[GUEST ACCESS MODE: Data is scrambled or limited to provide examples. Make requests using your API key to unlock full data. Check https://lunarcrush.ai/auth for authentication information.]  Robin Monotti [@robinmonotti](/creator/twitter/robinmonotti) on x 234K followers Created: 2025-07-27 07:37:14 UTC ANGUS DALGLEISH ON "VACCINE" INDUCED TURBOCANCERS: Professor of Oncology at St George's Hospital Medical School, London: "There are numerous reports in the literature of cancers arising within days of the vaccines being administered, especially in the case of lymphomas and leukaemias. There are several reports of PET scan mapped tumours exploding at the site and draining area of covid injections with the advice to inject covid vaccines away from known cancers! Outside my clinical observations, several friends have developed cancer after a totally unnecessary covid booster taken only to facilitate travel. T cell responses are suppressed after the boosters (not the first two injections) and that this is especially marked in some cancer patients. The antibody repertoire switches after the first booster from a protective IgG1 and IgG3 dominant B cell response to a tolerising IgG4 one, made worse by further boosters, as reported in a recent Science Immunology paper. As many cancers are controlled by effective T cell led immunity, the sudden perturbation of this control would clearly explain the development of B cell leukaemia and lymphomas, melanoma renal cell cancers and colorectal ones, all tumours which can respond to immunotherapy. Another report by Loacker et al in Clin Chem Lab Med shows that mRNA vaccines increase PD-L1 on granulocytes and monocytes, which means they effect the very opposite of what the immunotherapy agents do against these tumours, and whichin turn explains why many of these tumours appear to be resistant to this otherwise effective therapy. Taken together, the effect on the immune response of these boosters can easily explain the relapses and so-called turbo-charged cancers appearing. Other reports document the presence of DNA plasmids and SV XX (a known cancer-inducing gene) sequences, as well as the ability of mRNA to bind to important suppressor genes. Although this is controversial and has been challenged, it has led to the realisation of significant batch-to-batch variation that could enhance the cancer process yet probably not manifest itself for a few years. The very possibility that we could be sitting on a vaccine-inducing cancer time bomb means that we must never again get involved into a mass vaccine programme for another possible Disease X." Link in comments:  XXXXXX engagements  **Related Topics** [london](/topic/london) [robin](/topic/robin) [Post Link](https://x.com/robinmonotti/status/1949373500218565096)
[GUEST ACCESS MODE: Data is scrambled or limited to provide examples. Make requests using your API key to unlock full data. Check https://lunarcrush.ai/auth for authentication information.]
Robin Monotti @robinmonotti on x 234K followers
Created: 2025-07-27 07:37:14 UTC
ANGUS DALGLEISH ON "VACCINE" INDUCED TURBOCANCERS: Professor of Oncology at St George's Hospital Medical School, London:
"There are numerous reports in the literature of cancers arising within days of the vaccines being administered, especially in the case of lymphomas and leukaemias. There are several reports of PET scan mapped tumours exploding at the site and draining area of covid injections with the advice to inject covid vaccines away from known cancers! Outside my clinical observations, several friends have developed cancer after a totally unnecessary covid booster taken only to facilitate travel.
T cell responses are suppressed after the boosters (not the first two injections) and that this is especially marked in some cancer patients.
The antibody repertoire switches after the first booster from a protective IgG1 and IgG3 dominant B cell response to a tolerising IgG4 one, made worse by further boosters, as reported in a recent Science Immunology paper. As many cancers are controlled by effective T cell led immunity, the sudden perturbation of this control would clearly explain the development of B cell leukaemia and lymphomas, melanoma renal cell cancers and colorectal ones, all tumours which can respond to immunotherapy.
Another report by Loacker et al in Clin Chem Lab Med shows that mRNA vaccines increase PD-L1 on granulocytes and monocytes, which means they effect the very opposite of what the immunotherapy agents do against these tumours, and whichin turn explains why many of these tumours appear to be resistant to this otherwise effective therapy. Taken together, the effect on the immune response of these boosters can easily explain the relapses and so-called turbo-charged cancers appearing.
Other reports document the presence of DNA plasmids and SV XX (a known cancer-inducing gene) sequences, as well as the ability of mRNA to bind to important suppressor genes. Although this is controversial and has been challenged, it has led to the realisation of significant batch-to-batch variation that could enhance the cancer process yet probably not manifest itself for a few years. The very possibility that we could be sitting on a vaccine-inducing cancer time bomb means that we must never again get involved into a mass vaccine programme for another possible Disease X."
Link in comments:
XXXXXX engagements
