Evidence map›Paper›PMID 33450048›Full record

ArticleBritish journal of pharmacology2021

M351-0056 is a novel low MW compound modulating the actions of the immune-checkpoint protein VISTA.

Xinlei Hu, Chenxin Qie, Jingwei Jiang, Xiaoxue Xie, Wenting Chen, Wanmei Liu, Jun Liu

Open access · hybridAbstract read
In one paragraph

Article in British journal of pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 20 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

7 authors at 1 institution in 1 country.

Xinlei HuJiangsu Key Lab of Drug Screening, China Pharmaceutical University, Nanjing, China.ORCID 0000-0002-4144-8923
Chenxin QieJiangsu Key Lab of Drug Screening, China Pharmaceutical University, Nanjing, China.
Jingwei JiangJiangsu Key Lab of Drug Screening, China Pharmaceutical University, Nanjing, China.
Xiaoxue XieJiangsu Key Lab of Drug Screening, China Pharmaceutical University, Nanjing, China.
Wenting ChenJiangsu Key Lab of Drug Screening, China Pharmaceutical University, Nanjing, China.
Wanmei LiuJiangsu Key Lab of Drug Screening, China Pharmaceutical University, Nanjing, China.
Jun LiuJiangsu Key Lab of Drug Screening, China Pharmaceutical University, Nanjing, China.
China Pharmaceutical University · CN

Funding

National Natural Science Foundation of China 81673443National Natural Science Foundation of China 81973361Natural Science Foundation of Jiangsu Province BK20202009
6 · The paper itself

Abstract

background and purposeThe protein V-domain immunoglobulin suppressor of T-cell activation (VISTA) is a novel immune-checkpoint molecule that belongs to the B7 family and regulates a broad spectrum of immune responses. So far, low MW compounds targeting VISTA for the treatment of autoimmune diseases or inflammation, have not been identified. EXPERIMENTAL APPROACH: We developed a homology modelling for VISTA 3D structure and subsequent virtual screening for low MW ligands binding to VISTA. Visualization of the binding postures of docked ligands with protein VISTA indicated that compound M351-0056 targeted VISTA. The biological activities of compound M351-0056 targeting VISTA were investigated in vitro using monocytes and T cells and in vivo, using mice with imiquimod-induced dermatitis. KEY

resultsThe K CONCLUSION AND IMPLICATIONS: The compound M351-0056 showed high affinity for VISTA and may modulate its immune function in vitro and in vivo. Our finding provides a lead compound for therapeutically enhancing VISTA-mediated pathways to benefit the treatment of autoimmune diseases or inflammation.

Indexed as

Immune Checkpoint ProteinsLymphocyte ActivationAnimalsCytokinesDermatitisImiquimodInflammationLigandsMembrane ProteinsMiceCytokinesImiquimodImmune Checkpoint ProteinsLigandsMembrane ProteinsVsir protein, mouseM351-0056modulatorpsoriasis-like dermatitisVISTA

Identifiers

PMID33450048
PMCPMC9328666
OpenAlexW3118263771

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.