“…Their link with clinical prognosis has been reported in a variety of human solid tumors. The majority of these studies report that an extensive infiltration with DC is associated with increased OS and cover many tumors types, including melanoma (Gerber et al, 2014;Ladányi et al, 2007;Neagu et al, 2013;Simonetti et al, 2007), HCC (Cai et al, 2006;Yin et al, 2003), gallbladder (Furihata et al, 2005;Nakakubo et al, 2003), oral (Reichert et al, 2001), esophageal (Furihata et al, 1992;Ishigami et al, 2003a;Lu et al, 2013), gastric (Amoueian et al, 2015Ananiev et al, 2011;Kashimura et al, 2012;Tsukayama et al, 2005), NSCLC (Al-Shibli et al, 2009;Dai et al, 2010;Hald et al, 2013;Inoshima et al, 2002;Johnson et al, 2000), colorectal (Gulubova et al, 2012;McMullen et al, 2010;Nakayama et al, 2003;Väyrynen et al, 2014), bladder (Inoue et al, 1993), breast (Iwamoto et al, 2003;La Rocca et al, 2008;Lespagnard et al, 1999;Park et al, 2012), endometrial (Honig et al, 2005;Lijun et al, 2012), and ovarian cancer (Eisenthal et al, 2001;Zhang et al, 2015). Nevertheless, the infiltration with CD123 + plasmacytoid DC has been associated with shorter OS in breast cancer ( Jensen et al, 2012;Treilleux et al, 2004), as well as the presence of CD208 + and CD1a + DCs in colorectal (Sandel et al, 2005)...…”