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Microbiota long-term dynamics and prediction of acute graft-versus-host disease in pediatric allogeneic stem cell transplantation
by
Aarestrup, Frank M.
, Müller, Klaus Gottlob
, Kielsen, Katrine
, Mordhorst, Hanne
, Ingham, Anna Cäcilia
, Ifversen, Marianne
, Pamp, Sünje Johanna
in
Acute GvHD
/ Antibiotics
/ Antimicrobial agents
/ Bacteria
/ Bacterial infections
/ Bioinformatics
/ Biomedical and Life Sciences
/ Biomedicine
/ CD4 antigen
/ Children
/ Clinical outcomes
/ Community composition
/ Discriminant analysis
/ Feces
/ Graft versus host disease
/ Graft-versus-host reaction
/ Gut, oral, and nasal microbiota
/ Helper cells
/ Hematopoietic stem cells
/ Holobiont
/ Homeostasis
/ HSCT
/ Immune reconstitution
/ Immune system
/ Infections
/ Intestinal microflora
/ Lymphocytes B
/ Lymphocytes T
/ Machine learning
/ Medical Microbiology
/ Microbial Ecology
/ Microbial Genetics and Genomics
/ Microbiology
/ Microbiome
/ Microbiomes
/ Microbiota
/ Microorganisms
/ Mortality
/ Mouth
/ Nose
/ Pathogenesis
/ Patients
/ Pediatrics
/ Precision medicine
/ Stem cell transplantation
/ Virology
2021
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Microbiota long-term dynamics and prediction of acute graft-versus-host disease in pediatric allogeneic stem cell transplantation
by
Aarestrup, Frank M.
, Müller, Klaus Gottlob
, Kielsen, Katrine
, Mordhorst, Hanne
, Ingham, Anna Cäcilia
, Ifversen, Marianne
, Pamp, Sünje Johanna
in
Acute GvHD
/ Antibiotics
/ Antimicrobial agents
/ Bacteria
/ Bacterial infections
/ Bioinformatics
/ Biomedical and Life Sciences
/ Biomedicine
/ CD4 antigen
/ Children
/ Clinical outcomes
/ Community composition
/ Discriminant analysis
/ Feces
/ Graft versus host disease
/ Graft-versus-host reaction
/ Gut, oral, and nasal microbiota
/ Helper cells
/ Hematopoietic stem cells
/ Holobiont
/ Homeostasis
/ HSCT
/ Immune reconstitution
/ Immune system
/ Infections
/ Intestinal microflora
/ Lymphocytes B
/ Lymphocytes T
/ Machine learning
/ Medical Microbiology
/ Microbial Ecology
/ Microbial Genetics and Genomics
/ Microbiology
/ Microbiome
/ Microbiomes
/ Microbiota
/ Microorganisms
/ Mortality
/ Mouth
/ Nose
/ Pathogenesis
/ Patients
/ Pediatrics
/ Precision medicine
/ Stem cell transplantation
/ Virology
2021
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Microbiota long-term dynamics and prediction of acute graft-versus-host disease in pediatric allogeneic stem cell transplantation
by
Aarestrup, Frank M.
, Müller, Klaus Gottlob
, Kielsen, Katrine
, Mordhorst, Hanne
, Ingham, Anna Cäcilia
, Ifversen, Marianne
, Pamp, Sünje Johanna
in
Acute GvHD
/ Antibiotics
/ Antimicrobial agents
/ Bacteria
/ Bacterial infections
/ Bioinformatics
/ Biomedical and Life Sciences
/ Biomedicine
/ CD4 antigen
/ Children
/ Clinical outcomes
/ Community composition
/ Discriminant analysis
/ Feces
/ Graft versus host disease
/ Graft-versus-host reaction
/ Gut, oral, and nasal microbiota
/ Helper cells
/ Hematopoietic stem cells
/ Holobiont
/ Homeostasis
/ HSCT
/ Immune reconstitution
/ Immune system
/ Infections
/ Intestinal microflora
/ Lymphocytes B
/ Lymphocytes T
/ Machine learning
/ Medical Microbiology
/ Microbial Ecology
/ Microbial Genetics and Genomics
/ Microbiology
/ Microbiome
/ Microbiomes
/ Microbiota
/ Microorganisms
/ Mortality
/ Mouth
/ Nose
/ Pathogenesis
/ Patients
/ Pediatrics
/ Precision medicine
/ Stem cell transplantation
/ Virology
2021
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Microbiota long-term dynamics and prediction of acute graft-versus-host disease in pediatric allogeneic stem cell transplantation
Journal Article
Microbiota long-term dynamics and prediction of acute graft-versus-host disease in pediatric allogeneic stem cell transplantation
2021
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Overview
Background
Patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT) exhibit changes in their gut microbiota and are experiencing a range of complications, including acute graft-versus-host disease (aGvHD). It is unknown if, when, and under which conditions a re-establishment of microbial and immunological homeostasis occurs. It is also unclear whether microbiota long-term dynamics occur at other body sites than the gut such as the mouth or nose. Moreover, it is not known whether the patients’ microbiota prior to HSCT holds clues to whether the patient would suffer from severe complications subsequent to HSCT. Here, we take a holobiont perspective and performed an integrated host-microbiota analysis of the gut, oral, and nasal microbiota in 29 children undergoing allo-HSCT.
Results
The bacterial diversity decreased in the gut, nose, and mouth during the first month and reconstituted again 1–3 months after allo-HSCT. The microbial community composition traversed three phases over 1 year. Distinct taxa discriminated the microbiota temporally at all three body sides, including
Enterococcus
spp.,
Lactobacillus
spp., and
Blautia
spp. in the gut. Of note, certain microbial taxa appeared already changed in the patients prior to allo-HSCT as compared with healthy children. Acute GvHD occurring after allo-HSCT could be predicted from the microbiota composition at all three body sites prior to HSCT. The reconstitution of CD4
+
T cells, T
H
17, and B cells was associated with distinct taxa of the gut, oral, and nasal microbiota.
Conclusions
This study reveals for the first time bacteria in the mouth and nose that may predict aGvHD. Monitoring of the microbiota at different body sites in HSCT patients and particularly through involvement of samples prior to transplantation may be of prognostic value and could assist in guiding personalized treatment strategies. The identification of distinct bacteria that have a potential to predict post-transplant aGvHD might provide opportunities for an improved preventive clinical management, including a modulation of microbiomes. The host-microbiota associations shared between several body sites might also support an implementation of more feasible oral and nasal swab sampling-based analyses. Altogether, the findings suggest that the microbiota and host factors together could provide actionable information to guiding precision medicine.
92cAJ6KC3SeHUVAFGfZKuD
Video Abstract
Publisher
BioMed Central,Springer Nature B.V,BMC
Subject
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