Evidence map›Paper›PMID 38172339›Full record

ArticleNature cancer2024

Bacteria and bacteriophage consortia are associated with protective intestinal metabolites in patients receiving stem cell transplantation.

Erik Thiele Orberg, Elisabeth Meedt, Andreas Hiergeist, Jinling Xue, Paul Heinrich, Jinlong Ru, Sakhila Ghimire, Oriana Miltiadous, Sarah Lindner, Melanie Tiefgraber and 27 more

Abstract read
In one paragraph

Article in Nature cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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  13. Gut microbiota and acute graft-versus-host disease.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

37 authors at 10 institutions in 2 countries.

Erik Thiele Orberg *Department of Internal Medicine III, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany. e.orberg@tum.de.ORCID http://orcid.org/0000-0003-1969-8261
Elisabeth Meedt *Department of Internal Medicine III, Hematology and Medical Oncology, University Medical Center, Regensburg, Germany.
Andreas Hiergeist *Institute of Clinical Microbiology and Hygiene, University Medical Center, Regensburg, Germany.
Jinling Xue *Institute of Virology, Helmholtz Zentrum Munich, Munich, Germany.
Paul HeinrichDepartment of Internal Medicine III, Hematology and Medical Oncology, University Medical Center, Regensburg, Germany.ORCID http://orcid.org/0000-0002-6149-2083
Jinlong RuInstitute of Virology, Helmholtz Zentrum Munich, Munich, Germany.
Sakhila GhimireDepartment of Internal Medicine III, Hematology and Medical Oncology, University Medical Center, Regensburg, Germany.
Oriana MiltiadousDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-1571-3893
Sarah LindnerDepartment of Immunology, Sloan Kettering Institute, New York, NY, USA.
Melanie TiefgraberDepartment of Internal Medicine III, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.
Sophia GöldelDepartment of Internal Medicine III, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.
Tina EismannDepartment of Internal Medicine III, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.
Alix SchwarzDepartment of Internal Medicine III, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.
Sascha GöttertDepartment of Internal Medicine III, Hematology and Medical Oncology, University Medical Center, Regensburg, Germany.
Sebastian JaroschInstitute for Medical Microbiology, Immunology and Hygiene, School of Medicine, Technical University of Munich, Munich, Germany.ORCID http://orcid.org/0000-0002-2908-8590
Katja SteigerGerman Cancer Consortium (DKTK), partner-site Munich, a partnership between DKFZ and Klinikum rechts der Isar, Munich, Germany.ORCID http://orcid.org/0000-0002-7269-5433
Christian SchulzDepartment of Internal Medicine II, University Hospital, Ludwig-Maximilians-Universität, Munich, Germany.
Michael GiglBavarian Center for Biomolecular Mass Spectrometry, School of Life Sciences, Technical University of Munich, Freising, Germany.ORCID http://orcid.org/0000-0002-5617-9236
Julius C FischerDepartment of Radiation Oncology, School of Medicine, Technical University of Munich (TUM), Klinikum rechts der Isar TUM, Munich, Germany.ORCID http://orcid.org/0000-0002-6951-3416
Klaus-Peter JanssenDepartment of Surgery, School of Medicine, Technical University of Munich (TUM), Klinikum rechts der Isar TUM, Munich, Germany.ORCID http://orcid.org/0000-0002-4707-7887
Michael QuanteDepartment of Internal Medicine II, University Medical Center, Freiburg, Germany.
Simon HeideggerDepartment of Internal Medicine III, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.ORCID http://orcid.org/0000-0001-6394-5130
Peter HerhausDepartment of Internal Medicine III, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.
Mareike VerbeekDepartment of Internal Medicine III, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.
Jürgen RulandGerman Cancer Consortium (DKTK), partner-site Munich, a partnership between DKFZ and Klinikum rechts der Isar, Munich, Germany.ORCID http://orcid.org/0000-0002-8381-3597
Marcel R M van den BrinkDepartment of Immunology, Sloan Kettering Institute, New York, NY, USA.ORCID http://orcid.org/0000-0003-0696-4401
Daniela WeberDepartment of Internal Medicine III, Hematology and Medical Oncology, University Medical Center, Regensburg, Germany.
Matthias EdingerDepartment of Internal Medicine III, Hematology and Medical Oncology, University Medical Center, Regensburg, Germany.
Daniel WolffDepartment of Internal Medicine III, Hematology and Medical Oncology, University Medical Center, Regensburg, Germany.ORCID http://orcid.org/0000-0001-7015-3190
Dirk H BuschInstitute for Medical Microbiology, Immunology and Hygiene, School of Medicine, Technical University of Munich, Munich, Germany.ORCID http://orcid.org/0000-0001-8713-093X
Karin KleigreweBavarian Center for Biomolecular Mass Spectrometry, School of Life Sciences, Technical University of Munich, Freising, Germany.ORCID http://orcid.org/0000-0002-7718-0252
Wolfgang HerrDepartment of Internal Medicine III, Hematology and Medical Oncology, University Medical Center, Regensburg, Germany.
Florian BassermannDepartment of Internal Medicine III, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.ORCID http://orcid.org/0000-0003-4435-2609
André Gessner *Institute of Clinical Microbiology and Hygiene, University Medical Center, Regensburg, Germany.
Li Deng *Institute of Virology, Helmholtz Zentrum Munich, Munich, Germany.
Ernst Holler *Department of Internal Medicine III, Hematology and Medical Oncology, University Medical Center, Regensburg, Germany.
Hendrik Poeck *Department of Internal Medicine III, Hematology and Medical Oncology, University Medical Center, Regensburg, Germany. hendrik.poeck@ukr.de.ORCID http://orcid.org/0000-0002-0836-2095
TUM Klinikum · DEUniversity Hospital Regensburg · DEGerman Cancer Research Center · DEHelmholtz Zentrum München · DETechnical University of Munich · DEGerman Center for Infection Research · DEInstitute of Medical Microbiology and Hygiene · DEMemorial Sloan Kettering Cancer Center · USKettering University · USUniversity Medical Center Freiburg · DE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
The role of autophagy gene Atg16L1 in allogeneic hematopoietic stem cell transplantation - Resubmission - 1R01HL123340 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CADWELL, KEN HASHIGIWA, VAN DEN BRINK, MARCEL R M · 2015 to 2022
$5.2M
Deutsche Forschungsgemeinschaft (German Research Foundation) 324392634, 395357507Deutsche Forschungsgemeinschaft (German Research Foundation) 360372040Deutsche Forschungsgemeinschaft (German Research Foundation) 360372040, 395357507, 324392634Deutsche Forschungsgemeinschaft (German Research Foundation) 395357507Deutsche Forschungsgemeinschaft (German Research Foundation) 464797012Deutsche Forschungsgemeinschaft (German Research Foundation) BA 2851/6-1, 360372040Deutsche Forschungsgemeinschaft (German Research Foundation) DE 2360/1-1Deutsche Forschungsgemeinschaft (German Research Foundation) DE 2360/6-1Deutsche Krebshilfe (German Cancer Aid) 70114547Jos& Carreras Leuk&mie-Stiftung (Deutsche Jos& Carreras Leuk&mie-Stiftung) DJCLS 01 GvHD/2016NCI NIH HHS P30 CA008748U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01-HL123340, R01-HL147584Wilhelm Sander-Stiftung (Wilhelm Sander Foundation) 2021.040.1
6 · The paper itself

