Evidence map›Paper›PMID 38515751›Full record

ArticleFrontiers in immunology2024

CD81 and CD82 expressing tumor-infiltrating lymphocytes in the NSCLC tumor microenvironment play a crucial role in T-cell activation and cytokine production.

Kwangmin Na, Seul Lee, Dong Kwon Kim, Young Seob Kim, Joon Yeon Hwang, Seong-San Kang, Sujeong Baek, Chai Young Lee, Seung Min Yang, Yu Jin Han and 11 more

Open access · goldAbstract 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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. CD82-associated exhausted CD8Frontiers in immunology · 2025
    Article
  10. 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

21 authors at 3 institutions in 1 country.

Kwangmin Na *Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Seul Lee *Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Dong Kwon KimSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Young Seob KimYonsei New Il Han Institute for Integrative Lung Cancer Research, Yonsei University College of Medicine, Seoul, Republic of Korea.
Joon Yeon HwangSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Seong-San KangJEUK Institute for Cancer Research, JEUK Co., Ltd., Gumi-City, Republic of Korea.
Sujeong BaekSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Chai Young LeeSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Seung Min YangSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Yu Jin HanSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Mi Hyun KimSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Heekyung HanSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Youngtaek KimSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jae Hwan KimSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Seunghyun JeonSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Youngseon ByeonYonsei New Il Han Institute for Integrative Lung Cancer Research, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jii Bum LeeDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
Sun Min LimDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
Min Hee HongDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
Kyoung-Ho PyoSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Byoung Chul ChoYonsei New Il Han Institute for Integrative Lung Cancer Research, Yonsei University College of Medicine, Seoul, Republic of Korea.
Yonsei University · KRSeverance Hospital · KRJeuk (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: To understand the immune system within the tumor microenvironment (TME) of non-small cell lung cancer (NSCLC), it is crucial to elucidate the characteristics of molecules associated with T cell activation. Methods: We conducted an in-depth analysis using single-cell RNA sequencing data obtained from tissue samples of 19 NSCLC patients. T cells were classified based on the Tumor Proportion Score (TPS) within the tumor region, and molecular markers associated with activation and exhaustion were analyzed in T cells from high TPS areas. Results: Notably, tetraspanins CD81 and CD82, belonging to the tetraspanin protein family, were found to be expressed in activated T cells, particularly in cytotoxic T cells. These tetraspanins showed strong correlations with activation and exhaustion markers. Discussion: These findings highlight the multifaceted roles of CD81 and CD82 in T cell activation, cytokine production, memory subset accumulation, and target cell cytolysis. Therefore, these findings suggest the potential of CD81 and CD82 as promising candidates for co-stimulatory molecules in immune therapeutic strategies for cancer treatment within the intricate TME.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAntigens, CDCytokinesHumansInterleukin-2Kangai-1 ProteinLymphocytes, Tumor-InfiltratingTetraspanin 28TetraspaninsTumor MicroenvironmentAntigens, CDCD81 protein, humanCD82 protein, humanCytokinesInterleukin-2Kangai-1 ProteinTetraspanin 28Tetraspaninscell therapyimmunotherapytetraspaninsT lymphocytetumor-infiltrating lymphocyte

Identifiers

PMID38515751
PMCPMC10954780
OpenAlexW4392559496

What OpenQuestion holds

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Registered trials

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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.