to healthy subjects can prove to pose a heavier burden than cervical cancer [123].
There are at least 100 types of HPV strains, 15 of which have been pathologically associated with cancer. Two vaccines, Gardasil™ and Cervarix™, are commercially available against HPV. Both contain the L1 capsid proteins of several HPV strains as antigens. Gardasil™ contains serotypes 16, 18, 6, 11. These antigens are combined with aluminum (Al) hydroxyphosphate sulphate as an adjuvant. Cervarix™ contains a combination of the oil-based adjuvant monophosphoryl lipid A (MPL) and Al hydroxide (ASO4) as adjuvant and is directed at strains 16 and 18 [124].
There have been several reports of post-licensure adverse events, some of which have even been fatal [125]. Compared to other vaccines, an unusually high proportion of adverse drug reactions has been reported associated with HPV vaccines [126].
In 2008, Australia reported an annual ADR rate of 7.3/100,000, the highest since 2003. This increase was almost entirely due to ADRs reported following the commencement of the national HPV vaccination program for females aged 12–26 years in April 2007 (705 out of a total of 1538 ADRs records). The numbers only decreased after the cessation of the catch-up schedule. Although the percentage of convulsions attributable to the HPV vaccine decreased, the overall report remained comparable between 2007 and 2009 (51% and 40% respectively). These reports do not prove the association, but show that there is a higher frequency of ADRs related to HPV vaccines reported worldwide, and that they fit a consistent pattern (i.e., nervous system-related disorders rank the highest in frequency) that deserves further investigation [126], [127], [128].
Indeed, several autoimmune diseases have been linked to HPV immunization. Examples include GBS, MS, Acute disseminated encephalomyelitis (ADEM), Transverse Myelitis (TM), postural orthostatic tachycardia syndrome (POTS), SLE, primary ovarian failure (POF), pancreatitis, vasculitis, immune thrombocytopenic purpura (ITP) and Autoimmune hepatitis (AH) [123].
3.6. Influenza
Influenza is an acute viral infection that affects the respiratory tract and is caused by influenza type A–C viruses of the Orthomyxoviridae family [129].
H1N1 mortality rates in the 2009 outbreak showed high risk in those aged 70 years and older, presence of chronic diseases and delayed admission. Risk of infection was lower in those who had been vaccinated for seasonal influenza with 2008/9 trivalent inactivated vaccine [130].
Studies have demonstrated that influenza vaccine is safe and immunogenic in patients with SLE or rheumatoid arthritis (RA), diminishing the risk of respiratory infections [129].
It has been shown that adjuvanted vaccine had more local reactions but did not increase systemic adverse reactions [131].
Molecular mimicry has been suggested as a mechanism to explain an autoimmune response following influenza vaccination. However, a causal relationship between influenza vaccines and induction of autoimmune diseases remains unproved [129].
Diseases or symptoms reported after influenza vaccination include mostly neurological syndromes such as GBS [REF]. Nonetheless, influenza vaccines should be recommended for patients with MS, because influenza infection is associated with increased risk of exacerbations.
That being said, influenza vaccinations showed increased risk of autoimmune responses suggestive of ASIA [132], vasculitis [133] and APS [134] among others.
Autre risque potentiel surtout pour les jeunes enfants : Les nano-particules d’aluminium dans les adjuvants des vaccins :
Et qui fait souvent débat, un des problèmes est que les nano-particules ne se comporteraient pas comme les micro-particules d’aluminium et seraient en fait beaucoup plus toxiques car pas eliminées par le corps et pourraient pénétrer dans le cerveau:
Vaccine Aluminium Travels Into The Brain
“Parents can be reassured that the trace quantities of aluminum in vaccines can’t possibly do harm.“
-Dr Paul Offit: Vaccine promoter, vaccine patent licensor, and autism pundit, 2015
“…the existing evidence on the toxicology and pharmacokinetics of Al adjuvants…altogether strongly implicate these compounds as contributors to the rising prevalence of neurobehavioural disorders in children.”
-Dr Chris Shaw, Neuroscientist and aluminum researcher at University of British Columbia, 2013.
