Residual Viral Replication during Antiretroviral Therapy Boosts Human Immunodeficiency Virus Type 1-Specific CD8 + T-Cell Responses in Subjects Treated Early after Infection

Author:

Ortiz Gabriel M.1,Hu Jennifer1,Goldwitz Joshua A.1,Chandwani Rohit1,Larsson Marie2,Bhardwaj Nina2,Bonhoeffer Sebastian3,Ramratnam Bharat1,Zhang Linqi1,Markowitz Martin M.1,Nixon Douglas F.1

Affiliation:

1. Aaron Diamond AIDS Research Center, The Rockefeller University, New York, New York 10016

2. Laboratory for Cellular Immunology, The Rockefeller University, New York, New York 10021

3. Ecology and Evolution, ETH Zurich, CH-8092 Zurich, Switzerland

Abstract

ABSTRACT Human immunodeficiency virus type 1 (HIV-1)-infected subjects treated early after infection have preserved HIV-1-specific CD4 + T-cell function. We studied the effect of highly active antiretroviral therapy (HAART) on the frequency of HIV-1-specific CD8 + T cells in patients treated during early ( n = 31) or chronic ( n = 23) infection. The degree of viral suppression and time of initiation of treatment influenced the magnitude of the CD8 + T-cell response. HIV-1-specific CD8 + T cells can increase in number after HAART in subjects treated early after infection who have episodes of transient viremia.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference43 articles.

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