Yingbo Li
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Lighting up Macrophage Reprogramming Assists Immunosuppressive Niche Modulation in Primary Tumors and Tumor-Draining Lymph Nodes of Breast Cancer
1 Introduction Triple-negative breast cancer (TNBC) is the most aggressive subtype of breast cancer and is notorious for its rapid progression, early systemic spread, and lack of effective targeted therapies [1-4]. Its poor prognosis stems from a profoundly immunosuppressive tumor microenvironment (TME) that blunts the efficacy of chemotherapy, targeted therapy, and emerging immunotherapies [5, 6].
Programmable nanomicelles rewire myeloid immunity for durable control of primary and metastatic breast cancer
Abstract Immunosuppressive myeloid cells, including immature dendritic cells (DC) and tumor-promoting macrophages, drive tumor progression and immune evasion. Reprogramming these cells into immune effectors remains challenging. Here, we present a programmable nanomicelle platform that reconfigures myeloid immunity to combat both primary and metastatic breast cancer (BC). The nanomicelles co-deliver photosensitizers (IR825), anti-PD-L1 antibodies, and antagomiR-182 with spatiotemporal precision.
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