![]() |
Fifth International CongressDrug Therapy in HIV Infection22-26 October, 2000
|
PLASMA AND TISSUE HIV-1 AND HIV-2 VIRAL LOAD IN HIV-2 AND DUAL HIV-1/HIV-2 INFECTED INDIVIDUALS: IMPLICATIONS FOR STARTING HAART
M. Schutten, M.E. van der Ende, K. Tenner-Racz, P. Racz, H.G.M. Niesters and A.D.M.E. Osterhaus
University Hospital Rotterdam, Department of Virology, Dr Molewaterplein 40, 3015 GD Rotterdam, The Netherlands
Int Cong Drug Therapy HIV 2000 Oct 22-26;5:Abstract No. PL3.6
AIDS 2000, Oct 22-26;14(Suppl. 4);S3
PURPOSE OF STUDY: Within the Rotterdam area approximately 20 HIV-2 seropositive (HIV-2+) individuals have been reported. Quantitative plasma and tissue HIV-1/HIV-2 RNA levels were measured to determine the most optimal treatment strategy for HIV-2+ individuals.
METHODS: EDTA plasma samples were collected from HIV-1+, HIV-2+ and dual HIV-1/HIV-2+ individuals in 1999 and stored at –80C. HIV-2 plasma viral loads measured with a newly developed assay based on the Taqman realtime PCR detection method were compared with HIV-1 plasma viral loads measured with the Cobas Amplicor v1.5. The number of virus producing cells per mm2 of lymphoid tissue were determined by in situ hybridization.
RESULTS: The plasma and tissue HIV RNA load in HIV-2+ patients with < 200 CD4+ cells was significantly lower as compared to HIV-1+ patients. None of the HIV-2+ patients with > 200 CD4+ cells had plasma HIV-2 RNA levels that would urge starting therapy (> 5000 copies/ml). Two HIV- 1/HIV-2+ patients with < 200CD4+ cells proved to have significant levels of both HIV-1 and HIV-2 RNA before start of therapy. Interestingly after start of antiretroviral therapy (ART) in both patients (RTV/SQV and combivir/ NFV) the plasma HIV-1 RNA level decreased to and remained undetectable. The plasma HIV-2 RNA showed a rebound in both patients within 6 months despite a reported good adherence to their therapy [1].
CONCLUSIONS: On basis of these results and the limited options for treating HIV-2 (inadequate efficacy of NNRTIs and most probably also nelfinavir and amprenavir) we recommend starting ART as late as possible (CD4+ cells < 300/µl or plasma HIV-2 RNA levels > 5000 copies/ml). The fact that both HIV-1 and HIV-2 may actively replicate in dual HIV-1/HIV-2+ individuals also indicate that it is wise to refrain from treating such individuals with antivirals that are not efficacious against HIV-2.
Reference:
1. Schutten M, van der Ende ME, Osterhaus ADME. "Antiretroviral therapy in patients with dual infection with human immunodeficiency virus types 1 and 2", N Engl J Med. 2000 Jun 8;342(23):1758-60.
Presenting author:
Download Conferences Abstracts
2000-10-22
PL3-6
Originally published in AIDS Volume 14, Supplement 4 and hosted with permission of the publisher Lippincott Williams & Wilkins, 250 Waterloo Road, London, SE1 8RD, UK. Tel: +44 (0)20 7981 0700 Fax: +44 (0) 7981 0701
Copyright © 2000 - Lippincott Williams & Wilkins. All rights reserved. All abstracts from the Fifth International Congress Drug Therapy in HIV Infection, appearing on the AEGiS web site, are protected by United States copyright law and may not be reproduced, distributed, transmitted, displayed, or otherwise published without the prior written permission of Lippincott Williams & Wilkins. You may not alter or remove any trademark, copyright or other notice. However, provided that you maintain all copyright and other notices contained therein, you may download material (one machine readable copy and one print copy per page) for your personal, non-commercial use only.
http://www.aidsonline.com http://www.ovid.com
This information is designed to support, not replace, the relationship that exists between you and your doctor. ©1980, 2005. AEGiS.