Evidence map›Paper›PMID 38923327›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Manipulating the Crosstalk between Cancer and Immunosuppressive Cells with Phototherapeutic Gold-Nanohut for Reprogramming Tumor Microenvironment.

Hung-Wei Cheng, Wei Lee, Fei-Ting Hsu, Yen-Ho Lai, Shu-Rou Huang, Chris Seh Hong Lim, Zhen-Kai Lin, Shih-Chao Hsu, Chih-Sheng Chiang, Long-Bin Jeng and 2 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
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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

12 authors.

Hung-Wei ChengDepartment of Materials Science and Engineering, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.
Wei LeeCell Therapy Center, China Medical University Hospital, Taichung, 40447, Taiwan.
Fei-Ting HsuDepartment of Biological Science and Technology, China Medical University, Taichung, 406040, Taiwan.
Yen-Ho LaiCell Therapy Center, China Medical University Hospital, Taichung, 40447, Taiwan.
Shu-Rou HuangTranslational Medicine Research Center, New Drug development Center and Department of Neurology, China Medical University Hospital, Taichung, 40447, Taiwan.
Chris Seh Hong LimDepartment of Physician Assistant Studies, School of Health and Rehabilitation Sciences, MGH Institute, Boston, Massachusetts, 02114, USA.
Zhen-Kai LinDepartment of Materials Science and Engineering, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.
Shih-Chao HsuDepartment of Surgery, China Medical University Hospital, Taichung, 40447, Taiwan.
Chih-Sheng ChiangCell Therapy Center, China Medical University Hospital, Taichung, 40447, Taiwan.ORCID 0000-0002-4865-9395
Long-Bin JengCell Therapy Center, China Medical University Hospital, Taichung, 40447, Taiwan.
Woei-Cherng ShyuTranslational Medicine Research Center, New Drug development Center and Department of Neurology, China Medical University Hospital, Taichung, 40447, Taiwan.
San-Yuan ChenDepartment of Materials Science and Engineering, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.ORCID 0000-0002-6500-2993

Funding

China Medical University CMU104-S-10China Medical University CMU104-S-15-03China Medical University CMU111-MF-56China Medical University CMU111-N-03China Medical University and Hospital DMR-110-182National Science and Technology Council MOST 110-2314-B39-043-MY3National Science and Technology Council MOST 111-2221-E-A49-112-MY3National Science and Technology Council MOST 111-2314-B-039-009-MY3National Science and Technology Council MOST 111-2314-B-A49-051-MY3National Science and Technology Council MOST 111-2823-8-039-002National Science and Technology Council NSTC 112-2823-8-039-003National Yang Ming Chiao Tung University NYCU-KMU-113-I001
6 · The paper itself

Abstract

Photoimmunotherapy faces challenges due to insufficient intratumoral accumulation of photothermal agents and the reversion of the cancer-immunity cycle during treatment. In this study, an anti-PD-L1-immobilized magnetic gold nanohut, AuNH-2-Ab, with photoresponsive, thermosensitive, and immunomodulatory properties to effectively suppress the growth of primary tumors, elevate immunogenic cell death (ICD) levels, reverse the tumor immune microenvironment (TIME), and consequently inhibit metastases are developed. AuNH-2-Ab achieves high tumor accumulation (9.54% injected dose) following systemic administration, allowing the modulation of hyperthermia dose of over 50 °C in the tumor. By optimizing the hyperthermia dose, AuNH-2-Ab simultaneously target and eliminate cancer cells and tumor-associated macrophages, thereby activating potent antitumor immunity without being compromised by immunosuppressive elements. Hyperthermia/pH induced morphological transformation of AuNH-2-Ab involving the detachment of the surface antibody for in situ PD-L1 inhibition, and exposure of the inner fucoidan layer for natural killer (NK) cell activation. This precision photoimmunotherapy approach reprograms the TIME, significantly prolongs survival in a murine hepatocellular carcinoma model (Hep55.1c), and harnesses the synergistic effects of ICD production and checkpoint inhibitors by utilizing a single nanoplatform.

Indexed as

GoldImmunosuppression TherapyMetal NanoparticlesNeoplasmsPhototherapyTumor MicroenvironmentAnimalsB7-H1 AntigenCell Line, TumorImmunogenic Cell DeathMaleMice, Inbred C57BLTemperatureB7-H1 AntigenGoldcheckpoint immunotherapymagnetic navigationphotoimmunotherapytumor immune microenvironment

Identifiers

PMID38923327
PMCPMC11348132

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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.