Evidence map›Paper›PMID 33602926›Full record

ArticleNature communications2021

Gastrointestinal microbiota composition predicts peripheral inflammatory state during treatment of human tuberculosis.

Matthew F Wipperman, Shakti K Bhattarai, Charles Kyriakos Vorkas, Venkata Suhas Maringati, Ying Taur, Laurent Mathurin, Katherine McAulay, Stalz Charles Vilbrun, Daphie Francois, James Bean and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 2 syntheses or guidelines pooled it, 51 citations in OpenAlex.

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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

15 authors at 4 institutions in 2 countries.

Matthew F Wipperman *Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0003-1436-3366
Shakti K Bhattarai *Department of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA, USA.
Charles Kyriakos VorkasImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0003-4952-7041
Venkata Suhas MaringatiDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA, USA.
Ying TaurDivision of Infectious Diseases, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0002-6601-8284
Laurent MathurinHaitian Study Group for Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.
Katherine McAulayCenter for Global Health, Weill Cornell Medicine, New York, NY, USA.
Stalz Charles VilbrunHaitian Study Group for Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.
Daphie FrancoisHaitian Study Group for Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.
James BeanImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Kathleen F WalshCenter for Global Health, Weill Cornell Medicine, New York, NY, USA.ORCID 0000-0002-9001-3918
Carl NathanImmunology and Microbial Pathogenesis Graduate Program, Weill Cornell Graduate School, New York, NY, USA.
Daniel W FitzgeraldCenter for Global Health, Weill Cornell Medicine, New York, NY, USA.
Michael S GlickmanImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA. glickmam@mskcc.org.ORCID 0000-0001-7918-5164
Vanni BucciDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA, USA. vanni.bucci2@umassmed.edu.ORCID 0000-0002-3257-2922
Memorial Sloan Kettering Cancer Center · USCornell University · USGheskio Centers · HTUniversity of Massachusetts Chan Medical School · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Disparities in COVID Disease Severity and Outcomes in New York CityUL1TR002384 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JULIANNE L IMPERATO-MCGINLEY · 2017 to 2026
$86.2M
Viable but Nonculturable MtbU19AI111143 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI CASANOVA, JEAN-LAURENT, GLICKMAN, MICHAEL S · 2014 to 2020
$48.6M
J. NRSA Training CoreTL1TR002386 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI Genevieve Giny Fouda Amou ou · 2017 to 2026
$5.8M
The role of Mucosal-associated invariant T (MAIT) cells during the innate immune response to Mycobacterium tuberculosisK08AI132739 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI VORKAS, CHARLES KYRIAKOS · 2018 to 2022
$921k
NCATS NIH HHS TL1 TR002386NCATS NIH HHS UL1 TR002384NCI NIH HHS P30 CA008748NIAID NIH HHS K08 AI132739NIAID NIH HHS U19 AI111143
6 · The paper itself

Abstract

The composition of the gastrointestinal microbiota influences systemic immune responses, but how this affects infectious disease pathogenesis and antibiotic therapy outcome is poorly understood. This question is rarely examined in humans due to the difficulty in dissociating the immunologic effects of antibiotic-induced pathogen clearance and microbiome alteration. Here, we analyze data from two longitudinal studies of tuberculosis (TB) therapy (35 and 20 individuals) and a cross sectional study from 55 healthy controls, in which we collected fecal samples (for microbiome analysis), sputum (for determination of Mycobacterium tuberculosis (Mtb) bacterial load), and peripheral blood (for transcriptomic analysis). We decouple microbiome effects from pathogen sterilization by comparing standard TB therapy with an experimental TB treatment that did not reduce Mtb bacterial load. Random forest regression to the microbiome-transcriptome-sputum data from the two longitudinal datasets reveals that renormalization of the TB inflammatory state is associated with Mtb pathogen clearance, increased abundance of Clusters IV and XIVa Clostridia, and decreased abundance of Bacilli and Proteobacteria. We find similar associations when applying machine learning to peripheral gene expression and microbiota profiling in the independent cohort of healthy individuals. Our findings indicate that antibiotic-induced reduction in pathogen burden and changes in the microbiome are independently associated with treatment-induced changes of the inflammatory response of active TB, and the response to antibiotic therapy may be a combined effect of pathogen killing and microbiome driven immunomodulation.

Indexed as

Gastrointestinal MicrobiomeAdultAlgorithmsAnti-Bacterial AgentsAntitubercular AgentsBacterial LoadBiodiversityCase-Control StudiesCohort StudiesGene Expression RegulationHumansInflammationModels, BiologicalReproducibility of ResultsTuberculosisAnti-Bacterial AgentsAntitubercular Agents

Identifiers

PMID33602926
PMCPMC7892575
OpenAlexW3131850724

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.