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Blood, 15 August 2001, Vol. 98, No. 4, pp. 906-912
PLENARY PAPER
Depletion of circulating natural type 1 interferon-producing
cells in HIV-infected AIDS patients
Vassili Soumelis,
Iain Scott,
Ferdous Gheyas,
Damien Bouhour,
Gregoire Cozon,
Laurent Cotte,
Laurence Huang,
Jay A. Levy, and
Yong-Jun Liu
From the Department of Immunobiology, DNAX Research
Institute of Molecular and Cellular Biology, Palo Alto, CA; Department
of Medicine, University of California San Francisco; Department of
Biostatistics, Schering-Plough Research Institute, Kenilworth, NJ;
Hospices Civils de Lyon, Lyon, France; San Francisco General Hospital,
CA.
Natural interferon- producing cells (IPCs) are a newly
characterized blood cell type, which is the major source of type I interferons in antiviral innate immune responses. The relationship between the number of circulating IPCs, HIV disease progression, and
the occurrence of HIV-related complications was investigated. The study
of 25 healthy donors and 54 HIV-infected subjects demonstrated a direct
correlation between blood IPC number, interferon- production, and
clinical state of HIV-infected subjects. Asymptomatic long-term survivors had increased IPC number and function relative to uninfected controls and infected individuals with progressive disease. IPC numbers
were markedly reduced in AIDS patients developing opportunistic infections and cancer. A negative correlation was found between the IPC
number in the blood and the HIV viral load, suggesting that IPCs are
important in controlling HIV replication. This study provides the first
evidence that IPCs are being affected during the course of HIV
infection and suggests that these cells can play a vital role in the
protection against opportunistic pathogens and cancer.

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K. Abel, M. J. Alegria-Hartman, K. Rothaeusler, M. Marthas, and C. J. Miller
The Relationship between Simian Immunodeficiency Virus RNA Levels and the mRNA Levels of Alpha/Beta Interferons (IFN-{alpha}/{beta}) and IFN-{alpha}/{beta}-Inducible Mx in Lymphoid Tissues of Rhesus Macaques during Acute and Chronic Infection
J. Virol.,
July 17, 2002;
76(16):
8433 - 8445.
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J. K. Sandberg, N. M. Fast, E. H. Palacios, G. Fennelly, J. Dobroszycki, P. Palumbo, A. Wiznia, R. M. Grant, N. Bhardwaj, M. G. Rosenberg, et al.
Selective Loss of Innate CD4+ V{alpha}24 Natural Killer T Cells in Human Immunodeficiency Virus Infection
J. Virol.,
June 27, 2002;
76(15):
7528 - 7534.
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J. Chehimi, D. E. Campbell, L. Azzoni, D. Bacheller, E. Papasavvas, G. Jerandi, K. Mounzer, J. Kostman, G. Trinchieri, and L. J. Montaner
Persistent Decreases in Blood Plasmacytoid Dendritic Cell Number and Function Despite Effective Highly Active Antiretroviral Therapy and Increased Blood Myeloid Dendritic Cells in HIV-Infected Individuals
J. Immunol.,
May 1, 2002;
168(9):
4796 - 4801.
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M. I. Zimmer, A. T. Larregina, C. M. Castillo, S. Capuano III, L. D. Falo Jr, M. Murphey-Corb, T. A. Reinhart, and S. M. Barratt-Boyes
Disrupted homeostasis of Langerhans cells and interdigitating dendritic cells in monkeys with AIDS
Blood,
April 15, 2002;
99(8):
2859 - 2868.
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D. L. Brassard, M. J. Grace, and R. W. Bordens
Interferon-{alpha} as an immunotherapeutic protein
J. Leukoc. Biol.,
April 1, 2002;
71(4):
565 - 581.
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W. Barchet, M. Cella, B. Odermatt, C. Asselin-Paturel, M. Colonna, and U. Kalinke
Virus-induced Interferon {alpha} Production by a Dendritic Cell Subset in the Absence of Feedback Signaling In Vivo
J. Exp. Med.,
February 19, 2002;
195(4):
507 - 516.
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M. Gilliet, A. Boonstra, C. Paturel, S. Antonenko, X.-L. Xu, G. Trinchieri, A. O'Garra, and Y.-J. Liu
The Development of Murine Plasmacytoid Dendritic Cell Precursors Is Differentially Regulated by FLT3-ligand and Granulocyte/Macrophage Colony-Stimulating Factor
J. Exp. Med.,
April 1, 2002;
195(7):
953 - 958.
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