| Literature DB >> 31902676 |
Peter D Koch1, Christopher B Rodell1, Rainer H Kohler1, Mikael J Pittet1, Ralph Weissleder2.
Abstract
Immune-checkpoint blockers can promote sustained clinical responses in a subset of cancer patients. Recent research has shown that a subpopulation of tumor-infiltrating dendritic cells functions as gatekeepers, sensitizing tumors to anti-PD-1 treatment via production of interleukin-12 (IL-12). Hypothesizing that myeloid cell-targeted nanomaterials could be used to deliver small-molecule IL-12 inducers, we performed high-content image-based screening to identify the most efficacious small-molecule compounds. Using one lead candidate, LCL161, we created a myeloid-targeted nanoformulation that induced IL-12 production in intratumoral myeloid cells in vivo, slowed tumor growth as a monotherapy, and had no significant systemic toxicity. These results pave the way for developing combination immunotherapeutics by harnessing IL-12 production for immunostimulation.Entities:
Keywords: cancer; dendritic cells; drug delivery; high-content drug screening; immunotherapy; interleukin-12; nanoparticle
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Year: 2020 PMID: 31902676 PMCID: PMC7422681 DOI: 10.1016/j.chembiol.2019.12.007
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116