Evidence map›Paper›PMID 39514075›Full record

ReviewDiscover oncology2024

Advances and prospects in tumor infiltrating lymphocyte therapy.

Xu Qiu, Shengjun Li, Tianyu Fan, Yue Zhang, Bin Wang, Bei Zhang, Mingzhe Zhang, Li Zhang

Abstract readReview
In one paragraph

Review in Discover oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Cell-Based Therapies for Solid Tumors: Challenges and Advances.International journal of molecular sciences · 2025
    Review
  12. 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.

Xu QiuThe Department of Immunology, School of Basic Medicine, Qingdao University, Qingdao, Shandong, China.
Shengjun LiClinical Laboratory, Qingdao Women and Children's Hospital, Qingdao, Shandong, China.
Tianyu FanThe Department of Immunology, School of Basic Medicine, Qingdao University, Qingdao, Shandong, China.
Yue ZhangThe Department of Immunology, School of Basic Medicine, Qingdao University, Qingdao, Shandong, China.
Bin WangThe Department of Pathogenic Biology, School of Basic Medicine, Qingdao University, Qingdao, Shandong, China.
Bei ZhangThe Department of Immunology, School of Basic Medicine, Qingdao University, Qingdao, Shandong, China.
Mingzhe ZhangThe Cancer Institute, The Affiliated Hospital of Qingdao University, Qingdao, China.
Li ZhangThe Department of Immunology, School of Basic Medicine, Qingdao University, Qingdao, Shandong, China. 343918320@qq.com.ORCID http://orcid.org/0000-0002-7809-6378

Funding

China Postdoctoral Science Foundation 2016M592142Natural Science Foundation of Shandong Province ZR2021MH138
6 · The paper itself

Abstract

Tumor-infiltrating lymphocyte (TIL) therapy in adoptive T-cell therapy (ACT) has already caused durable regression in a variety of cancer types due to T-cell persistence, clinical activity, and duration of objective response and safety. TILs are composed of polyclonal effector T-cells specific to heterogenetic tumor antigens, reasonably providing a promising means for tumor therapy. In addition, their expansion in vitro can release them from the suppressive tumor microenvironment. Even though significant advances have been made in the procedure of TIL therapy, from TIL isolation, modification, expansion, and infusion back to the patient to target the tumor, strategy optimization is always ongoing to overcome drawbacks such as a complex process, options for the lineage differentiation status of TILs, and sufficient trafficking of TILs to the tumor. In this review, we summarize the current advances of TIL therapy, raise problem-based optimization strategies, and provide future perspectives on next-generation TIL therapy as a potential avenue for enhancing cell-based immunotherapy.

Indexed as

Adoptive cell therapy (ACT)ImmunotherapyT-cellsTumor infiltrating lymphocyte (TIL)Tumor treatment

Identifiers

PMID39514075
PMCPMC11549075

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.