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Journal of Virology, April 2008, p. 3997-4006, Vol. 82, No. 8
0022-538X/08/$08.00+0     doi:10.1128/JVI.01545-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Human Immunodeficiency Virus Viremia Induces Plasmacytoid Dendritic Cell Activation In Vivo and Diminished Alpha Interferon Production In Vitro{triangledown}

John C. Tilton,1 Maura M. Manion,1 Marlise R. Luskin,1 Alison J. Johnson,1 Andy A. Patamawenu,1 Claire W. Hallahan,1 Nancy A. Cogliano-Shutta,1 JoAnn M. Mican,1 Richard T. Davey Jr.,1 Shyam Kottilil,1 Jeffrey D. Lifson,2 Julia A. Metcalf,1 Richard A. Lempicki,2 and Mark Connors1*

Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland,1 Science Applications International Corporation—Frederick Inc., National Cancer Institute, Frederick, Maryland2

Received 16 July 2007/ Accepted 11 January 2008

Human immunodeficiency virus type 1 (HIV-1) infection has been associated with perturbations of plasmacytoid dendritic cells (PDC), including diminished frequencies in the peripheral blood and reduced production of type I interferons (IFNs) in response to in vitro stimulation. However, recent data suggest a paradoxical increase in production of type 1 interferons in vivo in HIV-infected patients compared to uninfected controls. Using a flow cytometric assay to detect IFN-{alpha}-producing cells within unseparated peripheral blood mononuclear cells, we observed that short-term interruptions of antiretroviral therapy are sufficient to result in significantly reduced IFN-{alpha} production by PDC in vitro in response to CpG A ligands or inactivated HIV particles. The primary cause of diminished IFN-{alpha} production was reduced responsiveness of PDC to de novo stimulation, not diminished per cell IFN-{alpha} production or migration of cells to lymphoid organs. Real-time PCR analysis of purified PDC from patients prior to and during treatment interruptions revealed that active HIV-1 replication is associated with upregulation of type I IFN-stimulated gene expression. Treatment of hepatitis C virus-infected patients with IFN-{alpha}2b and ribavirin for hepatitis C virus infection resulted in a profound suppression of de novo IFN-{alpha} production in response to CpG A or inactivated HIV particles, similar to the response observed in HIV-infected patients. Together, these results suggest that diminished production of type I interferons in vitro by PDC from HIV-1-infected patients may not represent diminished interferon production in vivo. Rather, diminished function in vitro is likely a consequence of prior activation via type I interferons or HIV virions in vivo.


* Corresponding author. Mailing address: LIR, NIAID, NIH, Bldg. 10, Rm. 11B-09, 10 Center Dr., MSC 1876, Bethesda, MD 20892-1876. Phone: (301) 496-8057. Fax: (301) 402-0070. E-mail: mconnors{at}niaid.nih.gov

{triangledown} Published ahead of print on 6 February 2008.


Journal of Virology, April 2008, p. 3997-4006, Vol. 82, No. 8
0022-538X/08/$08.00+0     doi:10.1128/JVI.01545-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







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