Evidence mapPaperPMID 41807467Full record

ArticleNature communications2026

A hierarchical theranostic nanoagent for multimodal imaging and targeted foam cell intervention in atherosclerosis.

Jianwen Song, Xiaoying Kang, Shuxuan Yang, Xue Meng, Zihang Shi, Wen Li, Ji Qi

Abstract read
In one paragraph

Article in Nature communications, 2026. 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

7 authors.

Jianwen Song *State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, and Academy for Advanced Interdisciplinary Studies, Nankai University, Tianjin, China.
Xiaoying Kang *State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, and Academy for Advanced Interdisciplinary Studies, Nankai University, Tianjin, China.
Shuxuan YangState Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, and Academy for Advanced Interdisciplinary Studies, Nankai University, Tianjin, China.
Xue MengState Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, and Academy for Advanced Interdisciplinary Studies, Nankai University, Tianjin, China.
Zihang ShiState Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, and Academy for Advanced Interdisciplinary Studies, Nankai University, Tianjin, China.
Wen LiState Key Laboratory of Advanced Medical Materials and Devices, Tianjin Key Laboratory of Biomedical Materials, Key Laboratory of Biomaterials and Nanotechnology for Cancer Immunotherapy, Institute of Biomedical Engineering, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China. liwen@bme.pumc.edu.cn.ORCID http://orcid.org/0000-0001-6783-1464
Ji QiState Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, and Academy for Advanced Interdisciplinary Studies, Nankai University, Tianjin, China. qiji@nankai.edu.cn.ORCID http://orcid.org/0000-0001-7597-9725

Funding

National Science Foundation of China | National Natural Science Foundation of China-Yunnan Joint Fund (NSFC-Yunnan Joint Fund) 32471462National Science Foundation of China | National Natural Science Foundation of China-Yunnan Joint Fund (NSFC-Yunnan Joint Fund) 82172081
6 · The paper itself

Abstract

Atherosclerosis (AS) is a leading cause of cardiovascular and cerebrovascular disease and is driven by lipid accumulation and chronic inflammation within arterial plaques. Foam cells play a central role in plaque growth and destabilization, yet their precise diagnosis and targeted regulation remain challenging. Here we present a hierarchical nanoagent that integrates multimodal imaging with selective foam cell intervention for improved AS management. The molecular probe enables near-infrared II fluorescence, photoacoustic, and magnetic resonance imaging, providing complementary information on plaque location, depth, and morphology. To achieve targeted therapy, the probe is co-encapsulated with atorvastatin using responsive nanocarriers camouflaged with macrophage membranes and equipped with a foam cell-targeting peptide. This hierarchical strategy enables precise targeting to inflamed plaques and foam cells, where controlled drug release promotes lipid efflux, reduces inflammatory signaling, and enhances plaque stabilization in female AS mouse models. This integrated imaging-guided therapeutic platform holds great promise for precise diagnosis and treatment of cardiovascular disease.

Indexed as

AtherosclerosisFoam CellsMultimodal ImagingTheranostic NanomedicineAnimalsAtorvastatinDisease Models, AnimalFemaleHumansMacrophagesMagnetic Resonance ImagingMiceNanoparticlesPhotoacoustic TechniquesPlaque, AtheroscleroticAtorvastatin

Identifiers

PMID41807467
PMCPMC13111603

What Socratic 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 Socratic graph.