Evidence map›Paper›PMID 30659053›Full record

ArticleCancer immunology research2019

TIGIT and PD-1 Mark Intratumoral T Cells with Reduced Effector Function in B-cell Non-Hodgkin Lymphoma.

Sarah E Josefsson, Klaus Beiske, Yngvild N Blaker, Mette S Førsund, Harald Holte, Bjørn Østenstad, Eva Kimby, Hakan Köksal, Sébastien Wälchli, Baoyan Bai and 5 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

73 citing papers in PubMed, 114 citations in OpenAlex.

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  15. Multimodal cell-cell communication driving CD8Frontiers in immunology · 2025
    Review
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13 more citing papers are in PubMed but not listed here.

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

15 authors at 3 institutions in 3 countries.

Sarah E JosefssonDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Klaus BeiskeDepartment of Pathology, Division of Cancer Medicine, Oslo University Hospital, Oslo, Norway.
Yngvild N BlakerDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Mette S FørsundDepartment of Pathology, Division of Cancer Medicine, Oslo University Hospital, Oslo, Norway.
Harald HolteKG Jebsen Centre for B-cell Malignancies, Institute for Clinical Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0001-9799-9428
Bjørn ØstenstadDepartment of Oncology, Division of Cancer Medicine, Oslo University Hospital, Oslo, Norway.
Eva KimbyDepartment of Hematology, Karolinska Institutet, Stockholm, Sweden.
Hakan KöksalKG Jebsen Centre for B-cell Malignancies, Institute for Clinical Medicine, University of Oslo, Oslo, Norway.
Sébastien WälchliKG Jebsen Centre for B-cell Malignancies, Institute for Clinical Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0001-5869-1746
Baoyan BaiDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Erlend B SmelandDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Ronald LevyDivision of Oncology, Stanford School of Medicine, Stanford, California.
Arne KolstadDepartment of Oncology, Division of Cancer Medicine, Oslo University Hospital, Oslo, Norway.
Kanutte HuseDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
June H MyklebustDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway. June.Helen.Myklebust@rr-research.no.
Oslo University Hospital · NOKarolinska Institutet · SEStanford Medicine · US

Funding

Enhancing Cancer Immunotherapy: Targeting the Tumor and Targeting the HostR35CA197353 · NCI · STANFORD UNIVERSITY · PI LEVY, RONALD · 2016 to 2022
$6.1M
NCI NIH HHS R35 CA197353
6 · The paper itself

Abstract

Checkpoint blockade can reverse T-cell exhaustion and promote antitumor responses. Although blocking the PD-1 pathway has been successful in Hodgkin lymphoma, response rates have been modest in B-cell non-Hodgkin lymphoma (NHL). Coblockade of checkpoint receptors may therefore be necessary to optimize antitumor T-cell responses. Here, characterization of coinhibitory receptor expression in intratumoral T cells from different NHL types identified TIGIT and PD-1 as frequently expressed coinhibitory receptors. Tumors from NHL patients were enriched in CD8

Indexed as

AdultAgedAged, 80 and overCell Line, TumorCytokinesFemaleHumansImmunologic MemoryLigandsLymphoma, Non-HodgkinMiddle AgedProgrammed Cell Death 1 ReceptorReceptors, ImmunologicT-Lymphocyte SubsetsTumor MicroenvironmentCytokinesLigandsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorReceptors, ImmunologicTIGIT protein, human

Identifiers

PMID30659053
PMCPMC6636339
OpenAlexW2909122278

What OpenQuestion holds

Textmetadata
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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.