1. Leukocyte immunoglobulin-like receptor B1 is critical for antibody-dependent dengue.
- Author
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Chan KR, Ong EZ, Tan HC, Zhang SL, Zhang Q, Tang KF, Kaliaperumal N, Lim AP, Hibberd ML, Chan SH, Connolly JE, Krishnan MN, Lok SM, Hanson BJ, Lin CN, and Ooi EE
- Subjects
- Antibody-Dependent Enhancement immunology, Blotting, Western, Cell Line, Dengue immunology, Dengue Virus physiology, Humans, Leukocyte Immunoglobulin-like Receptor B1, Microarray Analysis, RNA, Small Interfering genetics, Receptors, IgG metabolism, Antibody-Dependent Enhancement physiology, Antigens, CD metabolism, Dengue physiopathology, Dengue Virus metabolism, Receptors, Immunologic metabolism
- Abstract
Viruses must evade the host innate defenses for replication and dengue is no exception. During secondary infection with a heterologous dengue virus (DENV) serotype, DENV is opsonized with sub- or nonneutralizing antibodies that enhance infection of monocytes, macrophages, and dendritic cells via the Fc-gamma receptor (FcγR), a process termed antibody-dependent enhancement of DENV infection. However, this enhancement of DENV infection is curious as cross-linking of activating FcγRs signals an early antiviral response by inducing the type-I IFN-stimulated genes (ISGs). Entry through activating FcγR would thus place DENV in an intracellular environment unfavorable for enhanced replication. Here we demonstrate that, to escape this antiviral response, antibody-opsonized DENV coligates leukocyte Ig-like receptor-B1 (LILRB1) to inhibit FcγR signaling for ISG expression. This immunoreceptor tyrosine-based inhibition motif-bearing receptor recruits Src homology phosphatase-1 to dephosphorylate spleen tyrosine kinase (Syk). As Syk is a key intermediate of FcγR signaling, LILRB1 coligation resulted in reduced ISG expression for enhanced DENV replication. Our findings suggest a unique mechanism for DENV to evade an early antiviral response for enhanced infection.
- Published
- 2014
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