Evidence map›Paper›PMID 30063587›Full record

ArticleJournal of immunotherapy (Hagerstown, Md. : 1997)2018

Cancer Stem Cell Vaccination With PD-L1 and CTLA-4 Blockades Enhances the Eradication of Melanoma Stem Cells in a Mouse Tumor Model.

Fang Zheng, Jianzhong Dang, Hongyu Zhang, Fangzhou Xu, Diandian Ba, Bingyu Zhang, Fanjun Cheng, Alfred E Chang, Max S Wicha, Qiao Li

Open access · greenAbstract read
In one paragraph

Article in Journal of immunotherapy (Hagerstown, Md. : 1997), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

40 citing papers in PubMed, 72 citations in OpenAlex.

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  7. Breaking Immunosuppression to Enhance Cancer Stem Cell-Targeted Immunotherapy.International journal of biological sciences · 2025
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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

10 authors at 5 institutions in 2 countries.

Fang ZhengDepartment of Pediatrics.
Jianzhong DangDepartment of Geriatrics, Renmin Hospitial of Wuhan University, Wuhan.
Hongyu ZhangDepartment of Hematology.
Fangzhou XuThe Clinical Trial Institute, Peking University Shenzhen Hospital, Shenzhen.
Diandian BaDepartment of Pediatrics.
Bingyu ZhangDepartment of Pediatrics.
Fanjun ChengInstitute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology.
Alfred E ChangDepartment of Surgery, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI.
Max S WichaDepartment of Surgery, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI.
Qiao LiDepartment of Surgery, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI.
Michigan Center for Translational Pathology · USHuazhong University of Science and Technology · CNPeking University Shenzhen Hospital · CNUniversity of Michigan–Ann Arbor · USWuhan University · CN

Funding

Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
Intramural NIH HHS Z99 OD999999NCATS NIH HHS UL1 TR000433NCATS NIH HHS UL1 TR002240ODCDC CDC HHS Z99 OD999999
6 · The paper itself

Abstract

Immune checkpoint inhibitors and monoclonal antibodies reinvigorate cancer immunotherapy. However, these immunotherapies only benefit a subset of patients. We previously reported that ALDH tumor cells were highly enriched for cancer stem cells (CSCs), and ALDH CSC lysate-pulsed dendritic cell (CSC-DC) vaccine was shown to induce CSC-specific cytotoxic T lymphocytes. In this study, we investigated the CSC targeting effect of the CSC-DC vaccine combined with a dual blockade of programmed death-ligand 1 and cytotoxic T-lymphocyte-associated protein (CTLA-4) in B16-F10 murine melanoma tumor model. Our data showed that animals treated with the dual blockade of programmed death-ligand 1 and CTLA-4 and CSC-DC vaccine conferred significantly more tumor regression than the CSC-DC vaccine alone. Importantly, the triple combination treatment dramatically eliminated ALDH CSCs in vivo. We observed that CSC-DC vaccine in combination with anti-PD-L1 and anti-CTLA-4 administration resulted in ∼1.7-fold fewer PD-1CD8 T cells and ∼2.5-fold fewer CTLA-4CD8 T cells than the populations observed following the CSC-DC vaccination alone. Moreover, significant antitumor effects and dramatically eliminated ALDH CSCs following the triple combination treatment were accompanied by significantly enhanced T-cell expansion, suppressed transforming growth factor β secretion, enhanced IFN-γ secretion, and significantly enhanced host specific CD8 T-cell response against CSCs. Collectively, these data showed that administration of a-PD-L1 and a-CTLA-4 combined with CSC-DC vaccine may represent an effective immunotherapeutic strategy for cancer patients in clinical.

Indexed as

Cancer VaccinesAnimalsB7-H1 AntigenCombined Modality TherapyCTLA-4 AntigenCytokinesDendritic CellsFemaleMelanoma, ExperimentalMice, Inbred C57BLNeoplastic Stem CellsT-Lymphocytes, CytotoxicVaccinationB7-H1 AntigenCancer VaccinesCd274 protein, mouseCTLA-4 AntigenCtla4 protein, mouseCytokines

Identifiers

PMID30063587
PMCPMC6128768
OpenAlexW2886849359

What OpenQuestion holds

Textmetadata
LicenceTDM
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.