Low-Pressure Pulsed Focused Ultrasound with Microbubbles Promotes an Anticancer Immunological Response
Journal
Journal of Translational Medicine
Journal Volume
10
Journal Issue
221
Pages
1-12
Date Issued
2012
Author(s)
H-L Liu
H-Y Hsieh
L-A Lu
C-W Kang
M-F Wu
C-Y Lin
H-L Liu
H-Y Hsieh
L-A Lu
C-W Kang
M-F Wu
C-Y Lin
Abstract
Background: High-intensity focused-ultrasound (HIFU) has been successfully employed for thermal ablation of tumors in clinical settings. Continuous- or pulsed-mode HIFU may also induce a host antitumor immune response, mainly through expansion of antigen-presenting cells in response to increased cellular debris and through increased macrophage activation/infiltration. Here we demonstrated that another form of focused ultrasound delivery, using low-pressure, pulsed-mode exposure in the presence of microbubbles (MBs), may also trigger an antitumor immunological response and inhibit tumor growth.Methods: A total of 280 tumor-bearing animals were subjected to sonographically-guided FUS. Implanted tumors were exposed to low-pressure FUS (0.6 to 1.4 MPa) with MBs to increase the permeability of tumor microvasculature.Results: Tumor progression was suppressed by both 0.6 and 1.4-MPa MB-enhanced FUS exposures. We observed a transient increase in infiltration of non-T regulatory (non-Treg) tumor infiltrating lymphocytes (TILs) and continual infiltration of CD8+ cytotoxic T-lymphocytes (CTL). The ratio of CD8+/Treg increased significantly and tumor growth was inhibited.Conclusions: Our findings suggest that low-pressure FUS exposure with MBs may constitute a useful tool for triggering an anticancer immune response, for potential cancer immunotherapy. ? 2012 Liu et al.; licensee BioMed Central Ltd.
SDGs
Other Subjects
animal cell; animal experiment; animal model; animal tissue; article; cancer inhibition; CD8+ T lymphocyte; controlled study; cytotoxic T lymphocyte; echography; high intensity focused ultrasound; low pressure pulsed focused ultrasound; lymphocytic infiltration; microbubble; microvasculature; mouse; nonhuman; permeability; regulatory T lymphocyte; tumor immunity; tumor microvasculature; Animals; Computer Systems; Disease Progression; Flow Cytometry; Humans; Immunity; Mice; Mice, Inbred BALB C; Microbubbles; Microscopy, Fluorescence; Microvessels; Models, Immunological; Neoplasms; Permeability; Pressure; Temperature; Tumor Microenvironment; Ultrasonics
Type
journal article