ICAM-5 modulates cytokine/chemokine production in the CNS during the course of herpes simplex virus type 1 infection

Abstract Chemokines are important in HSE development in the CNS but underlying regulatory events are unknown. Two-hybrid binding assays identified that intercellular adhesion molecule 5 (ICAM-5), an immune modulator in the CNS, interacted with neurovirulence factor, UOL, of HSV-1. Viral load and int...

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Published in:Journal of neuroimmunology Vol. 213; no. 1; pp. 12 - 19
Main Authors: Tse, Margaret C.L, Lane, Crystal, Mott, Kevin, Onlamoon, Nattawat, Hsiao, Hui-Mien, Perng, Guey Chuen
Format: Journal Article
Language:English
Published: Netherlands Elsevier B.V 18-08-2009
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Summary:Abstract Chemokines are important in HSE development in the CNS but underlying regulatory events are unknown. Two-hybrid binding assays identified that intercellular adhesion molecule 5 (ICAM-5), an immune modulator in the CNS, interacted with neurovirulence factor, UOL, of HSV-1. Viral load and interleukin levels were similar in UOL deletion virus (ΔUOL), and wild type virus infected mouse brains. However, higher numbers of lymphocytes, but unaltered soluble ICAM-5 and chemokine levels were detected in ΔUOL infected mouse brains. In contrast, lower lymphocyte numbers, reduced soluble ICAM-5, and higher chemokine levels were detected in wild type virus infected brains. Our results suggest that ICAM-5 plays a critical role in modulating chemokine production in the CNS.
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ISSN:0165-5728
1872-8421
DOI:10.1016/j.jneuroim.2009.06.007