Wang et al. in 2018 wrote about the harms & adverse effects of nano-particles (NPs) on human reproductive system, so why did CDC, FDA, Fauci, Walensky, Francis Collins, Njoo, Tam & medical doctors

disregard this? NP accumulation damages organs (testis, epididymis, ovary & uterus) by destroying Sertoli cells, Leydig cells & germ cells, causing reproductive organ dysfunction

Seminal disregarded study:

‘NP accumulation damages organs (testis, epididymis, ovary, and uterus) by destroying Sertoli cells, Leydig cells, and germ cells, causing reproductive organ dysfunction that adversely affects sperm quality, quantity, morphology, and motility or reduces the number of mature oocytes (eggs) and disrupts primary and secondary follicular development. In addition, NPs can disrupt the levels of secreted hormones, causing changes in sexual behavior.’

So why the hell did they allow mRNA-DNA technology gene injections to be given to pregnant women, women of child-bearing age; injected them with a biologically active agent with no safety testing? Criminals IMO!

‘Previous studies have shown that numerous types of NPs are able to pass certain biological barriers and exert toxic effects on crucial organs, such as the brain, liver, and kidney.

SOURCE:

https://pubmed.ncbi.nlm.nih.gov/30587973/

‘Previous studies have shown that numerous types of NPs are able to pass certain biological barriers and exert toxic effects on crucial organs, such as the brain, liver, and kidney.

Only recently, attention has been directed toward the reproductive toxicity of nanomaterials.

NPs can pass through the blood-testis barrier, placental barrier, and epithelial barrier, which protect reproductive tissues, and then accumulate in reproductive organs.

NP accumulation damages organs (testis, epididymis, ovary, and uterus) by destroying Sertoli cells, Leydig cells, and germ cells, causing reproductive organ dysfunction that adversely affects sperm quality, quantity, morphology, and motility or reduces the number of mature oocytes and disrupts primary and secondary follicular development.

In addition, NPs can disrupt the levels of secreted hormones, causing changes in sexual behavior.

The molecular mechanisms involved in NP toxicity to the reproductive system are not fully understood, but possible mechanisms include oxidative stress, apoptosis, inflammation, and genotoxicity. Previous studies have shown that NPs can increase inflammation, oxidative stress, and apoptosis and induce ROS, causing damage at the molecular and genetic levels which results in cytotoxicity.’