Further substantiation that injury by shedding (bioweaponized HERV-K102) occurred
New data from Dr. Avindra Nath’s research group of the NIH mentioned in the Fauci diary.
Image 1. Proposed Mechanism for Pfizer-BioNTech’s Process II LNPs Compromising the HERV-K102 Protector Particles That INJURE AND KILL Third Parties Upon Transmission Rather than Provide Sterilizing and Herd Immunity
Image 2. Evidence that shedding affected the unvaccinated as well as the vaccinated.
See details in
https://rumble.com/v51idm2-dr.-marian-laderoute-jun-01-2024-regina-saskatchewan.html
Image 3. Evidence for Progressive Loss of Herd Immunity by Dose Eroded by the Pfizer-BioNTech’s spike mRNA GENE THERAPY Product used for Immunization in England
For Image 2, we can only follow the effects of the Pfizer vaccination on non-COVID-19 mortality as the spread of SARS-CoV-2 was highly variable and thus, COVID-19 mortality could not be used to track the role of vaccination dose on mortality rates in the unvaccinated.
The positive control Omicron shown in E validates that the methodology can detect changes in mortality rates in the population such as diminished death rates for either COVID-19 or non-COVID-19 deaths in the vaccinated or unvaccinated.
If we first examine the role of innate immunity in response to the first dose in the absence of the spike IgG antibodies that develop only after the second dose, we see in the unvaccinated that the mortality rate drops by about 75% (-75%) for COVID-19 and 21 % (-21%) for non-COVID-19. The first case shows the action of trained immunity of macrophages and how it generates herd immunity against COVID-19.
The mechanisms by which trained immunity of foamy macrophages (innate immunity) can protect against pathogens as well as chronic diseases more specifically are provided in this reference:
Marian P. Laderoute. Trained immunity of M1-like foamy macrophages: A key role of human endogenous retrovirus K102 particles. Global Translational Medicine 025370071. https://doi.org/10.36922/GTM025370071
with a lay summary provided here:
lay summary of the TI paper of June 26, 2026.
Image 4. The multitude of ways in which the launch of HERV-K102 particles by lysis of foamy macrophages can provide sterilizing and herd immunity as well as reduce chronic disease risks are summarized in this image.
Protection is by the induction of the interferon response and the induction of innate T and B cells to HERV-K102 envelope expressed on tumors and virally transformed cells. The HERV-K102 particles and/or IRF-1 released with the particles (used to make particles) upregulates PD-L1 on vascular endothelial cells which may protect against complement activation and vasculitis. The particles are believed to induce lysis in cancer cells and virus transformed cells. Sterilizing immunity (and pathogen clearance) is postulated to be due to HERV-K102 envelope on pathogens budding from the cells and inactivation/clearance by the IgG antibodies to HERV-K102 envelope.
We have learned of a putative case potentially involving the in vivo integration of a 22 bp seqment identical to spike protein, in an aggressive bladder cancer in a young woman
John A. Catanzaro, Nicolas Hulscher, & Peter A. McCullough. Genomic Integration and Molecular Dysregulation in Aggressive Stage IV Bladder Cancer Following COVID-19 mRNA Vaccination. Zenodo. September 15, 2025. (preprint) https://doi.org/10.5281/zenodo.17122912 and
published in International Journal of Innovative Research in Medical Science, 10:10, October 2025. https:doi.org/10.23958/ijirms/vol10-i10/2130.
This integration site held the calling card of integration by HERV-K102 (the same target site duplication (TSD) in the flanking sequence of the integration) as discussed here:
Image 5. HERV-K102 implicated in facilitating integration in Bladder Cancer in Vivo.
Tentatively this argues that the Pfizer vaccine and shedding was involved even though the woman only directly received the Modern LNPs with spike mRNA.
