Evidence map›Paper›PMID 37228440›Full record

ArticleNano research2023

Aerosolized immunotherapeutic nanoparticle inhalation potentiates PD-L1 blockade for locally advanced lung cancer.

Yang Liu, William N Crowe, Lulu Wang, W Jeffrey Petty, Amyn A Habib, Dawen Zhao

Open access · greenAbstract read
In one paragraph

Article in Nano research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Yang LiuDepartment of Biomedical Engineering, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
William N CroweDepartment of Biomedical Engineering, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Lulu WangDepartment of Biomedical Engineering, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
W Jeffrey PettyDepartment of Medicine, Section on Hematology and Oncology, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Amyn A HabibDepartment of Neurology, University of Texas Southwestern Medical Center and VA North Texas Medical Center, Dallas, TX 75390, USA.
Dawen ZhaoDepartment of Biomedical Engineering, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Wake Forest University · USThe University of Texas Southwestern Medical Center · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Intrapleural immunotherapeutic nanoparticles for MPE treatmentR01CA264102 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG, ZHAO, DAWEN · 2021 to 2025
$2.3M
The role of Nrf2 in mediating resistance to EGFR inhibition in glioblastomaR01CA244212 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HABIB, AMYN · 2020 to 2024
$1.9M
BLRD VA I01 BX002559NCI NIH HHS P30 CA012197NCI NIH HHS R01 CA244212NCI NIH HHS R01 CA264102
6 · The paper itself

Abstract

Despite therapeutic advancements, the prognosis of locally advanced non-small cell lung cancer (LANSCLC), which has invaded multiple lobes or the other lung and intrapulmonary lymph nodes, remains poor. The emergence of immunotherapy with immune checkpoint blockade (ICB) is transforming cancer treatment. However, only a fraction of lung cancer patients benefit from ICB. Significant clinical evidence suggests that the proinflammatory tumor microenvironment (TME) and programmed death-ligand 1 (PD-L1) expression correlate positively with response to the PD-1/PD-L1 blockade. We report here a liposomal nanoparticle loaded with cyclic dinucleotide and aerosolized (AeroNP-CDN) for inhalation delivery to deep-seated lung tumors and target CDN to activate stimulators of interferon (IFN) genes in macrophages and dendritic cells (DCs). Using a mouse model that recapitulates the clinical LANSCLC, we show that AeroNP-CDN efficiently mitigates the immunosuppressive TME by reprogramming tumor-associated macrophage from the M2 to M1 phenotype, activating DCs for effective tumor antigen presentation and increasing tumor-infiltrating CD8

Indexed as

aerosol inhalationlocally advanced non-small cell lung cancer (LANSCLC)nanoparticle immunotherapeuticprogrammed death 1/programmed death-ligand 1 (PD-1/PD-L1) blockadestimulator of interferon genes

Identifiers

PMID37228440
PMCPMC10208391
OpenAlexW4313400350

What OpenQuestion holds

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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.