COVID vaccine mRNA crosses placenta in mice, exposing fetuses to vaccine-induced spike protein risks

A new study titled “mRNA-1273 is placenta-permeable and immunogenic in the fetus” by Jeng-Chang Chen et al. presents a chilling revelation about the COVID-19 mRNA vaccines, specifically the mRNA-1273 (Moderna) formulation. While the authors frame their findings within the context of advancing prenatal mRNA molecular therapy, a closer examination of the data reveals a deeply troubling reality: The mRNA-1273 vaccine is not only capable of crossing the placental barrier but also induces an immune response in the fetus. This discovery raises alarming questions about the true intent behind these vaccines and their potential role as a depopulation bioweapon, as the fetus is vulnerable to the effects of the vaccine-induced toxicity from the spike protein.

Key findings and implications:

• Placental permeability: The study confirms that mRNA-1273, when administered to pregnant mice, rapidly circulates in maternal blood and crosses the placenta within one hour, spreading into fetal circulation. This finding shatters the narrative that mRNA vaccines remain localized at the injection site and are “safe” for pregnant women.

• Fetal accumulation and spike protein production: The mRNA accumulates in fetal tissues, particularly the liver, where it is translated into spike protein. This raises serious concerns about the long-term effects of spike protein expression in developing fetuses, including potential organ damage and autoimmune disorders.

• Fetal immunogenicity: The study reveals that mRNA-1273 is immunogenic in fetuses, leading to the production of anti-spike IgM and IgG antibodies, as well as heightened cellular immunity. This unnatural immune activation in utero could have devastating consequences for fetal development and long-term health.

• Dose-dependent effects: Higher doses of mRNA-1273 result in greater transplacental transfer and increased fetal immune responses, suggesting a direct correlation between vaccine dosage and potential harm to the unborn child.

A depopulation bioweapon in disguise, targeting fetuses

The findings of this study provide compelling evidence that mRNA-1273 is not merely a vaccine but a genetic weapon capable of infiltrating the most vulnerable population: unborn children. The ability of mRNA-1273 to cross the placenta and induce an immune response in the fetus is a hallmark of a depopulation bioweapon, designed to disrupt normal fetal development and compromise future generations.

The production of spike protein in fetal tissues is particularly concerning, given the well-documented toxicity of the spike protein. Studies have shown that the spike protein can cause inflammation, blood clotting, and damage to vital organs. By introducing this toxic protein into developing fetuses, mRNA-1273 may be setting the stage for a wave of chronic illnesses, infertility, and premature deaths in the coming decades.

The illusion of “protection”

The authors of the study attempt to frame their findings in a positive light, suggesting that maternal mRNA-1273 vaccination could provide newborns with “passive and active anti-spike immunity.” However, this narrative is deeply misleading. The immune system of a fetus is not designed to handle the artificial immune activation caused by mRNA vaccines. Forcing an immature immune system to produce antibodies against a synthetic spike protein could lead to immune dysregulation, autoimmune disorders, and increased susceptibility to infections.

Furthermore, the long-term consequences of fetal exposure to mRNA-1273 are entirely unknown. The study’s focus on short-term immunogenicity ignores the potential for delayed adverse effects, such as developmental abnormalities, cancer, and generational genetic damage.

This study serves as a wake-up call for humanity. The COVID-19 mRNA vaccines, far from being a tool for public health, are a dangerous genetic experiment with the potential to cause unprecedented harm. The fact that mRNA-1273 can cross the placenta and alter fetal development is a clear indication that these vaccines are not safe for pregnant women or their unborn children.

The global push to vaccinate pregnant women with mRNA-1273 must be immediately halted. Governments, health organizations, and medical professionals must be held accountable for promoting these experimental injections without fully understanding their long-term effects. The ability of mRNA-1273 to cross the placenta, produce spike protein in fetal tissues, and induce an immune response in the unborn is a chilling reminder of the dangers posed by these experimental injections. The lives of future generations are at stake, and we cannot afford to remain silent in the face of this unprecedented threat.

Sources include:

ChildrensHealthDefense.org

ScienceDirect.com

Pubmed.gov