Evidence map›Paper›PMID 40616101›Full record

ArticleCell communication and signaling : CCS2025

Enhanced immunotherapy response in lung adenocarcinoma patients with COPD: insights into tumor cells and immune microenvironment characteristics.

Yuji Huang, Boxuan Liang, Xuewei Chen, Zhiming Li, Yanhong Deng, Jiaxin Du, Yizhou Zhong, Xi Lin, Junjun Fu, Jieyu Xie and 2 more

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2025. 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

12 authors.

Yuji Huang *Department of Cardiovascular Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China.
Boxuan Liang *NMPA Key Laboratory for Safety Evaluation of Cosmetics, Guangdong Provincial Key Laboratory of Tropical Disease Research, Department of Toxicology, School of Public Health, Southern Medical University, Guangzhou, 510515, China.
Xuewei Chen *State Key Laboratory of Respiratory Disease & National Clinical Research Center for Respiratory Disease, Department of Thoracic Surgery and Oncology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510120, China.
Zhiming LiNMPA Key Laboratory for Safety Evaluation of Cosmetics, Guangdong Provincial Key Laboratory of Tropical Disease Research, Department of Toxicology, School of Public Health, Southern Medical University, Guangzhou, 510515, China.
Yanhong DengNMPA Key Laboratory for Safety Evaluation of Cosmetics, Guangdong Provincial Key Laboratory of Tropical Disease Research, Department of Toxicology, School of Public Health, Southern Medical University, Guangzhou, 510515, China.
Jiaxin DuNMPA Key Laboratory for Safety Evaluation of Cosmetics, Guangdong Provincial Key Laboratory of Tropical Disease Research, Department of Toxicology, School of Public Health, Southern Medical University, Guangzhou, 510515, China.
Yizhou ZhongDepartment of Cardiovascular Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China.
Xi LinNMPA Key Laboratory for Safety Evaluation of Cosmetics, Guangdong Provincial Key Laboratory of Tropical Disease Research, Department of Toxicology, School of Public Health, Southern Medical University, Guangzhou, 510515, China.
Junjun FuState Key Laboratory of Respiratory Disease & National Clinical Research Center for Respiratory Disease, Department of Thoracic Surgery and Oncology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510120, China.
Jieyu XieState Key Laboratory of Respiratory Disease & National Clinical Research Center for Respiratory Disease, Department of Thoracic Surgery and Oncology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510120, China.
Xin ZhangState Key Laboratory of Respiratory Disease & National Clinical Research Center for Respiratory Disease, Department of Thoracic Surgery and Oncology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510120, China. zhangxinpost@139.com.
Zhenlie HuangDepartment of Cardiovascular Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China. huangzhenlie858252@smu.edu.cn.

Funding

Guangdong-Dongguan Joint grant 2022A1515111098Guangzhou Municipal Health Commission Project 2023C-TS17the Chinese Postdoctoral Science Foundation 2022M721486the GDMPA Project of Scientific and Technological Innovation 2024ZDZ09the Guangdong Basic Applied Basic Research Foundation 2022A1515010610the Guangdong Provincial Key Laboratory of Tropical Disease Research 2017B030314035the National Natural Science Foundation of China 82273656the Open Project of State Key Laboratory of Respiratory Disease SKLRD-OP-202005the Science and Technology Project of Guangdong Province, China 2022A0505050035
6 · The paper itself

Abstract

backgroundLung cancer and chronic obstructive pulmonary disease (COPD) are major global health challenges, and their coexistence in patients presents unique clinical complexities. Interestingly, patients with both lung adenocarcinoma (LUAD) and COPD show reduced responses to conventional chemotherapy and targeted therapies but demonstrate enhanced sensitivity to immunotherapy.

methodsWe investigated this phenomenon using a cohort of 248 LUAD patients undergoing immunotherapy. Single-cell transcriptomic analysis was performed on 187,123 cells from tumor samples, adjacent normal tissues, and peripheral blood mononuclear cells from six treatment-naïve LUAD patients—three with COPD and three without. To further validate these findings, we conducted multiplex fluorescent immunohistochemical (mfIHC) analysis on 34 additional treatment-naïve LUAD patients and analyzed an independent cohort of 65 LUAD patients undergoing immunotherapy.

resultsWe found that COPD-associated LUAD tumors exhibited distinctive features, including elevated expression of human leukocyte antigen I (HLA-I) on malignant cells and a less aggressive tumor phenotype. The immune microenvironment in these tumors was more active, with increased infiltration of NK cells, effector CD4+ T cells, and effector CD8+ T cells. Additionally, we observed higher numbers of exhausted C-X-C motif chemokine ligand 13+ CD8+ T cells and mature dendritic cells enriched in immunoregulatory molecules expressing immune checkpoint genes. These findings were confirmed in both the mfIHC cohort and the independent immunotherapy cohort, where we observed that COPD-related features correlated with improved responses to immunotherapy.

conclusionOur study reveals that COPD leads to elevated HLA-I expression and a more active immune microenvironment in LUAD tumors, characterized by enhanced cytotoxic immune cell infiltration and a shift towards immunoregulatory profiles. These features correlate with improved immunotherapy responses, highlighting the potential for optimizing treatment strategies in LUAD patients with COPD.

Indexed as

Adenocarcinoma of LungImmunotherapyLung NeoplasmsPulmonary Disease, Chronic ObstructiveTumor MicroenvironmentAgedFemaleHumansMaleMiddle AgedC-X-C motif chemokine ligand 13Human leukocyte antigen ILung cancerMalignant cellsObstructive lung diseaseTumor immune microenvironment

Identifiers

PMID40616101
PMCPMC12232029

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.