Evidence map›Paper›PMID 38818122›Full record

ArticleBioengineering & translational medicine2024

Photothermal Prussian blue nanoparticles generate potent multi-targeted tumor-specific T cells as an adoptive cell therapy.

Elizabeth E Sweeney, Palak Sekhri, Nethaji Muniraj, Jie Chen, Sally Feng, Joshua Terao, Samantha J Chin, Danielle E Schmidt, Catherine M Bollard, Conrad Russell Y Cruz and 1 more

Abstract read
In one paragraph

Article in Bioengineering & translational medicine, 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. Article
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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

11 authors.

Elizabeth E SweeneyDepartment of Biochemistry & Molecular Medicine, School of Medicine and Health Sciences George Washington University Washington District of Columbia USA.
Palak SekhriCenter for Cancer and Immunology Research Children's National Hospital Washington District of Columbia USA.
Nethaji MunirajThe Integrated Biomedical Sciences Program, School of Medicine and Health Sciences George Washington University Washington District of Columbia USA.
Jie ChenCenter for Cancer and Immunology Research Children's National Hospital Washington District of Columbia USA.
Sally FengCenter for Cancer and Immunology Research Children's National Hospital Washington District of Columbia USA.
Joshua TeraoThe Integrated Biomedical Sciences Program, School of Medicine and Health Sciences George Washington University Washington District of Columbia USA.
Samantha J ChinCenter for Cancer and Immunology Research Children's National Hospital Washington District of Columbia USA.
Danielle E SchmidtCenter for Cancer and Immunology Research Children's National Hospital Washington District of Columbia USA.
Catherine M BollardCenter for Cancer and Immunology Research Children's National Hospital Washington District of Columbia USA.
Conrad Russell Y CruzCenter for Cancer and Immunology Research Children's National Hospital Washington District of Columbia USA.
Rohan FernandesCenter for Cancer and Immunology Research Children's National Hospital Washington District of Columbia USA.ORCID https://orcid.org/0000-0001-9439-4626

Funding

Engineered Ensemble Nanoimmunotherapies for CancerR37CA226171 · NCI · GEORGE WASHINGTON UNIVERSITY · PI FERNANDES, ROHAN · 2019 to 2024
$2.6M
NCI NIH HHS R37 CA226171
6 · The paper itself

Abstract

Prussian blue nanoparticle-based photothermal therapy (PBNP-PTT) is an effective tumor treatment capable of eliciting an antitumor immune response. Motivated by the ability of PBNP-PTT to potentiate endogenous immune responses, we recently demonstrated that PBNP-PTT could be used ex vivo to generate tumor-specific T cells against glioblastoma (GBM) cell lines as an adoptive T cell therapy (ATCT). In this study, we further developed this promising T cell development platform. First, we assessed the phenotype and function of T cells generated using PBNP-PTT. We observed that PBNP-PTT facilitated CD8+ T cell expansion from healthy donor PBMCs that secreted IFNγ and TNFα and upregulated CD107a in response to engagement with target U87 cells, suggesting specific antitumor T cell activation and degranulation. Further, CD8+ effector and effector memory T cell populations significantly expanded after co-culture with U87 cells, consistent with tumor-specific effector responses. In orthotopically implanted U87 GBM tumors in vivo, PBNP-PTT-derived T cells effectively reduced U87 tumor growth and generated long-term survival in >80% of tumor-bearing mice by Day 100, compared to 0% of mice treated with PBS, non-specific T cells, or T cells expanded from lysed U87 cells, demonstrating an enhanced antitumor efficacy of this ATCT platform. Finally, we tested the generalizability of our approach by generating T cells targeting medulloblastoma (D556), breast cancer (MDA-MB-231), neuroblastoma (SH-SY5Y), and acute monocytic leukemia (THP-1) cell lines. The resulting T cells secreted IFNγ and exerted increased tumor-specific cytolytic function relative to controls, demonstrating the versatility of PBNP-PTT in generating tumor-specific T cells for ATCT.

Indexed as

adoptive T cell therapycancerhematological malignanciesphotothermal therapyPrussian blue nanoparticlessolid tumorstumor‐specific T cells

Identifiers

PMID38818122
PMCPMC11135148

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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.