Modern child sacrificing continues

Vaccines

Michigan - full 9-hour deposition/(confession)
https://www.youtube.com/watch?v=DFTsd042M3o 

​"Aborted fetal tissues are used in vaccines. Vaccines have been experimentally tested on orphans and on mental handicapped children. Experimental tests on babies from mothers in prisons. Experimental tests on 1 million people in then colonial Belgian Congo."

'Babies Have To Remain Alive For Organs To Be Harvested In Vaccine (plus ALL DRUG) Development Experiments.' Aaron Siri says, 'You Can't Grow Viruses Using Dead Organ Tissue, They Have To Be Born Alive ... Dr. Stanley Plotkin Admits To All Under Oath ... Unborn Babies Are Alive At Tissue Extraction' ... Dr. Plotkin gladly admits, without remorse, to Lawyer Aaron Siri, that he accepts human sacrifice as a normal, acceptable consequence in order to further science' as he is 1st & foremost a scientist & practicing Atheist. Former Vaccine Researcher & Biologist Pamela Acker has stated, "The babies are alive when the researchers start extracting the tissue. Their hearts are still beating & they're not given any anesthetic because that would contaminate the organs being harvested that need to be alive, pure & free of toxins.' According to expert Dr. Theresa Deisher, PhD, 'Babies are born alive from five to six months old, with beating hearts cut out without anesthesia for research purposes. Researchers also cut through live babies' faces to collect brain tissue.'"

"Stanley Alan Plotkin is an American physician & vaccinologist renowned for his pivotal role in developing several critical vaccines. Born and raised in New York City, he attended The Bronx High School of Science, where at the age of 15, he was inspired by the books Arrowsmith by Sinclair Lewis and Microbe Hunters by Paul de Kruif to pursue a career in medicine and research. He earned his bachelor's degree from New York University in 1952 and his MD from SUNY Downstate Medical Center in 1956. Plotkin began his research career at the Wistar Institute in Philadelphia in the 1960s, where he played a key role in developing the rubella vaccine using the RA 27/3 strain of the virus, grown on the WI-38 fetal-derived human cell line ..."  AI-generated answer from multiple sources.

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Pharma Drugs & Gain-of-function (GOF) Gene Altering

Chimeric = Humanized Mice:
Humanized liver mouse models are increasingly being used in preclinical trials and have allowed for groundbreaking in-vivo research to evaluate everything from human-specific drug toxicity and efficacy to gene therapies. Hera Biolabs
Humanized mice, created by introducing human stem cells into mouse embryos. Human cells have been injected into the amniotic fluid of pregnant mice, where they migrated to fetal organs such as the intestines, liver, and brain, demonstrating a promising technique for creating humanized mouse models.  ​AI generated from multiple sources. https://med.stanford.edu/news/all-news/2012/10/mice-with-humanized-livers-improve-early-drug-testing-scientist-show.html

Harma: Drugs & Vaccines use Humanized Mice as a Valuable Pre-Clinical Model

• For Cancer Immunotherapy Research:  https://pmc.ncbi.nlm.nih.gov/articles/PMC8636317/
• For Cardiac Research: A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarction.  https://www.sciencedirect.com/science/article/pii/S2666379124005421
• ​For over-the-counter Antihistamines: Clemizole is a chemical compound originally developed as a first-generation antihistamine but is now being researched for its potential in treating other conditions, including Dravet syndrome, a rare form of epilepsy, as well as Hepatitis C.
• For Diabetes - Weight Loss: Ozempic, studies conducted on humanized mice have provided critical insights into how Ozempic (semaglutide) affects different bodily systems, going beyond its well-known weight loss effects.
• An exhaustive list of every drug tested on humanized mice is impossible to create - read below.

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Planned Parenthood

SWORN VIDEO TESTIMONY DESCRIBES INFANTICIDE IN FETAL ORGAN HARVESTING  
​Read & Listen  Planned Parenhood Procurment Managers

ABR https://www.centerformedicalprogress.org/human-capital/special-report-advanced-bioscience-resources/

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When did this begin? 

