targeting toll-like receptor signaling in plasmacytoid dendritic cells and autoreactive b cells as a therapy for lupus针对toll样受体信号在血浆树突细胞和autoreactive b细胞治疗红斑狼疮.pdfVIP
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targeting toll-like receptor signaling in plasmacytoid dendritic cells and autoreactive b cells as a therapy for lupus针对toll样受体信号在血浆树突细胞和autoreactive b细胞治疗红斑狼疮
Available online /content/8/1/203
Review
Targeting Toll-like receptor signaling in plasmacytoid dendritic
cells and autoreactive B cells as a therapy for lupus
Petar S Lenert
Assistant Professor, Division of Rheumatology, Department of Internal Medicine, Carver College of Medicine, The University of Iowa, Iowa City, Iowa, USA
Corresponding author: Petar S Lenert, petar-lenert@
Published: 10 January 2006 Arthritis Research Therapy 2006, 8:203 (doi:10.1186/ar1888)
This article is online at /content/8/1/203
© 2006 BioMed Central Ltd
Abstract limited heterogeneity [4] but they have potent capacity to
This review focuses on the role of Toll-like receptors (TLRs) in sense micro-organisms and alert body defense system about
lupus and on possibilities to treat lupus using TLR modulating the presence of infectious danger. This is achieved through
inhibitory oligodeoxynucleotides (INH-ODNs). TLRs bridge innate recognition of conserved microbial patterns such as
and adaptive immune responses and may play an important role in unmethylated CpG motifs in bacterial DNA [5], single-
the pathogenesis of systemic lupus erythematosus. Of particular stranded or double-stranded (ds) viral RNA, lipopoly-
interest are TLR3, -7, -8, and -9, which are localized intracellularly. saccharide, peptidoglycan, and bacterial flagellin (for review,
These TLRs recognize single-stranded or double-stranded RNA or
hypomethylated CpG-DNA. Exposure to higher order CpG-DNA see [6]). However, the role of TLRs extends beyond microbial
ligands or t
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