The dendritic cell subtype-restricted C-type lectin Clec9A is a target for vaccine enhancement
- Caminschi, I; Proietto, AI; Ahmet, F; Kitsoulis, S; Teh, JS; Lo, JCY; Rizzitelli, A; Wu, L; Vremec, D; van Dommelen, SLH; Campbell, IK; Maraskovsky, E; Braley, H; Davey, GM; Mottram, P; De Velde, NV; Jensen, K; Lew, AM; Wright, MD; Heath, WR; Shortman, K; Lahoud, MH;
Publication Year 2008-10-15, Volume 112, Issue #8, Page 3264-3273
- Journal Title
- Publication Type
- Journal Article
- A novel dendritic cell (DC)-restricted molecule, Clec9A, was identified by gene expression profiling of mouse DC subtypes. Based on sequence similarity, a human ortholog was identified. Clec9A encodes a type II membrane protein with a single extracellular C-type lectin domain. Both the mouse Clec9A and human CLEC9A were cloned and expressed, and monoclonal antibodies (mAbs) against each were generated. Surface staining revealed that Clec9A was selective for mouse DCs and was restricted to the CD8(+) conventional DC and plasmacytoid DC subtypes. A subset of human blood DCs also expressed CLEC9A. A single injection of mice with a mAb against Clec9A, which targets antigens (Ags) to the DCs, produced a striking enhancement of antibody responses in the absence of added adjuvants or danger signals, even in mice lacking Toll-like receptor signaling pathways. Such targeting also enhanced CD4 and CD8 T-cell responses. Thus, Clec9A serves as a new marker to distinguish subtypes of both mouse and human DCs. Furthermore, targeting Ags to DCs with antibodies to Clec9A is a promising strategy to enhance the efficiency of vaccines, even in the absence of adjuvants.
- AMER SOC HEMATOLOGY
- SUBSETS IN-VIVO; STEADY-STATE; CUTTING EDGE; T-CELLS; DC-SIGN; DIFFERENTIAL PRODUCTION; ANTIGEN PRESENTATION; CROSS-PRESENTATION; IFN-ALPHA; CD8(+)
- Publisher's Version
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Creation Date: 2008-10-15 12:00:00Last Modified: 0001-01-01 12:00:00