There is conflicting data on when this began - decades ago, according to AI searches: 
​
"The first documented use of humanized mice for drug testing involved the evaluation of Clemizole, a drug being developed for Hepatitis C. Scientists used chimeric mice with humanized livers to study the drug's metabolism and interactions" Clemizole was first described in the scientific literature in 1952 and was discovered in the 1950s as a first-generation ..."
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"The first reporting of humanized mouse models occurred in 1988, when three independent research groups successfully transplanted human hematopoietic cells into immunodeficient mice. Two of these studies utilized C.B17-SCID mice as recipients for either human peripheral blood or human fetal tissues." Humanized mice were first used in 1988 ... to model human immunodeficiency virus (HIV) infection and the human immune response to HIV.   https://pmc.ncbi.nlm.nih.gov/articles/PMC7265413/​

Stanford University scientists first used chimeric mice with humanized livers to predict human drug metabolism and drug-drug interactions in a landmark 2012 study.
The research, led by Gary Peltz, focused on clemizole, a drug in development for hepatitis C virus (HCV) infection. The team used TK-NOG mice—a model with livers largely replaced by human cells—to test how clemizole was metabolized and how it interacted with ritonavir, a known CYP3A4 inhibitor.

1996 Flu Shot

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US Government WITH Pharma Companies & Universities 

FDA, NIH Buying Aborted Human Fetal Parts for Experiments link to read
Judicial Watch reveals that the U.S. Food and Drug Administration (FDA) has paid tens of thousands of taxpayer dollars to obtain human fetal tissue from the California-based “procurement” firm Advanced Bioscience Resources (ABR), undoubtedly supplied by abortion providers such as Planned Parenthood. According to the report, the fetal tissue was used in a sort of Frankenstein project to create “humanized mice” to test “biologic drug products.” To this day, research continues unimpeded. 
E-mail dated September 27, 2012, Howard submitted an application to Larton for “tissue purchases” in the amount of $12,000. The contract reportedly requested tissue from an aborted fetus with a gestational age of 16 to 24 weeks and “One set of tissue (thymus/liver) approx. twice monthly.” Instructions stated that the tissues were to be shipped “fresh; on wet ice."

Judicial Watch - Freedom of Information Act (FOIA) documents Link to read

NIH Fetal Tissue Use
"The National Institutes of Health (NIH) has specific requirements for research involving human fetal tissue obtained from elective abortions, including the procurement and use of fresh fetal organs for pharmaceutical and medical research purposes. As of September 25, 2019, NIH implemented updated requirements for grant applications and research and development (R&D) contracts proposing the use of human fetal tissue (HFT) ..."  Multiple sources

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Covid Bioweapon "vaccines" created with aborted cells/tissue/organs 
Many people only view the HEK 293 cell line (derived from human embryonic kidney cells from an aborted baby in the 1970s: There is no statute of limitations on the issue), while ignoring the fresh tissue and organs being obtained for research of drugs: "vaccines", bioweapons, cancer drugs, "particularly the progagation of adenoviral-based ad retroviral-based vectors." 

"Independent testing and expert testimony have confirmed the presence of residual DNA fragments in vials of mRNA Covid-19 shots, levels exceeding safety guidelines. Molecular biologist and cancer geneticist Phillip Buckhaults presented to a South Carolina Senate committee on September 12, 2023, stating that DNA pieces were present in leftover Pfizer/BioNTech vaccine vials and expressing concern about the potential for genome integration and cancer risks. Similarly, genomic expert Kevin McKernan reported finding DNA contamination in Pfizer and Moderna bivalent vaccine vials."

"J&J uses a modified adenovirus, Adenovirus 26, as the vector to deliver the genetic material encoding the SARS-CoV-2 spike protein to cells. The mRNA is packaged within a modified virus, known as a viral vector. The double viral vector approach involves using two viruses: the adenovirus vector and the SARS-CoV-2 virus. The adenovirus vector carries the genetic material encoding the SARS-CoV-2 spike protein, which is then expressed by the cells."  From J&J website  "... it was developed using a cell line originally derived from fetal tissue obtained from an elective abortion in the 1970s, known as the PER.C6 cell line."

