Evidence map›Paper›PMID 37364933›Full record

ArticleJournal for immunotherapy of cancer2023

TIGIT is a key inhibitory checkpoint receptor in lymphoma.

James Godfrey, Xiufen Chen, Nicole Sunseri, Alan Cooper, Jovian Yu, Arina Varlamova, Dmitry Zarubin, Yuriy Popov, Connor Jacobson, Ekaterina Postovalova and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2023. 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
3.5field-weighted citation impact, top 7% 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, 15 citations in OpenAlex.

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  11. Targeting LAG-3, TIM-3, and TIGIT for cancer immunotherapy.Journal of hematology & oncology · 2023
    Review
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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

18 authors at 3 institutions in 1 country.

James Godfrey *Hematology, City of Hope Comprehensive Cancer Center, Duarte, California, USA.ORCID 0000-0002-4103-4288
Xiufen Chen *Comprehensive Cancer Center, University of Chicago, Chicago, Illinois, USA.
Nicole Sunseri *Comprehensive Cancer Center, University of Chicago, Chicago, Illinois, USA.
Alan CooperComprehensive Cancer Center, University of Chicago, Chicago, Illinois, USA.
Jovian YuComprehensive Cancer Center, University of Chicago, Chicago, Illinois, USA.
Arina VarlamovaBostonGene, Waltham, Massachusetts, USA.
Dmitry ZarubinBostonGene, Waltham, Massachusetts, USA.
Yuriy PopovBostonGene, Waltham, Massachusetts, USA.
Connor JacobsonBostonGene, Waltham, Massachusetts, USA.
Ekaterina PostovalovaBostonGene, Waltham, Massachusetts, USA.
Zhongmin XiangBostonGene, Waltham, Massachusetts, USA.
Krystle NomieBostonGene, Waltham, Massachusetts, USA.
Aleksander BagaevBostonGene, Waltham, Massachusetts, USA.
Girish VenkataramanComprehensive Cancer Center, University of Chicago, Chicago, Illinois, USA.
Yuanyuan ZhaComprehensive Cancer Center, University of Chicago, Chicago, Illinois, USA.
Sravya TumuluruComprehensive Cancer Center, University of Chicago, Chicago, Illinois, USA.
Sonali M SmithComprehensive Cancer Center, University of Chicago, Chicago, Illinois, USA.
Justin P KlineComprehensive Cancer Center, University of Chicago, Chicago, Illinois, USA jkline@medicine.bsd.uchicago.edu.
University of Chicago · USAddgene · USCity of Hope · US

Funding

Oncology Research Career Development ProgramK12CA001727 · NCI · CITY OF HOPE NATIONAL MEDICAL CENTER · PI MORTIMER, JOANNE E. · 1992 to 2024
$14.6M
NCI NIH HHS K12 CA001727
6 · The paper itself

Abstract

backgroundPD-1 checkpoint blockade therapy (CBT) has greatly benefited patients with select solid tumors and lymphomas but has limited efficacy against diffuse large B-cell lymphoma (DLBCL). Because numerous inhibitory checkpoint receptors have been implicated in driving tumor-specific T cell dysfunction, we hypothesized that combinatorial CBT would enhance the activity of anti-PD-1-based therapy in DLBCL. T cell immunoglobulin and immunoreceptor tyrosine-based inhibitory motif domain (TIGIT) is a coinhibitory receptor expressed on dysfunctional tumor-infiltrating T cells, and TIGIT blockade has demonstrated encouraging activity in combination with PD-1 blockade in murine tumor models and in clinical studies. However, the degree to which TIGIT mediates T cell dysfunction in DLBCL has not been fully explored.

resultsHere, we demonstrate that TIGIT is broadly expressed on lymphoma-infiltrating T cells (LITs) across a variety of human lymphomas and is frequently coexpressed with PD-1. TIGIT expression is particularly common on LITs in DLBCL, where TIGIT

conclusionsThese results provide rationale for clinical investigation of TIGIT and PD-1 blockade in lymphomas, including DLBCL.

Indexed as

Lymphoma, Large B-Cell, DiffuseProgrammed Cell Death 1 ReceptorAnimalsHumansMiceReceptors, ImmunologicProgrammed Cell Death 1 ReceptorReceptors, ImmunologicTIGIT protein, humanHematologic NeoplasmsImmune Checkpoint InhibitorsProgrammed Cell Death 1 Receptor

Identifiers

PMID37364933
PMCPMC10410806
OpenAlexW4382139154

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.