BDCA-2, a Novel Plasmacytoid Dendritic Cell–specific Type II C-type Lectin, Mediates Antigen Capture and Is a Potent Inhibitor of Interferon α/β Induction

Author:

Dzionek Andrzej1,Sohma Yoshiaki2,Nagafune Jun2,Cella Marina3,Colonna Marco3,Facchetti Fabio4,Günther Gritt1,Johnston Ian1,Lanzavecchia Antonio5,Nagasaka Tomoko2,Okada Tsutomu2,Vermi William4,Winkels Gregor1,Yamamoto Terumi2,Zysk Monika1,Yamaguchi Yasunori2,Schmitz Jürgen1

Affiliation:

1. Miltenyi Biotec GmbH, D-51429 Bergisch Gladbach, Germany

2. Pharmaceutical Research Laboratory, Kirin Brewery Company, Limited, Gunma 370-1295, Japan

3. Basel Institute for Immunology, CH-4005 Basel, Switzerland

4. Department of Pathology, University of Brescia, Spedali Civili Brescia, 1-25124 Brescia, Italy

5. Institute for Research in Biomedicine, CH-6500 Bellinzona, Switzerland

Abstract

Plasmacytoid dendritic cells are present in lymphoid and nonlymphoid tissue and contribute substantially to both innate and adaptive immunity. Recently, we have described several monoclonal antibodies that recognize a plasmacytoid dendritic cell-specific antigen, which we have termed BDCA-2. Molecular cloning of BDCA-2 revealed that BDCA-2 is a novel type II C-type lectin, which shows 50.7% sequence identity at the amino acid level to its putative murine ortholog, the murine dendritic cell–associated C-type lectin 2. Anti–BDCA-2 monoclonal antibodies are rapidly internalized and efficiently presented to T cells, indicating that BDCA-2 could play a role in ligand internalization and presentation. Furthermore, ligation of BDCA-2 potently suppresses induction of interferon α/β production in plasmacytoid dendritic cells, presumably by a mechanism dependent on calcium mobilization and protein-tyrosine phosphorylation by src-family protein-tyrosine kinases. Inasmuch as production of interferon α/β by plasmacytoid dendritic cells is considered to be a major pathophysiological factor in systemic lupus erythematosus, triggering of BDCA-2 should be evaluated as therapeutic strategy for blocking production of interferon α/β in systemic lupus erythematosus patients.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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