Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2009 Feb;25(2):135-9.
doi: 10.1089/aid.2008.0200.

Delaying a treatment switch in antiretroviral-treated HIV type 1-infected patients with detectable drug-resistant viremia does not have a profound effect on immune parameters: AIDS Clinical Trials Group Study A5115

Affiliations
Randomized Controlled Trial

Delaying a treatment switch in antiretroviral-treated HIV type 1-infected patients with detectable drug-resistant viremia does not have a profound effect on immune parameters: AIDS Clinical Trials Group Study A5115

Allan R Tenorio et al. AIDS Res Hum Retroviruses. 2009 Feb.

Abstract

Some patients are unable to achieve and maintain an undetectable plasma HIV-1 RNA level with combination antiretroviral therapy (ART) and are therefore maintained on a partially suppressive regimen. To determine the immune consequences of continuing ART despite persistent viremia, we randomized 47 ART-treated individuals with low to moderate plasma HIV-1 RNA levels (200-9999 copies/ml) to either an immediate switch in therapy or a delayed switch (when plasma HIV-1 RNA became > or =10,000 copies/ml). After 48 weeks of follow-up, naive and memory CD4+ T cell percents were comparable in the two groups. The proportion of subjects with a lymphocyte proliferative response to Candida, Mycobacterium avium-intracellulare complex, or HIV-gag was also not significantly different at week 48. Delaying a treatment switch in patients with partial virologic suppression and stable CD4+ T cells does not have profound effects on immune parameters.

PubMed Disclaimer

Similar articles

Cited by

References

    1. World Health Organization. Antiretroviral Therapy for HIV infection in Adults and Adolescents: Recommendations for a Public Health Approach, 2006 Rev. WHO Press; Geneva, Switzerland: 2006. pp. 34–35.
    1. Hatano H. Hunt P. Weidler J. Coakley E. Hoh R. Liegler T. Martin JN. Deeks SG. Rate of viral evolution and risk of losing future drug options in heavily pretreated, HIV-infected patients who continue to receive a stable, partially suppressive treatment regimen. Clin Infect Dis. 2006;43:1329–1336. - PubMed
    1. Deeks SG. Barbour JD. Martin JN. Swanson MS. Grant RM. Sustained CD4 + T cell response after virologic failure of protease inhibitor-based regimens in patients with human immunodeficiency virus infection. J Infect Dis. 2000;181:946–953. - PubMed
    1. Lawrence J. Mayers DL. Hullsiek KH. Collins G. Abrams DI. Reisler RB. Crane LR. Schmetter BS. Dionne TJ. Saldanha JM. Jones MC. Baxter JD. Structured treatment interruption in patients with multidrug-resistant human immunodeficiency virus. N Engl J Med. 2003;349:837–846. - PubMed
    1. Riddler SA. Jiang H. Tenorio A. Huang H. Kuritzkes DR. Acosta EP. Landay A. Bastow B. Haas DW. Tashima KT. Jain MK. Deeks SG. Bartlett JA. A randomized study of antiviral medication switch at lower- versus higher-switch thresholds: AIDS Clinical Trials Group Study A5115. Antiviral Ther. 2007;12:531–541. - PubMed

Publication types

MeSH terms