Evidence map›Paper›PMID 37345049›Full record

ArticleCancers2023

TIGIT Expression on Activated NK Cells Correlates with Greater Anti-Tumor Activity but Promotes Functional Decline upon Lung Cancer Exposure: Implications for Adoptive Cell Therapy and TIGIT-Targeted Therapies.

Md Faqrul Hasan, Tayler J Croom-Perez, Jeremiah L Oyer, Thomas A Dieffenthaller, Liza D Robles-Carrillo, Jonathan E Eloriaga, Sanjana Kumar, Brendan W Andersen, Alicja J Copik

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Emerging Immune-Based Therapeutic Strategies in Hepatocellular Carcinoma.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Immune checkpoint molecules beyond PD-1 and CTLA-4: emerging targets in autoimmune diseases and cancer immunotherapy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Natural killer cells: the immune frontline against circulating tumor cells.Journal of experimental & clinical cancer research : CR · 2025
    Review
  14. Article
  15. Review
  16. Primary and Acquired Resistance to Immunotherapy with Checkpoint Inhibitors in NSCLC: From Bedside to Bench and Back.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  17. Review
  18. Article
  19. Article
  20. 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

9 authors at 1 institution in 1 country.

Md Faqrul HasanBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Tayler J Croom-PerezBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Jeremiah L OyerBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Thomas A DieffenthallerBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Liza D Robles-CarrilloBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Jonathan E EloriagaBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Sanjana KumarBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Brendan W AndersenBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Alicja J CopikBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.ORCID 0000-0003-4109-5539
University of Central Florida · US

Funding

Florida Department of Health 9JK04University of Central Florida Preeminent Postdoctoral Program
6 · The paper itself

Abstract

Treatments targeting TIGIT have gained a lot of attention due to strong preclinical and early clinical results, particularly with anti-PD-(L)1 therapeutics. However, this combination has failed to meet progression-free survival endpoints in phase III trials. Most of our understanding of TIGIT comes from studies of T cell function. Yet, this inhibitory receptor is often upregulated to the same, or higher, extent on NK cells in cancers. Studies in murine models have demonstrated that TIGIT inhibits NK cells and promotes exhaustion, with its effects on tumor control also being dependent on NK cells. However, there are limited studies assessing the role of TIGIT on the function of human NK cells (hNK), particularly in lung cancer. Most studies used NK cell lines or tested TIGIT blockade to reactivate exhausted cells obtained from cancer patients. For therapeutic advancement, a better understanding of TIGIT in the context of activated hNK cells is crucial, which is different than exhausted NK cells, and critical in the context of adoptive NK cell therapeutics that may be combined with TIGIT blockade. In this study, the effect of TIGIT blockade on the anti-tumor activities of human ex vivo-expanded NK cells was evaluated in vitro in the context of lung cancer. TIGIT expression was higher on activated and/or expanded NK cells compared to resting NK cells. More TIGIT

Indexed as

cancer immune cell therapycheckpoint blockade immunotherapylung cancerNK cellTIGIT blockade

Identifiers

PMID37345049
PMCPMC10216728
OpenAlexW4381276489

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.