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<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <responseDate>2026-10-15T03:49:49Z</responseDate>
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    <identifier>10.57760/sciencedb.j00217.05985</identifier>
    <datestamp>2025-02-14T15:00:33Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2025-02-14</dc:date>
  <dc:title>ROS-Inducing Micelles Sensitize Tumor-Associated Dendritic cells to TLR3 Stimulation for Potent Immunotherapy</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.j00217.05985</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Objective To prepare ZnPP-PM nanoparticles based on peptide micelles (PM) loaded with zinc protoporphyrin IX (ZnPP) for targeted delivery of immune adjuvants, and to study their activation ability and anti-tumor effect on tumor associated dendritic cells (TADCs) derived from mouse bone marrow.Method ZnPP was connected to mannose functionalized PM block copolymers via amide bonds, self-assembled into ZnPP-PM with the ability to target DC and induce ROS, and loaded with PIC via electrostatic adsorption to form ZnPP-PM/PIC nanoparticles, which were characterized. Application of laser confocal microscopy and flow cytometry to detect the uptake ability of cells towards ZnPP-PM, as well as the effect of ZnPP-PM/PIC on the production and activation of reactive oxygen species (ROS) in TADCs. And verify the in vivo anti-tumor effect of ZnPP-PM/PIC through animal experiments.Result The particle sizes of ZnPP-PM and ZnPP-PM/PIC are approximately 33 &amp;plusmn; 3.55 nm and 30 &amp;plusmn; 2.47 nm, respectively, with no significant difference between the two. They have good dispersibility and stability, and exhibit specific targeting ability towards DC. In addition, ZnPP-PM/PIC can more effectively promote TADC activation by enhancing ROS production and PIC coordination (P&amp;lt;0.05), and induce more effective anti-tumor effects in vivo by increasing the activation of effector cells (CD8+CD69+, CD4+CD69+ or NK1.1+CD69+) in tumors and TDLNs.Conclusion Based on ZnPP-PM as a targeted transport immune adjuvant, promoting TADC activation can become a potential anti-tumor treatment strategy.</dc:description>
  <dc:subject>Tumor associated dendritic cells; Zinc protoporphyrin IX; Immune adjuvant; Peptide micelle</dc:subject>
  <dc:creator>Shao-wan.Su</dc:creator>
  <dc:creator>Ce.Wang</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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