Evidence map›Paper›PMID 37790403›Full record

ArticleResearch square2023

Rapid intestinal and systemic metabolic reprogramming in an immunosuppressed environment.

Bing Ma, Samuel J Gavzy, Michael France, Yang Song, Hnin Wai Lwin, Allison Kensiski, Vikas Saxena, Wenji Piao, Ram Lakhan, Jegan Iyyathurai and 7 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 1 institution in 1 country.

Bing MaUniversity of Maryland, Baltimore.
Samuel J GavzyUniversity of Maryland Medical Center.
Michael FranceUniversity of Maryland, Baltimore.
Yang SongUniversity of Maryland, Baltimore.
Hnin Wai LwinUniversity of Maryland, Baltimore.
Allison KensiskiUniversity of Maryland, Baltimore.
Vikas SaxenaUniversity of Maryland, Baltimore.
Wenji PiaoUniversity of Maryland, Baltimore.
Ram LakhanUniversity of Maryland, Baltimore.
Jegan IyyathuraiUniversity of Maryland, Baltimore.
Lushen LiUniversity of Maryland, Baltimore.
Christina PaluskieviczUniversity of Maryland, Baltimore.
Long WuUniversity of Maryland, Baltimore.
Marina WillsonShirkeyUniversity of Maryland, Baltimore.
Emmanuel F MongodinUniversity of Maryland, Baltimore.
Valeria R MasUniversity of Maryland Medical Center.
Jonathan BrombergUniversity of Maryland, Baltimore.
University of Maryland, Baltimore · US

Funding

Signaling Pathways in Innate ImmunityT32AI095190 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Stefanie N. Vogel · 2012 to 2026
$4.7M
Immunological and functional consequences triggered by the gut microbiota regulate alloimmunity and cardiac transplant outcomeR01HL148672 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI BROMBERG, JONATHAN S, MA, BING · 2019 to 2022
$2.3M
Mechanisms of microbiome-driven cardiac allograft outcomesU01AI170050 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Jonathan S Bromberg, Bing Ma · 2022 to 2026
$1.9M
NHLBI NIH HHS R01 HL148672NIAID NIH HHS T32 AI095190NIAID NIH HHS U01 AI170050
6 · The paper itself

Abstract

Intrinsic metabolism shapes the immune environment associated with immune suppression and tolerance in settings such as organ transplantation and cancer. However, little is known about the metabolic activities in an immunosuppressive environment. In this study, we employed metagenomic, metabolomic, and immunological approaches to profile the early effects of the immunosuppressant drug tacrolimus, antibiotics, or both in gut lumen and circulation using a murine model. Tacrolimus induced rapid and profound alterations in metabolic activities within two days of treatment, prior to alterations in gut microbiota composition and structure. The metabolic profile and gut microbiome after seven days of treatment was distinct from that after two days of treatment, indicating continuous drug effects on both gut microbial ecosystem and host metabolism. The most affected taxonomic groups are Clostriales and Verrucomicrobiae (i.e.,

Indexed as

antibioticsgut dysbiosisgut microbiomeimmune toleranceimmunosuppressionintegrative multi-omicsmetabolometransplantation

Identifiers

PMID37790403
PMCPMC10543476
OpenAlexW4386953752

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.