The dendritic cell subtype-restricted C-type lectin Clec9A is a target for vaccine enhancement

Author:

Caminschi Irina1,Proietto Anna I.1,Ahmet Fatma1,Kitsoulis Susie1,Shin Teh Joo1,Lo Jennifer C. Y.1,Rizzitelli Alexandra2,Wu Li1,Vremec David1,van Dommelen Serani L. H.1,Campbell Ian K.1,Maraskovsky Eugene3,Braley Hal3,Davey Gayle M.1,Mottram Patricia4,van de Velde Nicholas4,Jensen Kent5,Lew Andrew M.1,Wright Mark D.6,Heath William R.1,Shortman Ken1,Lahoud Mireille H.1

Affiliation:

1. The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia;

2. Department of Biochemistry and Molecular Biology, Monash University, Melbourne, Australia;

3. CSL Limited, Melbourne, Australia;

4. Burnet Institute, Austin Hospital, Melbourne, Australia;

5. Human Immunology Laboratory, Schering-Plough Biopharma, Palo Alto, CA; and

6. Department of Immunology, Monash University, Melbourne, Australia

Abstract

Abstract 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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