Journal
ADVANCED SCIENCE
Volume 10, Issue 10, Pages -Publisher
WILEY
DOI: 10.1002/advs.202205139
Keywords
breast cancer; cytokine; immune checkpoint inhibitor; immunotherapy; interleukin-12; metastatic tumor
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Researchers have developed a nanocytokine that can release active interleukin 12 (IL-12) specifically in tumor tissues, leading to localized antitumoral inflammation without causing systemic immune responses and toxicities. This strategy shows promising potential for safer and more effective immunotherapies.
Treatment of immunologically cold tumors is a major challenge for immune checkpoint inhibitors (ICIs). Interleukin 12 (IL-12) can invigorate ICIs against cold tumors by establishing a robust antitumor immunity. However, its toxicity and systemic induction of counteracting immunosuppressive signals have hindered translation. Here, IL-12 activity is spatiotemporally controlled for safely boosting efficacy without the stimulation of interfering immune responses by generating a nanocytokine that remains inactive at physiological pH, but unleashes its full activity at acidic tumor pH. The IL-12-based nanocytokine (Nano-IL-12) accumulate and release IL-12 in tumor tissues, eliciting localized antitumoral inflammation, while preventing systemic immune response, counteractive immune reactions, and adverse toxicities even after repeated intravenous administration. The Nano-IL-12-mediated spatiotemporal control of inflammation prompt superior anticancer efficacy, and synergize with ICIs to profoundly inflame the tumor microenvironment and completely eradicate ICI-resistant primary and metastatic tumors. The strategy could be a promising approach toward safer and more effective immunotherapies.
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