A new paper by the same research group
[Hulscher N, Schmidt V, Morz M, Rogers C, von Ranke N, Zhang W, Catanzaro JA, McCullough PA. Persistence of vaccine mRNA, plasmid DNA, spike protein, and dysregulation over 3.5 years post COVID-19 mRNA vaccination. Medical Research Archives, July 29, 2026. https;//doi.org/10.18103/mra2026.0351.]
reveals that not only is spike protein detectable over the 3.5 years but also other components of the Pfizer LNPs. This implies that shedding involving the bioweaponized/compromised HERV-K102 particles released from the upper respiratory tract (released as sebum from sebocytes), may generate a very high risk of host integration to third parties. We are talking the genetic modification of humans whether directly injected or not by the dirty Pfizer LNPs.
Judging by the clinical details, I would say this 55 year old male was shed upon on October 28, 2021 implying Pfizer shedding could be commonly implicated in the longer term post COVID-19 vaccination syndromes and not just mortality within 48 hours of vaccination or mortality beyond 60 days after the last shot.
But there is now evidence from 2022 consistent with the notion that a complex of spike antibody-antigen activated complement in the victims of shedding that characterized shedding injuries (see Image 1 above).
[Safavi F, Gustafson L, Walitt B, Lehky T, Dehbashi S, Amanda Wiebold A, Mina Y, Shin S, Pan B, Polydefkis M, Oaklander AL, Nath A. Neuropathic symptoms with SARS-CoV-2 vaccination. medRxiv preprint doi: https://doi.org/10.1101/2022.05.16.22274439; this version posted May 17, 2022. ]
In this paper 87 % of the cases with neuropathic symptoms had onset within 48 hours and where for most cases (60.9%) the injury occurred after the first dose. Only 8.7% did not receive the mRNA versions. Since the development of spike antibodies does not occur until after the second mRNA shot, this tends to rule out any role of antibody dependent enhancement (ADE) of infection into macrophages as playing a role in the genesis of the neuropathic symptoms. The latter helps to argue that shedding from the recently double-vaccinated vaccinator at the large clinics is more likely (environment causes) than immunological internal changes to the host (especially for reactions under 2 days as it take 2 days to identify spike protein in the blood). In Figure 1, the authors showed that the biopsies performed on the lower legs of patients (5) versus controls (9), had demonstrably higher deposits of C4d on endothelial cells.
C4d deposits on endothelial cells indicates an antibody-complex reaction that activates complement via the classical pathway.
Murata K, Baldwin WM 3rd. Mechanisms of complement activation, C4d deposition, and their contribution to the pathogenesis of antibody-mediated rejection. Transplant Rev (Orlando). 2009 Jul;23(3):139-50. doi: 10.1016/j.trre.2009.02.005.
Importantly, C4d deposition on the vascular endothelium is associated with influx of neutrophils and/or macrophages frequently involving IL-8 (CXCL8) a poor prognosis indicator for COVID-19 and for exposure to Pfizer but not Moderna LNPs (Image 6).
Image 6. Data from Cao X et al, 2025 implicates Pfizer but not Moderna LNPs in provoking IL-8 production in human macrophages.
Conclusions:
The new data from Dr. Avindra Nath’s research group of the NIH mentioned in the Fauci diary as a paper that should be restricted from publication by NIH as it would cause vaccine hesitancy, provides a new substantiation angle of the proposed shedding phenomenon unique to the Pfizer spike mRNA gene therapy lipid nanoparticles that caused injury and deaths within 48 hours of receipt of the mRNA “clot shots”.
Slowly accumulating evidence implicates the spike mRNA from Pfizer in the genetic modification of the host related to integration facilitated within HERV-K102 particles and which might provide the foundation for long term and persistent multi-organ system injuries recognized as Post COVID-19 Vaccination Syndrome.
The interference with the protector function of HERV-K102 particles in generating sterilizing and herd immunity by the Pfizer spike mRNA “dirty” LNPs could and has threaten the survival of the Homo sapiens species.
Moving forward, we MUST ban the inappropriate use of mRNA/cDNA gene therapy technologies for immunization purposes, if we are to learn from these horrendous “crimes against humanity”. This message is not only for HHS but for DoD (and the CIA), and DoJ.
Thank You, Dr. Laderoute. I am sorry to understand this so clearly. It is truly diabolical. ;-(
Marian, are you saying that shedding can result in exosomes or other particle entering the nucleus and modifying our dna?