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Enhancing cell-mediated immunity through dendritic cell activation: the role of Tri-GalNAc-modified PLGA-PEG nanoparticles encapsulating SR717
M. Tuberculosis fusion proteins (TP) and the STING agonist SR717 are co-encapsulated within Triantennary N-Acetylgalactosamine (Tri-GalNAc)-modified PLGA-PEG nanoparticles, denoted as TP/GPS. Following subcutaneous administration, these TP/GPS are effectively phagocytosed by dendritic cells (DCs). T...
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Published in: | Frontiers in immunology 2024-12, Vol.15 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | M. Tuberculosis
fusion proteins (TP) and the STING agonist SR717 are co-encapsulated within Triantennary N-Acetylgalactosamine (Tri-GalNAc)-modified PLGA-PEG nanoparticles, denoted as TP/GPS. Following subcutaneous administration, these TP/GPS are effectively phagocytosed by dendritic cells (DCs). The encapsulated TP and SR717 are then released, stimulating the DCs maturation and antigen presentation to T cells. This leads to the subsequent activation and differentiation of CD4
+
and CD8
+
T cells into memory T cells. |
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ISSN: | 1664-3224 1664-3224 |
DOI: | 10.3389/fimmu.2024.1490003 |