Scientific Reports (Apr 2022)

Bone marrow transplantation induces changes in the gut microbiota that chronically increase the cytokine response pattern of splenocytes

  • Saeed Katiraei,
  • Janna A. van Diepen,
  • Luciana P. Tavares,
  • Lisa R. Hoving,
  • Amanda Pronk,
  • Ineke Verschueren,
  • Patrick C. N. Rensen,
  • Jaap Jan Zwaginga,
  • Sarantos Kostidis,
  • Martin Giera,
  • Mauro Teixera,
  • Ko Willems van Dijk,
  • Mihai G. Netea,
  • Jimmy F. P. Berbée,
  • Vanessa van Harmelen

DOI
https://doi.org/10.1038/s41598-022-10637-7
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 12

Abstract

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Abstract Bone marrow transplantation (BMT) involves conditioning regimens which acutely induce side effects, including systemic inflammation, intestinal damage and shifts in the gut microbial composition, some of which may persist chronically. As the gut microbiota affect systemic immune responses, we aimed to investigate whether, post-BMT, the peripheral immune system is modulated as a direct consequence of alterations in the gut microbiota. We show that 24 weeks post-BMT, splenocytes but not peritoneal macrophages display increased cytokine response patterns upon ex-vivo stimulation with various pathogens as compared to untreated controls. The pattern of BMT-induced cytokine responses was transferred to splenocytes, and not to peritoneal macrophages, of healthy controls via co-housing and transferred to germfree mice via transplantation of cecum content. Thus, BMT induces changes in gut microbiota that in their turn increase cytokine responsiveness of splenocytes. Thus, BMT establishes a dominant microbiota that attenuates normalization of the immune-response.