Evidence map›Paper›PMID 21179470›Full record

ArticlePloS one2010

Photodynamic therapy of tumors can lead to development of systemic antigen-specific immune response.

Pawel Mroz, Angelika Szokalska, Mei X Wu, Michael R Hamblin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 5% 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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 138 citations in OpenAlex.

  1. TNF-β +252 A>G polymorphism and susceptibility to cancer.Journal of cancer research and clinical oncology · 2013
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  7. Enhancing antitumour immunity with photodynamic therapy.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2025
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13 more citing papers are in PubMed but not listed here.

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 2 countries.

Pawel MrozWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Angelika Szokalska
Mei X Wu
Michael R Hamblin
Harvard University · USHarvard–MIT Division of Health Sciences and Technology · USMassachusetts General Hospital · US

Funding

Photodynamic Therapy of Localized InfectionsR01AI050875 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI HAMBLIN, MICHAEL R · 2003 to 2017
$4.8M
Macrophage Targeted Photodynamic TherapyR01CA083882 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HAMBLIN, MICHAEL R · 2002 to 2004
$740k
NCI NIH HHS R01 CA083882NIAID NIH HHS R01 AI050875NIAID NIH HHS R01AI050875NIAID NIH HHS R01CA/AI838801
6 · The paper itself

Abstract

backgroundThe mechanism by which the immune system can effectively recognize and destroy tumors is dependent on recognition of tumor antigens. The molecular identity of a number of these antigens has recently been identified and several immunotherapies have explored them as targets. Photodynamic therapy (PDT) is an anti-cancer modality that uses a non-toxic photosensitizer and visible light to produce cytotoxic reactive oxygen species that destroy tumors. PDT has been shown to lead to local destruction of tumors as well as to induction of anti-tumor immune response. METHODOLOGY/PRINCIPAL

findingsWe used a pair of equally lethal BALB/c colon adenocarcinomas, CT26 wild-type (CT26WT) and CT26.CL25 that expressed a tumor antigen, β-galactosidase (β-gal), and we treated them with vascular PDT. All mice bearing antigen-positive, but not antigen-negative tumors were cured and resistant to rechallenge. T lymphocytes isolated from cured mice were able to specifically lyse antigen positive cells and recognize the epitope derived from beta-galactosidase antigen. PDT was capable of destroying distant, untreated, established, antigen-expressing tumors in 70% of the mice. The remaining 30% escaped destruction due to loss of expression of tumor antigen. The PDT anti-tumor effects were completely abrogated in the absence of the adaptive immune response.

conclusionUnderstanding the role of antigen-expression in PDT immune response may allow application of PDT in metastatic as well as localized disease. To the best of our knowledge, this is the first time that PDT has been shown to lead to systemic, antigen- specific anti-tumor immunity.

Indexed as

AnimalsAntigensAntineoplastic AgentsCD8-Positive T-LymphocytesCell Line, TumorColonic NeoplasmsDimerizationDisease Models, AnimalFlow CytometryImmune SystemInterferon-gammaMiceMice, Inbred BALB CPhotochemotherapyPhotosensitizing AgentsReactive Oxygen SpeciesAntigensAntineoplastic AgentsInterferon-gammaPhotosensitizing AgentsReactive Oxygen SpeciesTumor Necrosis Factor-alpha

Identifiers

PMID21179470
PMCPMC3001867
OpenAlexW2084906892

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.