Evidence map›Paper›PMID 35604411›Full record

ArticleThe Journal of experimental medicine2022

Tumor-induced double positive T cells display distinct lineage commitment mechanisms and functions.

Sara E Schad, Andrew Chow, Levi Mangarin, Heng Pan, Jiajia Zhang, Nicholas Ceglia, Justina X Caushi, Nicole Malandro, Roberta Zappasodi, Mathieu Gigoux and 16 more

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. The double-positive cells in the tumor microenvironment.Journal of translational internal medicine · 2026
    Article
  9. Functionally heterogeneous intratumoral CD4Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Pathological Proliferation of CD4Infection and drug resistance · 2026
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

26 authors.

Sara E SchadSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-2306-6999
Andrew ChowSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-1151-2450
Levi MangarinSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-1219-6998
Heng PanWeill Cornell Medical College, New York, NY.ORCID 0000-0002-5407-5687
Jiajia ZhangJohn Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0003-4623-6134
Nicholas CegliaComputational Oncology, Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-9387-103X
Justina X CaushiJohn Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0002-8009-3408
Nicole MalandroSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-3939-1195
Roberta ZappasodiSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-7031-6671
Mathieu GigouxSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-1831-7597
Daniel HirschhornSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-0467-7687
Sadna BudhuSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-3284-1408
Masataka AmisakiParker Institute for Cancer Immunotherapy, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-4153-4036
Monica ArniellaBroad Institute of MIT and Harvard, Cambridge, MA.ORCID 0000-0002-7286-0590
David RedmondWeill Cornell Medical College, New York, NY.ORCID 0000-0002-0983-8606
Jamie ChaftDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-5838-9982
Patrick M FordeJohn Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0001-6925-6344
Justin F GainorDepartment of Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0001-8697-4081
Matthew D HellmannDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-2670-9777
Vinod BalachandranSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-2956-223X
Sohrab ShahComputational Oncology, Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-6402-523X
Kellie N SmithJohn Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0002-6295-8930
Drew PardollJohn Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0001-6215-1013
Olivier ElementoWeill Cornell Medical College, New York, NY.ORCID 0000-0002-8061-9617
Jedd D WolchokSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-6718-2222
Taha MerghoubSwim Across America and Ludwig Collaborative Laboratory, Immunology Program, Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-1518-5111

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
TRAINING IN AREAS FUNDAMENTAL TO CANCER RESEARCHT32CA009110 · NCI · JOHNS HOPKINS UNIVERSITY · PI MATUNIS, MICHAEL J., WEERARATNA, ASHANI T · 1985 to 2025
$13.1M
IMMUNIZATION AGAINST MELANOMA DIFFERENTIATION ANTIGENSR01CA056821 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI WOLCHOK, JEDD D. · 1992 to 2020
$5.7M
Immunogenomic determinants of response and resistance to neoadjuvant anti-PD-1 in resectable NSCLCR37CA251447 · NCI · JOHNS HOPKINS UNIVERSITY · PI Kellie Nicole Smith · 2021 to 2026
$2.2M
Cancer Research InstituteNCI NIH HHS P30 CA008748NCI NIH HHS R01 CA056821NCI NIH HHS R37 CA251447NCI NIH HHS T32 CA009110NIH HHS P30 CA008748
6 · The paper itself

Abstract

Transcription factors ThPOK and Runx3 regulate the differentiation of "helper" CD4+ and "cytotoxic" CD8+ T cell lineages respectively, inducing single positive (SP) T cells that enter the periphery with the expression of either the CD4 or CD8 co-receptor. Despite the expectation that these cell fates are mutually exclusive and that mature CD4+CD8+ double positive (DP) T cells are present in healthy individuals and augmented in the context of disease, yet their molecular features and pathophysiologic role are disputed. Here, we show DP T cells in murine and human tumors as a heterogenous population originating from SP T cells which re-express the opposite co-receptor and acquire features of the opposite cell type's phenotype and function following TCR stimulation. We identified distinct clonally expanded DP T cells in human melanoma and lung cancer by scRNA sequencing and demonstrated their tumor reactivity in cytotoxicity assays. Our findings indicate that antigen stimulation induces SP T cells to differentiate into DP T cell subsets gaining in polyfunctional characteristics.

Indexed as

CD4-Positive T-LymphocytesMelanomaAnimalsCD4 AntigensCD8 AntigensCD8-Positive T-LymphocytesCell DifferentiationCell LineageMiceT-Lymphocyte SubsetsCD4 AntigensCD8 Antigens

Identifiers

PMID35604411
PMCPMC9130031

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.