Evidence map›Paper›PMID 26755821›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Low-Intensity Focused Ultrasound Induces Reversal of Tumor-Induced T Cell Tolerance and Prevents Immune Escape.

Sanmay Bandyopadhyay, Thomas J Quinn, Lisa Scandiuzzi, Indranil Basu, Ari Partanen, Wolfgang A Tomé, Fernando Macian, Chandan Guha

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 67 citations in OpenAlex.

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  10. Engineering Versatile Nanomedicines for Ultrasonic Tumor Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
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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

8 authors at 2 institutions in 1 country.

Sanmay BandyopadhyayDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461;ORCID http://orcid.org/0000-0002-1015-2388
Thomas J QuinnDepartment of Radiation Oncology, Albert Einstein College of Medicine, Bronx, NY 10461; and.ORCID http://orcid.org/0000-0002-5897-8111
Lisa ScandiuzziDepartment of Radiation Oncology, Albert Einstein College of Medicine, Bronx, NY 10461; and.
Indranil BasuDepartment of Radiation Oncology, Albert Einstein College of Medicine, Bronx, NY 10461; and.ORCID http://orcid.org/0000-0003-1057-8888
Ari PartanenPhilips Healthcare, Bethesda, MD 20817.
Wolfgang A ToméDepartment of Radiation Oncology, Albert Einstein College of Medicine, Bronx, NY 10461; and.
Fernando MacianDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461; Philips Healthcare, Bethesda, MD 20817 cguha@montefiore.org fernando.macian@einstein.yu.edu.
Chandan GuhaDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461; Department of Radiation Oncology, Albert Einstein College of Medicine, Bronx, NY 10461; and Philips Healthcare, Bethesda, MD 20817 cguha@montefiore.org fernando.macian@einstein.yu.edu.
Albert Einstein College of Medicine · USPhilips (United States) · US

Funding

Role of Autophagy in T Cell Function and Immunosenescence (Project 3)P01AG031782 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MACIAN, FERNANDO · 2009 to 2024
$36.2M
Special Animal CoreP30DK041296 · NIDDK · YESHIVA UNIVERSITY · PI WOLKOFF, ALLAN W · 1989 to 2018
$22.9M
Molecular mechanisms of T cell anergyR01AI059738 · NIAID · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI MACIAN, FERNANDO · 2004 to 2014
$3.9M
HIFU-enhanced tumor vaccinesR01EB009040 · NIBIB · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI GUHA, CHANDAN · 2008 to 2012
$2.2M
Molecular mechanisms of T cell anergyR56AI059738 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MACIAN, FERNANDO · 2016 to 2016
$418k
NIAID NIH HHS AI059738NIAID NIH HHS R01 AI059738NIAID NIH HHS R56 AI059738NIA NIH HHS P01 AG031782NIBIB NIH HHS EB009040NIBIB NIH HHS R01 EB009040NIDDK NIH HHS P30 DK041296
6 · The paper itself

Abstract

Immune responses against cancer cells are often hindered by immunosuppressive mechanisms that are developed in the tumor microenvironment. Induction of a hyporesponsive state in tumor Ag-specific T cells is one of the major events responsible for the inability of the adaptive immune system to mount an efficient antitumor response and frequently contributes to lessen the efficacy of immunotherapeutic approaches. Treatment of localized tumors by focused ultrasound (FUS) is a minimally invasive therapy that uses a range of input energy for in situ tumor ablation through the generation of thermal and cavitation effect. Using a murine B16 melanoma tumor model, we show that a variant of FUS that delivers a reduced level of energy at the focal point and generates mild mechanical and thermal stress in target cells has the ability to increase immunogenic presentation of tumor Ags, which results in reversal of tumor-induced T cell tolerance. Furthermore, we show that the combination of nonablative low-energy FUS with an ablative hypofractionated radiation therapy results in synergistic control of primary tumors and leads to a dramatic reduction in spontaneous pulmonary metastases while prolonging recurrence-free survival only in immunocompetent mice.

Indexed as

AnimalsCombined Modality TherapyEnzyme-Linked Immunosorbent AssayFlow CytometryMelanoma, ExperimentalMiceMice, Inbred C57BLMice, TransgenicNeoplasm MetastasisRadiotherapyReal-Time Polymerase Chain ReactionSkin NeoplasmsT-LymphocytesTumor EscapeUltrasonic Therapy

Identifiers

PMID26755821
PMCPMC4744543
OpenAlexW2233572073

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.