Increased Turnover of CCR5+and Redistribution of CCR5−CD4 T Lymphocytes during Primary Human Immunodeficiency Virus Type 1 Infection

Abstract

CCR5 is the major coreceptor for human immunodeficiency virus (HIV) type 1 during primary infection. CCR5⁺ CD4 T lymphocytes were studied in subjects with primary HIV-1 infection (PHI) or acute Epstein-Barr virus (EBV) infection and in HIV-uninfected controls. The early decline of CD4 T lymphocytes during PHI resulted from depletion of CCR5⁻ CD4 T lymphocytes. After antiretroviral therapy, Ki-67⁻ CCR5⁻ CD4 T cell counts rapidly increased in the circulation, which suggests that the initial decrease was due to an alteration in trafficking and/or sequestration. In the CCR5⁺ subset of CD4 T cells, there was an elevation in the proliferative (Ki-67⁺) fraction during PHI, yet their total number remained in the normal range. In contrast, in acute EBV infection, proliferating CCR5⁺ CD4 T cells accumulated to very high levels, suggesting they have an important role in the early antiviral response, which may be impaired in HIV-1 infection