Evidence map›Paper›PMID 42496031›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Immediate Growth Control in Response to Boiling Histotripsy is Prognostic for Intratumoral Immune Activation.

Lydia E Kitelinger, Matthew R DeWitt, Carly M Van Wagoner, Claire A Conarroe, Charles C Funk, Aaron B Streit, AeRyon Kim, Richard J Price, Timothy N J Bullock

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Lydia E KitelingerDepartment of Pathology, University of Virginia, Charlottesville, Virginia, USA.ORCID https://orcid.org/0000-0002-9167-1285
Matthew R DeWittDepartment of Radiology & Medical Imaging, Department of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, USA.
Carly M Van WagonerDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, Virginia, USA.ORCID https://orcid.org/0009-0009-2091-5762
Claire A ConarroeDepartment of Pathology, University of Virginia, Charlottesville, Virginia, USA.
Charles C FunkDepartment of Pathology, University of Virginia, Charlottesville, Virginia, USA.
Aaron B StreitDepartment of Pathology, University of Virginia, Charlottesville, Virginia, USA.ORCID https://orcid.org/0009-0003-7728-6553
AeRyon KimDepartment of Pathology, University of Virginia, Charlottesville, Virginia, USA.
Richard J PriceDepartment of Radiology & Medical Imaging, Department of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, USA.ORCID https://orcid.org/0000-0002-0237-2102
Timothy N J BullockDepartment of Pathology, University of Virginia, Charlottesville, Virginia, USA.ORCID https://orcid.org/0000-0001-6141-3261

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Dina Gould Halme · 1987 to 2026
$72.1M
Focused Ultrasound Regimens that Synergize with Melanoma ImmunotherapyR01EB030007 · NIBIB · UNIVERSITY OF VIRGINIA · PI BULLOCK, TIMOTHY N, PRICE, RICHARD J. · 2020 to 2023
$2.6M
MR Image-Guided Drug Delivery to Cerebral Cavernous Malformations with Focused UltrasoundR01CA279134 · NCI · UNIVERSITY OF VIRGINIA · PI Richard J. Price · 2024 to 2026
$1.8M
Augmenting focused ultrasound-mediated drug delivery to brain tumors with vascular normalizationR21CA286367 · NCI · UNIVERSITY OF VIRGINIA · PI PRICE, RICHARD J. · 2024 to 2024
$399k
Comprehensive Cancer CentersFocused Ultrasound Foundation NIH R01EB030007Focused Ultrasound Foundation R01CA279134Focused Ultrasound Foundation R21CA286367NCI NIH HHS P30 CA044579NCI NIH HHS R01 CA279134NCI NIH HHS R21 CA286367NIBIB NIH HHS R01 EB030007University of Virginia's Focused Ultrasound Immuno-Oncology
6 · The paper itself

Abstract

Despite the clear efficacy of immune checkpoint blockade, a subset of melanoma patients receives no clinical benefit from treatment. Boiling histotripsy (BH), a mechanical form of focused ultrasound, allows for non-invasive and non-ionizing tissue destruction. As mechanically fractionating tumors with BH may potentiate T cell-mediated anti-tumor responses, we addressed gaps in knowledge regarding the impact BH has on antigen-presenting cell (APC) presence in the tumor microenvironment (TME), antigen acquisition, and conventional dendritic cell (cDC) activation states in settings where BH does or does not induce a primary tumor growth response. When BH treatment immediately inhibited melanoma outgrowth, APC presence in the TME was significantly reduced, tumor antigen acquisition amongst APCs remained elevated when compared to controls, and intratumoral immune activation was observed distinctly in the cDC1 subset. Cavitation scoring based on real-time B-mode imaging signatures characteristic of BH-induced tissue destruction demonstrated that BH-mediated destruction strongly correlates with tumor antigen presence in the draining lymph nodes 24 h post-ablation. Collectively, these findings reveal that immediate BH-driven tumor growth control in a melanoma model stratifies distinct intratumoral immune states; positioning early growth response as a biologically informative prognostic indicator of BH-induced intratumoral immune activation.

Indexed as

antigen‐presenting cellsboiling histotripsycavitationmelanomatumor antigentumor microenvironment

Identifiers

PMID42496031
PMCPMC13398126

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Registered trials

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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.