Evidence map›Paper›PMID 40305288›Full record

ArticleCell reports2025

Single-cell transcriptomic profiling reveals diversity in human iNKT cells across hematologic tissues.

Reyka G Jayasinghe, Derek Hollingsworth, Nathan C Schedler, Emily Landy, Chaiyaporn Boonchalermvichian, Biki Gupta, Hao Yan, Jeanette Baker, Beruh Dejene, Kenneth I Weinberg and 2 more

Abstract read
In one paragraph

Article in Cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
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  5. Metabolic control of innate-like T cells.Nature reviews. Immunology · 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

12 authors.

Reyka G JayasingheDepartment of Medicine, Division of Oncology, Washington University School of Medicine, Saint Louis, MO, USA.
Derek HollingsworthDepartment of Pediatrics, Division of Hematology, Oncology, Stem Cell Transplantation and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Nathan C SchedlerDepartment of Pediatrics, Division of Hematology and Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Emily LandyDepartment of Pediatrics, Division of Hematology and Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Chaiyaporn BoonchalermvichianDepartment of Medicine, Division of Blood and Marrow Transplantation and Cellular Therapy, Stanford University School of Medicine, Stanford, CA, USA.
Biki GuptaDepartment of Medicine, Division of Blood and Marrow Transplantation and Cellular Therapy, Stanford University School of Medicine, Stanford, CA, USA.
Hao YanDepartment of Medicine, Division of Blood and Marrow Transplantation and Cellular Therapy, Stanford University School of Medicine, Stanford, CA, USA.
Jeanette BakerDepartment of Medicine, Division of Blood and Marrow Transplantation and Cellular Therapy, Stanford University School of Medicine, Stanford, CA, USA.
Beruh DejeneDepartment of Pediatrics, Division of Hematology, Oncology, Stem Cell Transplantation and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Kenneth I WeinbergDepartment of Pediatrics, Division of Hematology, Oncology, Stem Cell Transplantation and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Robert S NegrinDepartment of Medicine, Division of Blood and Marrow Transplantation and Cellular Therapy, Stanford University School of Medicine, Stanford, CA, USA.
Melissa MaversDepartment of Pediatrics, Division of Hematology, Oncology, Stem Cell Transplantation and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, USA; Department of Pediatrics, Division of Hematology and Oncology, Washington University School of Medicine, St. Louis, MO, USA. Electronic address: mmmavers@wustl.edu.

Funding

TUMOR SPECIFIC CYTOTOXIC T-LYMPHOCYTES IN BONE MARROW TRANSPLANTATIONP01CA049605 · NCI · STANFORD UNIVERSITY · PI David B. Miklos, Robert S Negrin · 1989 to 2026
$73.3M
TLI/ATG CONDTIONING: KIDNEY/BLOOD STEM CELL TRANSPLANTSP01HL075462 · NHLBI · STANFORD UNIVERSITY · PI MEYER, EVERETT · 2004 to 2020
$27.9M
TRAINING IN THE IMMUNOBIOLOGY AND MOLECULAR CELL BIOLOGY OF CANCERT32CA009547 · NCI · WASHINGTON UNIVERSITY · PI ROBERT DAVID SCHREIBER · 1986 to 2026
$12.1M
Washington University SPORE in Pancreatic CancerP50CA272213 · NCI · WASHINGTON UNIVERSITY · PI David G DeNardo, WILLIAM G HAWKINS · 2023 to 2026
$10.7M
Training Program in Hematopoietic Cell TransplantationT32HL007952 · NHLBI · STANFORD UNIVERSITY · PI NEGRIN, ROBERT S · 2001 to 2021
$2.1M
Immunosuppressive human invariant natural killer T cells for prevention of graft-versus-host diseaseK08HL151809 · NHLBI · WASHINGTON UNIVERSITY · PI MAVERS, MELISSA · 2020 to 2024
$833k
Four Laser, 18 Color Cell Sorter in the SSFFS10RR025518 · NCRR · STANFORD UNIVERSITY · PI HERZENBERG, LEONARD A · 2009 to 2009
$500k
NCI NIH HHS P01 CA049605NCI NIH HHS P50 CA272213NCI NIH HHS T32 CA009547NCRR NIH HHS S10 RR025518NHLBI NIH HHS K08 HL151809NHLBI NIH HHS P01 HL075462NHLBI NIH HHS T32 HL007952
6 · The paper itself

Abstract

Invariant natural killer T (iNKT) cells are evolutionarily conserved innate lymphocytes important for protection against pathogens, malignancies, and graft-versus-host disease, with potential for universal donor cellular therapies. While mouse studies reveal transcriptionally and functionally distinct subsets, a comprehensive understanding of human iNKT cell heterogeneity is limited. Herein, we delineate the transcriptomic diversity of human iNKT cells from multiple immunologically relevant hematologic tissues. Human iNKT cells express naive/precursor, transitional, and T helper (Th)1/17/NK-like transcriptional profiles, partially contrasting with findings in mice. Additionally, these data uncover transcription factor dynamics not previously described in mice and reveal a T effector memory RA

Indexed as

Gene Expression ProfilingNatural Killer T-CellsSingle-Cell AnalysisTranscriptomeAnimalsHumansMicecellular therapyCP: Cell biologyCP: Immunologygraft-versus-host diseaseiNKT cellsinnate lymphocytesinvariant natural killer T cellslymphocyte developmentlymphocyte subsetsT effector memory RATEMRATh differentiation

Identifiers

PMID40305288
PMCPMC12255272

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Registered trials

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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.