Can mRNA-LNP platform vaccines (thus via the mRNA COVID gene injection vaccine)pass down acquired immune traits to offspring? Yes, seem so via this mice study; can unvaccinated kids in close contact

with vaccinated parents, incorporate vaccine-induced antibodies? Shockingly, seems so via the displayed study; is this evidence of aerosol transfer of vaccine induced antibodies? maybe mRNA? spike?

These 2 studies, while not optimal methodologies and not ideal comparative effectiveness type research designs, do broaden the nefarious deadly potential of the COVID mRNA gene injections. The long-term implications. Needs to be considered as we assess these shots and we read and look at research as a means to inform us bit not everything we read is ‘as is’. Bear that in mind and we view research as a means to drive testable hypotheses. The makers of the gene injections however, did bring us death, from mRNA to complete vaccine, whether mRNA or DNA vector platforms.

1)

SOURCE:

https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1010830

‘The mRNA-LNP-based SARS-CoV-2 vaccine is highly inflammatory, and its synthetic ionizable lipid component responsible for the induction of inflammation has a long in vivo half-life. Since chronic inflammation can lead to immune exhaustion and non-responsiveness, we sought to determine the effects of pre-exposure to the mRNA-LNP on adaptive immune responses and innate immune fitness. We found that pre-exposure to mRNA-LNPs or LNP alone led to long-term inhibition of the adaptive immune response…Interestingly, mice pre-exposed to the mRNA-LNP platform can pass down the acquired immune traits to their offspring, providing better protection against influenza.’

2)

SOURCE:

https://www.medrxiv.org/content/10.1101/2022.04.28.22274443v1.full#F1

‘obtained nasal swabs from children living in households in which parents or family members had varying degrees of SARS-CoV2-specifc immunity, including those unvaccinated, vaccinated and COVID-19+. Initial comparison of nasal swabs acquired from children living in vaccinated households revealed readily detectable SARS-CoV-2-specific IgG (Fig 1E), especially when compared to the complete deficit of SARS-CoV-2-specific antibody detected in the few nasal swabs we obtained from children in non-vaccinated households.’ The methods in this study is weak IMO yet this raises some interesting troubling questions.

‘Evaluation of samples in this fashion revealed that high intranasal IgG in vaccinated parents was significantly associated (p-value = 0.01) with a 0.38 increase in the log transformed intranasal IgG gMFIs within a child from the same household (Fig 1F).’