Evidence map›Paper›PMID 36240285›Full record

ArticleScience immunology2022

Depletion of exhausted alloreactive T cells enables targeting of stem-like memory T cells to generate tumor-specific immunity.

Simone A Minnie, Olivia G Waltner, Kathleen S Ensbey, Nicole S Nemychenkov, Christine R Schmidt, Shruti S Bhise, Samuel R W Legg, Gabriela Campoy, Luke D Samson, Rachel D Kuns and 13 more

Open access · greenAbstract read
In one paragraph

Article in Science immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Circulating Tumor Cell PD-L1 and Peripheral Blood CD8Cancer management and research · 2026
    Article
  6. EomesoderminImmunity · 2025
    Article
  7. Targeting of the CD161 Inhibitory Receptor Enhances Bone-Marrow-Resident Memory CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  8. Article
  9. Article
  10. T Cells Dysfunction in Multiple Myeloma.ImmunoTargets and therapy · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. The Role of IL-18 in P2RX7-Mediated Antitumor Immunity.International journal of molecular sciences · 2023
    Review
  20. Review
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

23 authors at 5 institutions in 2 countries.

Simone A MinnieClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.ORCID 0000-0002-1314-9264
Olivia G WaltnerClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.ORCID 0000-0001-7021-0431
Kathleen S EnsbeyClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Nicole S NemychenkovClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Christine R SchmidtClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Shruti S BhiseClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Samuel R W LeggClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Gabriela CampoyClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Luke D SamsonClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Rachel D KunsQIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.ORCID 0000-0002-7465-7262
Ting ZhouDepartment of Immunobiology, Yale School of Medicine, New Haven, CT 06519, USA.
John D HuckDepartment of Immunobiology, Yale School of Medicine, New Haven, CT 06519, USA.ORCID 0000-0002-0755-3850
Slavica VuckovicQIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.ORCID 0000-0002-2803-0717
Danniel ZamoraDepartment of Medicine, University of Washington, Seattle, WA 98109, USA.ORCID 0000-0002-1318-2902
Albert YehClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.ORCID 0000-0003-3455-7360
Andrew SpencerAustralian Center for Blood Diseases, Monash University/the Alfred Hospital, Melbourne, VIC 3004, Australia.ORCID 0000-0002-0531-7424
Motoko KoyamaClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Kate A MarkeyClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.ORCID 0000-0002-7064-2362
Steven W LaneQIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.ORCID 0000-0002-8050-6209
Michael BoeckhClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.ORCID 0000-0003-1538-7984
Aaron M RingDepartment of Immunobiology, Yale School of Medicine, New Haven, CT 06519, USA.ORCID 0000-0003-3699-2446
Scott N FurlanClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.ORCID 0000-0003-3007-9840
Geoffrey R HillClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.ORCID 0000-0003-2994-0429
Fred Hutch Cancer Center · USUniversity of Washington · USQIMR Berghofer Medical Research Institute · AUYale University · USThe Alfred Hospital · AU

Funding

VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Geoffrey Roger HILL · 1985 to 2026
$128.4M
Project 3: Stem Cell Allografts for Lymphoid MalignanciesP01CA078902 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SANDMAIER, BRENDA MARIE · 1999 to 2025
$46.1M
Yale Cancer Biology Training GrantT32CA193200 · NCI · YALE UNIVERSITY · PI PETER M GLAZER, Qin Yan · 2016 to 2026
$3.6M
Cytomegalovirus-specific Immune Reconstitution after Hematopoietic Cell Transplantation in the Era of Modern Antiviral ProphylaxisK23AI163343 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Danniel Zamora · 2022 to 2026
$945k
NCI NIH HHS P01 CA018029NCI NIH HHS P01 CA078902NCI NIH HHS T32 CA193200NIAID NIH HHS K23 AI163343
6 · The paper itself

Abstract

Some hematological malignancies such as multiple myeloma are inherently resistant to immune-mediated antitumor responses, the cause of which remains unknown. Allogeneic bone marrow transplantation (alloBMT) is the only curative immunotherapy for hematological malignancies due to profound graft-versus-tumor (GVT) effects, but relapse remains the major cause of death. We developed murine models of alloBMT where the hematological malignancy is either sensitive [acute myeloid leukemia (AML)] or resistant (myeloma) to GVT effects. We found that CD8

Indexed as

Graft vs Host DiseaseHematologic NeoplasmsMultiple MyelomaAnimalsChromatinCyclophosphamideImmune Checkpoint InhibitorsInterleukin-18IsoantigensMemory T CellsMiceTransplantation, HomologousChromatinCyclophosphamideImmune Checkpoint InhibitorsInterleukin-18Isoantigens

Identifiers

PMID36240285
PMCPMC10184646
OpenAlexW4306182261

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.