Circulating microbial cell–free DNA is increased during neutropenia after hematopoietic stem cell transplantation

Author:

Blair Lily M.1,Akhund-Zade Jamilla1,Katsamakis Zoe A.2,Smibert Olivia C.345,Wolfe Alex E.6,Giardina Paul2,Slingerland John2,Bercovici Sivan1,Perales Miguel-Angel27,Taur Ying8,van den Brink Marcel R. M.279,Peled Jonathan U.27,Markey Kate A.2610

Affiliation:

1. 1Karius Inc, Redwood City, CA

2. 2Department of Medicine, Adult Bone Marrow Transplantation Service, Memorial Sloan Kettering Cancer Center, New York, NY

3. 3Department of Infectious Diseases, Austin Health, Heidelberg, VIC, Australia

4. 4Department of Infectious Diseases, Peter McCallum Cancer Centre, Melbourne, VIC, Australia

5. 5National Centre for Infections in Cancer, Peter McCallum Cancer Centre, Melbourne, VIC, Australia

6. 6Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA

7. 7Weill Cornell Medical College, New York, NY

8. 8Department of Medicine, Infectious Disease Service, Memorial Sloan Kettering Cancer Center, New York, NY

9. 9Sloan Kettering Institute, New York, NY

10. 10Division of Medicine, University of Washington, Seattle, WA

Abstract

Abstract We used a next-generation sequencing platform to characterize microbial cell–free DNA (mcfDNA) in plasma samples from patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HCT). In this observational study, we sought to characterize plasma mcfDNA in order to explore its potential association with the immunologic complications of transplantation. We compared serially collected patient samples with plasma collected from healthy control subjects. We observed changes in total mcfDNA burden in the plasma after transplantation, which was most striking during the early posttransplant neutropenic phase. This elevation could be attributed to a number of specific bacterial taxa, including Veillonella, Bacteroides, and Prevotella (genus level). For an additional cohort of patients, we compared the data of mcfDNA from plasma with 16s-ribosomal RNA sequencing data from stool samples collected at matched time points. In a number of patients, we confirmed that mcfDNA derived from specific microbial taxa (eg, Enterococcus) could also be observed in the matched stool sample. Quantification of mcfDNA may generate novel insights into mechanisms by which the intestinal microbiome influences systemic cell populations and, thus, has been associated with outcomes for patients with cancer.

Publisher

American Society of Hematology

Subject

Hematology

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