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Interferon-α But Not AZT Suppresses HIV Expression in Chronically Infected Cell Lines

Poli, Guido, Orenstein, Jan M., Kinter, Audrey, Folks, Thomas M., Fauci, Anthony S.·1989·Science

Abstract

Promonocytic (U1) and T lymphocytic (ACH-2) cell lines chronically infected with human immunodeficiency virus type 1 (HIV-1) constitutively express low levels of virus, but expression can be induced by phorbol esters and cytokines. Whereas ACH-2 cells produce infectious virions, U1 cells produce defective, noninfectious particles. Although 3′-azido-3′-deoxythimidine (AZT) prevented acute HIV infection of susceptible cells, it did not prevent the induction of HIV expression in the infected cell lines. In contrast, interferon alpha (IFN-α) inhibited the release of reverse transcriptase and viral antigens into the culture supernatant after phorbol ester stimulation of both cell lines. Further, IFN-α suppressed the production or release (or both) of whole HIV virions, but had no effect on the amount of cell-associated viral proteins. Also, after phorbol ester stimulation of ACH-2 cells, IFN-α reduced the number of infectious viral particles secreted into the culture supernatant, but had no effect on the infectivity of cell-associated virus. These findings lend support to the combined use of antiviral agents that have action at both the early (AZT) and the late (IFN-α) stages of HIV replication.

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Metadata

Authors
Poli, G., Orenstein, J. M., Kinter, A., Folks, T. M., & Fauci, A. S.
Venue
Science
Published
1989-05-05
Volume
244
Issue
4904
Pages
575-577
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2053905319
Cited by
328
References
1
FWCI
9.32
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Interferon-α But Not AZT Suppresses HIV Expression in Chronically Infected Cell Lines. https://app.cochat.ai/papers/10.1126/science.2470148
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Poli, G., Orenstein, J. M., Kinter, A., Folks, T. M., & Fauci, A. S. (1989). Interferon-α But Not AZT Suppresses HIV Expression in Chronically Infected Cell Lines. Science. https://doi.org/10.1126/science.2470148

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