ArticleCyborg and bionic systems (Washington, D.C.)2025
Reviving Dormant Immunity: Millimeter Waves Reprogram the Immunosuppressive Microenvironment to Potentiate Immunotherapy without Obvious Side Effects.
Article in Cyborg and bionic systems (Washington, D.C.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
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Who cites it
1 citing paper in PubMed.
- Ultrasound-Responsive Calcium Copper Phosphate Nanomaterials Induce Tumor Cell Death via the Synergistic Release of Copper and Calcium.International journal of molecular sciences · 2026Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Addressing the variability in cancer immunotherapeutic outcomes among patients and the challenge of devising safe strategies to overcome immune evasion in solid tumors are crucial in advancing cancer therapy. This study investigated the anti-tumor effect of millimeter waves (MMWs) alone and in combination with the anti-programmed cell death-ligand 1 (α-PD-L1) antibody in a 4T1 "cold tumor" model. The results show that MMWs not only inhibit tumor growth but also improve tumor metabolism and the immune microenvironment and enhance anti-tumor immune responses by inducing conformational changes of key immune proteins. Further experiments conducted on cellular and animal models demonstrated that the anti-tumor efficacy of MMWs, which plays a pivotal role, was substantially enhanced with the aid of α-PD-L1. This collaboration resulted in a synergistic effect that not only inhibited tumor progression but also promoted a sustained immune response and prevented recurrence. The additional CT26 "cold tumor" model validates the applicability of this strategy across other "cold tumor" types, particularly in reprogramming the immunosuppressed state of "cold tumor". These findings underscore the unique potential of MMWs as a nonionizing, nonthermal therapeutic tool that complements cancer immunotherapy, offering a novel approach for the precision treatment of solid tumors.
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Registered trials
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.