2021
DOI: 10.1186/s40824-021-00246-2
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Immune cell targeting nanoparticles: a review

Abstract: Immune cells are attractive targets for therapy as they are direct participants in a variety of diseases. Delivering a therapeutic agent only to cells that act on a disease by distinguishing them from other cells has the advantage of concentrating the therapeutic effect and lowering systemic side effects. Distinguishing each immune cell from other immune cells to deliver substances, including drugs and genes, can be achieved using nanotechnology. And also nanoparticles can ensure in vivo stability and sustaine… Show more

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Cited by 38 publications
(18 citation statements)
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References 72 publications
(68 reference statements)
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“…These groundbreaking advances were recognized by the 2018 Nobel Prize in Physiology or Medicine that was awarded to James Allison and Tasuku Honjo for “the discovery of cancer therapy by inhibition of negative immune regulation” [ 245 , 246 ]. In particular, the Nobel prize was awarded for the identification of immune checkpoints including cytotoxic T lymphocyte-associated antigen 4 (CTLA4) and programmed cell death-1/programmed death-ligand 1 (PD-1/PD-L1), leading the research boom for anticancer therapy by targeting these checkpoints [ 247 ]. In addition, nanomedicines prove to trigger the induction of immunogenic cell death (ICD), which is a specific mode of cell death with tumor antigens and danger-associated molecular patterns released to boost anticancer immunity [ 248 , 249 ].…”
Section: Hollow Nanoplatforms For Nir-ii Ptt-based Multi-modal Therapiesmentioning
confidence: 99%
“…These groundbreaking advances were recognized by the 2018 Nobel Prize in Physiology or Medicine that was awarded to James Allison and Tasuku Honjo for “the discovery of cancer therapy by inhibition of negative immune regulation” [ 245 , 246 ]. In particular, the Nobel prize was awarded for the identification of immune checkpoints including cytotoxic T lymphocyte-associated antigen 4 (CTLA4) and programmed cell death-1/programmed death-ligand 1 (PD-1/PD-L1), leading the research boom for anticancer therapy by targeting these checkpoints [ 247 ]. In addition, nanomedicines prove to trigger the induction of immunogenic cell death (ICD), which is a specific mode of cell death with tumor antigens and danger-associated molecular patterns released to boost anticancer immunity [ 248 , 249 ].…”
Section: Hollow Nanoplatforms For Nir-ii Ptt-based Multi-modal Therapiesmentioning
confidence: 99%
“…However, systemic administration provides liver, kidney, and spleen accumulation that compromise a preferential uptake by tumour-infiltrated MDSCs/TAMs. To avoid this important limitation, several studies have developed NP-based targeting systems employing surface markers to specifically target defined immune cell subsets [ 222 ]. For instance, polyethylene glycol (PEG)-sheddable, mannose-modified NPs were developed to target M2-like TAMs via mannose-CD206 binding after pH-sensitive PEG dissociation in the acidic TME [ 223 ].…”
Section: Conclusion and Future Perspectivementioning
confidence: 99%
“…The released DOX and PT activities of GO/MnWO4/PEG significantly ablated mouse tumors in vivo, suggesting the versatility of GO/MnWO4/PE for multimodal imaging-guided cancer synergistic therapy. On the other hand, AuNPs have tunable and enhanced adsorption cross-sections, making them preferred versatile imaging probes for MRI, CT, PA, and FL imaging [ 91 , 92 , 93 , 94 ]. However, a reduction in the cross-section of AuNPs hinders the acceptable level of PA signal amplitudes under the visible light range.…”
Section: Graphene-based Photoacoustic Imagingmentioning
confidence: 99%