Evidence map›Paper›PMID 39650651›Full record

ArticleFrontiers in immunology2024

Effect of hypoxia-induced mIL15 expression on expansion and memory progenitor stem-like TILs

Zhen Sun, Aotian Xu, Zhaojun Wu, Xiaohao Lan, Ganchen Gao, Bin Guo, Zhongjie Yu, Lin Shao, Hao Wu, Min Lv and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Zhen Sun *Department of Pathogenic Biology, School of Basic Medicine, Qingdao University, Qingdao, China.
Aotian Xu *Department of Research and Development, Qingdao Sino-Cell Biomed Co., Ltd., Qingdao, Shandong, China.
Zhaojun WuDepartment of Research and Development, Qingdao Sino-Cell Biomed Co., Ltd., Qingdao, Shandong, China.
Xiaohao LanDepartment of Research and Development, Qingdao Sino-Cell Biomed Co., Ltd., Qingdao, Shandong, China.
Ganchen GaoDepartment of Research and Development, Qingdao Sino-Cell Biomed Co., Ltd., Qingdao, Shandong, China.
Bin GuoDepartment of Research and Development, Qingdao Sino-Cell Biomed Co., Ltd., Qingdao, Shandong, China.
Zhongjie YuDepartment of Research and Development, Qingdao Sino-Cell Biomed Co., Ltd., Qingdao, Shandong, China.
Lin ShaoDepartment of Research and Development, Qingdao Sino-Cell Biomed Co., Ltd., Qingdao, Shandong, China.
Hao WuDepartment of Research and Development, Qingdao Sino-Cell Biomed Co., Ltd., Qingdao, Shandong, China.
Min LvDepartment of Research and Development, Qingdao Sino-Cell Biomed Co., Ltd., Qingdao, Shandong, China.
Yongjie WangDepartment of Thoracic Surgery, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Yi ZhaoDepartment of Research and Development, Qingdao Sino-Cell Biomed Co., Ltd., Qingdao, Shandong, China.
Bin WangDepartment of Pathogenic Biology, School of Basic Medicine, Qingdao University, Qingdao, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The adoptive cell transfer of tumor-infiltrating lymphocytes (TILs) has proven clinically beneficial in patients with non-small cell lung cancer refractory to checkpoint blockade immunotherapy, which has prompted interest in TIL-adoptive cell transfer. The transgenic expression of IL15 can promote the expansion, survival, and function of T cells Methods: Using TILs expanded from the tumor tissues of lung cancer patients, TILs with or without mIL15 expression (TIL-mIL15 or UN-TIL) were generated by lentiviral transduction. To reflect the advantages of mTIL15, the cells were divided into groups with IL2 (TIL-mIL15+IL2) or without IL2 (TIL-mIL15-IL2). Results: Compared to UN-TIL cells, mIL15 expression had a similar capacity for promoting TIL proliferation and maintaining cell viability. Our experimental findings indicate that, compared to UN-TIL and TIL-mIL15+IL2 cells, the expression of mIL15 in TIL-mIL15-IL2 cells promoted the formation of stem-like TILs (CD8 Discussion: This study demonstrates the superior persistence of TIL-mIL15-IL2 cells, which may serve as a novel treatment strategy for lung cancer patients.

Indexed as

Interleukin-15Lung NeoplasmsLymphocytes, Tumor-InfiltratingCarcinoma, Non-Small-Cell LungCell HypoxiaCell ProliferationHumansImmunologic MemoryImmunotherapy, AdoptiveMemory T CellsTumor MicroenvironmentInterleukin-15adoptive cell transferexpansionhypoxia regulationimmunotherapylung cancermembrane-bound interleukin 15tumor-infiltrating lymphocytes

Identifiers

PMID39650651
PMCPMC11621077

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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.