Evidence map›Paper›PMID 40261799›Full record

ReviewClinical and translational science2025

Promising New Anti-TIGIT Agents: Stealthy Allies in Cancer Immunotherapy.

Gatadi Srikanth, Durga Prasad Beda, Ashish Ranjan Dwivedi, Nandan Kumar Duddukuri, Srinivas Nanduri, Jitendra Patel

Abstract readReview
In one paragraph

Review in Clinical and translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Review
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  5. Article
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  8. Article
  9. Review
  10. Terminally exhausted CD8Frontiers in immunology · 2025
    Review
  11. 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

6 authors.

Gatadi SrikanthGITAM School of Pharmacy, GITAM (Deemed to Be University), Hyderabad, India.ORCID 0009-0005-4962-5030
Durga Prasad BedaGITAM School of Pharmacy, GITAM (Deemed to Be University), Hyderabad, India.
Ashish Ranjan DwivediGITAM School of Pharmacy, GITAM (Deemed to Be University), Hyderabad, India.
Nandan Kumar DuddukuriChemistry Division, Innatura Scientific Pvt. Ltd., Hyderabad, Telangana, India.
Srinivas NanduriDepartment of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Jitendra PatelDatta Meghe College of Pharmacy, Datta Meghe Institute of Higher Education, (Deemed to Be University), Wardha, Maharashtra, India.ORCID 0000-0001-8193-2878

Funding

SEED 2024/0306
6 · The paper itself

Abstract

TIGIT (T cell immunoreceptor with immunoglobulin and tyrosine-based inhibitory motif (ITIM) domain), Vstm3, and VSIG9, are newly recognized immunological checkpoints. They are prominently expressed on CD4+ and CD8+ T cells, tumor-infiltrating lymphocytes (TILs), natural killer (NK) cells, and regulatory T cells (Tregs). The TIGIT (TIGIT) protein is crucial for immune modulation since it diminishes NK cell populations and hinders T cell activity in cancer patients and experimental models. CD155, the principal ligand of TIGIT in humans, has been recognized as a pivotal target for immunotherapy owing to its interaction with TIGIT. CD155 is linked to the efficacy of anti-programmed cell death protein 1 (PD-1) therapy, even without TIGIT expression, underscoring its importance in immune checkpoint suppression. Anti-TIGIT medicines, either independently or in conjunction with anti-PD-1 treatments, have demonstrated potential in augmenting immune responses to malignancies. This review examines the structural and functional characteristics of the TIGIT protein, new developments in anti-TIGIT drugs, and their prospective use in cancer immunotherapy.

Indexed as

Immune Checkpoint InhibitorsImmunotherapyNeoplasmsReceptors, ImmunologicAnimalsHumansReceptors, VirusImmune Checkpoint Inhibitorspoliovirus receptorReceptors, ImmunologicReceptors, VirusTIGIT protein, humancancerimmunotherapyPD‐1resistanceTIGIT

Identifiers

PMID40261799
PMCPMC12013639

What OpenQuestion holds

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LicenceCC BY-NC
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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.