Evidence map›Paper›PMID 35720417›Full record

ReviewFrontiers in immunology2022

TIGIT as a Promising Therapeutic Target in Autoimmune Diseases.

Chenran Yue, Sheng Gao, Shuting Li, Zhouhang Xing, Hengrong Qian, Ying Hu, Wenqian Wang, Chunyan Hua

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Observational
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Landscape ofMolecular therapy. Methods & clinical development · 2025
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Reduced TIGITClinical rheumatology · 2025
    Article
  17. Review
  18. Article
  19. Article
  20. TIGIT deficiency promotes autoreactive CD4Nature communications · 2025
    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 2 institutions in 1 country.

Chenran YueSchool of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Sheng GaoLaboratory Animal Center, Wenzhou Medical University, Wenzhou, China.
Shuting LiSchool of the Second Clinical Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Zhouhang XingSchool of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Hengrong QianSchool of the Second Clinical Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Ying HuSchool of the Second Clinical Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Wenqian WangDepartment of Surgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University,  Wenzhou, China.
Chunyan HuaSchool of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Wenzhou Medical University · CNSecond Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Co-inhibitory receptors (IRs) are molecules that protect host against autoimmune reactions and maintain peripheral self-tolerance, playing an essential role in maintaining immune homeostasis. In view of the substantial clinical progresses of negative immune checkpoint blockade in cancer treatment, the role of IRs in autoimmune diseases is also obvious. Several advances highlighted the substantial impacts of T cell immunoglobulin and ITIM domain (TIGIT), a novel IR, in autoimmunity. Blockade of TIGIT pathway exacerbates multiple autoimmune diseases, whereas enhancement of TIGIT function has been shown to alleviate autoimmune settings in mice. These data suggested that TIGIT pathway can be manipulated to achieve durable tolerance to treat autoimmune disorders. In this review, we provide an overview of characteristics of TIGIT and its role in autoimmunity. We then discuss recent approaches and future directions to leverage our knowledge of TIGIT as therapeutic target in autoimmune diseases.

Indexed as

Autoimmune DiseasesReceptors, ImmunologicAnimalsAutoimmunityHumansImmune ToleranceMiceReceptors, Immunologicautoimmunityco-inhibitory receptorsimmune regulationtherapeutic targetTIGIT

Identifiers

PMID35720417
PMCPMC9203892
OpenAlexW4281717945

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.