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

生物 浆细胞样树突状细胞 干扰素 树突状细胞 C型凝集素 单克隆抗体 抗原 抗原呈递 抗原提呈细胞 α-干扰素 分子生物学 抗体 T细胞 免疫学 细胞生物学 凝集素 免疫系统
作者
Andrzej Dzionek,Yoshiaki Sohma,Jun Nagafune,Marina Cella,Marco Colonna,Fabio Facchetti,Gritt Günther,Ian Johnston,Antonio Lanzavecchia,T Nagasaka,Tsutomu Okada,William Vermi,Gregor Winkels,Terumi Yamamoto,Monika Zysk,Yasunori Yamaguchi,Jürgen Schmitz
出处
期刊:Journal of Experimental Medicine [Rockefeller University Press]
卷期号:194 (12): 1823-1834 被引量:749
标识
DOI:10.1084/jem.194.12.1823
摘要

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 alpha/beta 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 alpha/beta 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 alpha/beta in systemic lupus erythematosus patients.
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