An exhaustive list of every drug tested on humanized mice - aka dissected/sacrificed child organs or tissue put into animals aka abomination to God - is impossible to create because drug companies often keep preclinical data private. However, published scientific literature details numerous examples and classes of medicines tested in these models, particularly for research on immuno-oncology, infectious diseases, and drug metabolism. 
Humanized mice are immunocompromised mice that have been engrafted with human genes, cells, or tissues, allowing researchers to study human-specific biological responses and disease processes. 
Immuno-oncology.

Cancer immunotherapies (Chemo) are tested in humanized mouse models, which can be engineered with human immune cells and cancer cell lines (CDX) or patient-derived tumor tissue (PDX). 

• Immune checkpoint inhibitors (ICIs): These block checkpoint proteins on T-cells to help the immune system fight cancer. Tested ICIs include:
  • Nivolumab (anti-PD-1)
  • Pembrolizumab (anti-PD-1)
  • Atezolizumab (anti-PD-L1)
  • Ipilimumab (anti-CTLA-4)
  • Many ICI combination therapies, such as nivolumab and ipilimumab, have also been tested.
• Adoptive cell therapy (ACT): This involves using human immune cells to fight cancer, often genetically modified. Examples include:
  • CAR-T cell therapy: Anti-CD19 and EGFR CAR-T therapies.
  • CAR-NK cell therapy: Anti-GD2 CAR-NK therapy.
  • TCR-T cell therapy: WT-1 TCR-T therapy.
• Oncolytic viruses: These are genetically engineered viruses that selectively target and kill cancer cells. Examples tested in humanized mice include:
  • Herpes Simplex Virus (HSV-1 OV)
  • Oncolytic Vaccinia Virus
• Cytokine manipulation: Studies have explored therapies using cytokines, like IL-12, to influence the immune response against tumors.
• Monoclonal and bispecific antibodies: Humanized FcRn mouse models are used to test antibodies, which can be engineered to have a longer half-life in humans. An example is the CD19xCD28 bispecific antibody, RG6333.
• Small molecule inhibitors: These are also tested in combination with immunotherapies, such as a CDK4/6 inhibitor plus anti-PD-1. 

Infectious diseases
Humanized mice are essential for studying human-specific infectious agents and testing antiviral therapies. 

• HIV/SIV: Humanized mice are used for testing antiretroviral therapies and their efficacy against both HIV and SIV infections. Drug combinations tested include:
  • Emtricitabine (FTC), Bictegravir (BIC), and Tenofovir Alafenamide (TAF)
  • Emtricitabine (FTC), Elvitegravir (EVG), and Tenofovir Disoproxil Fumarate (TDF)
• Hepatitis C: In 2012, a drug developed to fight hepatitis C was tested in mice with humanized livers.
• Dengue Virus (DENV): Humanized mice have been used to study DENV infection and test new therapeutics.
• Malaria: Researchers have studied Plasmodium falciparum infection and tested new therapeutics in humanized mice with both humanized livers and blood.
• Ebola Virus: Humanized mice were used to study the pathogenesis of Ebola virus infection and test new drugs. 

Drug metabolism and toxicology
Humanized mice can be engineered with human liver or metabolic enzymes to predict how the human body will process and break down a drug. 

• Cytochrome P450 (CYP) enzymes: Mice engineered with human CYP enzymes (like CYP3A4) are used to test drug-drug interactions (DDIs). Drugs tested include:
  • Triazolam
  • Ritonavir
  • Ketoconazole
  • Midazolam
• Transport proteins: Models with human transport proteins, like MDR1 or OATP1B1, are used to study drug disposition and DDIs. Drugs tested include Digoxin and Atorvastatin.
• Chemotherapeutic drugs: Models with human hematopoietic systems are used to test the safety and lineage-specific toxicity of chemotherapy drugs like Oxilplatin, Topetecan, and Paclitaxel. 

Other diseases
Humanized models are also used for research into a variety of other conditions: 

• Autoimmune diseases: Models for conditions like psoriasis, atopic dermatitis, and rheumatoid arthritis are used to test drugs targeting specific human biomarkers.
• Metabolic disorders: Research into diabetes, obesity, and fatty liver disease uses humanized models targeting metabolic pathways.
• Neurological disorders: Models targeting pathways in neurological conditions like Alzheimer's and Parkinson's have been developed.