Evidence map›Paper›PMID 31424560›Full record

ArticlePhotochemistry and photobiology2020

Cancer Cell-targeted and Activatable Photoimmunotherapy Spares T Cells in a 3D Coculture Model.

Eric M Kercher, Shubhankar Nath, Imran Rizvi, Bryan Q Spring

Open access · greenAbstract read
In one paragraph

Article in Photochemistry and photobiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

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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

4 authors at 3 institutions in 1 country.

Eric M KercherTranslational Biophotonics Cluster, Northeastern University, Boston, MA.ORCID 0000-0002-4538-244X
Shubhankar NathWellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA.ORCID 0000-0001-5778-7615
Imran RizviJoint Department of Biomedical Engineering, University of North Carolina at Chapel Hill, North Carolina State University, Chapel Hill, NC.ORCID 0000-0001-9673-4700
Bryan Q SpringTranslational Biophotonics Cluster, Northeastern University, Boston, MA.
Northeastern University · USHarvard University · USUniversity of North Carolina at Chapel Hill · US

Funding

Small Molecule Enhancers of Photodynamic Therapy for Skin CancerP01CA084203 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Tayyaba Hasan · 2001 to 2026
$27.9M
Dual function theranostic constructs for photoacoustic guided surgery and photodynamic therapyR01CA231606 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA · 2019 to 2025
$3.1M
Ovarian Cancer PDT: Multi-intracellular targeting and Image-guided dosimetryR01CA160998 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA · 2011 to 2015
$2.0M
EXPERIMENTAL PHOTOIMMUNOTHERAPY OF OVARIAN CANCERR01AR040352 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA · 1992 to 2006
$1.6M
Targeted Photoactivatable Nanocells to Image and Treat Metastic Ovarian CancerRC1CA146337 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA · 2009 to 2010
$971k
Targeting Determinants of OvCa Metastases in Engineered 3D Microfluidic PlatformsR00CA175292 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RIZVI, IMRAN · 2016 to 2019
$746k
Online monitoring and image-guided treatment of chemoresistant micrometastasesK22CA181611 · NCI · NORTHEASTERN UNIVERSITY · PI SPRING, BRYAN QUILTY · 2015 to 2017
$559k
NCI NIH HHS K22 CA181611NCI NIH HHS P01 CA084203NCI NIH HHS R00 CA175292NCI NIH HHS R01 CA160998NCI NIH HHS R01 CA231606NCI NIH HHS RC1 CA146337NIAMS NIH HHS R01 AR040352NIH HHS R01AR40352
6 · The paper itself

Abstract

Photodynamic therapy (PDT) is an established therapeutic modality that uses nonionizing near-infrared light to activate photocytotoxicity of endogenous or exogenous photosensitizers (PSs). An ongoing avenue of cancer research involves leveraging PDT to stimulate antitumor immune responses; however, these effects appear to be best elicited in low-dose regimens that do not provide significant tumor reduction using conventional, nonspecific PSs. The loss of immune enhancement at higher PDT doses may arise in part from indiscriminate damage to local immune cell populations, including tumor-infiltrating T cells. We previously introduced "tumor-targeted, activatable photoimmunotherapy" (taPIT) using molecular-targeted and cell-activatable antibody-PS conjugates to realize precision tumor photodamage with microscale fidelity. Here, we investigate the immune cell sparing effect provided by taPIT in a 3D model of the tumor immune microenvironment. We report that high-dose taPIT spares 25% of the local immune cell population, five times more than the conventional PDT regimen, in a 3D coculture model incorporating epithelial ovarian cancer cells and T cells. These findings suggest that the enhanced selectivity of taPIT may be utilized to achieve local tumor reduction with sparing of intratumor effector immune cells that would otherwise be lost if treated with conventional PDT.

Indexed as

AnimalsCoculture TechniquesHumansImmunotherapyMiceNeoplasmsPhototherapyT-LymphocytesXenograft Model Antitumor Assays

Identifiers

PMID31424560
PMCPMC7028482
OpenAlexW2969961817

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.