Evidence map›Paper›PMID 39900923›Full record

ArticleNature communications2025

Plant-nanoparticles enhance anti-PD-L1 efficacy by shaping human commensal microbiota metabolites.

Yun Teng, Chao Luo, Xiaolan Qiu, Jingyao Mu, Mukesh K Sriwastva, Qingbo Xu, Minmin Liu, Xin Hu, Fangyi Xu, Lifeng Zhang and 10 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
–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

55 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

20 authors.

Yun Teng *Brown Cancer Center, University of Louisville School of Medicine, Louisville, USA. yun.teng@louisville.edu.ORCID 0000-0001-6428-2551
Chao Luo *Brown Cancer Center, University of Louisville School of Medicine, Louisville, USA.ORCID 0000-0002-6233-3287
Xiaolan Qiu *Brown Cancer Center, University of Louisville School of Medicine, Louisville, USA.
Jingyao MuBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA.
Mukesh K SriwastvaBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA.
Qingbo XuDepartment of Microbiology and Immunology, University of Louisville, Louisville, KY, USA.
Minmin LiuBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA.
Xin HuDepartment of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Fangyi XuBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA.
Lifeng ZhangBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA.
Juw Won ParkBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA.ORCID 0000-0002-4610-6893
Jae Yeon HwangBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA.ORCID 0000-0002-7247-0146
Maiying KongBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA.ORCID 0000-0002-7313-9084
Zhanxu LiuBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA.
Xiang ZhangDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY, USA.ORCID 0000-0003-1102-6313
Raobo XuDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY, USA.ORCID 0000-0002-7178-8961
Jun YanBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA.
Michael L MerchantKidney Disease Program and Clinical Proteomics Center, University of Louisville, Louisville, KY, USA.
Craig J McClainDepartment of Medicine, Division of Gastroenterology, Hepatology and Nutrition, University of Louisville School of Medicine, Louisville, KY, USA.ORCID 0000-0002-7219-8939
Huang-Ge ZhangBrown Cancer Center, University of Louisville School of Medicine, Louisville, USA. h0zhan17@louisville.edu.ORCID 0000-0001-9665-9202

Funding

WKU Lead Faculty AwardP20GM103436 · NIGMS · UNIVERSITY OF LOUISVILLE · PI ERIC C ROUCHKA · 2012 to 2026
$60.1M
Role of oxidized linoleic acid metabolites in the pathogenesis of alcoholic liver diseaseP20GM113226 · NIGMS · UNIVERSITY OF LOUISVILLE · PI BARVE, SHIRISH S · 2016 to 2025
$24.1M
The Role of Nutrition in the Development/Progression of Alcohol-Induced Organ InjuryP50AA024337 · NIAAA · UNIVERSITY OF LOUISVILLE · PI Xiang Zhang · 2016 to 2026
$17.9M
University of Louisville Center for Integrative Environmental Health SciencesP30ES030283 · NIEHS · UNIVERSITY OF LOUISVILLE · PI Amanda Jo LeBlanc · 2020 to 2026
$10.0M
Plant exosomes non-coding RNA-mediated anti-inflammatory mechanismsR01AT008617 · NCCIH · UNIVERSITY OF LOUISVILLE · PI HUANG-GE ZHANG · 2016 to 2026
$5.7M
BLRD VA I01 BX005254BLRD VA IK6 BX004199NCCIH NIH HHS R01 AT008617NIAAA NIH HHS P50 AA024337NIEHS NIH HHS P30 ES030283NIGMS NIH HHS P20 GM103436NIGMS NIH HHS P20 GM113226
6 · The paper itself

Abstract

Diet has emerged as a key impact factor for gut microbiota function. However, the complexity of dietary components makes it difficult to predict specific outcomes. Here we investigate the impact of plant-derived nanoparticles (PNP) on gut microbiota and metabolites in context of cancer immunotherapy with the humanized gnotobiotic mouse model. Specifically, we show that ginger-derived exosome-like nanoparticle (GELN) preferentially taken up by Lachnospiraceae and Lactobacillaceae mediated by digalactosyldiacylglycerol (DGDG) and glycine, respectively. We further demonstrate that GELN aly-miR159a-3p enhances anti-PD-L1 therapy in melanoma by inhibiting the expression of recipient bacterial phospholipase C (PLC) and increases the accumulation of docosahexaenoic acid (DHA). An increased level of circulating DHA inhibits PD-L1 expression in tumor cells by binding the PD-L1 promoter and subsequently prevents c-myc-initiated transcription of PD-L1. Colonization of germ-free male mice with gut bacteria from anti-PD-L1 non-responding patients supplemented with DHA enhances the efficacy of anti-PD-L1 therapy compared to controls. Our findings reveal a previously unknown mechanistic impact of PNP on human tumor immunotherapy by modulating gut bacterial metabolic pathways.

Indexed as

B7-H1 AntigenGastrointestinal MicrobiomeImmune Checkpoint InhibitorsNanoparticlesAnimalsCell Line, TumorDocosahexaenoic AcidsFemaleGerm-Free LifeHumansImmunotherapyMaleMelanomaMiceMicroRNAsB7-H1 AntigenCD274 protein, humanDocosahexaenoic AcidsImmune Checkpoint InhibitorsMicroRNAs

Identifiers

PMID39900923
PMCPMC11790884

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.