Please use this identifier to cite or link to this item: https://doi.org/10.1073/pnas.1105079108
Title: Immune surveillance by mast cells during dengue infection promotes natural killer (NK) and NKT-cell recruitment and viral clearance
Authors: St. John, A.L. 
Rathore, A.P.S. 
Yap, H.
Ng, M.-L.
Metcalfe, D.D.
Vasudevan, S.G. 
Abraham, S.N.
Issue Date: 31-May-2011
Source: St. John, A.L., Rathore, A.P.S., Yap, H., Ng, M.-L., Metcalfe, D.D., Vasudevan, S.G., Abraham, S.N. (2011-05-31). Immune surveillance by mast cells during dengue infection promotes natural killer (NK) and NKT-cell recruitment and viral clearance. Proceedings of the National Academy of Sciences of the United States of America 108 (22) : 9190-9195. ScholarBank@NUS Repository. https://doi.org/10.1073/pnas.1105079108
Abstract: A wealth of evidence supports the essential contributions of mast cells (MCs) to immune defense against bacteria and parasites; however, the role of MCs in viral infections has not been defined. We now report that rodent, monkey, and human MCs are able to detect dengue virus (DENV), a lymphotropic, enveloped, single-stranded, positive-sense RNA virus that results in MC activation and degranulation. We observe that the response of MCs to DENV also involves the activation of antiviral intracellular host response pathways, melanoma differentiation-associated gene 5 (MDA5) and retinoic acid inducible gene 1 (RIG-I), and the de novo transcription of cytokines, including TNF-α and IFN-α, and chemokines, such as CCL5, CXCL12, and CX3CL1. This multifaceted response of MCs to DENV is consequential to the containment of DENV in vivo because, after s.c. infection, MC-deficient mice show increased viral burden within draining lymph nodes, which are known to be targeted organs during DENV spread, compared with MC-sufficient mice. This containment of DENV is linked to the MC-driven recruitment of natural killer and natural killer T cells into the infected skin. These findings support expanding the defined role of immunosurveillance by MCs to include viral pathogens.
Source Title: Proceedings of the National Academy of Sciences of the United States of America
URI: http://scholarbank.nus.edu.sg/handle/10635/53445
ISSN: 00278424
DOI: 10.1073/pnas.1105079108
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