本則回應

• Lin標記此篇為：❌ 含有不實訊息

  理由

  假的。馬龍博士不曾創造或是發明RNA疫苗，這是反對疫苗者的陰謀論。
  Robert Malone雖然有醫生執照，曾做過將DNA及RNA轉入細胞和動物的研究，但卻從未成功研發過mRNA疫苗（即目標抗體的產生）。《mRNA疫苗發明者》是錯誤的權威陳述，疫苗也並不會讓人死亡或是免疫力下降。
  輝瑞及莫德納的疫苗所產生的刺突蛋白是有兩個重要的安全特性：第一，它帶有一個transmembrane anchor region（跨膜錨定區），所以會卡在細胞膜上，不會到處亂跑，第二，它的氨基酸序列已經被改變，從而失去細胞毒性。
  
  學界的研究上無法證實刺突蛋白對人體有害，以目前緊急授權之下所流通的疫苗與實際接種情況，疫苗是相當安全且能預防疾病的，刺突蛋白在動物上產生的實驗反應並不能推論到在人類身上也會如此。疫苗也並非大規模殺傷性生化武器，施打疫苗仍是目前最推薦保護自己的方法。

  出處

  
  
  https://healthfeedback.org/claimreview/b⋯n-and-vaccination-misrepresents-studies/
  
  https://www.mygopen.com/2021/05/Geert-Vanden-Bossche.html
  https://www.fda.gov/consumers/consumer-u⋯use-ivermectin-treat-or-prevent-covid-19
  https://www.who.int/news-room/feature-st⋯to-treat-covid-19-within-clinical-trials
  
  
  

  Byram Bridle’s claim that COVID-19 vaccines are toxic fails to account for key differences between the spike protein produced during infection and vaccination, misrepresents studies - Health Feedback

  https://healthfeedback.org/claimreview/byram-bridles-claim-that-covid-19-vaccines-are-toxic-fails-to-account-for-key-differences-between-the-spike-protein-produced-during-infection-and-vaccination-misrepresents-studies/

  The spike protein of SARS-CoV-2 allows the virus to bind to and infect cells, making it an ideal target for vaccine development. Recent studies suggested that the spike protein produced during infecti

  【誤導】大規模疫苗接種將導致免疫逃逸？全球免疫災難？專家：可能性低毋須過度擔心

  https://www.mygopen.com/2021/05/Geert-Vanden-Bossche.html

  網傳「大規模施打疫苗造成免疫逃逸」的訊息。MyGoPen 透過新興科技媒體中心邀請專家解析流傳內容。專家指出，目前還沒有證據能夠證明「大規模疫苗接種將導致免疫逃避機制出現」的情況，因此，對於新冠病毒的免疫逃避不需要太擔心。另外，專家也說，傳言稱「新冠疫苗會引發免疫逃避」其可能性非常低，由於人類長期用

  https://www.fda.gov/consumers/consumer-updates/why-you-should-not-use-ivermectin-treat-or-prevent-covid-19

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  https://www.who.int/news-room/feature-stories/detail/who-advises-that-ivermectin-only-be-used-to-treat-covid-19-within-clinical-trialshttps://www.who.int/news-room/feature-stories/detail/who-advises-that-ivermectin-only-be-used-to-treat-covid-19-within-clinical-trials

  Cannot get data from URL