Evidence map›Paper›PMID 41668092›Full record

ArticleCell communication and signaling : CCS2026

Extracellular vesicle-associated PD-L1 induces CD4

Junhong Huang, Yuanyuan Xia, Yingqin Zhang, Chunmei Zhang, Zhizai Chen, Xun Hou, Zheng Wang, Bei Hu, Hongke Zeng, Xin Li and 2 more

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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.

Junhong Huang *Emergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China.
Yuanyuan Xia *Department of Oncology, Key Laboratory of Biological Targeting Diagnosis, Therapy and Rehabilitation of Guangdong Higher Education Institutes, The Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, 510700, China.
Yingqin Zhang *Emergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China.
Chunmei ZhangEmergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China.
Zhizai ChenEmergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China.
Xun HouEmergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China.
Zheng WangEmergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China.
Bei HuEmergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China.
Hongke ZengEmergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China.
Xin LiEmergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China. xlidoct@qq.com.
Yuelin ZhangEmergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China. zhangyuelin1999@163.com.
Wenqiang JiangEmergency Intensive Care Unit, Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, 106 Zhongshan Er Road, Guangzhou, Guangdong, 510080, China. jiangwenqiang@gdph.org.cn.

Funding

the China International Medical Foundation-Clinical Development Z-2018-31-2102-2the National key research and development program intergovernmental key projects 2023YFE0114300the Natural Science Foundation for Distinguished Scholars of Guangdong Province 20022B1515020104the Natural Science Foundation of Guangdong 2022A1515012428Zhongnanshan Medical Foundation of Guangdong province ZNSXS-20240052
6 · The paper itself

Abstract

backgroundThe upregulation of PD-1 on T lymphocytes is one of the key mechanisms driving sepsis-induced immunosuppression. Nevertheless although it is known that PD-L1 on antigen-presenting cells acts as a ligand for PD-1 on T lymphocytes, it remains to be determined whether extracellular vesicle-associated PD-L1 also serves as its ligand.

methodsPlasma extracellular vesicles (EVs) were isolated via ultracentrifugation. We evaluated the relationship of EV-associated PD-L1 level to immune function and prognosis in septic patients. Additionally, we observed the effect of EV-associated PD-L1 on the proliferation and immune function of co-cultured CD4+ T cells in vitro. We further verified the role of EV-associated PD-L1 by knocking down PD-L1 in a mouse model.

resultsThe peripheral circulating EV levels were significantly increased in septic patients compared with healthy volunteers. Enhanced PD-L1 protein content on these EVs was evident in septic patients, particularly in those exhibiting adverse prognostic features and pronounced immunosuppression. EVs secreted by LPS-stimulated monocytes were enriched with more PD-L1 than monocytes alone. Co-culture of CD4+ T cells with sepsis-derived EVs significantly downregulated the expression of CD69, IFN-γ and cell viability but upregulated the level of IL-4 and TGF-β. This was accompanied by heightened PD-1 expression and an increased Tregs/CD4+ T cell ratio. Conversely, this effect was partially reversed by inhibition of EV production or knockout of PD-L1 in EVs. Compared with LPS-treated EVs, PD-L1 knockout LPS-treated EVs alleviated the immunosuppressive state in CLP mice.

conclusionThe elevated level of circulating EV-associated PD-L1 was closely associated with poor prognosis and immunosuppression in septic patients. EV-associated PD-L1 engaged CD4+ T cells to induce CD4+ T cell dysfunction and may be one of the key mechanisms inducing immunosuppression in sepsis.

Indexed as

B7-H1 AntigenCD4-Positive T-LymphocytesExtracellular VesiclesImmune ToleranceImmunosuppression TherapySepsisAnimalsCoculture TechniquesFemaleHumansMaleMiceMice, Inbred C57BLB7-H1 AntigenCD274 protein, humanExtracellular vesiclesImmunosuppressionPD-L1SepsisT lymphocyte

Identifiers

PMID41668092
PMCPMC12990564

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.