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Journal of Virology, September 2007, p. 10201-10206, Vol. 81, No. 18
0022-538X/07/$08.00+0 doi:10.1128/JVI.00419-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
Alpha Interferon Enhances TRIM5
-Mediated Antiviral Activities in Human and Rhesus Monkey Cells
Ryuta Sakuma,
Amber A. Mael, and
Yasuhiro Ikeda*
Molecular Medicine Program, Mayo Clinic College of Medicine, Rochester, Minnesota 55905
Received 27 February 2007/
Accepted 25 June 2007
Dominant, constitutively expressed antiretroviral factors, including TRIM5
and APOBEC3 proteins, are distinguished from the conventional innate immune systems and are classified as intrinsic immunity factors. Here, we demonstrate that interferon alpha (IFN-
) treatment upregulates TRIM5
mRNA in rhesus monkey cells, which correlates with the enhanced TRIM5
-mediated pre- and postintegration blocks of human immunodeficiency virus replication. In human cells, IFN-
increases the levels of TRIM5
mRNA, resulting in enhanced antiviral activity against N-tropic murine leukemia virus infection. These observations indicate that the TRIM5
-mediated antiviral effects can be orchestrated by the conventional innate immune response. It is conceivable that TRIM5
plays an essential role in controlling both the initial retroviral exposure and the subsequent viral dissemination in vivo.
* Corresponding author. Mailing address; Mayo Clinic College of Medicine, Molecular Medicine Program, Guggenheim 18-11c, 200 First Street SW, Rochester, MN 55905. Phone: (507) 538-0153. Fax: (507) 266-2122. E-mail:
ikeda.yasuhiro{at}mayo.edu
Published ahead of print on 3 July 2007.
Journal of Virology, September 2007, p. 10201-10206, Vol. 81, No. 18
0022-538X/07/$08.00+0 doi:10.1128/JVI.00419-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
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