Evidence map›Paper›PMID 36709251›Full record

ArticleBMC neurology2023

B.infantis enhances immunotherapy for Guillain-Barre syndrome through regulating PD-1.

Peng Shi, Di Nian, Hongdang Qu, Ming Ye, Chun Wang, Li Li, Qian Li

Open access · goldAbstract read
In one paragraph

Article in BMC neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Review
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

7 authors at 2 institutions in 1 country.

Peng ShiDepartment of Neurology, first Affiliated Hospital of Bengbu Medical College, Bengbu, 233004, Anhui, China.
Di NianDepartment of Medical Examination, Bengbu Medical College, Bengbu, 233030, Anhui, China. Niandi1234@126.com.
Hongdang QuDepartment of Neurology, first Affiliated Hospital of Bengbu Medical College, Bengbu, 233004, Anhui, China.
Ming YeDepartment of Neurology, first Affiliated Hospital of Bengbu Medical College, Bengbu, 233004, Anhui, China.
Chun WangDepartment of Neurology, first Affiliated Hospital of Bengbu Medical College, Bengbu, 233004, Anhui, China.
Li LiDepartment of Neurology, first Affiliated Hospital of Bengbu Medical College, Bengbu, 233004, Anhui, China.
Qian LiDepartment of Neurology, first Affiliated Hospital of Bengbu Medical College, Bengbu, 233004, Anhui, China.
First Affiliated Hospital of Bengbu Medical College · CNBengbu Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGuillain-Barré syndrome (GBS) is a rare, autoimmune disease. B.infantis is reported to be effective in alleviating GBS by regulating abnormal function of T helper (Th) cells.

objectivesIn this study, T cells were isolated from healthy and GBS patients. The therapeutic effect of Bifidobacterium infantis (B.infantis) and whether it is achieved by PD-1 was examined at cellular and animal models.

methodsWe used CCK-8, flow cytometry and real-time PCR to determine the differentiation of T cell subsets at cellular level. Then, an experimental autoimmune neuritis (EAN) animal model using six-week SD rats (n = 30, male) weighing 180-200 g was established to support the role of B. infantis in GBS through PD-1.

resultsB. infantis inhibited the proliferation and promoted apoptosis of T cells from GBS. At the same time, the expression levels of PD-1 increased, which was correlated with decreased T-bet (Th1) and ROR-γt (Th17) and increased Foxp3 (Treg) expression. Moreover, B. infantis alleviated the symptoms of GBS. Th1 and Th17 cells decreased while Treg cells increased after B. infantis treatment, which could be partly abrogated by PD-1 inhibitor.

conclusionsWe concluded from this study that B.infantis alleviated GBS partly through PD-1.

Indexed as

Guillain-Barre SyndromeAnimalsBifidobacterium longum subspecies infantisImmunotherapyMaleProgrammed Cell Death 1 ReceptorRatsRats, Sprague-DawleyProgrammed Cell Death 1 ReceptorB. infantis,experimental autoimmune neuritis animal modelGuillain-Barré syndromePD-1T helper cells

Identifiers

PMID36709251
PMCPMC9883859
OpenAlexW4318323783

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.