A simple self-adjuvanting biomimetic nanovaccine self-assembled with the conjugate of phospholipids and nucleotides can induce a strong cancer immunotherapeutic effect
Biomimetic nanoparticles have potential applications in many fields due to their favorable properties. Here, we developed a self-adjuvanting biomimetic anti-tumor nanovaccine, which was self-assembled with an amphiphilic conjugate synthesized with the phospholipids of 1,2-dioleoyl- sn-glycero -3-pho...
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Veröffentlicht in: | Biomaterials science 2021-01, Vol.9 (1), p.84-92 |
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Sprache: | eng |
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Zusammenfassung: | Biomimetic nanoparticles have potential applications in many fields due to their favorable properties. Here, we developed a self-adjuvanting biomimetic anti-tumor nanovaccine, which was self-assembled with an amphiphilic conjugate synthesized with the phospholipids of 1,2-dioleoyl-
sn-glycero
-3-phosphoethanolamine (DOPE) and hydrophilic Toll-like receptor (TLR9) agonist CpG ODN. The nanovaccine could not only provide effective initial antigen stimulation and sustained long-term antigen supply with a controlled release, but also induce antigen cross-presentation
via
the MHC-I pathway initiating CD8
+
T-cell responses. Moreover, the dense nucleotide shell around the nanovaccine could promote antigen endocytosis
via
various receptor-mediated pathways into dendritic cells. CpG ODN interacted with TLR9 triggering the cytokine secretion of TNF-α and IL-10, which further boosted the anti-tumor humoral and cellular immune responses, which led to a significant tumor suppressive effect and remarkable survival prolongation. So, this nanovaccine self-assembled with phospholipid-nucleotide amphiphiles can serve as a safe, simple and efficient approach for anti-tumor immunotherapy.
The biomimetic nanovaccines not only promoted antigens endocytosis into dendritic cells
via
receptor-mediated pathways but also induced antigens cross-presentation eliciting CD8
+
T-cell responses. CPG-ODN as an adjuvant further enhanced the anti-tumor immune responses. |
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ISSN: | 2047-4830 2047-4849 |
DOI: | 10.1039/d0bm01333a |