Evidence map›Paper›PMID 35230974›Full record

ArticleThe Journal of clinical investigation2022

Remodeling the tumor microenvironment via blockade of LAIR-1 and TGF-β signaling enables PD-L1-mediated tumor eradication.

Lucas A Horn, Paul L Chariou, Sofia R Gameiro, Haiyan Qin, Masafumi Iida, Kristen Fousek, Thomas J Meyer, Margaret Cam, Dallas Flies, Solomon Langermann and 2 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
13.6field-weighted citation impact, top 1% 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

98 citing papers in PubMed, 114 citations in OpenAlex.

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  10. Collagen remodeling in breast cancer progression: from molecular mechanisms to diagnostic and therapeutic opportunities.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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38 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

12 authors at 1 institution in 1 country.

Lucas A HornLaboratory of Tumor Immunology and Biology and.
Paul L ChariouLaboratory of Tumor Immunology and Biology and.
Sofia R GameiroLaboratory of Tumor Immunology and Biology and.
Haiyan QinLaboratory of Tumor Immunology and Biology and.
Masafumi IidaLaboratory of Tumor Immunology and Biology and.
Kristen FousekLaboratory of Tumor Immunology and Biology and.
Thomas J MeyerCCR Collaborative Bioinformatics Resource (CCBR), Center for Cancer Research, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Margaret CamCCR Collaborative Bioinformatics Resource (CCBR), Center for Cancer Research, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Dallas FliesNextCure, Inc., Beltsville, Maryland, USA.
Solomon LangermannNextCure, Inc., Beltsville, Maryland, USA.
Jeffrey SchlomLaboratory of Tumor Immunology and Biology and.
Claudia PalenaLaboratory of Tumor Immunology and Biology and.
National Cancer Institute · US

Funding

Strategies for Cancer Vaccine Development: Preclinical StudiesZIABC010944 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SCHLOM, JEFFREY · 2009 to 2025
$26.6M
Novel Targets for Vaccine TherapyZICBC010937 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PALENA, CLAUDIA · 2010 to 2022
$13.2M
6 · The paper itself

Abstract

Collagens in the extracellular matrix (ECM) provide a physical barrier to tumor immune infiltration, while also acting as a ligand for immune inhibitory receptors. Transforming growth factor-β (TGF-β) is a key contributor to shaping the ECM by stimulating the production and remodeling of collagens. TGF-β activation signatures and collagen-rich environments have both been associated with T cell exclusion and lack of responses to immunotherapy. Here, we describe the effect of targeting collagens that signal through the inhibitory leukocyte-associated immunoglobulin-like receptor-1 (LAIR-1) in combination with blockade of TGF-β and programmed cell death ligand 1 (PD-L1). This approach remodeled the tumor collagenous matrix, enhanced tumor infiltration and activation of CD8+ T cells, and repolarized suppressive macrophage populations, resulting in high cure rates and long-term tumor-specific protection across murine models of colon and mammary carcinoma. The results highlight the advantage of direct targeting of ECM components in combination with immune checkpoint blockade therapy.

Indexed as

B7-H1 AntigenNeoplasmsReceptors, ImmunologicTumor MicroenvironmentAnimalsImmunotherapyLigandsMiceTransforming Growth Factor betaB7-H1 Antigenleukocyte-associated immunoglobulin-like receptor 1LigandsReceptors, ImmunologicTransforming Growth Factor betaCancer immunotherapyImmunology

Identifiers

PMID35230974
PMCPMC9012291
OpenAlexW4214601193

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.