Note to Reader: In laymen's terms, these vaccines are designed to target aspects of the immune system in order to enhance the effects of respiratory (and other) disease particularly to cause acute lung injury after a respiratory infection.
This entire year was a run-through of what is yet to come. Read that again. It was ALL LIES. I have told you time and time again. They tell you things are the reality as they actively work to bring about those very things making them reality. Did you pay attention this time? This is what is happening to you. M'kay?
Everything that they told you about this "virus", the "pandemics", etc. Is what is to come, not what already was. Re-read Note to Reader.
I'm not here to tell other people what to think about the things that have transpired over the past several years. Not any of it. However, I want you to know that your life is an illusion and your environment an anomaly. The reality that is coming is the one that bore an individual like me.
Many of you are old and/or getting up there in age now but you are directly responsible for the pending calamity that will affect generations to come. It was the same lack of wherewithal that you exhibit even to this very day that caused it. We are not the same you and me. You DO NOT have my respect just because you walked a certain number of years on the face of this Earth, and that is because you walked and never saw. You have been the blind leading the blind to utter calamity.
I, a little white girl who grew up in extreme poverty in an urban environment where I and those like me were the outsiders, have been caused to point out your ass from a hole in the ground. Fuck you.
Dr. Judy Mikovits Exposes Anthony Fauci - Revolution Television Our girl Judy calling out the Leviathan.
If you come across important videos, download them, if you can, as we are in an information war and the dissemination of and preservation of information is paramount moving forward.
ADE may cause enhanced respiratory disease and acute lung injury after respiratory virus infection (ERD) with symptoms of monocytic infiltration and an excess of eosinophils in respiratory tract.[24] ADE along with type 2 T helper cell-dependent mechanisms may contribute to a development of the vaccine associated disease enhancement (VADE), which is not limited to respiratory disease.[24] Some vaccine candidates that targeted coronaviruses, RSV virus and Dengue virus elicited VADE, and were terminated from further development or became approved for use only for patients who have had those viruses before.
Recent Interview by Luc Montagnier.
Luc Montagnier is a French virologist and recipient of the 2008 Nobel Prize in Medicine for his discovery of the human immunodeficiency virus (HIV). On April 18, Professor Montagnier appeared on a French TV station (video in French with English subtitles) to comment on the origin of COVID-19, echoing what several other scientists have suggested in saying that the virus had been manipulated by researchers. He also mentioned in his appearance on the program that components of HIV had been inserted into the coronavirus sequence, perhaps in pursuit of an AIDS vaccine.
When asked by one of the commentators if the coronavirus under investigation may have come from a patient who is otherwise infected with HIV, Professor Montagnier said, “No. In order to insert an HIV sequence into this genome, molecular tools are needed, and that can only be done in a laboratory.”
Back in April and May of 2020 Dr. Montagnier told you -
"Don't Accept A Vaccine", Says Dr. Luc Montagnier - Nobel Prize Recipient 2008 for Discovering HIV
Nobel Prize Winner Dr. Luc Montagnier on the Coronavirus on a French mainstream channel CNEWS, April 17, 2020. For the full interview go to: https://www.youtube.com/watch?v=-a7nl... (choose cc for closed caption to be translated from French to English).
Antibody-Dependent Enhancement
Antibody-dependent enhancement (ADE), sometimes less precisely called immune enhancement or disease enhancement, is a phenomenon in which binding of a virus to suboptimal antibodies enhances its entry into host cells, followed by its replication.[1][2]
Antiviral antibodies promote viral infection of target immune cells by exploiting the phagocytic FcγR or complement pathway.[3] After interaction with the virus the antibody binds Fc receptors (FcR) expressed on certain immune cells or some of the complement proteins. FcγR binds antibody via its fragment crystallizable region (Fc).
Usually the process of phagocytosis is accompanied by the virus degradation, however, if the virus is not neutralized (either due to low affinity binding or targeting to a non-neutralizing epitope), antibody binding might result in a virus escape and therefore, enhanced infection. Thus, phagocytosis can cause viral replication, with the subsequent death of immune cells. The virus “deceives” the process of phagocytosis of immune cells and uses the host's antibodies as a Trojan horse.
ADE may occur due to the non-neutralizing characteristic of the antibody, which bind viral epitopes other than those involved in a host cell attachment and entry. ADE may also happen due to the presence of sub-neutralizing concentrations of antibodies (binding to viral epitopes below the threshold for neutralization).[4] In addition ADE can be induced when the strength of antibody-antigen interaction is below the certain threshold.[5][6] This phenomenon might lead to both increased virus infectivity and virulence.
The viruses that can cause ADE frequently share some common features such as antigenic diversity, abilities to replicate and establish persistence in immune cells.[1] ADE can occur during the development of a primary or secondary viral infection, as well as after vaccination with a subsequent virus challenge.[1][7][8] It has been observed mainly with positive-strand RNA viruses. Among them are Flaviviruses such as Dengue virus,[9]Yellow fever virus, Zika virus,[10][11]Coronaviruses, including alpha- and betacoronaviruses,[12]Orthomyxoviruses such as influenza,[13]Retroviruses such as HIV,[14][15][16] and Orthopneumoviruses such as RSV.[17][18][19]
The mechanism that involves phagocytosis of immune complexes via FcγRII / CD32 receptor is better understood compared to the complement receptor pathway.[20][21][22] Cells that express this receptor are represented by monocytes, macrophages, some categories of dendritic cells and B-cells. ADE is mainly mediated by IgG antibodies,[21] however, IgM along with complement,[23] and IgA antibodies[15][16] have also been shown to be trigger ADE.
ADE may cause enhanced respiratory disease and acute lung injury after respiratory virus infection (ERD) with symptoms of monocytic infiltration and an excess of eosinophils in respiratory tract.[24] ADE along with type 2 T helper cell-dependent mechanisms may contribute to a development of the vaccine associated disease enhancement (VADE), which is not limited to respiratory disease.[24] Some vaccine candidates that targeted coronaviruses, RSV virus and Dengue virus elicited VADE, and were terminated from further development or became approved for use only for patients who have had those viruses before.
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