Plasmacytoid DC (pDC) are bone marrow-derived leukocytes that secrete type I IFN (IFN-I) 1, 2. pDC detect selleck products RNA and DNA from viruses and RNA/DNA/immunocomplexes through two endosomal sensors, TLR7

and TLR9, respectively, both of which induce secretion of IFN-I through the MyD88-IRF7 signaling pathway 3–5. pDC were first identified in humans as CD4+, CD68+ and IL-3R+ (CD123) plasma cell-like cells 6. Initially, it was unclear what functions these cells perform in vivo; however, pDC’s prominent endoplasmic reticulum suggested a role in cytokine secretion. Later, it was demonstrated that this unique subset could differentiate into Ag-presenting cells 7, 8 and specialize in the secretion of IFN-I, thus corresponding to the human natural IFN-producing cells 9, 10. In 2001, cells that resembled human pDC were finally identified in the mouse 11. pDC originate in the bone marrow from common lymphoid/myeloid progenitors and are dependent on Flt3L, STAT3 and the transcription factor E2-2 for development 12. pDC, similar to committed precursors of classical DC, enter lymphoid organs directly from the blood through the high endothelial venules 13–15. Under homeostatic R788 order conditions, pDC also inhabit mucosal tissues and organs, albeit at low numbers. pDC accumulation in lymphoid tissues, mucosa and organs occurs during several human pathologies, particularly in LN of patients affected by

sarcoidosis, Mycobacterium tuberculosis infection 16, Kikuchi’s disease 17, and in the skin of patients affected by psoriasis 18, 19, systemic lupus erythematosus (SLE) 20 and lichen planus 21, 22. pDC accumulation has also been observed in brain lesions of patients with multiple sclerosis 23, in the salivary glands of patients with

Sjogren’s syndrome 24 and the synovia or inflamed muscle tissue/skin of people afflicted with rheumatoid arthritis 25, 26 or dermatomyositis 27, 28, respectively. pDC are over-represented in 3-oxoacyl-(acyl-carrier-protein) reductase the blood of patients with type I diabetes around the time of onset 29. pDC also infiltrate tumors 30–37 and are recruited to infected sites during viral infections caused by herpes zoster virus 38, HCV 39 and herpes simplex virus 40. The accumulation of pDC has been observed in many animal models of disease. During influenza 41–43 and RSV 44, 45 infections, pDC are recruited to the lungs and draining LN of mice. pDC numbers increase in the pancreatic LN around the onset of diabetes in NOD mice 46 and in the pancreas during lymphocytic choriomeningitis virus infection 47. In mouse models of HSV infection, pDC accumulate in the LN following footpad infection with HSV-1 48 and in the vaginal mucosa during HSV-2 infection 49. pDC are also recruited to the vaginal mucosa of rhesus macaques intravaginally infected with SIV 50. Furthermore, it has been reported that pDC infiltrate LN during SIV infection 51, 52.