Scientists in China Create New Vaccines Using Body Parts From Nine Aborted Babies
Due to dwindling capacity for existing aborted fetal cell lines to self-replicate, scientists in China have developed a new aborted fetal cell line, WALVAX 2 that will be used for viral vaccine production. The existing cell lines, MRC-5 and WI-38 are currently used in MMR, Varicella, Hepatitis-A, Shingles, some rabies and some polio vaccines.
WALVAX 2 is taken from the lung tissue of a 3 month gestation female who was ultimately selected from among 9 aborted babies. The scientists noted how they followed specific guidelines to mimic WI-38 and MRC-5 in selecting the aborted babies, ranging from 2-4 months gestation. They further noted how they induced labor using a “water bag” abortion to shorten the delivery time and prevent the death of the fetus to ensure live intact organs which were immediately sent to the labs for cell preparation.
According to the studies published earlier this year in the NIH Pub Med, scientists noted that Walvax-2 cells replicated more rapidly than MRC-5 cells, attained greater population doubling and performed better or equal to the existing cell lines for culturing viruses.
In 1964 Leonard Hayflick introduced what is known as the “Hayflick limit” – how all normal cells have a finite lifespan and limited capacity to replicate before going into senescence and eventually, become unstable and form tumors. (L. Hayflick, The Limited In Vitro Lifetime of Human Diploid Cell Strains, Experimental Cell Research, Vol 37, 1964) Attempts to immortalize these cells to extend their lifespan have likewise introduced problems with tumor formations, as in aborted fetal cell line PER C6, introduced into the US in 2001.
Study: Characteristics and viral propagation properties of a new human diploid cell line, walvax-2, and its suitability as a candidate cell substrate for vaccine production
Human diploid cell strains (HDCSs), possessing identical chromosome sets known to be free of all known adventitious agents, are of great use in developing human vaccines. However it is extremely difficult to obtain qualified HDCSs that can satisfy the requirements for the mass production of vaccines. We have developed a new HDCS, Walvax-2, which we derived from the lung tissue of a 3-month-old fetus. We established primary, master and working cell banks successfully from reconstituted frozen cells. Observations during the concurrent propagation of Walvax-2 and MRC-5 cells revealed differences in terms of growth rate, cell viability and viral sensitivities. Specifically, Walvax-2 cells replicated more rapidly than MRC-5 cells, with Walvax-2 cells attaining the same degree of confluence in 48 hours as was reached by MRC-5 cells in 72 hours. Moreover, Walvax-2 cells attained 58 passages of cell doublings whereas MRC-5 reached 48 passages during this period. We also assessed the susceptibility of these cells to rabies, hepatitis A, and Varicella viruses. Analysis of virus titers showed the Walvax-2 cells to be equal or superior to MRC-5 cells for cultivating these viruses. Furthermore, in order to characterize the Walvax-2 cell banks, a series of tests including cell identification, chromosomal characterization, tumorigenicity, as well as tests for the presence of microbial agents, exogenous viruses, and retroviruses, were conducted according to standard international protocols. In conclusion, results from this study show that Walvax-2 cell banks are a promising cell substrate and could potentially be used for the manufacturing of HDCVs.
Forsaking God For the Sake of Science
“What have you done? Listen: your brother’s blood cries out to me…” (Gn 4:10)
There are times in the history of mankind when we must take great pause and examine the path we have taken in the past and more importantly, what path we will take in the future to correct the twisted route that brought us here to begin with.
Such was the case where social elites, physicians and scientists in their zeal for power and glory saw nothing wrong in deliberately ending a fellow human being’s life for the so-called betterment of others who were deemed worthy of preserving.
This report will take us back to one of the most heinous, shameful eras in history beginning in the early 1900’s – back to a time that few reading this article will even know existed in the United States. And incredibly, what you are about to read was considered perfectly acceptable behavior in most circles.
The year was 1910 and a man by the name of Harry H. Laughlin was making the news with his influential positions as Director of the newly formed Eugenics Record Office which was funded by the Harriman and Rockefeller families and the Carnegie Institute. Known by both friends and foes as one of the most racist, anti-Semitics of the early 20th century, Laughlin was appointed to head the “master race project” which sought to weed out the undesirables in society. 
In his report to the Committee in 1914, Laughlin noted in no uncertain terms that, “defective parents must be stopped from having any children at all” and then described his proposed means of accomplishing that. In brief:
“Hence the selection of certain potential parents, and the elimination of others, is the only basis of a possible effective eugenics program of any sort….. That the present apparent tendency of society proposes to sterilize and thus cut off the lines of descent only of persons amply demonstrated in each particular case to be unable to understand, or, if understanding, morally unable to inhibit or control himself or herself in a manner preventing the continuance of his or her unworthy traits. To permit such individuals to reproduce their kind is neither merciful nor just.”
Within a decade, Laughlin introduced his state-level “Model Eugenical Sterilization Law” in 1922 requiring the forcible sterilization of those deemed unfit to breed. These would include the “feeble-minded”, mentally impaired, epileptics, the deaf, the blind, the homeless and chronic offenders of the law. By 1931 twenty eight states had enacted the legislation.