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

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...

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Detalles Bibliográficos
Autores principales: Katiraei, Saeed, van Diepen, Janna A., Tavares, Luciana P., Hoving, Lisa R., Pronk, Amanda, Verschueren, Ineke, Rensen, Patrick C. N., Zwaginga, Jaap Jan, Kostidis, Sarantos, Giera, Martin, Teixera, Mauro, van Dijk, Ko Willems, Netea, Mihai G., Berbée, Jimmy F. P., van Harmelen, Vanessa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046407/
https://www.ncbi.nlm.nih.gov/pubmed/35477719
http://dx.doi.org/10.1038/s41598-022-10637-7
Descripción
Sumario: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.