Oligonucleotide-Based Modulation of Macrophage Polarization: Emerging
Strategies in Immunotherapy
Abstract
Recent advancements in immunotherapy spotlight the pivotal role of
macrophages in disease treatment. The polarization of macrophages,
wherein these immune cells differentiate into either pro-inflammatory
(M1) or anti-inflammatory (M2) states, plays a vital role in the
therapeutic modulation of a spectrum of diseases. Oligonucleotides have
emerged as potent tools for modulating macrophage polarization with high
specificity and potential cost-effectiveness compared to traditional
therapies. In this review, we delve into the application of
oligonucleotides for steering macrophage polarization, introducing how
macrophage is polarized and how 4 different kinds of oligonucleotide
(ASO, siRNA, agomir/antagomir and aptamer) works, discusses their
therapeutic potentials and challenges associated with these strategies,
emphasizing the importance of precise, disease-specific interventions by
presenting actual examples. While the application of oligonucleotides in
clinical faces challenges, we also highlights some recent, significant
advances in current trials and the future potential in stimulating
macrophages for therapeutic advantages in immunotherapy, signaling a
frontier in disease treatment and management.