Abstract:
:Plasmacytoid dendritic cells (pDCs) are known mainly for their secretion of type I IFN upon viral encounter. We describe a CD2hiCD5+CD81+ pDC subset, distinguished by prominent dendrites and a mature phenotype, in human blood, bone marrow, and tonsil, which can be generated from CD34+ progenitors. These CD2hiCD5+CD81+ cells express classical pDC markers, as well as the toll-like receptors that enable conventional pDCs to respond to viral infection. However, their gene expression profile is distinct, and they produce little or no type I IFN upon stimulation with CpG oligonucleotides, likely due to their diminished expression of IFN regulatory factor 7. A similar population of CD5+CD81+ pDCs is present in mice and also does not produce type I IFN after CpG stimulation. In contrast to conventional CD5-CD81- pDCs, human CD5+CD81+ pDCs are potent stimulators of B-cell activation and antibody production and strong inducers of T-cell proliferation and Treg formation. These findings reveal the presence of a discrete pDC population that does not produce type I IFN and yet mediates important immune functions previously attributed to all pDCs.
journal_name
Proc Natl Acad Sci U S Aauthors
Zhang H,Gregorio JD,Iwahori T,Zhang X,Choi O,Tolentino LL,Prestwood T,Carmi Y,Engleman EGdoi
10.1073/pnas.1610630114subject
Has Abstractpub_date
2017-02-21 00:00:00pages
1988-1993issue
8eissn
0027-8424issn
1091-6490pii
1610630114journal_volume
114pub_type
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