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Καταχωρήθηκε: Τετάρτη 12 Οκτ 2022
Presenter: Prof Spyridonidis
Participants: Dr Liga, Dr Tsokanas, Dr Valera
Duration: 40 mins

https://www.thelancet.com/journals/lanhae/article/PIIS2352-3026(22)00223-X/fulltext?dgcid=hubspot_update_feature_updates22_lanhae&utm_campaign=update-lanhae&utm_medium=email&_hsmi=229262662&_hsenc=p2ANqtz-_4qThtytktyouVD9PQP8m6s2Fw61Pl4L4GAD65juL7jMS0i30Ms-ENPUL-k5yafQMCP8p8BUvXYXbK66-tdjlqjUP42w&utm_content=229205353&utm_source=hs_email

The effect of the gut microbiota on patients’ outcomes after allogeneic haematopoietic cell transplantation (HCT) is now well established. In particular, gut microbiota dysbiosis has been associated with acute graft-versus-host disease (GVHD). Furthermore, increasing data also suggest an effect of the gut microbiota on outcome after autologous HCT
and CAR T cells. In fact, the bacterial gut microbiota interplays with the immune system and contributes to immunological complication and antitumour response to treatment. Therefore, faecal microbiota transplantation has been evaluated in patients with haematological malignancies for various indications, including Clostridioides difficile
infection, eradication of multidrug-resistant bacteria, and steroid refractory acute GVHD. In addition, use of prophylactic faecal microbiota transplantation to restore the gut microbiota and improve patients’ outcomes is being developed in the setting of allogeneic HCT, but also probably very soon in patients receiving autologous HCT or CAR T cells.
 

 

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