Plasmacytoid dendritic cells cross-prime naive CD8 T cells by transferring antigen to conventional dendritic cells through exosomes
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Authors: Fu, Chunmei; Peng, Peng; Loschko, Jakob; Feng, Li; Phuong Pham; Cui, Weiguo; Lee, Kelvin P.; Krug, Anne B.; Jiang, Aimin
Abstract
Although plasmacytoid dendritic cells (pDCs) have been shown to play a critical role in generating viral immunity and promoting tolerance to suppress antitumor immunity, whether and how pDCs cross-prime CD8 T cells in vivo remain controversial. Using a pDC-targeted vaccine model to deliver antigens specifically to pDCs, we have demonstrated that pDC-targeted vaccination led to strong cross-priming and durable CD8 T cell immunity. Surprisingly, cross-presenting pDCs required conventional DCs (cDCs) to achieve cross-priming in vivo by transferring antigens to cDCs. Taking advantage of an in vitro system where only pDCs had access to antigens, we further demonstrated that cross-presenting pDCs were unable to efficiently prime CD8 T cells by themselves, but conferred antigennaive cDCs the capability of cross-priming CD8 T cells by transferring antigens to cDCs. Although both cDC1s and cDC2s exhibited similar efficiency in acquiring antigens from pDCs, cDC1s but not cDC2s were required for cross-priming upon pDC-targeted vaccination, suggesting that cDC1s played a critical role in pDC-mediated cross-priming independent of their function in antigen presentation. Antigen transfer from pDCs to cDCs was mediated by previously unreported pDC-derived exosomes (pDCexos), that were also produced by pDCs under various conditions. Importantly, all these pDCexos primed naive antigen-specific CD8 T cells only in the presence of bystander cDCs, similarly to cross-presenting pDCs, thus identifying pDCexo-mediated antigen transfer to cDCs as a mechanism for pDCs to achieve cross-priming. In summary, our data suggest that pDCs employ a unique mechanism of pDCexo-mediated antigen transfer to cDCs for cross-priming.
Design and implementation of detector control system for muon forward tracker at ALICE
JOURNAL OF INSTRUMENTATION
Authors: Yamakawa, K.; Augustinus, A.; Batigne, G.; Chochula, P.; Oya, M.; Panebianco, S.; Pinazza, O.; Shigaki, K.; Tieulent, R.; Yamaguchi, Y.
Abstract
ALICE is the experiment at the CERN LHC devoted to study heavy-ion collisions. An upgrade program of the ALICE detector is ongoing toward the LHC Run 3 starting in 2022 together with the upgrade of the data acquisition system and the detector control system (DCS). One of the main projects of the current ALICE upgrade program is the addition of the muon forward tracker (MFT), a new silicon pixel detector located at forward rapidity. In this paper, we describe the DCS of the MFT detector which is entirely controlled via a finite state machine in a hierarchical system.