Evidence map›Paper›PMID 35101945›Full record

ArticleJournal for immunotherapy of cancer2022

Generation of cDC-like cells from human induced pluripotent stem cells via Notch signaling.

Kenichi Makino, Mark D Long, Ryutaro Kajihara, Satoko Matsueda, Takaaki Oba, Kazunori Kanehira, Song Liu, Fumito Ito

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  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

8 authors at 2 institutions in 2 countries.

Kenichi Makino *Center for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Mark D Long *Department of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Ryutaro Kajihara *Center for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Satoko MatsuedaCenter for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Takaaki ObaCenter for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Kazunori KanehiraDepartment of Pathology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Song LiuDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Fumito ItoCenter for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA fumito.ito@med.usc.edu.ORCID 0000-0002-6866-671X
Roswell Park Comprehensive Cancer Center · USUniversity of Southern California · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Dean G. Tang · 1985 to 2026
$116.6M
Immuno-Oncology Translation Network: Data Management and Resource-Sharing Center at RPCIU24CA232979 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI HUTSON, ALAN DAVID, LIU, SONG · 2018 to 2024
$8.9M
In situ radioimmunotherapy to maximize the engagement of conventional type 1 dendritic cells against non-T cell-inflamed tumorsR01CA255240 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ITO, FUMITO · 2021 to 2025
$2.0M
Adoptive Cell Therapy with Rejuvenated Antigen-Specific T CellsK08CA197966 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ITO, FUMITO · 2015 to 2019
$875k
NCI NIH HHS K08 CA197966NCI NIH HHS P30 CA016056NCI NIH HHS R01 CA255240NCI NIH HHS U24 CA232979
6 · The paper itself

Abstract

backgroundDendritic cells (DCs) play critical roles in regulating the innate and adaptive immune responses, and have long been a major focus of cancer immunotherapy. Accumulating evidence suggests that conventional type 1 DCs (cDC1s) excel in cross-presentation of exogenous antigens on MHC-I molecules and induction of antitumor CD8

methodsHuman iPSCs established from peripheral blood T cells and monocytes were differentiated to myeloid cells under on-feeder or feeder-free culture conditions in vitro. Phenotype, genomic and transcriptomic signature, and function of human iPSC-derived DCs were analyzed. The role of Notch signaling for the generation of HLA-DR

resultsFlow cytometric analyses and single-cell profiling of HLA-DR

conclusionsOur study demonstrates a critical role of Notch signaling in regulating developmental pathway of human cDCs. These findings provide insights into the future development of personalized treatment with unlimited numbers of autologous cDCs from human iPSCs.

Indexed as

AnimalsCell DifferentiationCells, CulturedDendritic CellsHumansInduced Pluripotent Stem CellsMiceReceptors, NotchSequence Analysis, RNASignal TransductionSingle-Cell AnalysisTranscriptomeReceptors, Notchcell engineeringcellulardendritic cellsimmune reconstitutionimmunitysystems biology

Identifiers

PMID35101945
PMCPMC8804689
OpenAlexW4210424272

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.