Evidence map›Paper›PMID 34943884›Full record

ReviewCells2021

The Role of T Cell Immunotherapy in Acute Myeloid Leukemia.

Fang Hao, Christine Sholy, Chen Wang, Min Cao, Xunlei Kang

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. CAR-T cell therapy for cancer: current challenges and future directions.Signal transduction and targeted therapy · 2025
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. DOGMA-seq and multimodal, single-cell analysis in acute myeloid leukemia.International review of cell and molecular biology · 2025
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Higher TIGIT+ γδ TFrontiers in immunology · 2024
    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

5 authors at 1 institution in 1 country.

Fang HaoCenter for Precision Medicine, Department of Medicine, University of Missouri, 1 Hospital Drive, Columbia, MI 65212, USA.
Christine SholyCenter for Precision Medicine, Department of Medicine, University of Missouri, 1 Hospital Drive, Columbia, MI 65212, USA.
Chen WangCenter for Precision Medicine, Department of Medicine, University of Missouri, 1 Hospital Drive, Columbia, MI 65212, USA.
Min CaoCenter for Precision Medicine, Department of Medicine, University of Missouri, 1 Hospital Drive, Columbia, MI 65212, USA.
Xunlei KangCenter for Precision Medicine, Department of Medicine, University of Missouri, 1 Hospital Drive, Columbia, MI 65212, USA.
University of Missouri Hospital · US

Funding

Membrane protein target for leukemia therapyR37CA241603 · NCI · UNIVERSITY OF MISSOURI-COLUMBIA · PI KANG, XUNLEI · 2020 to 2025
$2.9M
American Heart Association 9CDA34770036NCI NIH HHS R37 CA241603
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a heterogeneous disease associated with various alterations in T cell phenotype and function leading to an abnormal cell population, ultimately leading to immune exhaustion. However, restoration of T cell function allows for the execution of cytotoxic mechanisms against leukemic cells in AML patients. Therefore, long-term disease control, which requires multiple therapeutic approaches, includes those aimed at the re-establishment of cytotoxic T cell activity. AML treatments that harness the power of T lymphocytes against tumor cells have rapidly evolved over the last 3 to 5 years through various stages of preclinical and clinical development. These include tissue-infiltrated lymphocytes (TILs), bispecific antibodies, immune checkpoint inhibitors (ICIs), chimeric antigen receptor T (CAR-T) cell therapy, and tumor-specific T cell receptor gene-transduced T (TCR-T) cells. In this review, these T cell-based immunotherapies and the potential of TILs as a novel antileukemic therapy will be discussed.

Indexed as

ImmunotherapyAnimalsClinical Trials as TopicHumansImmunotherapy, AdoptiveLeukemia, Myeloid, AcuteModels, BiologicalT-Lymphocytesacute myeloid leukemiabispecific antibodiesCAR-TT cell alterationT cell immunotherapyTCR-Ttissue-infiltrated lymphocytes

Identifiers

PMID34943884
PMCPMC8699747
OpenAlexW3217302674

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.