The Scientific Evidence
The scientific evidence for this “Trojan Horse” mechanism is unequivocal and overwhelming. Every step has been proven by multiple studies from well-known universities and government-funded laboratories: the ingestion of AANs by MFs, the movement of MFs into the brain, and the observation that MFs carry nanoparticles into the brain. Also, the entire process has been demonstrated. AANs injected into experimental animals have been detected and imaged in the brain. The ability of MFs to transport particles into the brain has even been used to deliver therapeutic drugs (formulated as particles) into the brain. The Trojan Horse mechanism is well established and recognized. It is not theoretical.
Dr. Larry Palevsky – Dangers of Aluminum in Vaccines
Vaccin et Placebo non-neutre:
Un problème largement méconnu de monsieur tout le monde et bien expliqué ici: le placebo est rarement neutre et ça rend difficile l’évaluation des effets secondaires. Donc oui quand les gens du groupe placebo ont également des réactions allergiques (107 vs. 137 pour le vrai vaccin Pfizer pour la covid) ce n’est pas juste dû à leur imagination mais au fait que le placebo est lui-même actif et pas juste de l’eau et du sucre comme on peut lire parfois
C’est d’ailleurs une des critiques faites dans cette étude scientifique indépendante sur les études des laboratoires pour les vaccins HPV, une autre est de remarquer que les les effets secondaires sérieux dans les bras vaccins ont été considérés comme non-relié au vaccin:
Serious adverse events after HPV vaccination: a critical review of randomized trials and post-marketing case series: https://pubmed.ncbi.nlm.nih.gov/28730271/ :
Most HPV vaccine randomized trials did not use inert placebo in the control group. Two of the largest randomized trials found significantly more severe adverse events in the tested HPV vaccine arm of the study. Compared to 2871 women receiving aluminum placebo, the group of 2881 women injected with the bivalent HPV vaccine had more deaths on follow-up (14 vs. 3, p = 0.012). Compared to 7078 girls injected with the 4-valent HPV vaccine, 7071 girls receiving the 9-valent dose had more serious systemic adverse events (3.3 vs. 2.6%, p = 0.01). For the 9-valent dose, our calculated number needed to seriously harm is 140 (95% CI, 79–653). The number needed to vaccinate is 1757 (95% CI, 131 to infinity). Practically, none of the serious adverse events occurring in any arm of both studies were judged to be vaccine-related.
Vaccins et fragment d’ADN issus de lignée de cellules foetales (en l’occurrence, avorté) :
Rappelons d’abord en quoi consiste une lignée de cellules foetales. Celle-ci s’obtient en prélevant une cellule sur un foetus (en l’occurrence, avorté) et en multipliant cette cellule en plusieurs cellules identiques. Ces cellules peuvent être cultivées et multipliées pendant plusieurs décennies, créant ainsi des « lignées cellulaires », souvent utilisées dans le cadre d’expériences scientifiques. Certaines lignées de cellules foetales remontent à plusieurs dizaines d’années et sont utilisées dans l’élaboration de nouveaux vaccins. Il s’agit en particulier des lignées HEK293 et PER.C6. L’utilisation de ces cellules ne requiert donc pas de nouveaux avortements. Elle tire son origine de d’avortements qui ont eu lieu dans les années ’60, ’70 et ’80, indépendamment d’un objectif pharmaceutique.
Vaccine Ingredients – Fetal Tissues
Varicella (chickenpox), rubella (the “R” in the MMR vaccine), hepatitis A, and one preparation of rabies vaccine are all made by growing the viruses in fetal embryo fibroblast cells.
https://www.chop.edu/centers-programs/vaccine-education-center/vaccine-ingredients/fetal-tissues
Epidemiologic and Molecular Relationship Between Vaccine Manufacture and Autism Spectrum Disorder Prevalence
Vaccines manufactured in human fetal cell lines contain unacceptably high levels of fetal DNA fragment contaminants. The human genome naturally contains regions that are susceptible to double strand break formation and DNA insertional mutagenesis. The « Wakefield Scare » created a natural experiment that may demonstrate a causal relationship between fetal cell-line manufactured vaccines and ASD prevalence.
La composition des vaccins :
Données publiées par le Center for Disease Control aux États-Unis
Aux Ames Citoyennes 
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