Abstract

The microbiome is a predictor of clinical outcome in patients receiving allogeneic hematopoietic stem cell transplantation (allo-SCT). Microbiota-derived metabolites can modulate these outcomes. How bacteria, fungi and viruses contribute to the production of intestinal metabolites is still unclear. We combined amplicon sequencing, viral metagenomics and targeted metabolomics from stool samples of patients receiving allo-SCT (n = 78) and uncovered a microbiome signature of Lachnospiraceae and Oscillospiraceae and their associated bacteriophages, correlating with the production of immunomodulatory metabolites (IMMs). Moreover, we established the IMM risk index (IMM-RI), which was associated with improved survival and reduced relapse. A high abundance of short-chain fatty acid-biosynthesis pathways, specifically butyric acid via butyryl-coenzyme A (CoA):acetate CoA-transferase (BCoAT, which catalyzes EC 2.8.3.8) was detected in IMM-RI low-risk patients, and virome genome assembly identified two bacteriophages encoding BCoAT as an auxiliary metabolic gene. In conclusion, our study identifies a microbiome signature associated with protective IMMs and provides a rationale for considering metabolite-producing consortia and metabolite formulations as microbiome-based therapies.

Indexed as

BacteriophagesHematopoietic Stem Cell TransplantationBacteriaButyric AcidFecesHumansButyric Acid

Identifiers

PMID38172339
PMCPMC12063274
OpenAlexW4390571169

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.