Dynamics of hepatitis C viremia after plasma exchange
Background/Aims: The dynamics of hepatitis C viremia after perturbation by plasma exchange was addressed in two infected patients with symptomatic cryoglobulinemia. This approach may offer an alternative to studying patients treated with antivirals in order to understand the dynamics of hepatitis C...
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Veröffentlicht in: | Journal of hepatology 1999-09, Vol.31 (3), p.389-393 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background/Aims: The dynamics of hepatitis C viremia after perturbation by plasma exchange was addressed in two infected patients with symptomatic cryoglobulinemia. This approach may offer an alternative to studying patients treated with antivirals in order to understand the dynamics of hepatitis C virion exchange among different compartments
in vivo.
Methods: Plasma exchange sessions were conducted every 24 h for 3 consecutive days; hepatitis C virus RNA copy numbers were evaluated in sequential plasma samples collected before (−24, −12, −8, and 0 h) and at short intervals (at 1, 3, 6, and 12 h) after each session.
Results: After each plasma exchange session viremia dropped by 45.3–93.3% in patient 1, and by 60.5–72.7% in patient 2, paralleling (or, in some cases, exceeding) the amount of fluid exchanged. No mobilization of cell-free hepatitis C virus from extra-vascular sites was documented during the 2-h plasma exchange. The dynamics of hepatitis C viremia after each procedure was also evaluated. Pre-plasma exchange levels were restored within 3–6 h in both patients, and the mean doubling times of residual viremia were 4.6 h and 4.5 h for patients 1 and 2, respectively.
Conclusions: The results, in agreement with recent evidence indicating that the turnover of hepatitis C virions is a highly dynamic process, extend previous evaluations by documenting that large amounts of newly-produced virions are introduced into the vascular compartment within a few hours of the drop in hepatitis C viremia caused by plasma exchange. |
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ISSN: | 0168-8278 1600-0641 |
DOI: | 10.1016/S0168-8278(99)80027-0 |