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Decay characteristics of HIV-1-infected compartments during combination therapy

Author

Listed:
  • Alan S. Perelson

    (Los Alamos National Laboratory)

  • Paulina Essunger

    (Los Alamos National Laboratory)

  • Yunzhen Cao

    (Los Alamos National Laboratory)

  • Mika Vesanen

    (Los Alamos National Laboratory)

  • Arlene Hurley

    (Los Alamos National Laboratory)

  • Kalle Saksela

    (Los Alamos National Laboratory)

  • Martin Markowitz

    (Los Alamos National Laboratory)

  • David D. Ho

    (Los Alamos National Laboratory)

Abstract

Analysis of changes in viral load after initiation of treatment with potent antiretroviral agents has provided substantial insight into the dynamics of human immunodeficiency virus type 1 (HIV-1)1–3. The concentration of HIV-1 in plasma drops by ∼99% in the first two weeks of treatment owing to the rapid elimination of free virus with a half-life (t1/2) of ≤6 hours and loss of productively infected cells with a t1/2 of 1.6 days3. Here we show that with combination therapy this initial decrease is followed by a slower second-phase decay of plasma viraemia. Detailed mathematical analysis shows that the loss of long-lived infected cells (t1/2of1–4weeks) is a major contributor to the second phase, whereas the activation of latently infected lymphocytes (t1/2 of 0.5–2 weeks) is only a minor source. Based on these decay characteristics, we estimate that 2.3–3.1 years of a completely inhibitory treatment would be required to eliminate HIV-1 from these compartments. To eradicate HIV-1 completely, even longer treatment may be needed because of the possible existence of undetected viral compartments or sanctuary sites.

Suggested Citation

  • Alan S. Perelson & Paulina Essunger & Yunzhen Cao & Mika Vesanen & Arlene Hurley & Kalle Saksela & Martin Markowitz & David D. Ho, 1997. "Decay characteristics of HIV-1-infected compartments during combination therapy," Nature, Nature, vol. 387(6629), pages 188-191, May.
  • Handle: RePEc:nat:nature:v:387:y:1997:i:6629:d:10.1038_387188a0
    DOI: 10.1038/387188a0
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