Selective Susceptibility of Human Skin Antigen Presenting Cells to Productive Dengue Virus Infection

被引:80
作者
Cerny, Daniela [1 ,2 ]
Haniffa, Muzlifah [3 ]
Shin, Amanda [1 ]
Bigliardi, Paul [4 ,5 ]
Tan, Bien Keem [6 ]
Lee, Bernett [1 ]
Poidinger, Michael [1 ]
Tan, Ern Yu [7 ]
Ginhoux, Florent [1 ]
Fink, Katja [1 ]
机构
[1] Agcy Sci Technol & Res, Singapore Immunol Network, Singapore, Singapore
[2] Nanyang Technol Univ, Sch Biol Sci, Singapore 639798, Singapore
[3] Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[4] Agcy Sci Technol & Res, Inst Mol Biol, Singapore, Singapore
[5] Natl Univ Hlth Syst, Univ Med Cluster, Div Rheumatol, Singapore, Singapore
[6] Singapore Gen Hosp, Dept Plast Surg, Singapore, Singapore
[7] Tan Tock Seng Hosp, Dept Gen Surg, Singapore, Singapore
关键词
HUMAN DENDRITIC CELLS; EPIDERMAL LANGERHANS CELLS; REGULATORY T-CELLS; DC-SIGN; PHOSPHATIDYLSERINE RECEPTORS; FUNCTIONAL SPECIALIZATION; HEMORRHAGIC-FEVER; PERIPHERAL-BLOOD; IMMUNE-RESPONSES; SEVERE DISEASE;
D O I
10.1371/journal.ppat.1004548
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dengue is a growing global concern with 390 million people infected each year. Dengue virus (DENV) is transmitted by mosquitoes, thus host cells in the skin are the first point of contact with the virus. Human skin contains several populations of antigen-presenting cells which could drive the immune response to DENV in vivo: epidermal Langerhans cells (LCs), three populations of dermal dendritic cells (DCs), and macrophages. Using samples of normal human skin we detected productive infection of CD14(+) and CD1c(+) DCs, LCs and dermal macrophages, which was independent of DC-SIGN expression. LCs produced the highest viral titers and were less sensitive to IFN-beta. Nanostring gene expression data showed significant up-regulation of IFN-beta, STAT-1 and CCL5 upon viral exposure in susceptible DC populations. In mice infected intra-dermally with DENV we detected parallel populations of infected DCs originating from the dermis and migrating to the skin-draining lymph nodes. Therefore dermal DCs may simultaneously facilitate systemic spread of DENV and initiate the adaptive antiviral immune response.
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页数:15
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