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10.1021/acsomega.6b00436

http://scihub22266oqcxt.onion/10.1021/acsomega.6b00436
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C5377267!5377267!28393131
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suck abstract from ncbi


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pmid28393131      ACS+Omega 2017 ; 2 (3): 937-45
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  • Controlling T-Cell Activation with Synthetic Dendritic Cells Using the Multivalency Effect #MMPMID28393131
  • Hammink R; Mandal S; Eggermont LJ; Nooteboom M; Willems PHGM; Tel J; Rowan AE; Figdor CG; Blank KG
  • ACS Omega 2017[Mar]; 2 (3): 937-45 PMID28393131show ga
  • Artificial antigen-presenting cells (aAPCs) have recently gained a lot of attention. They efficiently activate T cells and serve as powerful replacements for dendritic cells in cancer immunotherapy. Focusing on a specific class of polymer-based aAPCs, so-called synthetic dendritic cells (sDCs), we have investigated the importance of multivalent binding on T-cell activation. Using antibody-functionalized sDCs, we have tested the influence of polymer length and antibody density. Increasing the multivalent character of the antibody-functionalized polymer lowered the effective concentration required for T-cell activation. This was evidenced for both early and late stages of activation. The most important effect observed was the significantly prolonged activation of the stimulated T cells, indicating that multivalent sDCs sustain T-cell signaling. Our results highlight the importance of multivalency for the design of aAPCs and will ultimately allow for better mimics of natural dendritic cells that can be used as vaccines in cancer treatment.
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