Evidence map›Paper›PMID 35027427›Full record

ArticleJournal for immunotherapy of cancer2022

Cell membrane-anchored and tumor-targeted IL-12 (attIL12)-T cell therapy for eliminating large and heterogeneous solid tumors.

Jiemiao Hu, Qing Yang, Wendong Zhang, Hongwei Du, Yuhui Chen, Qingnan Zhao, Long Dao, Xueqing Xia, Fowlkes Natalie Wall, Zhongting Zhang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 50 citations in OpenAlex.

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  11. Therapeutic application of IL-12 for cancer therapy.Translational cancer research · 2026
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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

15 authors at 2 institutions in 1 country.

Jiemiao HuDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-5142-0641
Qing YangDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Wendong ZhangDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Hongwei DuLineberger Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.ORCID 0000-0002-7997-4507
Yuhui ChenLineberger Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Qingnan ZhaoDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Long DaoDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Xueqing XiaDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Fowlkes Natalie WallVeterinary Medicine & Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Zhongting ZhangDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Kris MahadeoDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Richard GorlickDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
S KopetzDepartment of Gastrointestinal Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Gianpietro DottiLineberger Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Shulin LiDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA sli4@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USUniversity of North Carolina at Chapel Hill · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Gene-Product Auto-Targeting to Tumor VesselsR01CA120895 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, SHULIN · 2007 to 2025
$4.8M
Cellular Immunotherapy of Ovarian CancerR01CA243543 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DOTTI, GIANPIETRO · 2019 to 2023
$2.0M
Tumor-Targeted Chemo-Immunotherapy for Osteosarcoma MetastasisR01CA200574 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LI, SHULIN, ZHANG, LIANGFANG · 2016 to 2020
$1.8M
NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA120895NCI NIH HHS R01 CA200574NCI NIH HHS R01 CA243543
6 · The paper itself

Abstract

backgroundAdoptive T-cell transfer has become an attractive therapeutic approach for hematological malignancies but shows poor activity against large and heterogeneous solid tumors. Interleukin-12 (IL-12) exhibits potent antitumor efficacy against solid tumors, but its clinical application has been stalled because of toxicity. Here, we aimed to develop a safe approach to IL-12 T-cell therapy for eliminating large solid tumors.

methodsWe generated a cell membrane-anchored IL-12 (aIL12), a tumor-targeted IL-12 (ttIL12), and a cell membrane-anchored and ttIL-12 (attIL12) and a cell membrane-anchored and tumor-targeted ttIL-12 (attIL12) armed T cells, chimeric antigen receptor-T cells, and T cell receptor-T (TCR-T) cells with each. We compared the safety and efficacy of these armed T cells in treating osteosarcoma patient-derived xenograft tumors and mouse melanoma tumors after intravenous infusions of the armed T cells.

resultsattIL12-T cell infusion showed remarkable antitumor efficacy in human and mouse large solid tumor models. Mechanistically, attIL12-T cells targeted tumor cells expressing cell-surface vimentin, enriching effector T cell and interferon γ production in tumors, which in turn stimulates dendritic cell maturation for activating secondary T-cell responses and tumor antigen spreading. Both attIL12- and aIL12-T-cell transfer eliminated peripheral cytokine release and the associated toxic effects.

conclusionsThis novel approach sheds light on the safe application of IL-12-based T-cell therapy for large and heterogeneous solid tumors.

Indexed as

AnimalsCell- and Tissue-Based TherapyDisease Models, AnimalHumansImmunotherapyInterleukin-12MiceNeoplasmsReceptors, Antigen, T-CellInterleukin-12Receptors, Antigen, T-Cellcostimulatory and Inhibitory T-cell receptorscytokinesdendritic cellsimmunotherapylymphocytestumor-infiltrating

Identifiers

PMID35027427
PMCPMC8762133
OpenAlexW4206280295

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.