Long-term Virologic and Immunologic Responses in Human Immunodeficiency Virus Type 1-Infected Children Treated with Indinavir, Zidovudine, and Lamivudine

Virologic and immunologic responses were examined for 33 human immunodeficiency virus (HIV)–infected children who participated for ⩾96 weeks in a phase 1/2 protocol of 16 weeks of indinavir monotherapy, followed by the addition of zidovudine and lamivudine. At week 96, a median increase of 199 CD4+...

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Published inThe Journal of infectious diseases Vol. 183; no. 7; pp. 1116 - 1120
Main Authors Jankelevich, Shirley, Mueller, Brigitta U., Mackall, Crystal L., Smith, Sharon, Zwerski, Sheryl, Wood, Lauren V., Zeichner, Steven L., Serchuck, Leslie, Steinberg, Seth M., Nelson, Robert P., Sleasman, John W., Nguyen, Bach-Yen, Pizzo, Philip A., Yarchoan, Robert
Format Journal Article
LanguageEnglish
Published Chicago, IL The University of Chicago Press 01.04.2001
University of Chicago Press
Oxford University Press
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Summary:Virologic and immunologic responses were examined for 33 human immunodeficiency virus (HIV)–infected children who participated for ⩾96 weeks in a phase 1/2 protocol of 16 weeks of indinavir monotherapy, followed by the addition of zidovudine and lamivudine. At week 96, a median increase of 199 CD4+ T cells/μL and a median decrease of 0.74 log10 HIV RNA copies/mL were observed. The relationship between control of viral replication and CD4+ T cell count was examined. Patients were categorized into 3 response groups on the basis of duration and extent of control of viral replication. Of 21 children with a transient decrease in virus load of ⩾0.7 log10 HIV RNA copies/mL from baseline, 7 experienced sustained increases in CD4+, CD4+CD45RA+, and CD4+CD45RO+ T cell counts. CD4+CD45RA+ (naive) T cells were the major contributor to CD4+ T cell expansion. Continued long-term immunologic benefit may be experienced by a subset of children, despite only transient virologic suppression
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ISSN:0022-1899
1537-6613
DOI:10.1086/319274