已證實 mRNA 疫苗所產生嘅棘蛋白會導致血管病變
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希望藍絲打科興，黃絲打复星，香港有救
屌你咁mrna係chur鳩你免疫系統㗎嘛，
本身咁廢咪會死埋囉
本身咁廢咪會死埋囉
打完毒針身體一年內不斷生產棘蛋白攻擊自己血管，但中武肺好多幾日就可以出院了。
mRNA疫苗可以話自損1000萬殺敵100。
mRNA疫苗可以話自損1000萬殺敵100。
然後就可以將港豬大換血
咁講係咪即係滅活既科興好啲
武肺病毒本身冇棘蛋白
The Long Road to Perdition
COVID19 vaccines are injected into the deltoid where they are taken up by muscle cells. The vaccine remains largely contained near the site of injection. Local muscle cells that take in the vaccine produce the spike protein and place it on the surface of the cell where it is recognized by the immune system. Vaccine that is not taken up by muscle is drained into the local lymph nodes where lymphatic cells absorb the vaccine and similarly make spike protein. The lymphatic cells are responsible for activating T and B cells, which are important steps in generating immunity.
In order to damage the endothelium of blood vessels, COVID-19 vaccines have to enter the vascular system and infect cells that circulate in the blood. Data collected by the European Medicines Agency shows that no significant amount of vaccine enters the circulation. The confinement of the expressed spike protein away from the circulatory system significant prevents it from causing damage to the vascular endothelium.
Redesigning the Spike Protein
The spike protein attaches SARS-CoV2 to cells through a receptor called ACE2. In order to fully interact, the spike protein must undergo a conformational change.
A research team lead by Dr. Barney Graham from the Vaccine Research Center at the NIH National Institute of Allergy and Infectious Diseases created an engineered form of the spike protein that is unable to make the shape change required to effectively bind to cells. The Pfizer/BioNTech, Moderna, Novavax, and Johnson&Johnson vaccines all use this inactivated spike protein, which means any spike protein that is produced by the vaccine is not able to be activated. This safety-switch limits the ability of the spike protein to bind ACE2 and limits its ability to cause damage.
https://www.science20.com/w_glen_pyle/the_thorny_problem_of_covid19_vaccines_and_spike_proteins-254373
有科學研究證明疫苗既spike protein已被deactivated, 不會對血管做成傷害。但又唔見你貼
COVID19 vaccines are injected into the deltoid where they are taken up by muscle cells. The vaccine remains largely contained near the site of injection. Local muscle cells that take in the vaccine produce the spike protein and place it on the surface of the cell where it is recognized by the immune system. Vaccine that is not taken up by muscle is drained into the local lymph nodes where lymphatic cells absorb the vaccine and similarly make spike protein. The lymphatic cells are responsible for activating T and B cells, which are important steps in generating immunity.
In order to damage the endothelium of blood vessels, COVID-19 vaccines have to enter the vascular system and infect cells that circulate in the blood. Data collected by the European Medicines Agency shows that no significant amount of vaccine enters the circulation. The confinement of the expressed spike protein away from the circulatory system significant prevents it from causing damage to the vascular endothelium.
Redesigning the Spike Protein
The spike protein attaches SARS-CoV2 to cells through a receptor called ACE2. In order to fully interact, the spike protein must undergo a conformational change.
A research team lead by Dr. Barney Graham from the Vaccine Research Center at the NIH National Institute of Allergy and Infectious Diseases created an engineered form of the spike protein that is unable to make the shape change required to effectively bind to cells. The Pfizer/BioNTech, Moderna, Novavax, and Johnson&Johnson vaccines all use this inactivated spike protein, which means any spike protein that is produced by the vaccine is not able to be activated. This safety-switch limits the ability of the spike protein to bind ACE2 and limits its ability to cause damage.
https://www.science20.com/w_glen_pyle/the_thorny_problem_of_covid19_vaccines_and_spike_proteins-254373
有科學研究證明疫苗既spike protein已被deactivated, 不會對血管做成傷害。但又唔見你貼
同埋個問題就係，打mrna點都有風險。
我當手biontech係0.1，打科興係0.2，*中左*武肺係0.8。
但喺香港，暫時中武肺機會可能都係0.2。
變左你打疫苗係1*0.1 or 1*0.2，但唔打疫苗係0.2*0.8。
所有數字我亂吹啦，唔可以作比較。但個問題唔係biontech危險，係香港呢一刻本身唔危險，所以唔主動接受另一個風險都尚可理解。
但我唔撚會留喺香港囉。
或者之後冇左biontech，港共會通關，之後迫你班人打科興同上海復星
我當手biontech係0.1，打科興係0.2，*中左*武肺係0.8。
但喺香港，暫時中武肺機會可能都係0.2。
變左你打疫苗係1*0.1 or 1*0.2，但唔打疫苗係0.2*0.8。
所有數字我亂吹啦，唔可以作比較。但個問題唔係biontech危險，係香港呢一刻本身唔危險，所以唔主動接受另一個風險都尚可理解。
但我唔撚會留喺香港囉。
或者之後冇左biontech，港共會通關，之後迫你班人打科興同上海復星
選擇性失明 
移民其實焗打
當你去英國到時得返啲AZ你打咪仲驚
當你去英國到時得返啲AZ你打咪仲驚
佢地唔係唔知
不過係要跟國家指示做
一話關疫苗事仲邊有人去打
不過係要跟國家指示做
一話關疫苗事仲邊有人去打
Biontech係用復星技術，睇嚟你谷緊針
而家嗰d係歐洲生產，之後會轉上海。
最好你喺香港一世都有得揀唔打啦，共享中國人榮耀。
最好你喺香港一世都有得揀唔打啦，共享中國人榮耀。
咁搞笑，bind 唔到去 ACE2 仲算唔算係武肺病毒抗原？產生嘅抗體對真正嘅 antigen 仲會唔會有效？
mRNA translates into proteins = enzymes that can modify genes to make spike proteins on human cell surface ，另外現時有self-amplifying mRNA 可以永生咁無限自動copy
basically mRNA疫苗係將人做成GMO，令人細胞表面express viral spike proteins 去產生 LONG LASTING specific antibody，一嚟 out compete 你其他 innate immune antibody，咁你對其他病毒病菌就變成immunocompromised無左抵抗能力，二嚟呢d specific antibody 有機會反target 人細胞表面嗰d viral spike proteins，引致其他autoimmune diseases
basically mRNA疫苗係將人做成GMO，令人細胞表面express viral spike proteins 去產生 LONG LASTING specific antibody，一嚟 out compete 你其他 innate immune antibody，咁你對其他病毒病菌就變成immunocompromised無左抵抗能力，二嚟呢d specific antibody 有機會反target 人細胞表面嗰d viral spike proteins，引致其他autoimmune diseases
嘩 好似打咗啲針刺入自己血管咁
咁打哂兩劑嘅咪好危險
咁打哂兩劑嘅咪好危險
滅活疫苗即係將棘蛋白打入身體，一樣會造成破壞 ....
FAKE NEWS
信連燈仔嘅下場你知係點啦
樓豬上年出晒名deep state陰謀論撚，專放假消息