Fetal Cell use in the Pfizer and Moderna mRNA Covid-19 Vaccines

An in depth discussion with citations of the role that aborted fetal cell lines play in the mRNA vaccines currently in use is warranted. We begin to wade into that discussion here.

The HEK 293 cell line was used in the medical sector’s initial understanding of the spike protein itself, and is the foundation for all of the vaccines in use.

They were used in the process of mapping the SARS-Cov-2 S protein, and subsequently, that information was then used by Pfizer, Moderna, Johnson & Johnson, and all other vaccine makers creating products that target the spike protein. The initial paper describing the structure of the S protein itself, Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation, states that:

“We obtained ~0.5 mg/liter of the recombinant prefusion-stabilized S ectodomain from FreeStyle 293 cells and purified the protein to homogeneity by affinity chromatography and size-exclusion chromatography (fig. S1).” 

Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation

The supplemental materials it show that they use it twice in the process:

“These expression vectors were used to transiently transfect FreeStyle293F cells (Thermo Fisher) using polyethylenimine.”

“Plasmids encoding the heavy and light chains of S230, 80R and m396 IgG were transiently transfected into Expi293cells (Thermo Fisher) using polyethylenimine.”

Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation

Both mRNA vaccines, not only use the cell line for testing the vaccine, but they are both downstream from the use of this cell line, thus can be considered morally tainted vaccines. 

Believers who are pro-life deserve informed consent on this matter.  If we are serious about ending the use of beloved children in this way, we have to stop buying products that in anyway used their bodies.  Ending the profit model of aborted fetal cell use in medicine is the only language that a fallen medical industry understands.