Evidence map›Paper›PMID 33506015›Full record

ArticleBioMed research international2021

Inhibition of PD-1 Protects against TNBS-Induced Colitis via Alteration of Enteric Microbiota.

Hao-Ming Xu, You-Lian Zhou, Jing Xu, Ying-Fei Li, Chong Zhao, Hong-Li Huang, Yan-Lei Du, Jie He, Yong-Jian Zhou, Yu-Qiang Nie

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 12 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

10 authors at 1 institution in 1 country.

Hao-Ming XuDepartment of Gastroenterology and Hepatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-8131-7477
You-Lian ZhouDepartment of Gastroenterology and Hepatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-7107-3288
Jing XuDepartment of Gastroenterology and Hepatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-5371-1899
Ying-Fei LiDepartment of Gastroenterology and Hepatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-8437-3191
Chong ZhaoDepartment of Gastroenterology and Hepatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-9941-8049
Hong-Li HuangDepartment of Gastroenterology and Hepatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-5882-1106
Yan-Lei DuDepartment of Gastroenterology and Hepatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-7868-2158
Jie HeDepartment of Gastroenterology and Hepatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-5880-8112
Yong-Jian ZhouDepartment of Gastroenterology and Hepatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-4036-4592
Yu-Qiang NieDepartment of Gastroenterology and Hepatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0001-7037-5340
Guangzhou First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

methodsColitis was induced in mice using 2,4,6-trinitrobenzene-sulfonic acid (TNBS), and mice were subsequently treated with either a PD-1 inhibitor or 5-amino-salicylic acid (ASA) as a positive control. Body weight, disease activity index (DAI), colon length, and tissue damage were evaluated, and the enteric microbiota was profiled using high-throughput 16S rRNA sequencing of fecal samples from the experimental mice.

resultsTNBS caused mice to experience IBD-like symptoms, which were attenuated by the PD-1 inhibitor, as indicated by a decrease in DAI scores (

conclusionPD-1 inhibition can partly mitigate TNBS-induced colitis and restore the enteric microbiota by enriching the abundance of SCFA-producing bacteria.

Indexed as

AnimalsColitisColonDisease Models, AnimalGastrointestinal MicrobiomeImmune Checkpoint InhibitorsMaleMesalamineMiceMice, Inbred BALB CProgrammed Cell Death 1 ReceptorProtective AgentsTrinitrobenzenesulfonic AcidImmune Checkpoint InhibitorsMesalaminePdcd1 protein, mouseProgrammed Cell Death 1 ReceptorProtective AgentsTrinitrobenzenesulfonic Acid

Identifiers

PMID33506015
PMCPMC7810563
OpenAlexW3120291425

What OpenQuestion holds

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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.