Evidence map›Paper›PMID 38424167›Full record

ArticleBritish journal of cancer2024

Single-cell RNA sequencing reveals myeloid and T cell co-stimulation mediated by IL-7 anti-cancer immunotherapy.

Hye Hyeon Eum, Dasom Jeong, Nayoung Kim, Areum Jo, Minsu Na, Huiram Kang, Yourae Hong, Jin-Sun Kong, Gi Heon Jeong, Seung-Ah Yoo and 1 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

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

11 authors at 2 institutions in 2 countries.

Hye Hyeon Eum *Department of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.ORCID 0000-0002-8081-4121
Dasom Jeong *Department of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Nayoung Kim *Department of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.ORCID 0000-0003-3202-750X
Areum JoDepartment of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.ORCID 0000-0001-7815-8439
Minsu NaDepartment of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Huiram KangDepartment of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Yourae HongDigestive Oncology, Department of Oncology, Katholieke Universiteit Leuven, Leuven, Belgium.
Jin-Sun KongDepartment of Biomedicine and Health Sciences, Graduate School, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Gi Heon JeongDepartment of Biomedicine and Health Sciences, Graduate School, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Seung-Ah YooDepartment of Biomedicine and Health Sciences, Graduate School, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Hae-Ock LeeDepartment of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea. haeocklee@catholic.ac.kr.ORCID 0000-0001-5123-0322
Catholic University of Korea · KRKU Leuven · BE

Funding

National Research Foundation of Korea (NRF) NRF-2019M3A9B6064691
6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors unleash inhibitory signals on T cells conferred by tumors and surrounding stromal cells. Despite the clinical efficacy of checkpoint inhibitors, the lack of target expression and persistence of immunosuppressive cells limit the pervasive effectiveness of the therapy. These limitations may be overcome by alternative approaches that co-stimulate T cells and the immune microenvironment.

methodsWe analyzed single-cell RNA sequencing data from multiple human cancers and a mouse tumor transplant model to discover the pleiotropic expression of the Interleukin 7 (IL-7) receptor on T cells, macrophages, and dendritic cells.

resultsOur experiment on the mouse model demonstrated that recombinant IL-7 therapy induces tumor regression, expansion of effector CD8 T cells, and pro-inflammatory activation of macrophages. Moreover, spatial transcriptomic data support immunostimulatory interactions between macrophages and T cells.

conclusionThese results indicate that IL-7 therapy induces anti-tumor immunity by activating T cells and pro-inflammatory myeloid cells, which may have diverse therapeutic applicability.

Indexed as

Interleukin-7NeoplasmsAnimalsCD8-Positive T-LymphocytesHumansImmunotherapyMiceSequence Analysis, RNAT-LymphocytesTumor MicroenvironmentInterleukin-7

Identifiers

PMID38424167
PMCPMC11014989
OpenAlexW4392282837

What Socratic 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 Socratic graph.