CLEC10A expression defines functionally distinct subsets of conventional type 2 dendritic cells (cDC2) in the mouse lung.Anal. functional differences between two cDC2 subsets classified by CLEC10A expression in a mouse model of ovalbumin (OVA) stimulated asthma.Conventional LDC subsets were isolated as previously described7 and classified by flow cytometry (FACS) based on XCR1 and CD172a expression.CDC2 could be further subdivided into CLEC10A and CLEC10A cDC2 based on their CLEC10A expression.We generated sensitized mice with OVA and identified cDC subsets in the spleen, mediastinal lymph nodes (MLN), and lungs. CLEC10A and CLEC10A cDC2 increased in proportion in the MLN and lungs more than in the spleen after OVA sensitization with significant increases in cell counts in the two cDC2 subsets compared to cDC1.To understand the genetic makeup of two cDC2 subsets, RNA sequencing was conducted on purified CLEC10A and CLEC10A cDC2 from OVA-primed lung.Addnl., CLEC10A cDC2 had higher expression of transcription factors related to cDC2 differentiation (Sirpa, Irf4, and Klf4) and costimulatory mols. (Cd40, Cd80, Cd86, and Icosl), whereas CLEC10A cDC2 had elevated levels of RNA associated with particular cytokines and receptors (Il6, Il10, Il23a, Il27, and Il17ra).Regarding pattern recognition receptors, RNA expression levels of various CLRs except for Clec7a and Clec9a were higher in CLEC10Ab cDC2 than in CLEC10A cDC2, and RNA expression levels of each Tolllike receptor also differed between the two cDC2 subsets.However, with respect to cytokine production capacity, CLEC10A cDC2 secreted significantly more IL-6 and TNF to various TLR ligands than CLEC10A cDC2, while there were no significant differences in IL-12p70 and IFN-g levels and no IL-10 was detected.These data suggest that CLEC10A expression defines two functionally distinct cDC2 subsets in the mouse lung and that CLEC10A cDC2 can induce Tcell immunity more efficiently.