Effect of combination antiretroviral therapy on T-cell immunity in acute human immunodeficiency virus type 1 infection

U Malhotra, MM Berrey, Y Huang… - The Journal of …, 2000 - academic.oup.com
U Malhotra, MM Berrey, Y Huang, J Markee, DJ Brown, S Ap, L Musey, T Schacker, L Corey…
The Journal of infectious diseases, 2000academic.oup.com
T-cell responses were evaluated prospectively in 41 patients with acute human
immunodeficiency virus type 1 (HIV-1) infection (30 untreated and 11 receiving zidovudine,
lamivudine, and indinavir) and in 38 uninfected adults. By 6–12 months, treated patients had
significantly greater median Candida and tetanus lymphoproliferative responses (stimulation
index [SI], 76 and 55, respectively) than did untreated patients (SI, 7 and 6, P=. 02 and. 001,
respectively), and the responses of treated patients surpassed those of uninfected adults (SI …
Abstract
T-cell responses were evaluated prospectively in 41 patients with acute human immunodeficiency virus type 1 (HIV-1) infection (30 untreated and 11 receiving zidovudine, lamivudine, and indinavir) and in 38 uninfected adults. By 6–12 months, treated patients had significantly greater median Candida and tetanus lymphoproliferative responses (stimulation index [SI], 76 and 55, respectively) than did untreated patients (SI, 7 and 6, P = .02 and .001, respectively), and the responses of treated patients surpassed those of uninfected adults (SI, 19 and 32, P= .002 and .101, respectively). Unlike the patients in the untreated group, the patients in the treated group mounted a 6-fold increased HIV-1 p24 response (SI increase, 1.0 to 5.7, P = .01) within 3 months. HIV-1-specific cytotoxicity remained detectable in most treated patients. Thus, combination therapy administered within 3–4 months of infection was associated with improved T-cell memory responses that were distinct from those of untreated patients. The amplified HIV-1-specific T-cell responses may help maintain cytotoxic activities.
Oxford University Press