Evidence map›Paper›PMID 35961291›Full record

ArticleNanotechnology2022

Intravital optical imaging for immune cell tracking after photoimmunotherapy with plasmonic gold nanostars.

Ericka Chorniak, Yang Liu, Ren Odion, Wiguins Etienne, Aidan Canning, Smita K Nair, Paolo Maccarini, Gregory M Palmer, Brant A Inman, Tuan Vo-Dinh

Open access · greenAbstract read
In one paragraph

Article in Nanotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

10 authors at 2 institutions in 1 country.

Ericka ChorniakDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, United States of America.
Yang LiuDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, United States of America.
Ren OdionDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, United States of America.ORCID 0000-0002-8290-3865
Wiguins EtienneDivision of Urology, Duke University Medical Center, Durham, NC 27710, United States of America.
Aidan CanningDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, United States of America.
Smita K NairDepartment of Surgery, Duke University Medical Center, Durham, NC 27710, United States of America.
Paolo MaccariniFitzpatrick Institute of Photonics, Duke University, Durham, NC 27708, United States of America.
Gregory M PalmerDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, United States of America.
Brant A InmanFitzpatrick Institute of Photonics, Duke University, Durham, NC 27708, United States of America.
Tuan Vo-DinhDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, United States of America.ORCID 0000-0003-3701-3326
Duke University · USDuke Medical Center · US

Funding

Plasmonic nanoparticle-mediated immunotherapy to treat metastatic cancerR01EB028078 · NIBIB · DUKE UNIVERSITY · PI VO-DINH, TUAN · 2019 to 2022
$2.1M
NIBIB NIH HHS R01 EB028078
6 · The paper itself

Abstract

Bladder cancer has been ranked as one of the most commonly occurring cancers in men and women with approximately half of the diagnoses being the late stage and/or metastatic diseases. We have developed a novel cancer treatment by combining gold nanostar-mediated photothermal therapy with checkpoint inhibitor immunotherapy to treat bladder cancer. Experiment results with a murine animal model demonstrated that our developed photoimmunotherapy therapy is more efficacious than any individual studied treatment. In addition, we used intravital optical imaging with a dorsal skinfold window chamber animal model to study immune responses and immune cell accumulation in a distant tumor following our photoimmunotherapy. The mice used have the CX3CR1-GFP receptor on monocytes, natural killer cells, and dendritic cells allowing us to dynamically track their presence by fluorescence imaging. Our proof-of-principle study results showed that the photoimmunotherapy triggered anti-cancer immune responses to generate anti-cancer immune cells which accumulate in metastatic tumors. Our study results illustrate that intravital optical imaging is an efficient and versatile tool to investigate immune responses and mechanisms of photoimmunotherapy in future studies.

Indexed as

GoldUrinary Bladder NeoplasmsAnimalsCell TrackingImmunotherapyMiceOptical ImagingPhototherapyGoldgold nanostars (GNS)immune cell trackingimmune responseintravital optical imagingphotoimmunotherapy

Identifiers

PMID35961291
PMCPMC9725032
OpenAlexW4290964314

What OpenQuestion holds

Textmetadata
LicenceTDM
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.