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Interleukin 15-Presenting Nanovesicles with Doxorubicin-Loaded Ferritin Cores for Cancer Immunochemotherapy. | LitMetric

Interleukin 15-Presenting Nanovesicles with Doxorubicin-Loaded Ferritin Cores for Cancer Immunochemotherapy.

Adv Sci (Weinh)

State Key Laboratory of Drug Research & Center of Pharmaceutics, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 501 Haike Road, Shanghai, 201203, China.

Published: December 2024

AI Article Synopsis

  • Interleukin 15 (IL15) is vital for supporting the growth and survival of immune cells like NK cells and CTLs, but its therapy faces issues like inflammation and unintended cancer cell activation.
  • The researchers created a specialized nanovesicle called DoxFILN, which combines IL15/IL15 receptor α complexes with a core of doxorubicin-loaded ferritin, significantly boosting the activity of immune cells in tumors.
  • In acidic tumor environments, DoxFILN releases its components to selectively target cancer cells, leading to targeted drug release and increased immune cell activation, showing potential as an innovative cancer treatment strategy.

Article Abstract

Interleukin 15 (IL15) is crucial for fostering the survival and proliferation of nature killer (NK) cells and cytotoxic T lymphocytes (CTLs), playing a pivotal role in tumor control. However, IL15 supplementary therapy encounters challenges such as systemic inflammation and non-specific stimulation of cancer cells. Herein, a nanovesicle termed DoxFILN, comprising a membrane presenting IL15/IL15 receptor α complexes (IL15c) and a core of doxorubicin-loaded ferritin (Dox-Fn) are reported. The DoxFILN significantly enhances the densities and activities of intratumoral CTLs and NK cells. Mechanistically, DoxFILN undergoes deshelling in the acidic tumor microenvironment, releasing Dox-Fn and membrane-bound IL15c. Dox-Fn selectively target transferrin receptors on cancerous cells, facilitating intracellular Dox release and inducing immunogenic cell death. Concurrently, membrane-bound IL15c recognizes and activates IL15 receptor β/γc heterodimers, leading to a remarkable increase in the proliferation and activation of CTLs (16-fold and 28-fold) and NK cells (37-fold and 50-fold). The IL15-displaying nanovesicle introduced here holds promise as a potential platform for immunochemotherapy in the treatment of cancer.

Download full-text PDF

Source
http://dx.doi.org/10.1002/advs.202409194DOI Listing

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