AI Article Synopsis

  • The study examined memory antiviral responses of CD4 T-cells in 16 patients with primary HIV-1 infection, including some with primary CMV infection, and compared them to patients with chronic HIV-1 and CMV coinfection.
  • Researchers found HIV-1 and CMV-specific CD4 T-cells were present in both primary and chronic infections, but a greater CMV-specific response was observed in the primary phase, while HIV-1 response showed no significant differences.
  • A notable portion of the CD4(+)CCR7(-) T cells were found to be infected with HIV-1, providing insights into the challenges of generating a strong CD4 T-cell immune response during primary infections.

Article Abstract

CD4 T-cell-specific memory antiviral responses to human immunodeficiency virus type 1 (HIV-1) and cytomegalovirus (CMV) were investigated in 16 patients with documented primary HIV-1 infection (4 of the 16 subjects also had primary CMV infection) and compared with those observed in patients with chronic HIV-1 and CMV coinfection. Virus-specific memory CD4 T cells were characterized on the basis of the expression of the chemokine receptor CCR7. HIV-1- and CMV-specific interferon-gamma-secreting CD4 T cells were detected in patients with primary and chronic HIV-1 and CMV coinfection and were mostly contained in the cell population lacking expression of CCR7. The magnitude of the primary CMV-specific CD4 T-cell response was significantly greater than that of chronic CMV infection, whereas there were no differences between primary and chronic HIV-1-specific CD4 T-cell responses. A substantial proportion of CD4(+)CCR7(-) T cells were infected with HIV-1. These results advance the characterization of antiviral memory CD4 T-cell response and the delineation of the potential mechanisms that likely prevent the generation of a robust CD4 T-cell immune response during primary infection.

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http://dx.doi.org/10.1182/blood-2001-11-0080DOI Listing

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