Evidence map›Paper›PMID 41605536›Full record

ReviewEuropean respiratory review : an official journal of the European Respiratory Society2026

The dual promise of extracellular vesicles in lung diseases: towards reliable biomarkers and drug delivery vectors.

Vanitha Sampath, Carmela Pablo-Torres, Faria Khan, Olivia A Kline, Quan Lu, Adam L Haber, Kari C Nadeau, Ronald Allan Panganiban, Jin-Ah Park

Abstract readReview
In one paragraph

Review in European respiratory review : an official journal of the European Respiratory Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Vanitha SampathDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Carmela Pablo-TorresDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Faria KhanDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.ORCID 0000-0001-6539-888X
Olivia A KlineDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Quan LuDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Adam L HaberDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Kari C NadeauDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Ronald Allan PanganibanDivisions of Asthma Research and Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.ORCID 0000-0003-0894-1318
Jin-Ah ParkDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA jpark@hsph.harvard.edu.ORCID 0000-0002-8930-9287

Funding

Treatment of Peanut Allergy with Intradermal Administration of ASP0892 (ARA-LAMP-vax): A Randomized, Double-Blind, Placebo-Controlled, Phase I/II StudyUM2AI130836 · NIAID · JOHNS HOPKINS UNIVERSITY · PI WOOD, ROBERT A · 2017 to 2023
$62.1M
Translational Research Support CoreP30ES000002 · NIEHS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI JAIME ELIZABETH HART · 1985 to 2026
$44.6M
The effects of immune-age on immune-response and the molecular mechanisms which drive itP01AI153559 · NIAID · STANFORD UNIVERSITY · PI DAVIS, MARK MORRIS · 2021 to 2025
$17.8M
Vaccination and infection: indicators of immunological health and responsivenessU19AI090019 · NIAID · STANFORD UNIVERSITY · PI DAVIS, MARK MORRIS · 2010 to 2015
$17.3M
Training Program in Molecular and Integrative Physiological SciencesT32HL007118 · NHLBI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI LU, QUAN · 1985 to 2025
$14.3M
Systems biological assessment of T cell responses to vaccinationU19AI167903 · NIAID · STANFORD UNIVERSITY · PI BALI PULENDRAN · 2022 to 2026
$13.2M
Project 3: T CellsU54CA260517 · NCI · STANFORD UNIVERSITY · PI WANG, TAIA · 2020 to 2024
$10.4M
Scientific Human Biomarker Exposure Monitoring Core (HEMC) for the Air pollution disrupts Inflammasome Regulation in HEart And Lung Total Health (AIRHEALTH) StudyP01HL152953 · NHLBI · STANFORD UNIVERSITY · PI JOHNSON, MARY · 2021 to 2025
$9.8M
Research ProjectP20TW013028 · FIC · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Christopher DeWeir Golden, Mary B Rice · 2024 to 2026
$4.8M
FUNCTIONAL ANALYSIS OF PATHOGENIC AND PROTECTIVE PEANUT ALLERGEN-SPECIFIC HUMAN ANTIBODIESR01AI125567 · NIAID · STANFORD UNIVERSITY · PI BOYD, SCOTT DEXTER · 2017 to 2022
$2.6M
Immune Tolerance Dysfunction in Pregnancy due to Ambient Air Pollution ExposureR01ES032253 · NIEHS · STANFORD UNIVERSITY · PI NADEAU, KARI C. · 2020 to 2024
$2.2M
T Cell Reagent Research for Monitoring T Cell in Food AllergyU01AI140498 · NIAID · STANFORD UNIVERSITY · PI NADEAU, KARI C. · 2018 to 2022
$1.8M
FIC NIH HHS P20 TW013028NCI NIH HHS U54 CA260517NHLBI NIH HHS P01 HL152953NHLBI NIH HHS T32 HL007118NIAID NIH HHS P01 AI153559NIAID NIH HHS R01 AI125567NIAID NIH HHS U01 AI140498NIAID NIH HHS U19 AI090019NIAID NIH HHS U19 AI167903NIAID NIH HHS UM2 AI130836NIEHS NIH HHS P30 ES000002NIEHS NIH HHS R01 ES032253
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are small, membrane-bound particles released by cells into the extracellular space. Once considered as cellular waste disposal organelles, EVs are now recognised as functional cellular components because they carry a variety of cargo biomolecules, including nucleic acids, proteins and lipids. EVs are constitutively released under homeostatic conditions, but their numbers increase and their cargo composition is altered under nonhomeostatic conditions, such as exposure to environmental pollutants, viral infections or disease states. Therefore, EVs are being actively explored as noninvasive biomarkers for many diseases, including lung diseases. In addition, EVs are key mediators of intercellular communication through the transfer of their cargo biomolecules from EV-releasing donor cells to recipient (target) cells through membrane fusion, endocytosis or receptor-ligand interactions. This intercellular communication between the cells positions EVs as novel drug delivery vectors because of their low immunogenicity, high biocompatibility and unique cargo compositions. While EV-based drugs have not yet been approved by regulatory authorities, numerous clinical trials are evaluating their use either as therapeutics or as delivery systems. In this review, we discuss EVs, with particular emphasis on recent advances in identifying reliable and sensitive biomarkers for lung diseases, and on their emerging role as targeted drug delivery systems.

Indexed as

Drug CarriersDrug Delivery SystemsExtracellular VesiclesLungLung DiseasesAnimalsBiomarkersCell CommunicationHumansBiomarkersDrug Carriers

Identifiers

PMID41605536
PMCPMC12848582

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.