Evidence map›Paper›PMID 34081628›Full record

ArticleJCI insight2021

Natural killer cells and cytotoxic T lymphocytes are required to clear solid tumor in a patient-derived xenograft.

Duy Tri Le, Tridu R Huynh, Bryan Burt, George Van Buren, Shawn A Abeynaike, Cristina Zalfa, Rana Nikzad, Farrah Kheradmand, John J Tyner, Silke Paust

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Transcriptomic analysis of the immune response toMolecular therapy. Nucleic acids · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. CXCR6Frontiers in immunology · 2022
    Article
  11. 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

10 authors at 5 institutions in 1 country.

Duy Tri LeDepartment of Pediatrics, Texas Children's Hospital, Houston, Texas, USA.
Tridu R HuynhScripps Research Translational Institute, La Jolla, California, USA.
Bryan BurtDivision of General Thoracic Surgery and.
George Van BurenDivision of Surgical Oncology, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas, USA.
Shawn A AbeynaikeDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, California, USA.
Cristina ZalfaDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, California, USA.
Rana NikzadDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, California, USA.
Farrah KheradmandMargaret M. and Albert B. Alkek Department of Medicine, Baylor College of Medicine and Michael E. DeBakey VA Medical Center, US Department of Veterans Affairs, Houston, Texas, USA.
John J TynerDivision of Cardiovascular/Thoracic Surgery, Scripps Clinic, La Jolla, California, USA.
Silke PaustDepartment of Pediatrics, Texas Children's Hospital, Houston, Texas, USA.
Scripps Research Institute · USBaylor College of Medicine · USMichael E. DeBakey VA Medical Center · USScripps Clinic · USTexas Children's Hospital · US

Funding

Scripps Translational Science InstituteUL1TR002550 · NCATS · SCRIPPS RESEARCH INSTITUTE, THE · PI TOPOL, ERIC JEFFREY · 2018 to 2022
$28.9M
Institutional Career Development CoreKL2TR002552 · NCATS · SCRIPPS RESEARCH INSTITUTE, THE · PI NICHOLSON, LAURA · 2018 to 2022
$5.2M
NCATS NIH HHS KL2 TR002552NCATS NIH HHS UL1 TR002550
6 · The paper itself

Abstract

Existing patient-derived xenograft (PDX) mouse models of solid tumors lack a fully tumor donor-matched, syngeneic, and functional immune system. We developed a model that overcomes these limitations by engrafting lymphopenic recipient mice with a fresh, undisrupted piece of solid tumor, whereby tumor-infiltrating lymphocytes (TILs) persisted in the recipient mice for several weeks. Successful tumor engraftment was achieved in 83% to 89% of TIL-PDX mice, and these were seen to harbor exhausted immuno-effector as well as functional immunoregulatory cells persisting for at least 6 months postengraftment. Combined treatment with interleukin-15 stimulation and immune checkpoint inhibition resulted in complete or partial tumor response in this model. Further, depletion of cytotoxic T lymphocytes and/or natural killer cells before combined immunotherapy revealed that both cell types were required for maximal tumor regression. Our TIL-PDX model provides a valuable resource for powerful mechanistic and therapeutic studies in solid tumors.

Indexed as

HeterograftsNeoplasmsNeoplasm TransplantationAdjuvants, ImmunologicAnimalsDisease Models, AnimalHumansImmune Checkpoint InhibitorsImmunotherapyInterleukin-15Killer Cells, NaturalMiceT-Lymphocytes, CytotoxicTransplantation, HeterologousXenograft Model Antitumor AssaysAdjuvants, ImmunologicImmune Checkpoint InhibitorsInterleukin-15Cancer immunotherapyImmunologyNK cellsT cells

Identifiers

PMID34081628
PMCPMC8410059
OpenAlexW3165505419

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.