Here is a video interview with Professor Angus Dalgleish, a respected UK oncologist with a background in immunotherapy and HIV research:
https://www.thefocalpoints.com/p/covid-19-vaccines-and-cancer-interview
Dalgleish's key points:
He has observed excess melanoma relapses and "rare/aggressive" cancers in younger patients after boosters in his practice.
Main proposed mechanism for cancer: T-cell suppression/exhaustion from repeated mRNA doses, plus IgG4 class switching that makes the response "tolerogenic" (the immune system stops attacking the "foreign" spike, and by extension fails to surveil cancers). He compares it to allowing a "transplant" (i.e., cancer) to grow unchecked.
Spike protein itself promotes inflammation/microclots that could aid metastatic spread.
Additional concerns: potential mRNA/DNA integration disrupting genes (e.g., p53, BRCA), SV40 promoter fragments, and bone-marrow effects.
He has repeatedly called mRNA COVID vaccines "an absolute disaster" that "should be completely, utterly banned," citing regulatory failure and what he sees as one of the largest carcinogenic exposures in history.
While that is all alarming, there was also a thought provoking post to the article by Kelly Reardon, taking these points further, and arguing that the dangers are real and must be met by banning the mRNA tech:
Kelly Reardon: The COVID modified mRNA-LNP genetic transfection injections MUST be recalled and the injurious and potentially deadly mRNA transfection platform MUST be banned. Even if there was no E. coli DNA plasmid "contamination" with no carcinogenic SV-40 promotor sequence, even if they had not deceptively injected shots into the public that were made by Process 2, even if the spike protein was not inflammatory & pathogenic... these mRNA transfection injections would have still injured and killed people. The mRNA transfection platform itself is irreparably flawed & inherently dangerous and the platform itself IS the primary problem. The mechanism of action (using mRNA instructions to turn one's own cells into foreign non-self "spike protein factories") IS the primary mechanism of harm. This triggers an immune system attack response, starting with the Killer T-Lymphocyte cells which will target & destroy one's formerly healthy cells, ANYWHERE in the body, that are now expressing non-self proteins... starting a cascade of damage at the deepest biological/cellular level. Due to the proven systemic biodistribution properties of the (toxic & inflammatory) lipid nanoparticles, the encased (designed to be long-lasting) n1-methyl pseudouridine modified mRNA can go anywhere in the body, including crossing the blood-brain & placental barriers. The LNP "delivery vehicles" travelled to different parts of the body in different people. Expressing any foreign non-self-protein is fatal to the cell doing the expressing. Some people will express lots of foreign proteins in vulnerable locations. Others express less in less vulnerable areas. The location of expression defines the adverse event: if you get foreign protein expression in your heart cells, you could get myocarditis & experience cardiac arrest; if the expression is in your brain, spinal cord, or peripheral nervous system, you could get one or more of a variety of neurological conditions; if in your eye, possible blindness; if in your ovaries, possible infertility; if in the placenta, possible miscarriage, stillbirth, or birth defects; if in the endothelial cells that line your blood vessels, possible vascular &/or microvascular injuries like clots/microclots or the long white fibrous clots, leading to strokes, heart attacks, or pulmonary embolisms… If the expression of foreign proteins is in your own immune cells, you could experience immune dysfunction, dysregulation, & suppression including repeated infections, immune tolerance of a pathogenic foreign protein due to antibody subclass switch to IgG4 & increased IgG4-related diseases, T cell exhaustion, interference with & suppression of innate immunity, persistent systemic inflammation, dysregulation of toll-like receptors and reduced cancer surveillance or the suppression of tumor-suppressing immune system activities & cell-signalling (increasing your risk of fast-growing and aggressive cancers). And more… Pathology reports, including from autopsies, have revealed & confirmed the Killer T Lymphocyte infiltration & destruction of cells, oftentimes in vital organs. These modified mRNA-LNP genetic transfection injections never would have passed proper safety studies required for gene therapy products. Safety studies (including biodistribution, immunogenicity, immunotoxicity, genotoxicity, carcinogenicity, reproductive toxicity, shedding, long-term effects, & more) that were bypassed because of the mislabeling as "vaccines". (And because of the EUA & "countermeasure" designations under the Project BioShield Act & PREP Act). The danger is NOT limited to just getting more COVID "boosters". ANY mRNA gene "therapy" product that transfects your cells & instructs those cells to produce non-self proteins (ANY non-self protein) will trigger an immune system attack response against your own cells & tissues. This makes EVERY mRNA-based transfection product harmful by design. This immune response to one's own cells being instructed to express non-self proteins (ANY non-self protein) triggers autoimmune responses, & then T-cell exhaustion & immune system dysfunction, regardless of whether or not the foreign protein is toxic itself.