Evidence map›Paper›PMID 37314518›Full record

ReviewInflammation research : official journal of the European Histamine Research Society ... [et al.]2023

From bench to bedside: targeting lymphocyte activation gene 3 as a therapeutic strategy for autoimmune diseases.

Xueyin Zhou, Yiming Gu, Huihong Wang, Wei Zhou, Lei Zou, Shuting Li, Chunyan Hua, Sheng Gao

Abstract readReview
PubMed Publisher
In one paragraph

Review in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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

8 authors at 1 institution in 1 country.

Xueyin ZhouSchool of the 2nd Clinical Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Yiming GuSchool of the 2nd Clinical Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Huihong WangSchool of the 2nd Clinical Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Wei ZhouSchool of the 2nd Clinical Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Lei ZouSchool of the 2nd Clinical Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Shuting LiSchool of the 2nd Clinical Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Chunyan HuaSchool of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China. huachunyan@wmu.edu.cn.
Sheng GaoLaboratory Animal Center, Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China. 4869335@qq.com.
Wenzhou Medical University · CN

Funding

China Scholarship Council 201808330646National Natural Science Foundation of China 81901660
6 · The paper itself

Abstract

backgroundImmune checkpoints negatively regulate immune response, thereby playing an important role in maintaining immune homeostasis. Substantial studies have confirmed that blockade or deficiency of immune checkpoint pathways contributes to the deterioration of autoimmune diseases. In this context, focusing on immune checkpoints might provide alternative strategies for the treatment of autoimmunity. Lymphocyte activation gene 3 (LAG3), as a member of immune checkpoint, is critical in regulating immune responses as manifested in multiple preclinical studies and clinical trials. Recent success of dual-blockade of LAG3 and programmed death-1 in melanoma also supports the notion that LAG3 is a crucial regulator in immune tolerance.

methodsWe wrote this review article by searching the PubMed, Web of Science and Google Scholar databases.

conclusionIn this review, we summarize the molecular structure and the action mechanisms of LAG3. Additionally, we highlight its roles in diverse autoimmune diseases and discuss how the manipulation of the LAG3 pathway can serve as a promising therapeutic strategy as well as its specific mechanism with the aim of filling the gaps from bench to bedside.

Indexed as

Autoimmune DiseasesNeoplasmsAntigens, CDHumansLymphocyte ActivationLymphocyte Activation Gene 3 ProteinAntigens, CDLymphocyte Activation Gene 3 ProteinAutoimmune diseaseImmune checkpointImmune regulationLAG3Therapy

Identifiers

PMID37314518
OpenAlexW4380576654

What OpenQuestion holds

Textmetadata
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.