Je ne sais pas si les propos, que l'on prête au pape, sont de lui ou pas, mais voici quelques informations en anglais.

Lien 1 sur téléchargement document de 2012

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335060/pdf/pone.0035421.pdf

Caution in proceeding to application of a SARS-CoV vaccine in humans is indicated

Lien 2 sur téléchargement document de 2020

https://pubmed.ncbi.nlm.nih.gov/33113270/


Conclusions drawn from the study and clinical implications: The specific and significant COVID-19 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in vaccine trials, as well as those being recruited for the trials and future patients after vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.

Pour ADE (Antibody-dependent enhancement)


Lien 2 complet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645850/pdf/IJCP-9999-e13795.pdf

Medical ethics standards required that, given the extent of evidence in the medical literature
reviewed above, the risk of ADE should be clearly and emphatically distinguished in the
informed consent from risks observed rarely as well as the more obvious risk of lack of
efficacy, which is unrelated to the specific risk of ADE. Based on the published literature, it
should have been obvious to any skilled medical practitioner in 2019 that there is a
significant risk to vaccine research subjects that they may experience severe disease once
vaccinated, while they might only have experienced a mild, self-limited disease if not
vaccinated. The consent should also clearly distinguish the specific risk of worsened COVID-
19 disease from generic statements about risk of death and generic risk of lack of efficacy of
the vaccine.

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