Evidence map›Paper›PMID 36027915›Full record

ArticleCancer cell2022

Induction of tumor cell autosis by myxoma virus-infected CAR-T and TCR-T cells to overcome primary and acquired resistance.

Ningbo Zheng, Jing Fang, Gang Xue, Ziyu Wang, Xiaoyin Li, Mengshi Zhou, Guangxu Jin, Masmudur M Rahman, Grant McFadden, Yong Lu

Open access · greenAbstract read
In one paragraph

Article in Cancer cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
6.9field-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

55 citing papers in PubMed, 72 citations in OpenAlex.

  1. FOXP1 Knockdown Reprograms Th9 CAR-T Cells to Overcome Antigen Escape.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Review
  3. Review
  4. Regulated cell death programs shaping cancer therapy.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Intravenous infusion of engineered megakaryocytes to produce oncolytic platelets in vivo for enhanced cancer immunotherapy.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  9. Oncolytic viruses: advanced strategies in cancer therapy.Signal transduction and targeted therapy · 2026
    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

10 authors at 3 institutions in 1 country.

Ningbo ZhengDepartment of Microbiology & Immunology, Wake Forest School of Medicine, Winston-Salem, NC 27101, USA.
Jing FangDepartment of Microbiology & Immunology, Wake Forest School of Medicine, Winston-Salem, NC 27101, USA.
Gang XueDepartment of Microbiology & Immunology, Wake Forest School of Medicine, Winston-Salem, NC 27101, USA.
Ziyu WangDepartment of Microbiology & Immunology, Wake Forest School of Medicine, Winston-Salem, NC 27101, USA.
Xiaoyin LiDepartment of Mathematics and Statistics, St. Cloud State University, St Cloud, MN 56301, USA.
Mengshi ZhouDepartment of Mathematics and Statistics, St. Cloud State University, St Cloud, MN 56301, USA.
Guangxu JinDepartment of Microbiology & Immunology, Wake Forest School of Medicine, Winston-Salem, NC 27101, USA.
Masmudur M RahmanBiodesign Center for Immunotherapy Vaccines and Virotherapy, Arizona State University, Tempe, AZ 85287, USA.
Grant McFaddenBiodesign Center for Immunotherapy Vaccines and Virotherapy, Arizona State University, Tempe, AZ 85287, USA. Electronic address: grantmcf@asu.edu.
Yong LuDepartment of Microbiology & Immunology, Wake Forest School of Medicine, Winston-Salem, NC 27101, USA. Electronic address: ylu2@houstonmethodist.org.
Wake Forest University · USArizona State University · USSt. Cloud State University · US

Funding

Studies in Poxvirus Host Range Genes and TropismR01AI080607 · NIAID · UNIVERSITY OF FLORIDA · PI RAHMAN, MASMUDUR MOHAMMED · 2009 to 2025
$5.6M
Intrapleural immunotherapeutic nanoparticles for MPE treatmentR01CA264102 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG, ZHAO, DAWEN · 2021 to 2025
$2.3M
The Unique Roles of Tumor-Specific Th9 Cells for Solid Tumor EradicationR01CA258477 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG · 2021 to 2025
$1.9M
Eradication of Escaped Variant Tumor Cells for Cancer ImmunotherapyR01CA248111 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG · 2021 to 2025
$1.9M
P38 MAPK is a molecular switch that controls the acquired resistance in adoptive cell therapyR37CA251318 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG · 2020 to 2024
$1.8M
NCI NIH HHS R01 CA248111NCI NIH HHS R01 CA258477NCI NIH HHS R01 CA264102NCI NIH HHS R37 CA251318NIAID NIH HHS R01 AI080607
6 · The paper itself

Abstract

Cytotoxicity of tumor-specific T cells requires tumor cell-to-T cell contact-dependent induction of classic tumor cell apoptosis and pyroptosis. However, this may not trigger sufficient primary responses of solid tumors to adoptive cell therapy or prevent tumor antigen escape-mediated acquired resistance. Here we test myxoma virus (MYXV)-infected tumor-specific T (T

Indexed as

Myxoma virusNeoplasmsReceptors, Chimeric AntigenHumansImmunotherapy, AdoptiveReceptors, Antigen, T-CellT-LymphocytesReceptors, Antigen, T-CellReceptors, Chimeric Antigenacquired resistanceautosisCAR-T cellsmyxoma virus

Identifiers

PMID36027915
PMCPMC9489043
OpenAlexW4293044445

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.