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A stable latent reservoir for HIV-1 in resting CD4+ T lymphocytes in infected children
Deborah Persaud, … , Stuart Ray, Robert F. Siliciano
Deborah Persaud, … , Stuart Ray, Robert F. Siliciano
Published April 1, 2000
Citation Information: J Clin Invest. 2000;105(7):995-1003. https://doi.org/10.1172/JCI9006.
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Article

A stable latent reservoir for HIV-1 in resting CD4+ T lymphocytes in infected children

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Abstract

HIV-1 persists in a latent state in resting CD4+ T lymphocytes of infected adults despite prolonged highly active antiretroviral therapy (HAART). To determine whether a latent reservoir for HIV-1 exists in infected children, we performed a quantitative viral culture assay on highly purified resting CD4+ T cells from 21 children with perinatally acquired infection. Replication-competent HIV-1 was recovered from all 18 children from whom sufficient cells were obtained. The frequency of latently infected resting CD4+ T cells directly correlated with plasma virus levels, suggesting that in children with ongoing viral replication, most latently infected cells are in the labile preintegration state of latency. However, in each of 7 children who had suppression of viral replication to undetectable levels for 1–3 years on HAART, latent replication-competent HIV-1 persisted with little decay, owing to a stable reservoir of infected cells in the postintegration stage of latency. Drug-resistance mutations generated by previous nonsuppressive regimens persisted in this compartment despite more than 1 year of fully suppressive HAART, rendering untenable the idea of recycling drugs that were part of failed regimens. Thus the latent reservoir for HIV-1 in resting CD4+ T cells will be a major obstacle to HIV-1 eradication in children.

Authors

Deborah Persaud, Theodore Pierson, Christian Ruff, Diana Finzi, Karen R. Chadwick, Joseph B. Margolick, Andrea Ruff, Nancy Hutton, Stuart Ray, Robert F. Siliciano

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Figure 1

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Representative flow cytometric analysis of CD4 and HLA-DR antigen expres...
Representative flow cytometric analysis of CD4 and HLA-DR antigen expression on monocyte-depleted PBMCs before (a) and after (b) sequential magnetic bead depletion and cell sorting.

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