Jiménez-Periáñez A, Abos Gracia B, López Relaño J, Diez-Rivero C M, Reche P A, Martínez-Naves E, Matveyeva E, Gómez del Moral M
EM-Silicon Nano-Technologies SL, Nat. R. Cisternas 8, 46010 Valencia, Spain.
Clin Dev Immunol. 2013;2013:362163. doi: 10.1155/2013/362163. Epub 2013 Nov 10.
The mesoporous silicon microparticles (MSMPs) are excellent vehicles for releasing molecules inside the cell. The aim of this work was to use MSMPs to deliver viral specific MHC class I restricted epitopes into human antigen presenting cells (monocyte derived dendritic cells, MDDCs) to facilitate their capture, processing, and presentation to CD8+ (cytotoxic) T lymphocytes. We show for the first time that MSMPs vehiculation of antigenic peptides enhances their MHC class I presentation by human MDDCs to CD8 T lymphocytes.
介孔硅微粒(MSMPs)是在细胞内释放分子的优良载体。本研究的目的是利用MSMPs将病毒特异性MHC I类限制性表位递送至人抗原呈递细胞(单核细胞衍生树突状细胞,MDDCs),以促进其捕获、加工并呈递给CD8+(细胞毒性)T淋巴细胞。我们首次表明,MSMPs运载抗原肽可增强人MDDCs将其MHC I类呈递给CD8 T淋巴细胞的能力。